General Information of Disease (ID: DIS5OIP1)

Disease Name Coronary heart disease
Synonyms
coronary arteriosclerosis; coronary artery disease; CHD (coronary heart disease); coronary disease; disease or disorder of coronary artery; coronary artery disease or disorder; disorder of coronary artery; CAD; coronary heart disease; disease of coronary artery; CHD
Disease Class BA80: Coronary atherosclerosis
Definition
Narrowing of the coronary arteries due to fatty deposits inside the arterial walls. The diagnostic criteria may include documented history of any of the following: documented coronary artery stenosis greater than or equal to 50% (by cardiac catheterization or other modality of direct imaging of the coronary arteries); previous coronary artery bypass surgery (CABG); previous percutaneous coronary intervention (PCI); previous myocardial infarction. (ACC)
Disease Hierarchy
DISLG4XS: Arterial disorder
DISWD40R: Disease
DISVO1I5: Cardiac disease
DIS5OIP1: Coronary heart disease
ICD Code
ICD-11
ICD-11: BA80.Z
ICD-9
ICD-9: 414
Expand ICD-9
414
Disease Identifiers
MONDO ID
MONDO_0005010
MESH ID
D003324
UMLS CUI
C1956346
MedGen ID
365486
SNOMED CT ID
414024009

Drug-Interaction Atlas (DIA) of This Disease

Drug-Interaction Atlas (DIA)
This Disease is Treated as An Indication in 4 Approved Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
Probucol DMVZQ2M Approved Small molecular drug [1]
Sertraline DM0FB1J Approved Small molecular drug [2]
Simvastatin DM30SGU Approved Small molecular drug [3]
LAROPIPRANT DM5FABJ Phase 4 Small molecular drug [4]
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This Disease is Treated as An Indication in 1 Drugs in Phase 2 Trial
Drug Name Drug ID Highest Status Drug Type REF
Heparin DM4ZP3W Phase 2/3 Trial Small molecular drug [5]
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This Disease is Treated as An Indication in 3 Clinical Trial Drug(s)
Drug Name Drug ID Highest Status Drug Type REF
CVBT-141H DMYPXQ2 Phase 2 NA [6]
FGF-1 DMXMC8I Phase 2 NA [7]
MEDI6570 DML8S0W Phase 2 Antibody [8]
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Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 359 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
ACE2 TTUI5H7 Limited Altered Expression [9]
ACR TTAHE2N Limited Biomarker [10]
ACTG1 TTGAZF9 Limited Biomarker [11]
ADAM10 TTVXEGU Limited Biomarker [12]
ADAM33 TTQICM2 Limited Genetic Variation [13]
ADAMTS1 TTS2TEI Limited Genetic Variation [14]
ADAMTS4 TTYG6BU Limited Biomarker [15]
ADORA3 TTJFY5U Limited Genetic Variation [16]
ADRA2A TTWG9A4 Limited Genetic Variation [17]
ADRB3 TTMXGCW Limited Genetic Variation [18]
AGTR2 TTQVOEI Limited Genetic Variation [19]
ALDH2 TTFLN4T Limited Genetic Variation [20]
ALOX5 TTSJ6Q4 Limited Biomarker [21]
ANGPTL3 TT59GO7 Limited Genetic Variation [22]
APOA2 TTGQA9W Limited Biomarker [23]
ARSA TTYQANR Limited Biomarker [24]
ATXN3 TT6A17J Limited Genetic Variation [25]
BLVRA TTJBPN3 Limited Genetic Variation [26]
BMPR2 TTGKF90 Limited Genetic Variation [27]
C3AR1 TTI6B3F Limited Biomarker [28]
C5AR1 TTHXFA1 Limited Altered Expression [29]
CA2 TTANPDJ Limited Biomarker [30]
CASP1 TTCQIBE Limited Altered Expression [31]
CCL11 TTCF05Y Limited Genetic Variation [32]
CCL17 TTMPHAE Limited Genetic Variation [33]
CCL21 TTLZK1U Limited Biomarker [34]
CD1A TTBGTFN Limited Altered Expression [35]
CD59 TTBGTEJ Limited Altered Expression [36]
CES1 TTMF541 Limited Genetic Variation [37]
CPB2 TTP18AY Limited Genetic Variation [38]
CPE TTXPWO6 Limited Genetic Variation [39]
CPS1 TT42M75 Limited Biomarker [40]
CTSS TTUMQVO Limited Biomarker [41]
CX3CL1 TT1OFBQ Limited Genetic Variation [42]
CYP3A5 TTHS0OK Limited Genetic Variation [43]
ELANE TTPLTSQ Limited Biomarker [44]
ENPP1 TTZTIWS Limited Genetic Variation [45]
EPO TTQG4NR Limited Biomarker [46]
ESR2 TTOM3J0 Limited Biomarker [47]
F11 TTDM4ZU Limited Biomarker [48]
F11R TT3C8EG Limited Genetic Variation [49]
F12 TTRJSMV Limited Genetic Variation [50]
F8 TT1290U Limited Altered Expression [51]
FCGR2B TT5RWKQ Limited Biomarker [52]
FGG TTR31L7 Limited Genetic Variation [53]
FN1 TTPJ921 Limited Altered Expression [54]
G3BP1 TTG0R8Z Limited Biomarker [55]
GCG TT6Y4PN Limited Altered Expression [56]
GGT1 TTZVT7O Limited Altered Expression [57]
GLP2R TT1YWO5 Limited Biomarker [58]
GRIK4 TTQV6BO Limited Biomarker [59]
GSTA1 TT4P8DE Limited Genetic Variation [60]
HNF1A TT01M3K Limited Genetic Variation [61]
HSPA8 TTMQL3K Limited Genetic Variation [62]
IFNL3 TTRF4Q2 Limited Genetic Variation [63]
IL15 TTJFA35 Limited Biomarker [64]
IL15RA TTGN89I Limited Altered Expression [65]
IL16 TTW4R0B Limited Genetic Variation [66]
IL18 TTRICUF Limited Altered Expression [31]
IL1RL1 TT4GZA4 Limited Biomarker [67]
IL23R TT6H4QR Limited Genetic Variation [68]
IL5 TTPREZD Limited Biomarker [69]
IRF8 TTHUBNK Limited Genetic Variation [70]
ITGA2 TTSJ542 Limited Genetic Variation [71]
JUP TTREN0G Limited Biomarker [72]
KLK1 TT5T3P6 Limited Biomarker [73]
LAG3 TTNVXAW Limited Altered Expression [74]
LAMP2 TTULDG7 Limited Biomarker [75]
LBP TTVQJLY Limited Biomarker [76]
LCAT TTGZ91P Limited Genetic Variation [77]
LIPA TTS8T1M Limited Biomarker [78]
LTA4H TTXZEAJ Limited Altered Expression [79]
MAP2K2 TT8H9GB Limited Altered Expression [80]
MAP3K8 TTGECUM Limited Altered Expression [81]
MIA TT5HNVS Limited Genetic Variation [82]
MSR1 TT2TDH9 Limited Altered Expression [83]
MTNR1A TT0WAIE Limited Genetic Variation [84]
MTTP TTUS1RD Limited Biomarker [85]
MUC16 TTC1PS3 Limited Biomarker [86]
MVD TTE5J6X Limited Genetic Variation [87]
MVK TT5DFHW Limited Genetic Variation [88]
MYBPC3 TT9WOBN Limited Genetic Variation [89]
NFKB1 TTUIZKC Limited Genetic Variation [90]
NPFFR2 TTXYNDJ Limited Altered Expression [91]
NPR1 TTM9IYA Limited Genetic Variation [92]
NPR3 TTWVLS6 Limited Altered Expression [93]
NR1H3 TTECBXN Limited Genetic Variation [94]
NR3C2 TT26PHO Limited Biomarker [95]
OGDH TTH8T6I Limited Altered Expression [96]
OPA1 TTTU49Q Limited Biomarker [97]
P2RY12 TTZ1DT0 Limited Biomarker [98]
PCSK1 TTED9LZ Limited Genetic Variation [99]
PECAM1 TT4EZB2 Limited Genetic Variation [61]
PF4 TTSG7Q5 Limited Biomarker [100]
PLG TTP86E2 Limited Biomarker [101]
PPIA TTL2ADK Limited Genetic Variation [102]
PRKCH TTONI0R Limited Genetic Variation [103]
PYY TTVFJLX Limited Altered Expression [104]
RENBP TTZCG0Q Limited Biomarker [105]
SAA1 TTY0DN9 Limited Genetic Variation [106]
SCARB1 TTRE324 Limited Genetic Variation [107]
SELL TT2IYXF Limited Biomarker [108]
SENP1 TTW9HY5 Limited Biomarker [109]
SERPINC1 TT4QPUL Limited Genetic Variation [25]
SFRP4 TTX8I1Y Limited Altered Expression [110]
SH2B3 TT36N7Z Limited Genetic Variation [61]
SLC2A4 TTP6MT5 Limited Altered Expression [111]
SLCO1B1 TTFGXEB Limited Genetic Variation [112]
SPOCK1 TTF23RE Limited Altered Expression [113]
SRGN TTCHB06 Limited Altered Expression [114]
SUV39H1 TTUWQTK Limited Biomarker [115]
TBXA2R TT2O84V Limited Altered Expression [116]
TCF7L2 TT80QAL Limited Altered Expression [117]
TERF2 TT5XSLT Limited Altered Expression [118]
THRA TTTSEPU Limited Genetic Variation [119]
TIAM1 TTNU6I5 Limited Genetic Variation [120]
TLR1 TTW14D0 Limited Genetic Variation [121]
TLR8 TT8CWFK Limited Genetic Variation [122]
TNC TTUCPMY Limited Biomarker [123]
TNFAIP3 TT5W0IO Limited Genetic Variation [124]
TNFRSF11B TT2CJ75 Limited Biomarker [125]
TNFRSF4 TTL31H0 Limited Biomarker [126]
TNFSF4 TTBW580 Limited Biomarker [127]
TREM1 TTHZQP0 Limited Genetic Variation [121]
TRPA1 TTELV3W Limited Genetic Variation [128]
UBC TTBP3XA Limited Altered Expression [129]
UCP1 TTI12YJ Limited Biomarker [93]
UCP2 TTSC2YM Limited Genetic Variation [130]
UCP3 TT12RJK Limited Genetic Variation [131]
VIP TTGTWLF Limited Biomarker [132]
VKORC1 TTEUC8H Limited Genetic Variation [133]
ZNF217 TTY3BRA Limited Genetic Variation [134]
ACACB TTY84UG Disputed Genetic Variation [135]
ACAT1 TTK3C21 Disputed Genetic Variation [37]
ALCAM TT2AFT6 Disputed Biomarker [136]
CTH TTLQUZS Disputed Genetic Variation [137]
IFNGR2 TT13TL0 Disputed Biomarker [138]
LTC4S TTW7OTG Disputed Biomarker [79]
NPPC TTRK0B9 Disputed Biomarker [139]
PADI4 TTQHAXM Disputed Biomarker [140]
SLC25A1 TTTD730 Disputed Biomarker [141]
SLC27A4 TT20AYF Disputed Biomarker [142]
SOAT2 TTAK0IN Disputed Genetic Variation [143]
TNFSF14 TTKVENM Disputed Biomarker [144]
ABL2 TT1A6HL moderate Genetic Variation [145]
ADAM8 TTQWYMD moderate Altered Expression [146]
ATXN2 TTPQJ7P moderate Genetic Variation [61]
BMP1 TT0L58T moderate Genetic Variation [61]
C1S TT7LRQH moderate Genetic Variation [61]
C5 TTKANGO moderate Genetic Variation [61]
CA13 TTQPHSR moderate Genetic Variation [147]
CALCRL TTY6O0Q moderate Altered Expression [148]
CD36 TTPJMCU moderate Genetic Variation [149]
CDH2 TT1WS0T moderate Genetic Variation [150]
CFB TTA0P7K moderate Genetic Variation [61]
CHRNB4 TTTVAFQ moderate Genetic Variation [151]
CSK TTX6F0Q moderate Genetic Variation [152]
CXCL11 TTWG0RE moderate Altered Expression [153]
CYP21A2 TTP4GLG moderate Genetic Variation [61]
DAGLB TTXZDEN moderate Genetic Variation [61]
DCLK2 TTHK3MO moderate Genetic Variation [128]
DMPK TTZQTY2 moderate Biomarker [154]
FER TTRA9G0 moderate Genetic Variation [155]
FES TTLBY21 moderate Genetic Variation [61]
FKBP5 TT0J5KQ moderate Genetic Variation [61]
FUT3 TTUPAD7 moderate Genetic Variation [156]
GCH1 TTLSWP6 moderate Genetic Variation [157]
GGCX TT76OLR moderate Genetic Variation [158]
GGT7 TT62BC7 moderate Genetic Variation [61]
GJA4 TTQO1VY moderate Biomarker [159]
HBEGF TT15SL0 moderate Altered Expression [160]
HCAR2 TTWNV8U moderate Biomarker [161]
HGFAC TTD96RW moderate Genetic Variation [61]
HMGCR TTPADOQ moderate Genetic Variation [162]
HTRA1 TT8POQR moderate Genetic Variation [61]
MAD1L1 TTNE9U7 moderate Genetic Variation [61]
MAS1 TTOISYB moderate Biomarker [9]
MAT2A TTSMPXQ moderate Genetic Variation [163]
NEDD9 TT1UREA moderate Genetic Variation [61]
NEK9 TTM57AW moderate Genetic Variation [61]
NOD1 TTYSRXM moderate Genetic Variation [164]
PAX5 TTA4REJ moderate Genetic Variation [165]
PDGFA TTSM78N moderate Genetic Variation [166]
PEPD TTLZXI0 moderate Altered Expression [167]
PHB TT6U071 moderate Genetic Variation [61]
PLCG1 TT6T4JI moderate Genetic Variation [61]
PPARA TTJ584C moderate Biomarker [168]
PROC TTZUXYS moderate Genetic Variation [169]
PTGER2 TT1ZAVI moderate Genetic Variation [170]
PTK7 TTXH2ZN moderate Genetic Variation [61]
RHOA TTP2U16 moderate Genetic Variation [61]
RPH3A TT9L4J8 moderate Genetic Variation [151]
SELP TTE5VG0 moderate Genetic Variation [171]
SERPINH1 TTPSWQG moderate Genetic Variation [61]
SLC22A3 TTG2UMS moderate Genetic Variation [172]
SLC26A4 TT7X02I moderate Genetic Variation [173]
SLC2A12 TTZO36H moderate Genetic Variation [61]
ST8SIA4 TTDP8YM moderate Genetic Variation [174]
TENT4A TT0XZ4Q moderate Genetic Variation [61]
TNNT2 TTWAS18 moderate Biomarker [175]
TOR1A TTF85KW moderate Altered Expression [176]
TRPC3 TTNVC34 moderate Biomarker [177]
TRPM3 TTO3TD8 moderate Genetic Variation [163]
UMPS TTAFJUD moderate Genetic Variation [61]
ZEB2 TTT2WK4 moderate Genetic Variation [61]
ABCG5 TTKZ7WY Strong Genetic Variation [178]
ACHE TT1RS9F Strong Altered Expression [179]
ADA TTLP57V Strong Altered Expression [180]
ADAMTS13 TTUREBK Strong Biomarker [181]
ADAMTS5 TTXSU2Y Strong Biomarker [182]
ADRA2B TTWM4TY Strong Biomarker [183]
ADRB1 TTR6W5O Strong Genetic Variation [184]
AHSG TTKF4WV Strong Altered Expression [185]
ALOX15 TTN9T81 Strong Genetic Variation [186]
ALPL TTMR5UV Strong Altered Expression [187]
ANPEP TTPHMWB Strong Biomarker [188]
AOC3 TT7HC21 Strong Biomarker [189]
APLN TT87D3J Strong Altered Expression [190]
APLNR TTJ8E43 Strong Genetic Variation [191]
APOA4 TTNC3WS Strong Biomarker [192]
APOC3 TTXOZQ1 Strong Biomarker [193]
ARG1 TT7ZQEV Strong Altered Expression [194]
ARRB2 TT8SO2I Strong Biomarker [195]
ASGR1 TTYM94H Strong Altered Expression [196]
BCHE TT3MSAO Strong Altered Expression [197]
BDKRB1 TTG5QIA Strong Altered Expression [198]
BDKRB2 TTGY8IW Strong Altered Expression [198]
CACNA1C TTZIFHC Strong Genetic Variation [199]
CCN1 TTPK79J Strong Biomarker [200]
CCR7 TT2GIDQ Strong Genetic Variation [201]
CD28 TTQ13FT Strong Biomarker [42]
CD40 TT1ERKL Strong Genetic Variation [202]
CD69 TTPQE9F Strong Biomarker [203]
CDK18 TTUMFAR Strong Genetic Variation [165]
CFTR TTRLZHP Strong Genetic Variation [61]
CR1 TTEA8OW Strong Altered Expression [36]
CTSG TTQAJF1 Strong Biomarker [204]
CXCL12 TT4UGTF Strong Genetic Variation [205]
CYP17A1 TTRA5BZ Strong Genetic Variation [206]
CYP2B6 TTMH124 Strong Genetic Variation [207]
CYP2C9 TTR40YJ Strong Genetic Variation [208]
CYP3A4 TTWP7HQ Strong Biomarker [209]
DFFA TTYVQ9C Strong Biomarker [210]
DIO1 TTU3X26 Strong Genetic Variation [211]
ECE1 TTQ9RYT Strong Genetic Variation [212]
EHMT1 TTOFXD7 Strong Genetic Variation [213]
F10 TTCIHJA Strong Biomarker [214]
F2R TTL935N Strong Genetic Variation [215]
F2RL3 TTD0652 Strong Posttranslational Modification [216]
F3 TT38MDJ Strong Biomarker [217]
F7 TTF0EGX Strong Genetic Variation [218]
FABP3 TT3TGLR Strong Biomarker [219]
FCGR2A TTXT21W Strong Biomarker [220]
FCGR3A TTIFOC0 Strong Biomarker [221]
FGF21 TTQ916P Strong Altered Expression [222]
FGFR4 TT1KX2S Strong Genetic Variation [223]
FOLH1 TT9G4N0 Strong Genetic Variation [224]
FURIN TTH9WF6 Strong Genetic Variation [61]
GCLM TTNFESW Strong Biomarker [225]
GDF15 TT4MXVG Strong Altered Expression [226]
GDF2 TTAP4T1 Strong Biomarker [227]
GIP TT40HS5 Strong Genetic Variation [61]
GLP1R TTVIMDE Strong Genetic Variation [213]
GP1BA TTVB0Q9 Strong Genetic Variation [228]
GPX1 TTYAHBP Strong Biomarker [229]
GREM1 TTOUZN5 Strong Altered Expression [230]
HDAC9 TT8M4E1 Strong Genetic Variation [231]
HMGB1 TTWQYB7 Strong Biomarker [232]
HPGDS TTCYE56 Strong Genetic Variation [233]
HPSE TTR7GJO Strong Biomarker [234]
HSPD1 TT9HL5R Strong Genetic Variation [235]
IGF2R TTPNE41 Strong Biomarker [236]
IL1R2 TT51DEV Strong Biomarker [195]
IL33 TT5MD4P Strong Altered Expression [237]
IL37 TTQTX98 Strong Altered Expression [238]
IRS1 TTAJSQ0 Strong Altered Expression [239]
ITGA1 TTPERWV Strong Genetic Variation [128]
KDM3A TTKXS4A Strong Biomarker [240]
KNG1 TTDJ4MY Strong Biomarker [241]
LCK TT860QF Strong Genetic Variation [242]
LEPR TT0HD6V Strong Genetic Variation [243]
LGALS2 TTRHK90 Strong Altered Expression [244]
LOX TTQHNAM Strong Genetic Variation [245]
LRP6 TTSXOWE Strong Biomarker [117]
MARK2 TTAJ45Y Strong Genetic Variation [246]
MBL2 TTMQDZ5 Strong Genetic Variation [247]
MC4R TTD0CIQ Strong Genetic Variation [248]
MFGE8 TT1GLAJ Strong Altered Expression [249]
MGAM TTXWASR Strong Biomarker [250]
MMP12 TTXZ0KQ Strong Altered Expression [251]
MMP7 TTMTWOS Strong Genetic Variation [252]
MMP8 TTGA1IV Strong Biomarker [253]
MTR TTUTO39 Strong Genetic Variation [254]
MUSK TT6SA0X Strong Genetic Variation [255]
NAGLU TTDM6HZ Strong Biomarker [11]
NAMPT TTD1WIG Strong Altered Expression [256]
NPC1L1 TTPD1CN Strong Altered Expression [257]
NPPB TTY63XT Strong Genetic Variation [258]
NPR2 TTNB7IF Strong Altered Expression [93]
NRG4 TTWAGKJ Strong Altered Expression [259]
NTF3 TTZHKV9 Strong Biomarker [136]
NTN1 TT0AH4L Strong Altered Expression [238]
OTC TT5KIO9 Strong Biomarker [260]
P2RY1 TTA93TL Strong Genetic Variation [261]
PCSK6 TT75LN9 Strong Altered Expression [262]
PDE3B TTN34SQ Strong Genetic Variation [263]
PDE4D TTSKMI8 Strong Genetic Variation [264]
PDGFD TTSN0GA Strong Genetic Variation [265]
PLTP TTZF6SN Strong Altered Expression [266]
PPARD TT2JWF6 Strong Altered Expression [267]
PRKCE TT57MT2 Strong Genetic Variation [61]
PTGS2 TTVKILB Strong Altered Expression [268]
PTH TT6F7GZ Strong Biomarker [269]
PTPRC TTUS45N Strong Biomarker [270]
RBP4 TT0C8BY Strong Altered Expression [238]
RTN4 TT7GXMU Strong Altered Expression [182]
S100A12 TTQ4ESF Strong Biomarker [271]
S100A8 TT4AF6N Strong Biomarker [195]
S1PR4 TTZ8C5Q Strong Biomarker [272]
SCD TT6RIOV Strong Genetic Variation [255]
SERPINF1 TTR59S1 Strong Altered Expression [273]
SLC52A2 TT6TKEN Strong Genetic Variation [246]
SLC5A2 TTF8JAT Strong Genetic Variation [274]
SLCO1C1 TT340CE Strong Genetic Variation [211]
SMAD3 TTHQZV7 Strong Genetic Variation [61]
SORT1 TTRX9AV Strong Biomarker [275]
SREBF1 TTER0UB Strong Biomarker [276]
SREBF2 TTRQ4AP Strong Biomarker [277]
TEK TT9VGXW Strong Genetic Variation [61]
TERF1 TT1Y6J2 Strong Altered Expression [278]
TERT TTQY2EJ Strong Biomarker [279]
TFPI TT068JH Strong Genetic Variation [280]
THBS1 TTKI0H1 Strong Genetic Variation [281]
TMSB4X TTMVAIU Strong Genetic Variation [282]
TNFRSF1A TTG043C Strong Biomarker [283]
TNFRSF1B TT63WSF Strong Biomarker [283]
TNFSF15 TTEST6I Strong Biomarker [284]
TNNI3 TTNLDK6 Strong Altered Expression [285]
TRAF6 TTCDR6M Strong Genetic Variation [286]
UTS2 TTERU0T Strong Altered Expression [287]
VCAM1 TTHCEF6 Strong Altered Expression [288]
YOD1 TTFSH0K Strong Biomarker [289]
CDH3 TTARMD9 Definitive Genetic Variation [290]
CEL TTTRNQW Definitive Biomarker [291]
CFD TT8D13I Definitive Biomarker [292]
CRLF2 TTRMZ0N Definitive Biomarker [293]
FCGR1A TTZK4I3 Definitive Altered Expression [294]
FGF19 TTGCH11 Definitive Biomarker [295]
HMGB2 TTA78JQ Definitive Altered Expression [296]
JMJD1C TTBISK4 Definitive Genetic Variation [297]
LCT TTA0OSE Definitive Biomarker [298]
MAG TT9XFON Definitive Biomarker [299]
POR TTOQ9GZ Definitive Altered Expression [300]
PTAFR TTQL5VC Definitive Genetic Variation [301]
RRM1 TTWP0NS Definitive Genetic Variation [302]
SETD7 TTJ0FSU Definitive Biomarker [303]
SIRT5 TTH0IOD Definitive Genetic Variation [304]
TNFRSF13C TT7NJSE Definitive Biomarker [305]
ZAP70 TTUMHT8 Definitive Biomarker [306]
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⏷ Show the Full List of 359 DTT(s)
This Disease Is Related to 12 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
ABCB5 DTKVEXO Limited Genetic Variation [307]
ATP2B1 DTJWQ1L Limited Biomarker [308]
SLC25A20 DTQOUM4 Limited Biomarker [30]
SLC2A6 DTS4MKQ Limited Genetic Variation [309]
SLC7A13 DTMWE5P Limited Biomarker [310]
ABCC10 DTPS120 moderate Genetic Variation [61]
ANXA11 DTGQ2CF moderate Genetic Variation [151]
KCNH7 DT3WXPI moderate Genetic Variation [61]
SLC22A4 DT2EG60 moderate Genetic Variation [61]
ABCC6 DT582KR Strong Genetic Variation [311]
SLC35A1 DTVZIRG Strong Biomarker [312]
SLCO6A1 DTIFXNS Strong Genetic Variation [313]
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⏷ Show the Full List of 12 DTP(s)
This Disease Is Related to 32 DME Molecule(s)
Gene Name DME ID Evidence Level Mode of Inheritance REF
ADH1B DEEN9RD Limited Genetic Variation [314]
ALDH1B1 DEXI4UQ Limited Genetic Variation [315]
CYP27A1 DEBS639 Limited Genetic Variation [316]
CYP2C18 DEZMWRE Limited Genetic Variation [317]
CYP2R1 DEBIHM3 Limited Genetic Variation [318]
CYP4A11 DE2XQGW Limited Biomarker [319]
DDAH1 DEY0TQC Limited Genetic Variation [320]
MSRA DEU2ZBY Limited Genetic Variation [321]
MT2A DEFKGT7 Limited Genetic Variation [322]
SULT1E1 DESTKG6 Limited Biomarker [323]
ACSS2 DEE76VW Strong Biomarker [324]
ADH1C DEM1HNL Strong Genetic Variation [325]
AKR1A1 DED2FW3 Strong Genetic Variation [326]
AOC2 DE8DP90 Strong Biomarker [189]
AS3MT DE9KJP3 Strong Genetic Variation [61]
CES2 DETHCPD Strong Biomarker [327]
CPA4 DEXKD7J Strong Biomarker [204]
CYP4F2 DE3GT9C Strong Biomarker [319]
CYP7A1 DEDZRQ1 Strong Genetic Variation [328]
DHCR7 DEL7GFA Strong Genetic Variation [329]
FAAH DEUM1EX Strong Biomarker [330]
FADS1 DE05S8C Strong Genetic Variation [255]
GCLC DESYL1F Strong Biomarker [225]
GSTM1 DEYZEJA Strong Biomarker [233]
GSTT1 DE3PKUG Strong Genetic Variation [233]
MTARC2 DE6QH2D Strong Biomarker [331]
NADSYN1 DELF8BA Strong Genetic Variation [329]
NAT2 DER7TA0 Strong Genetic Variation [332]
NNMT DECVGJ3 Strong Genetic Variation [333]
PON2 DEHJU7E Strong Biomarker [334]
SI DE5EO4Y Strong Biomarker [250]
ACP5 DESITDW Definitive Biomarker [335]
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⏷ Show the Full List of 32 DME(s)
This Disease Is Related to 566 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ABCG8 OTIJ76XW Limited Genetic Variation [61]
ABRAXAS2 OTAW1I4C Limited Altered Expression [336]
ACACA OT5CQPZY Limited Biomarker [337]
ACKR2 OTWYY14H Limited Biomarker [338]
ADAMTSL4 OTBILJMW Limited Genetic Variation [339]
ADAR OTQNOHR8 Limited Altered Expression [340]
ADD1 OTTF68DC Limited Genetic Variation [341]
ADIPOR2 OT2HDTL8 Limited Altered Expression [342]
AGGF1 OTA7U2T8 Limited Biomarker [343]
AGXT2 OTO6QUTM Limited Genetic Variation [320]
AIDA OTMRLWGT Limited Altered Expression [344]
ALOX15B OTWQQ08W Limited Genetic Variation [345]
AMFR OTQRX7LC Limited Genetic Variation [346]
ANP32B OT3SQMLU Limited Altered Expression [347]
APEX2 OTJ22LIT Limited Genetic Variation [53]
APOC4 OTE8ZUXY Limited Genetic Variation [348]
APPL1 OT8VR95S Limited Genetic Variation [349]
APPL2 OT9S4C4K Limited Genetic Variation [349]
ARHGAP31 OTUYTF4I Limited Biomarker [350]
ARHGEF7 OT9BPJCL Limited Genetic Variation [351]
ASCC1 OTH4VAP9 Limited Genetic Variation [351]
ASXL1 OTX931AW Limited Biomarker [352]
ATP6AP2 OT0IABVV Limited Genetic Variation [353]
B4GALNT1 OTCY80HS Limited Biomarker [354]
BCAR1 OTKT2C2N Limited Genetic Variation [355]
BHMT OTYB6PXZ Limited Genetic Variation [356]
BMS1 OTEGQ8ZO Limited Biomarker [337]
BRINP3 OT4VFHWN Limited Genetic Variation [357]
BTN2A1 OTUYPMZJ Limited Genetic Variation [358]
C1QL3 OT4TZH3J Limited Altered Expression [359]
C1QTNF1 OT7I7KHC Limited Altered Expression [360]
C1QTNF3 OTOJMWW0 Limited Biomarker [361]
C1QTNF9 OTLI3VA3 Limited Biomarker [362]
CAMTA1 OTAN1S5B Limited Biomarker [363]
CAP1 OTYM8A2N Limited Biomarker [364]
CBLIF OTNE20WU Limited Altered Expression [365]
CCL13 OTNX0JD0 Limited Biomarker [366]
CCL19 OTQ2UJMH Limited Biomarker [34]
CD93 OT6HZT6H Limited Biomarker [367]
CDKAL1 OTA0SGNE Limited Biomarker [368]
CHGA OTXYX5JH Limited Altered Expression [369]
CIDEB OT873IYM Limited Biomarker [370]
CLOCK OTNEOJY7 Limited Altered Expression [371]
CMTM5 OTMS7NDP Limited Biomarker [372]
CNBP OTTGM9NK Limited Genetic Variation [373]
COG6 OTDLQITC Limited Genetic Variation [374]
COL14A1 OTLNJ13O Limited Posttranslational Modification [375]
COMP OTS2FPMI Limited Altered Expression [376]
CORT OTX3GUHB Limited Biomarker [377]
COX1 OTG3O9BN Limited Altered Expression [378]
COX5A OTP0961M Limited Genetic Variation [379]
CPOX OTIAY121 Limited Genetic Variation [379]
CXCL6 OTFTCQ4O Limited Genetic Variation [380]
CYTB OTAHB98A Limited Biomarker [381]
DCLRE1C OTW3KB1I Limited Biomarker [382]
DLD OT378CU9 Limited Biomarker [383]
DNTT OTFSEF12 Limited Biomarker [384]
DOCK11 OTFSTN6A Limited Genetic Variation [385]
DUOX1 OTQ2AEW0 Limited Genetic Variation [386]
DUOX2 OTU14HCN Limited Genetic Variation [386]
DYM OTQ670WI Limited Biomarker [387]
EGR3 OTGPJIRA Limited Genetic Variation [388]
ELAVL2 OT6EJ8MQ Limited Biomarker [389]
ELMO1 OTY2ORXK Limited Biomarker [390]
ELOVL2 OTDAF6U3 Limited Genetic Variation [391]
ENHO OT91QASK Limited Biomarker [392]
ERCC5 OTQAKFJM Limited Genetic Variation [393]
ESYT3 OTG5H3YF Limited Genetic Variation [394]
FAT4 OT7QONNV Limited Altered Expression [116]
FBN2 OT3KYJQL Limited Genetic Variation [15]
FCGR2C OTNLMNYB Limited Biomarker [52]
FEN1 OT6QGG7O Limited Genetic Variation [395]
FLOT2 OTZ0QR5L Limited Genetic Variation [396]
FLYWCH1 OTWZVRX2 Limited Biomarker [55]
FSD1 OT8P6PT3 Limited Biomarker [397]
FSD1L OTBQ48RF Limited Biomarker [397]
GALNT3 OT7M67WT Limited Genetic Variation [398]
GGTLC1 OTWJKUHQ Limited Genetic Variation [399]
GOLGA4 OTCMEHNJ Limited Genetic Variation [380]
GPD1L OTVLWW9T Limited Biomarker [400]
GPIHBP1 OTDF8R2M Limited Biomarker [401]
GRK4 OTUU8V2S Limited Genetic Variation [402]
GSTM2 OTG4WT05 Limited Genetic Variation [403]
GUCY1A1 OTPTCBUN Limited Genetic Variation [404]
HAND2 OTCXYW4Y Limited Genetic Variation [405]
HBG2 OT4J48JJ Limited Altered Expression [406]
HHEX OTLIUVYX Limited Biomarker [368]
HLA-E OTX1CTFB Limited Genetic Variation [407]
HLA-F OT76CM19 Limited Genetic Variation [407]
HNRNPUL1 OTJP4U7K Limited Genetic Variation [408]
HPSE2 OTGEPP8V Limited Genetic Variation [409]
HSPA14 OTZCA5LK Limited Genetic Variation [235]
HTRA2 OTC7616F Limited Biomarker [410]
IARS1 OT9WXH5N Limited Genetic Variation [411]
IFNE OTXO5MHZ Limited Genetic Variation [412]
IL34 OTZ15VVK Limited Altered Expression [413]
IL6R OTCQL07Z Limited Genetic Variation [61]
IRF2 OTAZRUW3 Limited Biomarker [370]
IRF2BP2 OTSSRRCA Limited Altered Expression [414]
IRF6 OTKJ44EV Limited Biomarker [415]
ITLN1 OT7ZLJVV Limited Altered Expression [416]
JCAD OT7G1WJW Limited Genetic Variation [417]
KALRN OT8WRCBH Limited Genetic Variation [418]
KCTD10 OT5HFZXU Limited Genetic Variation [419]
KIDINS220 OTLBH2MA Limited Genetic Variation [420]
KIF2B OTLPAX4N Limited Genetic Variation [421]
KIF2C OTJ8G3NP Limited Genetic Variation [422]
KRT5 OTVGI9HT Limited Biomarker [423]
LAD1 OT6YGTVX Limited Biomarker [383]
LDB2 OT6Y8IEK Limited Altered Expression [424]
LMAN1 OTYHKDEO Limited Genetic Variation [425]
LSAMP OTYXVQX2 Limited Biomarker [426]
LUM OTSRC874 Limited Biomarker [11]
MADD OTUFYVGG Limited Genetic Variation [224]
MAFB OTH2N3T8 Limited Genetic Variation [427]
MAP1B OTVXW089 Limited Biomarker [428]
MAX OTKZ0YKM Limited Biomarker [370]
MCFD2 OTM0XU0U Limited Genetic Variation [425]
MIA3 OTBVIZQD Limited Genetic Variation [205]
MIP OTEBLU3E Limited Altered Expression [429]
MMD OTB5I4OC Limited Biomarker [430]
MON2 OTCSVMAR Limited Biomarker [221]
MPHOSPH6 OT6E2S48 Limited Biomarker [431]
MPI OTBH6ZK1 Limited Biomarker [432]
MVP OTJGHJRB Limited Genetic Variation [433]
MYLIP OTL0PFGV Limited Genetic Variation [434]
NANOS3 OTGX9IQU Limited Genetic Variation [435]
NCF2 OTAUW7L2 Limited Biomarker [272]
NDST4 OTEKG7JJ Limited Genetic Variation [436]
NDUFAB1 OTF906UR Limited Genetic Variation [437]
NEXN OTKB0B0H Limited Altered Expression [438]
NOX5 OTHTH59G Limited Biomarker [439]
NUCB2 OTHO6JWN Limited Altered Expression [440]
NUMB OTMB586Q Limited Genetic Variation [441]
OGFOD1 OTTUQ5O3 Limited Genetic Variation [442]
PAFAH2 OTSHD5M5 Limited Biomarker [443]
PCLAF OTMVIOUU Limited Genetic Variation [444]
PF4V1 OT2CXM6L Limited Biomarker [100]
PLA2G2D OTU604XM Limited Biomarker [445]
PLA2G5 OTQRSKCZ Limited Genetic Variation [446]
PLEKHG5 OTL0S21W Limited Genetic Variation [120]
PLIN2 OTRXJ9UN Limited Altered Expression [447]
PLPP3 OTSSF7BK Limited Genetic Variation [448]
PPBP OT1FHGQS Limited Biomarker [449]
PPIG OTZ8BTTM Limited Biomarker [450]
PRDM10 OTDDWU5Q Limited Genetic Variation [451]
PRORP OTWIS44P Limited Genetic Variation [452]
PTPRA OTZA82J1 Limited Genetic Variation [433]
PTPRD OTZPJ3GX Limited Biomarker [453]
QRSL1 OTJDU2UG Limited Genetic Variation [338]
RECQL5 OTVZMP1Q Limited Autosomal recessive [454]
RHOJ OTWI65OA Limited Biomarker [455]
RNF13 OT7HNYF4 Limited Genetic Variation [128]
RNF39 OTUQA9JT Limited Biomarker [456]
RPN1 OTEG4KU9 Limited Biomarker [338]
RSPH6A OTJ96T2F Limited Genetic Variation [457]
S100A7 OTJFVJRF Limited Biomarker [458]
SCAI OTAK3TMO Limited Genetic Variation [459]
SH2B1 OTJZO2CI Limited Genetic Variation [460]
SHC1 OT1J5IRN Limited Altered Expression [461]
SKIL OTNBXH32 Limited Altered Expression [462]
SNRNP70 OTP52YZ3 Limited Genetic Variation [463]
SOD3 OTIOZQAB Limited Genetic Variation [464]
SPESP1 OTWXKKTJ Limited Genetic Variation [465]
SRSF1 OTF61HOV Limited Genetic Variation [466]
SRSF2 OTVDHO6U Limited Genetic Variation [466]
ST6GAL1 OT7US3NO Limited Biomarker [453]
ST6GALNAC5 OTH91ETM Limited Biomarker [467]
SUGP1 OT7W0EB8 Limited Genetic Variation [468]
SUMO4 OT9B447E Limited Genetic Variation [469]
TADA1 OTV9RKSL Limited Biomarker [470]
TBPL1 OT4I143E Limited Biomarker [471]
TBX5 OT70PISV Limited Altered Expression [472]
TCN2 OT41D0L3 Limited Genetic Variation [473]
TCP1 OT1MGUX9 Limited Biomarker [474]
TES OTL8PP6V Limited Altered Expression [475]
TFAP2B OTR1T8E9 Limited Altered Expression [476]
TFEC OTUST8MR Limited Biomarker [113]
TGFBRAP1 OT80QNR5 Limited Genetic Variation [363]
TIMP4 OT8A68SW Limited Genetic Variation [477]
TLL1 OTK9NM7G Limited Genetic Variation [478]
TMEM132A OTNUI7O1 Limited Altered Expression [479]
TMEM170A OT65DTBD Limited Genetic Variation [355]
TNIP1 OTRAOTEW Limited Genetic Variation [431]
TNNT1 OT8PBOAR Limited Genetic Variation [480]
TRAF5 OTSBTLO0 Limited Altered Expression [481]
TRIB3 OTG5OS7X Limited Genetic Variation [482]
ACAT2 OTZ092ZJ Disputed Genetic Variation [143]
ANGPTL2 OTB6JG41 Disputed Posttranslational Modification [483]
APOD OTT77XW8 Disputed Biomarker [484]
CFAP97 OT0RSQO4 Disputed Altered Expression [485]
CHRNA3 OTCZQY1U Disputed Genetic Variation [486]
COG2 OTKQH4N4 Disputed Biomarker [487]
DHX40 OTOL02QN Disputed Biomarker [140]
EFNA5 OTOH4DRR Disputed Biomarker [138]
ERLIN1 OTUOOODY Disputed Genetic Variation [135]
FASTK OTTHFZMP Disputed Altered Expression [488]
FETUB OT7V07NI Disputed Biomarker [489]
MAP1LC3A OTPMGIU4 Disputed Biomarker [490]
MCIDAS OTK1JVAH Disputed Biomarker [491]
MYOCD OTSJNHTH Disputed Biomarker [492]
OXCT1 OT536PE7 Disputed Genetic Variation [493]
PPP3R1 OTGQNFJQ Disputed Genetic Variation [494]
PSMD4 OTH1VZTM Disputed Biomarker [138]
RFX1 OTZUDMPR Disputed Altered Expression [495]
SOSTDC1 OTAKDNSM Disputed Genetic Variation [496]
ADA2 OTGCV24S moderate Genetic Variation [497]
ANKRD13B OTJMS7MX moderate Genetic Variation [61]
APH1B OTQHPTGC moderate Genetic Variation [498]
AQP5 OT77GBY8 moderate Altered Expression [499]
ARHGAP15 OT9CKHDC moderate Genetic Variation [61]
ARHGAP26 OTNGQU7A moderate Genetic Variation [61]
ARHGAP4 OTXV053R moderate Biomarker [500]
ARHGAP42 OTIDSJMK moderate Genetic Variation [61]
ARHGEF12 OTM2D3LT moderate Genetic Variation [163]
ARID4A OT1XKBZ0 moderate Genetic Variation [61]
ARL2BP OT7REEDA moderate Genetic Variation [501]
ASZ1 OTLM93UO moderate Genetic Variation [61]
ATAD1 OTJ02XFL moderate Genetic Variation [502]
ATP1B1 OTTO6ZP4 moderate Genetic Variation [61]
ATP4B OTIP2EYJ moderate Biomarker [161]
ATPAF2 OTOMEQX6 moderate Genetic Variation [151]
ATXN2L OTP5M3R9 moderate Altered Expression [503]
B4GALNT2 OT85V4QV moderate Genetic Variation [61]
BCAP29 OTLUBG86 moderate Genetic Variation [61]
BCAS3 OTDVAX6B moderate Genetic Variation [61]
BMPR1B OTGFN0OD moderate Genetic Variation [61]
BRAP OTB7BAFQ moderate Biomarker [504]
BSND OTYWZWPD moderate Genetic Variation [501]
C2 OTHMF4YM moderate Genetic Variation [61]
CAPN10 OTS9LJW4 moderate Biomarker [505]
CARF OTWE0T6Q moderate Genetic Variation [158]
CCDC97 OTZSX6TF moderate Genetic Variation [61]
CCM2 OT2I5DOW moderate Genetic Variation [61]
CD300LF OTQWJGSR moderate Genetic Variation [61]
CENPO OTXAH83Y moderate Genetic Variation [61]
CHD1L OT7CZK7C moderate Altered Expression [506]
COG5 OTZEG7K0 moderate Genetic Variation [158]
CORO1C OTXDF9T3 moderate Genetic Variation [152]
CORO6 OT9TFSVB moderate Genetic Variation [61]
CPQ OTTNZNLD moderate Biomarker [500]
CST3 OTNZ6AO4 moderate Biomarker [507]
CWF19L2 OT08RTB4 moderate Genetic Variation [61]
DAB1 OTPL9MA3 moderate Genetic Variation [508]
DECR1 OTCDIR6X moderate Biomarker [509]
DHX38 OTBVB3W5 moderate Genetic Variation [61]
DHX58 OT19BYB1 moderate Genetic Variation [61]
DOK3 OT842U3C moderate Genetic Variation [61]
DRC3 OTOV0W5A moderate Genetic Variation [151]
EARS2 OTNCJKY7 moderate Biomarker [510]
EHBP1L1 OTZMO30X moderate Genetic Variation [61]
EHD3 OTOKC2G5 moderate Genetic Variation [511]
ELL OTCBN5LF moderate Genetic Variation [61]
EML1 OTOP2E01 moderate Genetic Variation [61]
EPRS1 OTXK0FLB moderate Genetic Variation [512]
FBF1 OTKA7EZI moderate Genetic Variation [61]
FBN1 OTYCJT63 moderate Biomarker [513]
FBRSL1 OT4BPXGG moderate Genetic Variation [152]
FGD5 OT5VIRP2 moderate Genetic Variation [61]
FGD6 OTI0T62C moderate Genetic Variation [61]
FHL5 OT6C00Z1 moderate Genetic Variation [61]
FNDC3B OTBILGDR moderate Genetic Variation [61]
FOXA3 OTRGT2OT moderate Genetic Variation [61]
GOSR2 OTYHIYN2 moderate Genetic Variation [61]
GPR149 OTN36PTI moderate Genetic Variation [61]
HEATR6 OTD3MYS0 moderate Genetic Variation [514]
HIVEP2 OTVOMCW4 moderate Genetic Variation [61]
HNRNPM OTFU3OEZ moderate Genetic Variation [61]
HS3ST1 OT5DVN9P moderate SusceptibilityMutation [515]
IGF2BP1 OT9G360P moderate Genetic Variation [158]
ILRUN OTE8FHQD moderate Genetic Variation [61]
INSIG1 OTZF5X1D moderate Genetic Variation [516]
KANK2 OT3SZIWM moderate Genetic Variation [61]
KAT2A OTN0W2SW moderate Genetic Variation [61]
KCNAB1 OT25GJE9 moderate Genetic Variation [128]
KDELR2 OT9QW7Q0 moderate Genetic Variation [61]
KIAA1217 OTRMK3PU moderate Genetic Variation [61]
KSR2 OTSMUL59 moderate Genetic Variation [517]
LIPC OTZY5SC9 moderate Altered Expression [518]
LPCAT3 OTWI96P4 moderate Biomarker [519]
LTBP1 OTR7Q75L moderate Altered Expression [520]
MAP1S OT5WUD4C moderate Genetic Variation [61]
MARK4 OT6Z2TGV moderate Genetic Variation [61]
MAST4 OT3LOE2J moderate Genetic Variation [61]
MCF2L OTEURA8N moderate Genetic Variation [61]
MORF4L1 OTEA6FYJ moderate Genetic Variation [61]
MPZL2 OTKFNDUI moderate Genetic Variation [173]
MSL2 OTVPQYBG moderate Genetic Variation [61]
MYH11 OTVNVWY3 moderate Genetic Variation [61]
MYO9B OTQ94R5K moderate Genetic Variation [61]
N4BP2L2 OTV2F04G moderate Genetic Variation [61]
NAA25 OTS3QVF1 moderate Genetic Variation [163]
NBEAL1 OTLJ11N3 moderate Genetic Variation [61]
NCOA6 OTOMIGTV moderate Genetic Variation [61]
NDUFA12 OTCD6I5M moderate Genetic Variation [61]
NME7 OTYMBK3Q moderate Genetic Variation [61]
NOA1 OT9GTOAC moderate Genetic Variation [61]
NUP210 OT3BLQ9M moderate Genetic Variation [165]
PALLD OTZ2MUJZ moderate Genetic Variation [61]
PARL OT7DMHSA moderate Genetic Variation [521]
PARP12 OTCQTYIO moderate Genetic Variation [61]
PCNX3 OTOM3GHH moderate Genetic Variation [61]
PDLIM5 OTLQVV22 moderate Genetic Variation [61]
PDS5B OT3U3X8Z moderate Genetic Variation [61]
PLCG2 OTGVC9MY moderate Genetic Variation [61]
PLCL1 OTJL2C79 moderate Genetic Variation [128]
PLEKHA7 OTNUMAZ0 moderate Genetic Variation [61]
PLEKHG1 OTDVYW2F moderate Genetic Variation [61]
PMAIP1 OTXEE550 moderate Genetic Variation [522]
PRB2 OTAD4JZ0 moderate Genetic Variation [523]
PRDM6 OTKY12D9 moderate Genetic Variation [61]
QRICH1 OTPVAX04 moderate Genetic Variation [61]
R3HDM2 OTMJ3S6J moderate Genetic Variation [61]
RAB37 OTRL8IUO moderate Genetic Variation [61]
RAMP2 OTGQXLH5 moderate Altered Expression [148]
RAMP3 OTX6XLLM moderate Altered Expression [148]
RASGEF1B OT56BBU0 moderate Genetic Variation [61]
RERE OT3G4GBZ moderate Genetic Variation [145]
REST OTLL92LQ moderate Genetic Variation [61]
RETN OTW5Z1NH moderate Biomarker [524]
RPA1 OT76POLP moderate Genetic Variation [525]
RRBP1 OT4ZTPTM moderate Genetic Variation [61]
RRP1B OTHDRVML moderate Genetic Variation [61]
SACM1L OT6ORKTD moderate Genetic Variation [526]
SARS1 OTFKXQ1O moderate Genetic Variation [151]
SCAF11 OTX59D0X moderate Genetic Variation [61]
SCG2 OTXWUQQL moderate Biomarker [527]
SELENOI OTX2A47A moderate Genetic Variation [61]
SELENOS OTUEWIU9 moderate Genetic Variation [528]
SEMA5A OTUOIOJV moderate Genetic Variation [61]
SERPINA2 OT7UW9HA moderate Genetic Variation [61]
SHOC1 OTP51XIP moderate Genetic Variation [128]
SHROOM3 OTQKC5X2 moderate Genetic Variation [61]
SMG6 OTRCEJQL moderate Genetic Variation [61]
SOX6 OTT0W0LE moderate Genetic Variation [61]
SPAG11A OTNQ9UB0 moderate Genetic Variation [170]
SRFBP1 OTI8518R moderate Genetic Variation [61]
ST3GAL4 OTNENJZQ moderate Genetic Variation [61]
STAG1 OT564IX4 moderate Genetic Variation [61]
STOML1 OTSIO2QA moderate Genetic Variation [61]
SUSD2 OTSJTAZP moderate Genetic Variation [61]
SWAP70 OTPHT2QD moderate Genetic Variation [61]
TADA2A OTXUMEL9 moderate Genetic Variation [497]
TBL1Y OTA0F7TM moderate Genetic Variation [529]
TBX20 OTMPU2XQ moderate Genetic Variation [61]
TDRKH OTV21BN1 moderate Genetic Variation [61]
TENT5A OTSYF511 moderate Genetic Variation [163]
THADA OTYZQX0F moderate Genetic Variation [61]
TMEM106B OTUWA6NW moderate Genetic Variation [61]
TMEM163 OTCT1Y1L moderate Genetic Variation [530]
TNS1 OTZ8S1PL moderate Genetic Variation [61]
TPTE2 OTR3K733 moderate Genetic Variation [530]
TRIM5 OTMZH7EJ moderate Genetic Variation [61]
TSPAN14 OT29167O moderate Genetic Variation [61]
TSPAN9 OT3DI3NH moderate Genetic Variation [61]
ABHD2 OTCRUOCS Strong Genetic Variation [249]
ACADS OTGFANYQ Strong Biomarker [531]
ACCS OTHIHI9D Strong Biomarker [324]
ACP1 OTJ9CKLU Strong Genetic Variation [532]
ACTA2 OTEDLG8E Strong Genetic Variation [533]
ADAMTS7 OTVKZ1DV Strong Genetic Variation [534]
ADIPOR1 OT65ZFZN Strong Genetic Variation [535]
ADTRP OTFI2BQX Strong Biomarker [536]
AFG3L2 OTRPMAUX Strong Posttranslational Modification [537]
AKAP13 OTOZAR14 Strong Genetic Variation [61]
AMPD1 OTU17BCI Strong Genetic Variation [538]
ANKS1A OTYZP3MP Strong Genetic Variation [165]
AP1S2 OTZHJFYI Strong Biomarker [539]
ARHGEF26 OTX0U8PX Strong Genetic Variation [61]
ARID5B OTUQ4CQY Strong Genetic Variation [540]
ARL15 OT00YSWZ Strong Genetic Variation [61]
ARPP21 OTWXZN5I Strong Biomarker [541]
BCL3 OT1M5B95 Strong Genetic Variation [542]
BGLAP OTK1YLWQ Strong Biomarker [543]
BID OTOSHSHU Strong Genetic Variation [544]
BMPR1A OTQOA4ZH Strong Biomarker [545]
BTBD8 OT3A3RD7 Strong Genetic Variation [546]
BTNL2 OTTTEMZA Strong Biomarker [547]
BUD13 OTXG6MX5 Strong Genetic Variation [548]
C16orf82 OT77Z5Y5 Strong Genetic Variation [480]
C1QTNF12 OTFAIQHR Strong Altered Expression [549]
C5AR2 OTP1Q82J Strong Genetic Variation [550]
CACUL1 OT6P1ZVP Strong Genetic Variation [551]
CAMK2N1 OTKCR5XL Strong Altered Expression [552]
CAPG OTJ86KI6 Strong Biomarker [553]
CASP8AP2 OTTWT68S Strong Biomarker [554]
CASQ2 OT09MNQ8 Strong Genetic Variation [555]
CASZ1 OTWJ2OR8 Strong Biomarker [312]
CAV2 OT1FGRQX Strong Altered Expression [556]
CCDC92 OT1YHLOR Strong Genetic Variation [61]
CCHCR1 OT22C116 Strong Biomarker [557]
CDH13 OTD2CYM5 Strong Genetic Variation [61]
CDH4 OT8LH3HN Strong Biomarker [558]
CDKN2B OTAG24N1 Strong Genetic Variation [559]
CELSR2 OTON6JSZ Strong Genetic Variation [61]
CFDP1 OTXY7J96 Strong Genetic Variation [457]
CHI3L1 OT2Z7VJH Strong Biomarker [560]
CHST9 OT1DEZRM Strong Genetic Variation [561]
CLEC1B OTO38TRG Strong Biomarker [562]
CNNM2 OTZHO8WU Strong Genetic Variation [61]
COL4A1 OTL6D1YE Strong Genetic Variation [61]
COX10 OTCYIS0L Strong Biomarker [563]
COX8A OTU0NR39 Strong Altered Expression [564]
CPA3 OTOK8M0V Strong Biomarker [204]
CPN2 OTYOYP14 Strong Biomarker [11]
CPNE3 OTCR3WG2 Strong Altered Expression [565]
CTRB1 OTFFF738 Strong Genetic Variation [566]
CTRL OTB6NA5O Strong Biomarker [567]
CXCL5 OTZOUPCA Strong Altered Expression [568]
DAB2IP OTF456VC Strong Genetic Variation [61]
DBP OTE0W7LN Strong Biomarker [569]
DDAH2 OT8Q40G2 Strong Genetic Variation [570]
DIO2 OTGPNSLH Strong Genetic Variation [211]
DOCK7 OTINNVQV Strong Genetic Variation [571]
EBF1 OTZ61YYH Strong Genetic Variation [572]
ERCC2 OT1C8HQ4 Strong Genetic Variation [302]
ERFE OTSES1HA Strong Biomarker [573]
ESM1 OT331Y8V Strong Altered Expression [574]
FCGR3B OTSLSPZG Strong Biomarker [221]
FCN1 OTK6ZHXH Strong Biomarker [272]
FLAD1 OTY8R02L Strong Genetic Variation [255]
GAL3ST1 OTSFFZRD Strong Biomarker [312]
GALNT2 OTZZ5386 Strong Genetic Variation [61]
GALNT4 OT6WKC13 Strong Genetic Variation [575]
GC OTWS63BY Strong Genetic Variation [576]
GCA OTAJ7ZHG Strong Biomarker [225]
GCKR OTSIWXGG Strong Genetic Variation [577]
GIGYF2 OTFNVEJ4 Strong Genetic Variation [61]
GMCL1 OTRZHUFV Strong Biomarker [225]
GNB3 OTA6HYBA Strong Genetic Variation [578]
GPR162 OTK4LT3K Strong Biomarker [579]
GSTK1 OTDNGWAF Strong Genetic Variation [313]
HHIPL1 OT3GMU2X Strong Biomarker [580]
HSPA2 OTSDET7B Strong Genetic Variation [581]
HSPH1 OTVRR73T Strong Biomarker [195]
IGFBP4 OT2HZRBD Strong Biomarker [582]
IL17RA OTVVI8ER Strong Biomarker [583]
ISYNA1 OT49ONSE Strong Biomarker [142]
ITGA2B OT4Y17PY Strong Genetic Variation [584]
JPH3 OTHTJO2I Strong Genetic Variation [585]
KCNE2 OTUO214Y Strong Biomarker [522]
KCNJ13 OTG1CNND Strong Genetic Variation [61]
KCNK5 OT68V64E Strong Genetic Variation [61]
KDM5D OTEKG0KD Strong Biomarker [586]
KL OTD4VWU6 Strong Biomarker [587]
KLF14 OT8BXLBS Strong Biomarker [588]
KLF15 OTGMQMVR Strong Altered Expression [589]
KLF2 OTIP1UFX Strong Genetic Variation [590]
KLLN OTV3FPH0 Strong Biomarker [591]
LGALS3BP OT9AGQKH Strong Biomarker [592]
LMOD1 OTZ2MEMG Strong Genetic Variation [61]
LRP8 OTZ71YV2 Strong Genetic Variation [593]
MAP3K7CL OT9J7RLC Strong Genetic Variation [61]
MARCHF1 OTI2EYO6 Strong Biomarker [594]
MEFV OTRJ6S6K Strong Altered Expression [31]
MEGF8 OT5G38CH Strong Biomarker [595]
METRN OTI2645G Strong Altered Expression [596]
METRNL OTB0DDL0 Strong Altered Expression [596]
MLKL OTDSLC81 Strong Biomarker [597]
MLXIPL OTR9MLLW Strong Genetic Variation [598]
MMP23B OT2OR6TS Strong Biomarker [599]
MMRN1 OT7ZNYHT Strong Genetic Variation [600]
MPRIP OT5FV5NS Strong Altered Expression [601]
MRTFA OTCVXASM Strong Genetic Variation [61]
MTHFD1L OTV01EFP Strong Genetic Variation [602]
MYO1F OTOAV4AR Strong Biomarker [272]
NBL1 OTT37U4O Strong Altered Expression [603]
NECTIN2 OTIE0W6O Strong Biomarker [542]
NFKBIZ OTU728KS Strong Genetic Variation [90]
NLN OTFRITPU Strong Altered Expression [604]
NLRP12 OTGR132Z Strong Genetic Variation [605]
NOS1AP OTDFOBRU Strong Genetic Variation [606]
NPC1 OTRIPICX Strong Genetic Variation [61]
NPPA OTMQNTNX Strong Genetic Variation [258]
NUS1 OT4DQ82L Strong Altered Expression [182]
OGN OTKP5S4L Strong Altered Expression [607]
OPN4 OT1LZ7TS Strong Altered Expression [604]
ORM2 OTRJGZP8 Strong Biomarker [11]
PAPPA OTTTG9PG Strong Genetic Variation [608]
PEAR1 OT2XLTB2 Strong Genetic Variation [609]
PHACTR1 OTAMPX9V Strong Genetic Variation [610]
PIK3C2A OTFBU4GD Strong Altered Expression [611]
PKP2 OTJOVF68 Strong Biomarker [612]
PLA2G10 OTRZ2L5A Strong Altered Expression [613]
PLA2G15 OT6VJTPA Strong Biomarker [324]
PLB1 OTZ6TTYV Strong Biomarker [614]
POC1A OTXAG4PL Strong Genetic Variation [615]
POU2F3 OTIOOJWD Strong Genetic Variation [616]
PPARGC1A OTHCDQ22 Strong Altered Expression [617]
PPIC OTY5Q42N Strong Altered Expression [618]
PQBP1 OTXCBEAH Strong Biomarker [619]
PRDM16 OT0BGA27 Strong Genetic Variation [61]
PRKAB2 OTLVN68B Strong Biomarker [620]
PRKX OTDAC6Z0 Strong Genetic Variation [195]
PROCR OTRHED17 Strong Genetic Variation [61]
PSRC1 OT7MDJMN Strong Genetic Variation [621]
RAPSN OTGMSWDQ Strong Genetic Variation [255]
RARRES2 OT1BJE8K Strong Genetic Variation [622]
RGN OTD04KB1 Strong Biomarker [619]
RGS5 OTUY0Q2I Strong Genetic Variation [623]
RLN1 OTL6QNHG Strong Altered Expression [624]
RNLS OTVP2WJM Strong Genetic Variation [625]
RRAD OTW2O4GD Strong Genetic Variation [626]
RYR2 OT0PF19E Strong Genetic Variation [555]
RYR3 OT4EHIP4 Strong Genetic Variation [627]
SCML4 OTSZJST3 Strong Genetic Variation [508]
SELENBP1 OT3NZNTR Strong Biomarker [557]
SEMA3F OTQFMS8S Strong Altered Expression [628]
SERPINB2 OT72QLZB Strong Genetic Variation [629]
SERPINE2 OTYF5340 Strong Biomarker [630]
SFRP5 OTLCVVSH Strong Altered Expression [631]
SHBG OTPWU5IW Strong Biomarker [557]
SP6 OTRAB1PN Strong Biomarker [588]
SPAAR OTWXG2R8 Strong Altered Expression [632]
SRF OTW18FQN Strong Biomarker [492]
STARD7 OTDUZ296 Strong Biomarker [183]
STN1 OT8UWRA3 Strong Genetic Variation [61]
SVEP1 OTOBICRD Strong Genetic Variation [61]
TFR2 OTMYCCEO Strong Genetic Variation [633]
THAP5 OT6ZMFYF Strong Biomarker [634]
THSD7A OT7249HH Strong Genetic Variation [508]
TMEM54 OTPQEFR0 Strong Genetic Variation [551]
TNFAIP6 OT1SLUZH Strong Biomarker [635]
TNFRSF6B OTKAN9G7 Strong Biomarker [636]
TOMM40 OTZDQ29F Strong Genetic Variation [637]
TREML4 OT2VLMTL Strong Biomarker [638]
TRIB1 OTPEO17G Strong Altered Expression [639]
TRPS1 OT7XPPEL Strong Genetic Variation [639]
AP2A2 OTD1UGUN Definitive Genetic Variation [640]
ARIH1 OTO3XDR2 Definitive Biomarker [641]
C1QTNF5 OTLKU5I2 Definitive Altered Expression [642]
CAPN3 OTCHG3YK Definitive Genetic Variation [643]
CCS OTXHT3QO Definitive Biomarker [644]
CKMT2 OT1KNPI1 Definitive Biomarker [645]
CPT1A OTI862QH Definitive Biomarker [168]
CRISPLD1 OT38HXJP Definitive Genetic Variation [646]
DEFA1 OT5N1B9B Definitive Biomarker [647]
DEFA3 OTO3N8E1 Definitive Biomarker [647]
EIF4A3 OTYYFE7K Definitive Altered Expression [648]
FADS3 OT9RVXGE Definitive Genetic Variation [649]
GDF10 OTEVXGJ7 Definitive Genetic Variation [650]
GOLGA6A OTHU9MRX Definitive Genetic Variation [213]
HABP2 OTAUIPW0 Definitive Biomarker [651]
HDLBP OTKDEEYX Definitive Biomarker [652]
HPR OTXSC9UB Definitive Genetic Variation [643]
HRG OTPLUFOG Definitive Biomarker [653]
INPP5K OTQFLQKA Definitive Biomarker [415]
INTS4 OT5JQ913 Definitive Biomarker [654]
ITSN1 OT8YF3S5 Definitive Altered Expression [655]
LRG1 OTLD0KWA Definitive Biomarker [653]
LRRC3B OT9VDGPR Definitive Biomarker [645]
MACIR OTPSW8Y8 Definitive Genetic Variation [656]
MFRP OTHY9ZA5 Definitive Altered Expression [642]
MRPS6 OTKFY73U Definitive Biomarker [657]
MTHFD2 OT1LQSGX Definitive Genetic Variation [658]
PPP4C OT4B0TNV Definitive Biomarker [306]
RASGRF2 OT67DAGF Definitive Biomarker [645]
RCBTB1 OTAYELI8 Definitive Genetic Variation [213]
RNF213 OT4OVE9O Definitive Genetic Variation [659]
RPS3A OTUEP7CL Definitive Biomarker [660]
RTCA OTSJRVTD Definitive Biomarker [661]
SELENOP OT02B8IR Definitive Altered Expression [662]
SIPA1 OTXY5RXC Definitive Biomarker [663]
SIRT4 OT5S0J23 Definitive Altered Expression [664]
SIX5 OTT1I9WY Definitive Genetic Variation [643]
SORBS3 OTVEUODC Definitive Altered Expression [665]
------------------------------------------------------------------------------------
⏷ Show the Full List of 566 DOT(s)

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34 Contribution of homeostatic chemokines CCL19 and CCL21 and their receptor CCR7 to coronary artery disease.Arterioscler Thromb Vasc Biol. 2014 Sep;34(9):1933-41. doi: 10.1161/ATVBAHA.113.303081. Epub 2014 Jul 2.
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36 Altered Expression of Complement Regulatory Proteins CD35, CD46, CD55, and CD59 on Leukocyte Subsets in Individuals Suffering From Coronary Artery Disease.Front Immunol. 2019 Aug 29;10:2072. doi: 10.3389/fimmu.2019.02072. eCollection 2019.
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38 Association of TAFI gene polymorphisms with severity of coronary stenosis in stable coronary artery disease.Thromb Res. 2018 Nov;171:171-176. doi: 10.1016/j.thromres.2018.10.001. Epub 2018 Oct 3.
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41 Cysteine Protease Cathepsins in Atherosclerotic Cardiovascular Diseases.J Atheroscler Thromb. 2018 Feb 1;25(2):111-123. doi: 10.5551/jat.RV17016. Epub 2017 Oct 5.
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44 Longitudinal associations between 4-hydroxynonenal and depression in coronary artery disease patients.Psychiatry Res. 2018 Dec;270:219-224. doi: 10.1016/j.psychres.2018.09.046. Epub 2018 Sep 21.
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48 Relation of coagulation factor XI with incident coronary heart disease and stroke: the Cardiovascular Health Study.Blood Coagul Fibrinolysis. 2017 Jul;28(5):389-392. doi: 10.1097/MBC.0000000000000616.
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50 Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls.Med Princ Pract. 2009;18(2):137-42. doi: 10.1159/000189812. Epub 2009 Feb 10.
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52 C-reactive protein-derived peptide 201-206 inhibits neutrophil adhesion to endothelial cells and platelets through CD32.J Leukoc Biol. 2011 Dec;90(6):1167-75. doi: 10.1189/jlb.0111032. Epub 2011 Sep 20.
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54 Role of tumor necrosis factor- in epithelial-to-mesenchymal transition in transplanted kidney cells in recipients with chronic allograft dysfunction.Gene. 2018 Feb 5;642:483-490. doi: 10.1016/j.gene.2017.11.059. Epub 2017 Nov 23.
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78 Lysosomal Acid Lipase in Lipid Metabolism and Beyond.Arterioscler Thromb Vasc Biol. 2019 May;39(5):850-856. doi: 10.1161/ATVBAHA.119.312136.
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80 Role of extracellular signal-regulated kinase for endothelial progenitor cell dysfunction in coronary artery disease.Basic Res Cardiol. 2009 Sep;104(5):613-20. doi: 10.1007/s00395-009-0022-6. Epub 2009 Apr 12.
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82 Extended evidence for association between the melanoma inhibitory activity 3 gene and myocardial infarction.Thromb Haemost. 2011 Apr;105(4):670-5. doi: 10.1160/TH10-10-0641. Epub 2011 Jan 25.
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85 Gene polymorphisms associated with non-alcoholic fatty liver disease and coronary artery disease: a concise review.Lipids Health Dis. 2016 Mar 10;15:53. doi: 10.1186/s12944-016-0221-8.
86 Serum Tumor Marker Carbohydrate Antigen 125 Levels and Carotid Atherosclerosis in Patients with Coronary Artery Disease.Open Med (Wars). 2018 Dec 24;13:534-538. doi: 10.1515/med-2018-0078. eCollection 2018.
87 Lack of association of interleukin-1 gene cluster polymorphisms with angiographically documented coronary artery disease: demonstration of association with hypertension in the Polish population.Arch Med Res. 2011 Jul;42(5):426-32. doi: 10.1016/j.arcmed.2011.08.002. Epub 2011 Aug 12.
88 The effect of MVK-MMAB variants, their haplotypes and GE interactions on serum lipid levels and the risk of coronary heart disease and ischemic stroke.Oncotarget. 2017 Aug 18;8(42):72801-72817. doi: 10.18632/oncotarget.20349. eCollection 2017 Sep 22.
89 Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients.PLoS One. 2011;6(9):e24123. doi: 10.1371/journal.pone.0024123. Epub 2011 Sep 7.
90 Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease.Immunol Lett. 2019 Apr;208:39-43. doi: 10.1016/j.imlet.2019.02.007. Epub 2019 Mar 19.
91 Genetics of adipose tissue biology.Prog Mol Biol Transl Sci. 2010;94:39-74. doi: 10.1016/B978-0-12-375003-7.00003-0.
92 Polymorphisms of renin-angiotensin system and natriuretic peptide receptor A genes in patients of Greek origin with a history of myocardial infarction.Angiology. 2010 Nov;61(8):737-43. doi: 10.1177/0003319710373091. Epub 2010 Jun 7.
93 Role of epicardial adipose tissue NPR-C in acute coronary syndrome.Atherosclerosis. 2019 Jul;286:79-87. doi: 10.1016/j.atherosclerosis.2019.05.010. Epub 2019 May 9.
94 Association of combined genetic variations in PPAR, PGC-1, and LXR with coronary artery disease and severity in Thai population.Atherosclerosis. 2016 May;248:140-8. doi: 10.1016/j.atherosclerosis.2016.03.005. Epub 2016 Mar 4.
95 Medications that reduce emergency hospital admissions: an overview of systematic reviews and prioritisation of treatments.BMC Med. 2018 Jul 26;16(1):115. doi: 10.1186/s12916-018-1104-9.
96 Proteome of platelets in patients with coronary artery disease.Exp Hematol. 2010 May;38(5):341-50. doi: 10.1016/j.exphem.2010.03.001. Epub 2010 Mar 11.
97 Effect of Nitroglycerin on the Performance of MR Coronary Angiography.J Magn Reson Imaging. 2017 May;45(5):1419-1428. doi: 10.1002/jmri.25483. Epub 2016 Oct 12.
98 Successful intravenous thrombolysis for ischemic stroke as a complication of coronary intervention in patients with ticagrelor pretreatment.J Clin Neurosci. 2020 Jan;71:283-286. doi: 10.1016/j.jocn.2019.10.007. Epub 2019 Oct 26.
99 Genetic variants in PCSK1 gene are associated with the risk of coronary artery disease in type 2 diabetes in a Chinese Han population: a case control study.PLoS One. 2014 Jan 28;9(1):e87168. doi: 10.1371/journal.pone.0087168. eCollection 2014.
100 PF-4var/CXCL4L1 predicts outcome in stable coronary artery disease patients with preserved left ventricular function.PLoS One. 2012;7(2):e31343. doi: 10.1371/journal.pone.0031343. Epub 2012 Feb 23.
101 Dual-reporter high-throughput screen for small-molecule in vivo inhibitors of plasminogen activator inhibitor type-1 yields a clinical lead candidate.J Biol Chem. 2019 Feb 1;294(5):1464-1477. doi: 10.1074/jbc.RA118.004885. Epub 2018 Dec 3.
102 Platelet surface expression of cyclophilin A is associated with increased mortality in patients with symptomatic coronary artery disease.J Thromb Haemost. 2020 Jan;18(1):234-242. doi: 10.1111/jth.14635. Epub 2019 Oct 20.
103 The role of PRKCH gene variants in coronary artery disease in a Chinese population.Mol Biol Rep. 2012 Feb;39(2):1777-82. doi: 10.1007/s11033-011-0918-8. Epub 2011 May 29.
104 Identifying functional modules for coronary artery disease by a prior knowledge-based approach.Gene. 2014 Mar 10;537(2):260-8. doi: 10.1016/j.gene.2013.12.049. Epub 2013 Dec 31.
105 DNA methylation GrimAge strongly predicts lifespan and healthspan.Aging (Albany NY). 2019 Jan 21;11(2):303-327. doi: 10.18632/aging.101684.
106 Genetic polymorphisms of serum amyloid A1 and coronary artery disease risk.Tissue Antigens. 2015 Mar;85(3):168-76. doi: 10.1111/tan.12516. Epub 2015 Feb 6.
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121 Association of TLR and TREM-1 gene polymorphisms with risk of coronary artery disease in a Russian population.Gene. 2014 Oct 15;550(1):101-9. doi: 10.1016/j.gene.2014.08.022. Epub 2014 Aug 13.
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130 Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease.BMC Med Genet. 2013 Mar 27;14:40. doi: 10.1186/1471-2350-14-40.
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144 Circulating TNFSF14 (Tumor Necrosis Factor Superfamily 14) Predicts Clinical Outcome in Patients With Stable Coronary Artery Disease.Arterioscler Thromb Vasc Biol. 2019 Jun;39(6):1240-1252. doi: 10.1161/ATVBAHA.118.312166.
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148 Expression of adrenomedullin in human epicardial adipose tissue: role of coronary status.Am J Physiol Endocrinol Metab. 2007 Nov;293(5):E1443-50. doi: 10.1152/ajpendo.00273.2007. Epub 2007 Sep 18.
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155 Atherogenic lipoprotein profile in families with and without history of early myocardial infarction.Physiol Res. 2001;50(1):1-8.
156 Fucosyltransferase 3 polymorphism and atherothrombotic disease in the Framingham Offspring Study.Am Heart J. 2007 Apr;153(4):636-9. doi: 10.1016/j.ahj.2006.12.015.
157 GCH1 haplotype determines vascular and plasma biopterin availability in coronary artery disease effects on vascular superoxide production and endothelial function.J Am Coll Cardiol. 2008 Jul 8;52(2):158-65. doi: 10.1016/j.jacc.2007.12.062.
158 Association analyses based on false discovery rate implicate new loci for coronary artery disease.Nat Genet. 2017 Sep;49(9):1385-1391. doi: 10.1038/ng.3913. Epub 2017 Jul 17.
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160 Increased plasma HB-EGF associated with obesity and coronary artery disease.Biochem Biophys Res Commun. 2002 Apr 5;292(3):781-6. doi: 10.1006/bbrc.2002.6720.
161 Pharmacological effects of lipid-lowering drugs recapitulate with a larger amplitude the phenotypic effects of common variants within their target genes.Pharmacogenet Genomics. 2008 Dec;18(12):1051-7. doi: 10.1097/FPC.0b013e32831270eb.
162 Association of Genetically Enhanced Lipoprotein Lipase-Mediated Lipolysis and Low-Density Lipoprotein Cholesterol-Lowering Alleles With Risk of Coronary Disease and Type 2 Diabetes.JAMA Cardiol. 2018 Oct 1;3(10):957-966. doi: 10.1001/jamacardio.2018.2866.
163 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.Nat Genet. 2018 Sep;50(9):1335-1341. doi: 10.1038/s41588-018-0184-y. Epub 2018 Aug 13.
164 A functional variant in the CARD4 gene and risk of premature coronary heart disease.Int J Immunogenet. 2006 Aug;33(4):307-11. doi: 10.1111/j.1744-313X.2006.00618.x.
165 Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.Cardiovasc Diabetol. 2018 Apr 25;17(1):61. doi: 10.1186/s12933-018-0705-0.
166 Polymorphisms in the genes encoding platelet-derived growth factor A and alpha receptor.J Mol Med (Berl). 2000;78(5):287-92. doi: 10.1007/s001090000111.
167 The association of serum prolidase activity with the presence and severity of coronary artery disease.Coron Artery Dis. 2008 Aug;19(5):319-25. doi: 10.1097/MCA.0b013e32830042ba.
168 Pro-angiogenic Role of Danqi Pill Through Activating Fatty Acids Oxidation Pathway Against Coronary Artery Disease.Front Pharmacol. 2018 Dec 4;9:1414. doi: 10.3389/fphar.2018.01414. eCollection 2018.
169 Association of the R485K polymorphism of the factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population.Clin Genet. 2000 Apr;57(4):296-303. doi: 10.1034/j.1399-0004.2000.570409.x.
170 Common polymorphisms of cyclooxygenase-2 and prostaglandin E2 receptor and increased risk for acute coronary syndrome in coronary artery disease.Thromb Haemost. 2008 Nov;100(5):893-8.
171 SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis.Mol Biol Rep. 2014 May;41(5):3369-80. doi: 10.1007/s11033-014-3199-1. Epub 2014 Feb 7.
172 PHACTR1 and SLC22A3 gene polymorphisms are associated with reduced coronary artery disease risk in the male Chinese Han population.Oncotarget. 2017 Jan 3;8(1):658-663. doi: 10.18632/oncotarget.13506.
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174 Hypoalphalipoproteinaemia and polymorphisms associated with reduced expression of the apolipoprotein A-I gene and resolution of disputed paternity in a large English family.Clin Genet. 1993 Jan;43(1):39-43. doi: 10.1111/j.1399-0004.1993.tb04424.x.
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176 Impact of salusin-alpha and -beta on human macrophage foam cell formation and coronary atherosclerosis.Circulation. 2008 Feb 5;117(5):638-48. doi: 10.1161/CIRCULATIONAHA.107.712539. Epub 2008 Jan 22.
177 Involvement of native TRPC3 proteins in ATP-dependent expression of VCAM-1 and monocyte adherence in coronary artery endothelial cells.Arterioscler Thromb Vasc Biol. 2008 Nov;28(11):2049-55. doi: 10.1161/ATVBAHA.108.175356. Epub 2008 Sep 11.
178 ABCG5/8 variants are associated with susceptibility to coronary heart disease.Mol Med Rep. 2014 Jun;9(6):2512-20. doi: 10.3892/mmr.2014.2098. Epub 2014 Apr 1.
179 AChE mRNA expression as a possible novel biomarker for the diagnosis of coronary artery disease and Alzheimer's disease, and its association with oxidative stress.Arch Physiol Biochem. 2022 Apr;128(2):352-359. doi: 10.1080/13813455.2019.1683584. Epub 2019 Nov 14.
180 Serum adenosine deaminase activity and coronary artery disease: a retrospective case-control study based on 9929 participants.Ther Adv Chronic Dis. 2019 Dec 6;10:2040622319891539. doi: 10.1177/2040622319891539. eCollection 2019.
181 Role of CD40 and ADAMTS13 in von Willebrand factor-mediated endothelial cell-platelet-monocyte interaction.Proc Natl Acad Sci U S A. 2018 Jun 12;115(24):E5556-E5565. doi: 10.1073/pnas.1801366115. Epub 2018 May 23.
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183 Association of Improvement in Fractional Flow Reserve With Outcomes, Including Symptomatic Relief, After Percutaneous Coronary Intervention.JAMA Cardiol. 2019 Apr 1;4(4):370-374. doi: 10.1001/jamacardio.2019.0175.
184 (2)-Adrenergic Receptor Gene Polymorphisms Are Associated with Cardiovascular Events But not All-Cause Mortality in Coronary Artery Disease Patients: A Meta-Analysis of Prospective Studies.Genet Test Mol Biomarkers. 2019 Feb;23(2):124-137. doi: 10.1089/gtmb.2018.0153. Epub 2019 Jan 22.
185 Association between fetuin-A and prognosis of CAD: A systematic review and meta-analysis.Eur J Clin Invest. 2019 May;49(5):e13091. doi: 10.1111/eci.13091. Epub 2019 Mar 12.
186 Interaction between ALOX15 polymorphisms and coronary artery disease in North Indian population.Clin Exp Hypertens. 2018;40(4):398-405. doi: 10.1080/10641963.2017.1384485. Epub 2017 Oct 25.
187 Homoarginine Supplementation Prevents Left Ventricular Dilatation and Preserves Systolic Function in a Model of Coronary Artery Disease.J Am Heart Assoc. 2019 Jul 16;8(14):e012486. doi: 10.1161/JAHA.119.012486. Epub 2019 Jul 15.
188 Cystatin C-Adiponectin Complex in Plasma Associates with Coronary Plaque Instability.J Atheroscler Thromb. 2017 Sep 1;24(9):970-979. doi: 10.5551/jat.39545. Epub 2017 Mar 17.
189 Inhibition of semicarbazide-sensitive amine oxidase reduces atherosclerosis in apolipoprotein E-deficient mice.Transl Res. 2018 Jul;197:12-31. doi: 10.1016/j.trsl.2018.03.001. Epub 2018 Mar 27.
190 Serum levels of chemerin, apelin, vaspin, and omentin-1 in obese type 2 diabetic Egyptian patients with coronary artery stenosis.Can J Physiol Pharmacol. 2018 Jan;96(1):38-44. doi: 10.1139/cjpp-2017-0272. Epub 2017 Sep 28.
191 Association of polymorphisms of leptin, leptin receptor and apelin receptor genes with susceptibility to coronary artery disease and hypertension.Life Sci. 2018 Aug 15;207:166-171. doi: 10.1016/j.lfs.2018.06.007. Epub 2018 Jun 6.
192 Glycated Apolipoprotein A-IV Induces Atherogenesis in Patients With CAD inType 2 Diabetes.J Am Coll Cardiol. 2017 Oct 17;70(16):2006-2019. doi: 10.1016/j.jacc.2017.08.053.
193 Relationship of lipoprotein-associated apolipoprotein C-III with lipid variables and coronary artery disease risk: The EPIC-Norfolk prospective population study.J Clin Lipidol. 2018 Nov-Dec;12(6):1493-1501.e11. doi: 10.1016/j.jacl.2018.08.010. Epub 2018 Aug 29.
194 Arginase-1 Variants and the Risk of Familial Coronary Artery Disease in Subjects Originating from Pakistan.Genet Test Mol Biomarkers. 2019 Jan;23(1):32-38. doi: 10.1089/gtmb.2018.0227. Epub 2018 Dec 8.
195 Screening hub genes in coronary artery disease based on integrated analysis.Cardiol J. 2018;25(3):403-411. doi: 10.5603/CJ.a2017.0106. Epub 2017 Oct 5.
196 ASGR1 but not FOXM1 expression decreases in the peripheral blood mononuclear cells of diabetic atherosclerotic patients.J Diabetes Complications. 2019 Aug;33(8):539-546. doi: 10.1016/j.jdiacomp.2019.05.008. Epub 2019 May 17.
197 Effect of intensive lipid-lowering therapies on cholinesterase activity in patients with coronary artery disease.Pharmacol Rep. 2017 Feb;69(1):150-155. doi: 10.1016/j.pharep.2016.09.016. Epub 2016 Sep 21.
198 Bradykinin receptors gene expression in white adipose tissue in nondiabetic patients with coronary artery disease.Coron Artery Dis. 2018 Jun;29(4):329-335. doi: 10.1097/MCA.0000000000000604.
199 CACNA1C gene polymorphisms, cardiovascular disease outcomes, and treatment response. Circ Cardiovasc Genet. 2009 Aug;2(4):362-70. doi: 10.1161/CIRCGENETICS.109.857839. Epub 2009 Jun 3.
200 Association of Cyr61-cysteine-rich protein 61 and short-term mortality in patients with acute heart failure and coronary heart disease.Biomark Med. 2019 Dec;13(18):1589-1597. doi: 10.2217/bmm-2019-0111. Epub 2019 Oct 29.
201 Polymorphism in the chemokine receptor 7 gene (CCR7) is associated with previous myocardial infarction in patients undergoing elective coronary angiography.Int J Immunogenet. 2016 Aug;43(4):218-25. doi: 10.1111/iji.12270. Epub 2016 Jun 17.
202 Functional association of a CD40 gene single-nucleotide polymorphism with the pathogenesis of coronary heart disease.Cardiovasc Res. 2020 May 1;116(6):1214-1225. doi: 10.1093/cvr/cvz206.
203 Value analysis of CD69 combined with EGR1 in the diagnosis of coronary heart disease.Exp Ther Med. 2019 Mar;17(3):2047-2052. doi: 10.3892/etm.2019.7175. Epub 2019 Jan 15.
204 Mast cell derived carboxypeptidase A3 is decreased among patients with advanced coronary artery disease.Cardiol J. 2019;26(6):680-686. doi: 10.5603/CJ.a2018.0018. Epub 2018 Mar 7.
205 Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease.Cytokine. 2019 Oct;122:154060. doi: 10.1016/j.cyto.2017.05.013. Epub 2017 Jul 10.
206 CYP17A1 Polymorphisms Are Linked to the Risk of Coronary Heart Disease in a Case-Control Study.J Cardiovasc Pharmacol. 2019 Aug;74(2):98-104. doi: 10.1097/FJC.0000000000000687.
207 Relationship of Genetic Polymorphisms of Aldosterone Synthase Gene Cytochrome P450 11B2 and Mineralocorticoid Receptors with Coronary Artery Disease in Taiwan.Int J Med Sci. 2016 Feb 1;13(2):117-23. doi: 10.7150/ijms.13862. eCollection 2016.
208 Polymorphisms of CYP2C8, CYP2C9 and CYP2C19 and risk of coronary heart disease in Russian population.Gene. 2017 Sep 5;627:451-459. doi: 10.1016/j.gene.2017.07.004. Epub 2017 Jul 4.
209 Plasma miR-142 accounting for the missing heritability of CYP3A4/5 functionality is associated with pharmacokinetics of clopidogrel.Pharmacogenomics. 2016 Sep;17(14):1503-17. doi: 10.2217/pgs-2016-0027. Epub 2016 Aug 24.
210 Expression pattern of miR-21, miR-25 and PTEN in peripheral blood mononuclear cells of patients with significant or insignificant coronary stenosis.Gene. 2019 May 25;698:170-178. doi: 10.1016/j.gene.2019.02.074. Epub 2019 Mar 6.
211 Deiodinases, Organic Anion Transporter Polypeptide Polymorphisms, and Thyroid Hormones in Patients with Myocardial Infarction.Genet Test Mol Biomarkers. 2018 Apr;22(4):270-278. doi: 10.1089/gtmb.2017.0283. Epub 2018 Mar 20.
212 C-338A polymorphism of the endothelin-converting enzyme (ECE-1) gene and the susceptibility to sporadic late-onset Alzheimer's disease and coronary artery disease.Dis Markers. 2008;24(3):175-9. doi: 10.1155/2008/578304.
213 Polymorphisms in the Glucagon-Like Peptide 1 Receptor (GLP-1R) Gene Are Associated with the Risk of Coronary Artery Disease in Chinese Han Patients with Type 2 Diabetes Mellitus: A Case-Control Study.J Diabetes Res. 2018 Sep 9;2018:1054192. doi: 10.1155/2018/1054192. eCollection 2018.
214 Efficacy and safety of adding rivaroxaban to the anti-platelet regimen in patients with coronary artery disease: a systematic review and meta-analysis of randomized controlled trials.BMC Pharmacol Toxicol. 2018 May 2;19(1):19. doi: 10.1186/s40360-018-0209-2.
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216 Correlation of hypertension and F2RL3 gene methylation with Prognosis of coronary heart disease.J Biol Regul Homeost Agents. 2018 Nov-Dec;32(6):1539-1544.
217 Identification of a new adtrp1-tfpi regulatory axis for the specification of primitive myelopoiesis and definitive hematopoiesis.FASEB J. 2018 Jan;32(1):183-194. doi: 10.1096/fj.201700166RR. Epub 2017 Sep 6.
218 Contribution of coagulation factor VII R353Q, -323P0/10 and HVR4 polymorphisms to coronary artery disease in Tunisians.J Thromb Thrombolysis. 2013 Feb;35(2):243-9. doi: 10.1007/s11239-012-0800-0.
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220 Role of activating FcR gene polymorphisms in Kawasaki disease susceptibility and intravenous immunoglobulin response.Circ Cardiovasc Genet. 2012 Jun;5(3):309-16. doi: 10.1161/CIRCGENETICS.111.962464. Epub 2012 May 7.
221 Impact of Mon2 monocyte-platelet aggregates on human coronary artery disease.Eur J Clin Invest. 2018 May;48(5):e12911. doi: 10.1111/eci.12911. Epub 2018 Mar 7.
222 Fibroblast growth factor 21 in cardio-metabolic disorders: a systematic review and meta-analysis.Metabolism. 2018 Jun;83:11-17. doi: 10.1016/j.metabol.2018.01.017. Epub 2018 Feb 2.
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224 MADD-FOLH1 Polymorphisms and Their Haplotypes with Serum Lipid Levels and the Risk of Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population.Nutrients. 2016 Apr 8;8(4):208. doi: 10.3390/nu8040208.
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226 Potential relation between soluble growth differentiation factor-15 and testosterone deficiency in male patients with coronary artery disease.Cardiovasc Diabetol. 2019 Feb 28;18(1):21. doi: 10.1186/s12933-019-0823-3.
227 Association of circulating BMP9 with coronary heart disease and hypertension in Chinese populations.BMC Cardiovasc Disord. 2019 May 30;19(1):131. doi: 10.1186/s12872-019-1095-2.
228 Association between polymorphisms of platelet membrane glycoprotein Ib and risk of coronary heart disease in Han Chinese, Henan, China.Int J Clin Exp Pathol. 2015 May 1;8(5):6005-11. eCollection 2015.
229 Association between Polymorphisms of Antioxidant Gene (MnSOD, CAT, and GPx1) and Risk of Coronary Artery Disease.Biomed Res Int. 2018 Aug 26;2018:5086869. doi: 10.1155/2018/5086869. eCollection 2018.
230 Platelets as a novel source of Gremlin-1: Implications for thromboinflammation.Thromb Haemost. 2017 Jan 26;117(2):311-324. doi: 10.1160/TH16-08-0665. Epub 2016 Dec 8.
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232 Upregulation of microRNA-218 reduces cardiac microvascular endothelial cells injury induced by coronary artery disease through the inhibition of HMGB1.J Cell Physiol. 2020 Mar;235(3):3079-3095. doi: 10.1002/jcp.29214. Epub 2019 Sep 30.
233 Genetic susceptibility of glutathione S-transferase genes (GSTM1/T1 and P1) to coronary artery disease in Asian Indians.Ann Hum Genet. 2018 Nov;82(6):448-456. doi: 10.1111/ahg.12274. Epub 2018 Jul 24.
234 Serum Heparanase Level Is Decreased in Stable Coronary Artery Disease.Med Princ Pract. 2019;28(6):573-580. doi: 10.1159/000503085. Epub 2019 Sep 4.
235 Salivary IgA to MAA-LDL and Oral Pathogens Are Linked to Coronary Disease.J Dent Res. 2019 Mar;98(3):296-303. doi: 10.1177/0022034518818445. Epub 2019 Jan 22.
236 Diagnosis of Microvascular Angina Using Cardiac Magnetic Resonance.J Am Coll Cardiol. 2018 Mar 6;71(9):969-979. doi: 10.1016/j.jacc.2017.12.046.
237 Interleukin-33 levels are elevated in chronic allograft dysfunction of kidney transplant recipients and promotes epithelial to mesenchymal transition of human kidney (HK-2) cells.Gene. 2018 Feb 20;644:113-121. doi: 10.1016/j.gene.2017.11.010. Epub 2017 Nov 6.
238 Association between new circulating proinflammatory and anti-inflammatory adipocytokines with coronary artery disease.Coron Artery Dis. 2019 Nov;30(7):528-535. doi: 10.1097/MCA.0000000000000778.
239 MicroRNA-128 confers protection against cardiac microvascular endothelial cell injury in coronary heart disease via negative regulation of IRS1.J Cell Physiol. 2019 Aug;234(8):13452-13463. doi: 10.1002/jcp.28025. Epub 2019 Jan 30.
240 Histone demethylase KDM3a, a novel regulator of vascular smooth muscle cells, controls vascular neointimal hyperplasia in diabetic rats.Atherosclerosis. 2017 Feb;257:152-163. doi: 10.1016/j.atherosclerosis.2016.12.007. Epub 2016 Dec 9.
241 Prospective study of plasma high molecular weight kininogen and prekallikrein and incidence of coronary heart disease, ischemic stroke and heart failure.Thromb Res. 2019 Oct;182:89-94. doi: 10.1016/j.thromres.2019.08.009. Epub 2019 Aug 22.
242 Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing.Gene. 2019 Dec 30;721:144107. doi: 10.1016/j.gene.2019.144107. Epub 2019 Sep 6.
243 Associations of leptin and leptin receptor genetic variants with coronary artery disease: a meta-analysis.Biosci Rep. 2019 Jun 10;39(6):BSR20190466. doi: 10.1042/BSR20190466. Print 2019 Jun 28.
244 Galectin-2 induces a proinflammatory, anti-arteriogenic phenotype in monocytes and macrophages.PLoS One. 2015 Apr 17;10(4):e0124347. doi: 10.1371/journal.pone.0124347. eCollection 2015.
245 Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.Nat Genet. 2017 Sep;49(9):1392-1397. doi: 10.1038/ng.3914. Epub 2017 Jul 17.
246 PAR-1 genotype influences platelet aggregation and procoagulant responses in patients with coronary artery disease prior to and during clopidogrel therapy. Platelets. 2005 Sep;16(6):340-5. doi: 10.1080/00207230500120294.
247 Mannose binding lectin 2 haplotypes do not affect the progression of coronary atherosclerosis in men with proven coronary artery disease treated with pravastatin.Atherosclerosis. 2011 Mar;215(1):125-9. doi: 10.1016/j.atherosclerosis.2010.11.041. Epub 2010 Dec 8.
248 Human Gain-of-Function MC4R Variants Show Signaling Bias and Protect against Obesity.Cell. 2019 Apr 18;177(3):597-607.e9. doi: 10.1016/j.cell.2019.03.044.
249 Regulation of MFGE8 by the intergenic coronary artery disease locus on 15q26.1.Atherosclerosis. 2019 May;284:11-17. doi: 10.1016/j.atherosclerosis.2019.02.012. Epub 2019 Feb 22.
250 Effect of Sitagliptin on Coronary Flow Reserve Assessed by Magnetic Resonance Imaging in Type 2 Diabetic Patients With Coronary Artery Disease.Circ J. 2018 Jul 25;82(8):2119-2127. doi: 10.1253/circj.CJ-18-0083. Epub 2018 May 12.
251 Expression of matrix metalloproteinase-12 in aortic dissection.BMC Cardiovasc Disord. 2013 May 3;13:34. doi: 10.1186/1471-2261-13-34.
252 Analysis of MMP-7 and TIMP-2 gene polymorphisms in coronary artery disease and myocardial infarction: A Turkish case-control study.Kaohsiung J Med Sci. 2017 Feb;33(2):78-85. doi: 10.1016/j.kjms.2016.12.002. Epub 2017 Jan 12.
253 Matrix metalloproteinase-8 and tissue inhibitor of matrix metalloproteinase-1 predict incident cardiovascular disease events and all-cause mortality in a population-based cohort.Eur J Prev Cardiol. 2017 Jul;24(11):1136-1144. doi: 10.1177/2047487317706585. Epub 2017 Apr 21.
254 Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients.Clin Chem Lab Med. 2008;46(10):1364-8. doi: 10.1515/CCLM.2008.306.
255 -5 Fatty Acid Desaturase FADS1 Impacts Metabolic Disease by Balancing Proinflammatory and Proresolving Lipid Mediators.Arterioscler Thromb Vasc Biol. 2018 Jan;38(1):218-231. doi: 10.1161/ATVBAHA.117.309660. Epub 2017 Oct 26.
256 The mRNA Expression and Circulating Levels of Visfatin and Their Correlation with Coronary Artery Disease Severity and 25-Hydroxyvitamin D.Horm Metab Res. 2016 Apr;48(4):269-74. doi: 10.1055/s-0035-1564133. Epub 2015 Oct 14.
257 Mechanisms of Niemann-Pick type C1 Like 1 protein degradation in intestinal epithelial cells.Am J Physiol Cell Physiol. 2019 Apr 1;316(4):C559-C566. doi: 10.1152/ajpcell.00465.2018. Epub 2019 Feb 21.
258 Association of natriuretic peptide polymorphisms with left ventricular dysfunction in southern Han Chinese coronary artery disease patients.Int J Clin Exp Pathol. 2014 Sep 15;7(10):7148-57. eCollection 2014.
259 Association of Circulating Neuregulin-4 with Presence and Severity of Coronary Artery Disease.Int Heart J. 2019 Jan 25;60(1):45-49. doi: 10.1536/ihj.18-130. Epub 2018 Nov 5.
260 Low-dose daily aspirin reduces topical minoxidil efficacy in androgenetic alopecia patients.Dermatol Ther. 2018 Nov;31(6):e12741. doi: 10.1111/dth.12741. Epub 2018 Oct 8.
261 Clopidogrel resistance in North Indian patients of coronary artery disease and lack of its association with platelet ADP receptors P2Y1 and P2Y12 gene polymorphisms.Platelets. 2013;24(4):297-302. doi: 10.3109/09537104.2012.693992. Epub 2012 Jun 21.
262 Serum PCSK6 and corin levels are not associated with cardiovascular outcomes in patients undergoing coronary angiography.PLoS One. 2019 Dec 11;14(12):e0226129. doi: 10.1371/journal.pone.0226129. eCollection 2019.
263 Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.Nat Commun. 2018 Apr 24;9(1):1613. doi: 10.1038/s41467-018-03911-8.
264 PDE4D gene polymorphisms and coronary heart disease: a case-control study in a north Indian population.J Clin Lab Anal. 2013 Jul;27(4):297-300. doi: 10.1002/jcla.21601.
265 A genome-wide association study of a coronary artery disease risk variant.J Hum Genet. 2013 Mar;58(3):120-6. doi: 10.1038/jhg.2012.124. Epub 2013 Jan 31.
266 Increased phospholipid transfer protein activity associated with the impaired cellular cholesterol efflux in type 2 diabetic subjects with coronary artery disease.Tohoku J Exp Med. 2007 Oct;213(2):129-37. doi: 10.1620/tjem.213.129.
267 Nrf2, NF-B and PPAR/ mRNA Expression Profile in Patients with Coronary Artery Disease.Arq Bras Cardiol. 2019 Dec;113(6):1121-1127. doi: 10.5935/abc.20190125.
268 Predicting significance of COX-2 expression of peripheral blood monocyte in patients with coronary artery disease.Ann Transl Med. 2019 Sep;7(18):483. doi: 10.21037/atm.2019.08.75.
269 Serum Parathyroid Hormone and Risk of Coronary Artery Disease: Exploring Causality Using Mendelian Randomization.J Clin Endocrinol Metab. 2019 Nov 1;104(11):5595-5600. doi: 10.1210/jc.2019-01063.
270 Novel Biomarkers for Coronary Restenosis Occurrence After Drug-Eluting Stent Implantation in Patients With Diabetes Having Stable Coronary Artery Disease.Clin Appl Thromb Hemost. 2018 Nov;24(8):1308-1314. doi: 10.1177/1076029618771752. Epub 2018 May 1.
271 S100 proteins in atherosclerosis.Clin Chim Acta. 2020 Mar;502:293-304. doi: 10.1016/j.cca.2019.11.019. Epub 2019 Nov 30.
272 NCF2, MYO1F, S1PR4, and FCN1 as potential noninvasive diagnostic biomarkers in patients with obstructive coronary artery: A weighted gene co-expression network analysis.J Cell Biochem. 2019 Oct;120(10):18219-18235. doi: 10.1002/jcb.29128. Epub 2019 Jun 27.
273 Correlation Between Pigment Epithelium-Derived Factor (PEDF) level and Degree of Coronary Angiography and Severity of Coronary Artery Disease in a Chinese Population.Med Sci Monit. 2018 Mar 25;24:1751-1758. doi: 10.12659/msm.908534.
274 Are SGLT2 polymorphisms linked to diabetes mellitus and cardiovascular disease? Prospective study and meta-analysis.Biosci Rep. 2019 Aug 7;39(8):BSR20190299. doi: 10.1042/BSR20190299. Print 2019 Aug 30.
275 Role of sortilin in lipid metabolism.Curr Opin Lipidol. 2019 Jun;30(3):198-204. doi: 10.1097/MOL.0000000000000598.
276 Down-regulated of SREBP-1 in circulating leukocyte is a risk factor for atherosclerosis: a case control study.Lipids Health Dis. 2019 Oct 14;18(1):177. doi: 10.1186/s12944-019-1125-1.
277 Expression of Sterol Regulatory Element-Binding Proteins in epicardial adipose tissue in patients with coronary artery disease and diabetes mellitus: preliminary study.Int J Med Sci. 2017 Feb 23;14(3):268-274. doi: 10.7150/ijms.17821. eCollection 2017.
278 Expression of telomere repeat binding factor 1 and TRF2 in Alzheimer's disease and correlation with clinical parameters.Neurol Res. 2019 Jun;41(6):504-509. doi: 10.1080/01616412.2019.1580456. Epub 2019 Feb 14.
279 Potential associations of testosterone/estradiol ratio, leukocyte hTERT expression and PBMC telomerase activity with aging and the presence of coronary artery disease in men.Exp Gerontol. 2019 Mar;117:38-44. doi: 10.1016/j.exger.2018.08.008. Epub 2018 Sep 1.
280 Significant genetic association of a functional TFPI variant with circulating fibrinogen levels and coronary artery disease.Mol Genet Genomics. 2018 Feb;293(1):119-128. doi: 10.1007/s00438-017-1365-6. Epub 2017 Sep 11.
281 Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis.Thromb Res. 2015 Jul;136(1):45-51. doi: 10.1016/j.thromres.2015.04.019. Epub 2015 Apr 23.
282 T4 Increases Neovascularization and Cardiac Function in Chronic Myocardial Ischemia of Normo- and Hypercholesterolemic Pigs.Mol Ther. 2018 Jul 5;26(7):1706-1714. doi: 10.1016/j.ymthe.2018.06.004. Epub 2018 Jun 19.
283 10-Year Associations Between Tumor Necrosis Factor Receptors 1 and 2 and Cardiovascular Events in Patients With Stable Coronary Heart Disease: A CLARICOR (Effect of Clarithromycin on Mortality and Morbidity in Patients With Ischemic Heart Disease) Trial Substudy.J Am Heart Assoc. 2018 Apr 23;7(9):e008299. doi: 10.1161/JAHA.117.008299.
284 Tumour necrosis factor like cytokine 1A levels and lesion complexity in non-smoking patients with coronary artery disease.Biomarkers. 2019 Dec;24(8):764-770. doi: 10.1080/1354750X.2019.1685004. Epub 2019 Nov 5.
285 Free fatty acids as a marker for predicting periprocedural myocardial injury after coronary intervention.Postgrad Med J. 2019 Jan;95(1119):18-22. doi: 10.1136/postgradmedj-2018-136137. Epub 2019 Jan 30.
286 miR-146a polymorphism influences levels of miR-146a, IRAK-1, and TRAF-6 in young patients with coronary artery disease.Cell Biochem Biophys. 2014 Mar;68(2):259-66. doi: 10.1007/s12013-013-9704-7.
287 Urotensin-II and cardiovascular remodeling.Peptides. 2008 May;29(5):764-9. doi: 10.1016/j.peptides.2007.09.012. Epub 2007 Sep 29.
288 Antibodies against HDL Components in Ischaemic Stroke and Coronary Artery Disease.Thromb Haemost. 2018 Jun;118(6):1088-1100. doi: 10.1055/s-0038-1645857. Epub 2018 May 3.
289 A novel circRNA-miRNA-mRNA network identifies circ-YOD1 as a biomarker for coronary artery disease.Sci Rep. 2019 Dec 4;9(1):18314. doi: 10.1038/s41598-019-54603-2.
290 Familial hypercholesterolemia screening program in Bosnia and Herzegovina and cardiovascular morbidity.Atherosclerosis. 2018 Oct;277:278-281. doi: 10.1016/j.atherosclerosis.2018.06.880.
291 -Phthalimidoalkyl Aryl Ureas as Potent and Selective Inhibitors of Cholesterol Esterase.ChemMedChem. 2018 Sep 6;13(17):1833-1847. doi: 10.1002/cmdc.201800388. Epub 2018 Aug 13.
292 Haemodynamic assessment of human coronary arteries is affected by degree of freedom of artery movement.Comput Methods Biomech Biomed Engin. 2017 Feb;20(3):260-272. doi: 10.1080/10255842.2016.1215439. Epub 2016 Jul 28.
293 Genetic Regulation of the Thymic Stromal Lymphopoietin (TSLP)/TSLP Receptor (TSLPR) Gene Expression and Influence of Epistatic Interactions Between IL-33 and the TSLP/TSLPR Axis on Risk of Coronary Artery Disease.Front Immunol. 2018 Aug 3;9:1775. doi: 10.3389/fimmu.2018.01775. eCollection 2018.
294 Altered human neutrophil FcRI and FcRIII but not FcRII expression is associated with the acute coronary event in patients with coronary artery disease.Coron Artery Dis. 2017 Jan;28(1):63-69. doi: 10.1097/MCA.0000000000000425.
295 Age-Biomarkers-Clinical Risk Factors for Prediction of Cardiovascular Events in Patients With Coronary Artery Disease.Arterioscler Thromb Vasc Biol. 2018 Oct;38(10):2519-2527. doi: 10.1161/ATVBAHA.118.311726.
296 Association of Serum HMGB2 Levels With In-Stent Restenosis: HMGB2 Promotes Neointimal Hyperplasia in Mice With Femoral Artery Injury and Proliferation and Migration of VSMCs.Arterioscler Thromb Vasc Biol. 2017 Apr;37(4):717-729. doi: 10.1161/ATVBAHA.116.308210. Epub 2017 Feb 9.
297 Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation.Int J Cardiol. 2018 Sep 15;267:171-176. doi: 10.1016/j.ijcard.2018.05.051. Epub 2018 May 18.
298 Oxidative stress predicts depressive symptom changes with omega-3 fatty acid treatment in coronary artery disease patients.Brain Behav Immun. 2017 Feb;60:136-141. doi: 10.1016/j.bbi.2016.10.005. Epub 2016 Oct 11.
299 Meta-Analysis Comparing Outcomes of Drug Eluting Stents Versus Single and Multiarterial Coronary Artery Bypass Grafting.Am J Cardiol. 2018 Dec 15;122(12):2018-2025. doi: 10.1016/j.amjcard.2018.09.005. Epub 2018 Sep 13.
300 The relationship between insulin resistance, adiponectin and C-reactive protein and vascular endothelial injury in diabetic patients with coronary heart disease.Exp Ther Med. 2018 Sep;16(3):2022-2026. doi: 10.3892/etm.2018.6407. Epub 2018 Jul 4.
301 Association of platelet-activating factor receptor gene rs5938 (G/T) and rs313152 (T/C) polymorphisms with coronary heart disease and blood stasis syndrome in a Chinese Han population.Chin J Integr Med. 2017 Dec;23(12):893-900. doi: 10.1007/s11655-017-2802-4. Epub 2017 Feb 15.
302 RRM1, RRM2 and ERCC2 Gene Polymorphisms in Coronary Artery Disease.In Vivo. 2016 09-10;30(5):611-5.
303 Novel epigenetic-sensitive clinical challenges both in type 1 and type 2 diabetes.J Diabetes Complications. 2018 Nov;32(11):1076-1084. doi: 10.1016/j.jdiacomp.2018.08.012. Epub 2018 Aug 19.
304 Functional genetic variants in the SIRT5 gene promoter in acute myocardial infarction.Gene. 2018 Oct 30;675:233-239. doi: 10.1016/j.gene.2018.07.010. Epub 2018 Jul 4.
305 B Cell-Activating Factor Neutralization Aggravates Atherosclerosis.Circulation. 2018 Nov 13;138(20):2263-2273. doi: 10.1161/CIRCULATIONAHA.117.032790.
306 Integrative analysis of promising molecular biomarkers and pathways for coronary artery disease using WGCNA and MetaDE methods.Mol Med Rep. 2018 Sep;18(3):2789-2797. doi: 10.3892/mmr.2018.9277. Epub 2018 Jul 16.
307 ABCA1 impacts athero-thrombotic risk and 10-year survival in a contemporary secondary prevention setting.Atherosclerosis. 2011 Oct;218(2):457-63. doi: 10.1016/j.atherosclerosis.2011.07.008. Epub 2011 Jul 20.
308 Association of ATP2B1 common variants with asymptomatic intracranial and extracranial large artery stenosis in hypertension patients.Clin Exp Hypertens. 2019;41(4):323-329. doi: 10.1080/10641963.2018.1481421. Epub 2018 Jun 14.
309 Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study.PLoS One. 2008 Apr 9;3(4):e1948. doi: 10.1371/journal.pone.0001948.
310 Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases.PLoS Genet. 2011 Mar;7(3):e1001338. doi: 10.1371/journal.pgen.1001338. Epub 2011 Mar 17.
311 Atorvastatin counteracts aberrant soft tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6??.J Mol Med (Berl). 2013 Oct;91(10):1177-84. doi: 10.1007/s00109-013-1066-5. Epub 2013 Jun 27.
312 Decreased circulating catestatin levels are associated with coronary artery disease: The emerging anti-inflammatory role.Atherosclerosis. 2019 Feb;281:78-88. doi: 10.1016/j.atherosclerosis.2018.12.025. Epub 2018 Dec 24.
313 Glutathione Transferase P1 Polymorphism Might Be a Risk Determinant in Heart Failure.Dis Markers. 2019 Jun 2;2019:6984845. doi: 10.1155/2019/6984845. eCollection 2019.
314 Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.BMJ. 2014 Jul 10;349:g4164. doi: 10.1136/bmj.g4164.
315 Synergistic association between two alcohol metabolism relevant genes and coronary artery disease among Chinese hypertensive patients.PLoS One. 2014 Jul 21;9(7):e103161. doi: 10.1371/journal.pone.0103161. eCollection 2014.
316 Mutation in CYP27A1 identified in family with coronary artery disease.Eur J Med Genet. 2013 Dec;56(12):655-60. doi: 10.1016/j.ejmg.2013.09.008. Epub 2013 Sep 28.
317 The roles of cytochrome p450 in ischemic heart disease.Curr Drug Metab. 2011 Jul;12(6):526-32. doi: 10.2174/138920011795713715.
318 Triangular relationship between single nucleotide polymorphisms in the CYP2R1 gene (rs10741657 and rs12794714), 25-hydroxyvitamin d levels, and coronary artery disease incidence.Biomarkers. 2014 Sep;19(6):488-92. doi: 10.3109/1354750X.2014.939226. Epub 2014 Jul 8.
319 A Novel Polymorphism in the Promoter of the CYP4A11 Gene Is Associated with Susceptibility to Coronary Artery Disease.Dis Markers. 2018 Feb 1;2018:5812802. doi: 10.1155/2018/5812802. eCollection 2018.
320 AGXT2 and DDAH-1 genetic variants are highly correlated with serum ADMA and SDMA levels and with incidence of coronary artery disease in Egyptians.Mol Biol Rep. 2018 Dec;45(6):2411-2419. doi: 10.1007/s11033-018-4407-1. Epub 2018 Oct 3.
321 Methionine sulfoxide reductase A rs10903323 G/A polymorphism is associated with increased risk of coronary artery disease in a Chinese population.Clin Biochem. 2013 Nov;46(16-17):1668-72. doi: 10.1016/j.clinbiochem.2013.07.011. Epub 2013 Jul 21.
322 Metallothionein 2A genetic polymorphism and its correlation to coronary heart disease.Eur Rev Med Pharmacol Sci. 2014;18(24):3747-53.
323 3D-speckle tracking echocardiography for assessment of coronary artery disease severity in stable angina pectoris.Echocardiography. 2019 Feb;36(2):320-327. doi: 10.1111/echo.14214. Epub 2018 Dec 4.
324 Predictive value of global and territorial longitudinal strain imaging in detecting significant coronary artery disease in patients with myocardial infarction without persistent ST-segment elevation.Echocardiography. 2019 Mar;36(3):512-520. doi: 10.1111/echo.14275. Epub 2019 Feb 25.
325 Genetic variation of alcohol dehydrogenase type 1C (ADH1C), alcohol consumption, and metabolic cardiovascular risk factors: results from the IMMIDIET study.Atherosclerosis. 2009 Nov;207(1):284-90. doi: 10.1016/j.atherosclerosis.2009.04.022. Epub 2009 Apr 24.
326 Alcohol dehydrogenase type 1C (ADH1C) variants, alcohol consumption traits, HDL-cholesterol and risk of coronary heart disease in women and men: British Women's Heart and Health Study and Caerphilly cohorts.Atherosclerosis. 2008 Feb;196(2):871-8. doi: 10.1016/j.atherosclerosis.2007.02.002. Epub 2007 Mar 26.
327 Low, borderline and normal ankle-brachial index as a predictor of incidents outcomes in the Mediterranean based-population ARTPER cohort after 9 years follow-up.PLoS One. 2019 Jan 23;14(1):e0209163. doi: 10.1371/journal.pone.0209163. eCollection 2019.
328 Interactions Between Regulatory Variants in CYP7A1 (Cholesterol 7-Hydroxylase) Promoter and Enhancer Regions Regulate CYP7A1 Expression.Circ Genom Precis Med. 2018 Oct;11(10):e002082. doi: 10.1161/CIRCGEN.118.002082.
329 Effect of polymorphisms in the NADSYN1/DHCR7 locus (rs12785878 and rs1790349) on plasma 25-hydroxyvitamin D levels and coronary artery disease incidence.J Nutrigenet Nutrigenomics. 2013;6(6):327-35. doi: 10.1159/000360422. Epub 2014 Mar 15.
330 Lipid Hydrolase Enzymes: Pragmatic Prolongevity Targets for Improved Human Healthspan?.Rejuvenation Res. 2020 Apr;23(2):107-121. doi: 10.1089/rej.2019.2211. Epub 2019 Oct 8.
331 Coronary microvascular dysfunction in patients with stable coronary artery disease: The CE-MARC 2 coronary physiology sub-study.Int J Cardiol. 2018 Sep 1;266:7-14. doi: 10.1016/j.ijcard.2018.04.061. Epub 2018 Apr 19.
332 Association of N-acetyltransferase-2 polymorphism with an increased risk of coronary heart disease in a Chinese population.Genet Mol Res. 2016 Mar 4;15(1):15016954. doi: 10.4238/gmr.15016954.
333 Serum N(1)-methylnicotinamide is Associated with Left Ventricular Systolic Dysfunction in Chinese.Sci Rep. 2018 Jun 5;8(1):8581. doi: 10.1038/s41598-018-26956-7.
334 Paraoxonase 3: Structure and Its Role in Pathophysiology of Coronary Artery Disease.Biomolecules. 2019 Dec 3;9(12):817. doi: 10.3390/biom9120817.
335 Serum Tartrate-resistant Acid Phosphatase-5b Levels are Associated with the Severity and Extent of Coronary Atherosclerosis in Patients with Coronary Artery Disease.J Atheroscler Thromb. 2017 Oct 1;24(10):1058-1068. doi: 10.5551/jat.39339. Epub 2017 Apr 19.
336 Regulation of Abro1/KIAA0157 during myocardial infarction and cell death reveals a novel cardioprotective mechanism for Lys63-specific deubiquitination.J Mol Cell Cardiol. 2011 Apr;50(4):652-61. doi: 10.1016/j.yjmcc.2010.12.015. Epub 2010 Dec 30.
337 Nonobstructive Coronary Artery Disease by Coronary CT Angiography ImprovesRisk Stratification and Allocationof StatinTherapy.JACC Cardiovasc Imaging. 2017 Sep;10(9):1031-1038. doi: 10.1016/j.jcmg.2016.10.022. Epub 2017 Mar 15.
338 Genetic variation associated with circulating monocyte count in the eMERGE Network.Hum Mol Genet. 2013 May 15;22(10):2119-27. doi: 10.1093/hmg/ddt010. Epub 2013 Jan 12.
339 Whole-exome sequencing in individuals with multiple cardiovascular risk factors and normal coronary arteries.Coron Artery Dis. 2016 Jun;27(4):257-66. doi: 10.1097/MCA.0000000000000357.
340 Adenosine-to-inosine RNA editing controls cathepsin S expression in atherosclerosis by enabling HuR-mediated post-transcriptional regulation.Nat Med. 2016 Oct;22(10):1140-1150. doi: 10.1038/nm.4172. Epub 2016 Sep 5.
341 Alpha-adducin polymorphism associated with increased risk of adverse cardiovascular outcomes: results from GENEtic Substudy of the INternational VErapamil SR-trandolapril STudy (INVEST-GENES).Am Heart J. 2008 Aug;156(2):397-404. doi: 10.1016/j.ahj.2008.03.007. Epub 2008 Jun 20.
342 Are decreased AdipoR1 mRNA levels associated with adiponectin resistance in coronary artery disease patients?.Clin Exp Pharmacol Physiol. 2015 Apr;42(4):331-6. doi: 10.1111/1440-1681.12361.
343 Angiogenic Factor AGGF1 Activates Autophagy with an Essential Role in Therapeutic Angiogenesis for Heart Disease.PLoS Biol. 2016 Aug 11;14(8):e1002529. doi: 10.1371/journal.pbio.1002529. eCollection 2016 Aug.
344 Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate gene.Genome Biol. 2019 Jul 8;20(1):133. doi: 10.1186/s13059-019-1749-5.
345 Association of polymorphisms in the ALOX15B gene with coronary artery disease.Clin Biochem. 2014 Apr;47(6):349-55. doi: 10.1016/j.clinbiochem.2013.12.013. Epub 2013 Dec 27.
346 A novel polymorphism of the GP78 gene is associated with coronary artery disease in Han population in China.Lipids Health Dis. 2014 Sep 9;13:147. doi: 10.1186/1476-511X-13-147.
347 The tumour necrosis factor superfamily ligand APRIL (TNFSF13) is released upon platelet activation and expressed in atherosclerosis.Thromb Haemost. 2009 Oct;102(4):704-10. doi: 10.1160/TH08-10-0665.
348 The association of APOC4 polymorphisms with premature coronary artery disease in a Chinese Han population.Lipids Health Dis. 2015 Jun 28;14:63. doi: 10.1186/s12944-015-0065-7.
349 Genetic variability in adapter proteins with APPL1/2 is associated with the risk of coronary artery disease in type 2 diabetes mellitus in Chinese Han population.Chin Med J (Engl). 2011 Nov;124(22):3618-21.
350 Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking.Ann Hum Genet. 2009 Nov;73(Pt 6):551-8. doi: 10.1111/j.1469-1809.2009.00540.x. Epub 2009 Aug 25.
351 -94 ATTG insertion/deletion polymorphism of the NFKB1 gene is associated with coronary artery disease in Han and Uygur women in China.Genet Test Mol Biomarkers. 2014 Jun;18(6):430-8. doi: 10.1089/gtmb.2013.0431. Epub 2014 May 12.
352 Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease.N Engl J Med. 2017 Jul 13;377(2):111-121. doi: 10.1056/NEJMoa1701719. Epub 2017 Jun 21.
353 A pharmacogenetic analysis of determinants of hypertension and blood pressure response to angiotensin-converting enzyme inhibitor therapy in patients with vascular disease and healthy individuals.J Hypertens. 2011 Mar;29(3):509-19. doi: 10.1097/HJH.0b013e328341d117.
354 Down regulation of GALNT3 contributes to endothelial cell injury via activation of p38 MAPK signaling pathway.Atherosclerosis. 2016 Feb;245:94-100. doi: 10.1016/j.atherosclerosis.2015.12.019. Epub 2015 Dec 17.
355 Functional Analysis of a Carotid Intima-Media Thickness Locus Implicates BCAR1 and Suggests a Causal Variant.Circ Cardiovasc Genet. 2015 Oct;8(5):696-706. doi: 10.1161/CIRCGENETICS.115.001062. Epub 2015 Aug 14.
356 Folate gene polymorphisms MTR A2756G, MTRR A66G, and BHMT G742A and risk for coronary artery disease: a meta-analysis.Genet Test Mol Biomarkers. 2012 Jun;16(6):471-5. doi: 10.1089/gtmb.2011.0237. Epub 2012 Feb 17.
357 The relationships between FAM5C SNP (rs10920501) variability and metabolic syndrome and inflammation in women with coronary heart disease.Biol Res Nurs. 2013 Apr;15(2):160-6. doi: 10.1177/1099800411424487. Epub 2011 Oct 18.
358 Association of a polymorphism of BTN2A1 with dyslipidemia in community-dwelling individuals.Mol Med Rep. 2014 Mar;9(3):808-12. doi: 10.3892/mmr.2014.1902. Epub 2014 Jan 16.
359 CTRP13 inhibits atherosclerosis via autophagy-lysosome-dependent degradation of CD36.FASEB J. 2019 Feb;33(2):2290-2300. doi: 10.1096/fj.201801267RR. Epub 2018 Sep 17.
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362 Autoantibodies Against (1)-Adrenoceptor Exaggerated Ventricular Remodeling by Inhibiting CTRP9 Expression.J Am Heart Assoc. 2019 Feb 19;8(4):e010475. doi: 10.1161/JAHA.118.010475.
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371 Does exercise training impact clock genes in patients with coronary artery disease and type 2 diabetes mellitus?.Eur J Prev Cardiol. 2016 Sep;23(13):1375-82. doi: 10.1177/2047487316639682. Epub 2016 Mar 21.
372 Validation of aspirin response-related transcripts in patients with coronary artery disease and preliminary investigation on CMTM5 function.Gene. 2017 Aug 15;624:56-65. doi: 10.1016/j.gene.2017.04.041. Epub 2017 Apr 28.
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375 A study in familial hypercholesterolemia suggests reduced methylomic plasticity in men with coronary artery disease.Epigenomics. 2015;7(1):17-34. doi: 10.2217/epi.14.64.
376 Altered serum level of cartilage oligomeric matrix protein and its association with coronary calcification in patients with coronary heart disease.J Geriatr Cardiol. 2017 Feb;14(2):87-92. doi: 10.11909/j.issn.1671-5411.2017.02.002.
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380 Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians.Clin Chim Acta. 2009 Jul;405(1-2):127-31. doi: 10.1016/j.cca.2009.04.015. Epub 2009 Apr 24.
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382 Home Monitoring of Heart Rate as a Predictor of Imminent Cardiovascular Events.Front Physiol. 2019 Mar 27;10:341. doi: 10.3389/fphys.2019.00341. eCollection 2019.
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386 Association of nicotinamide adenine dinucleotide phosphate oxidase p22phox gene 549C>T polymorphism with coronary artery disease.Chin Med J (Engl). 2012 Apr;125(8):1416-9.
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392 Adropin: Connection between Nonalcoholic Fatty Liver Disease and Coronary Artery Disease.Med Princ Pract. 2020;29(1):97. doi: 10.1159/000502039. Epub 2019 Jul 11.
393 Association between genetic variants of DNA repair genes and coronary artery disease.Genet Test Mol Biomarkers. 2013 Apr;17(4):307-13. doi: 10.1089/gtmb.2012.0383. Epub 2013 Jan 31.
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395 Interactions between the APOA5 -1131T>C and the FEN1 10154G>T polymorphisms on 6 polyunsaturated fatty acids in serum phospholipids and coronary artery disease.J Lipid Res. 2010 Nov;51(11):3281-8. doi: 10.1194/jlr.M010330. Epub 2010 Aug 27.
396 Flotillin-2 Gene Is Associated with Coronary Artery Disease in Chinese Han Population.Genet Test Mol Biomarkers. 2015 Dec;19(12):679-83. doi: 10.1089/gtmb.2015.0121. Epub 2015 Nov 10.
397 Upregulation of Circulating Cardiomyocyte-Enriched miR-1 and miR-133 Associate with the Risk of Coronary Artery Disease in Type 2 Diabetes Patients and Serve as Potential Biomarkers.J Cardiovasc Transl Res. 2019 Aug;12(4):347-357. doi: 10.1007/s12265-018-9857-2. Epub 2019 Jan 4.
398 Variant in GALNT3 Gene Linked with Reduced Coronary Artery Disease Risk in Chinese Population.DNA Cell Biol. 2017 Jul;36(7):529-534. doi: 10.1089/dna.2017.3688. Epub 2017 Apr 28.
399 Monocyte chemoattractant protein-1 gene (MCP-1) polymorphisms are associated with risk of premature coronary artery disease in Mexican patients from the Genetics of Atherosclerotic Disease (GEA) study.Immunol Lett. 2015 Oct;167(2):125-30. doi: 10.1016/j.imlet.2015.08.003. Epub 2015 Aug 12.
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402 G protein receptor kinase 4 polymorphisms: -blocker pharmacogenetics and treatment-related outcomes in hypertension.Hypertension. 2012 Oct;60(4):957-64. doi: 10.1161/HYPERTENSIONAHA.112.198721. Epub 2012 Sep 4.
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404 Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention.Cardiovasc Res. 2019 Aug 1;115(10):1512-1518. doi: 10.1093/cvr/cvz015.
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406 Upward trend of dapsone-induced methemoglobinemia in renal transplant community?"Salim SA. Palabindala V
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408 Gene polymorphisms associated with susceptibility to coronary artery disease in Han Chinese people.Genet Mol Res. 2014 Apr 8;13(2):2619-27. doi: 10.4238/2014.April.8.4.
409 Polymorphisms of human platelet alloantigens HPA-1 and HPA-2 associated with severe coronary artery disease.Cardiovasc Pathol. 2010 Sep-Oct;19(5):302-7. doi: 10.1016/j.carpath.2009.04.003. Epub 2009 Jun 9.
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413 IL-34 promotes foam cell formation by enhancing CD36 expression through p38 MAPK pathway.Sci Rep. 2018 Nov 26;8(1):17347. doi: 10.1038/s41598-018-35485-2.
414 IRF2BP2 Reduces Macrophage Inflammation and Susceptibility to Atherosclerosis.Circ Res. 2015 Sep 25;117(8):671-83. doi: 10.1161/CIRCRESAHA.114.305777. Epub 2015 Jul 20.
415 Sports-related sudden cardiac deaths in the young population of Switzerland.PLoS One. 2017 Mar 28;12(3):e0174434. doi: 10.1371/journal.pone.0174434. eCollection 2017.
416 Joint analysis of left ventricular expression and circulating plasma levels of Omentin after myocardial ischemia.Cardiovasc Diabetol. 2017 Jul 7;16(1):87. doi: 10.1186/s12933-017-0567-x.
417 The novel coronary artery disease risk gene JCAD/KIAA1462 promotes endothelial dysfunction and atherosclerosis.Eur Heart J. 2019 Aug 1;40(29):2398-2408. doi: 10.1093/eurheartj/ehz303.
418 Association of KALRN, ADIPOQ, and FTO gene polymorphism in type 2 diabetic patients with coronary artery disease: possible predisposing markers.Coron Artery Dis. 2016 Sep;27(6):490-6. doi: 10.1097/MCA.0000000000000386.
419 Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population.Lipids Health Dis. 2016 Oct 4;15(1):171. doi: 10.1186/s12944-016-0348-7.
420 Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease.Mol Cell Biochem. 2011 Sep;355(1-2):289-97. doi: 10.1007/s11010-011-0866-6. Epub 2011 May 13.
421 Impact of KIF6 Polymorphism rs20455 on Coronary Heart Disease Risk and Effectiveness of Statin Therapy in 100 Patients from Southern Iran.Arch Iran Med. 2015 Oct;18(10):683-7.
422 Survival bias and drug interaction can attenuate cross-sectional case-control comparisons of genes with health outcomes. An example of the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism and coronary heart disease.BMC Med Genet. 2011 Mar 24;12:42. doi: 10.1186/1471-2350-12-42.
423 The effect of anti-rheumatic medications for coronary artery diseases risk in patients with rheumatoid arthritis might be changed over time: A nationwide population-based cohort study.PLoS One. 2017 Jun 28;12(6):e0179081. doi: 10.1371/journal.pone.0179081. eCollection 2017.
424 Lim domain binding 2: a key driver of transendothelial migration of leukocytes and atherosclerosis.Arterioscler Thromb Vasc Biol. 2014 Sep;34(9):2068-77. doi: 10.1161/ATVBAHA.113.302709. Epub 2014 Jun 12.
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426 Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.Ann Hum Genet. 2008 Jul;72(Pt 4):443-53. doi: 10.1111/j.1469-1809.2008.00433.x. Epub 2008 Jul 3.
427 Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study.Lipids Health Dis. 2015 Jul 25;14:79. doi: 10.1186/s12944-015-0078-2.
428 CDKN2B-AS may indirectly regulate coronary artery disease-associated genes via targeting miR-92a.Gene. 2017 Sep 20;629:101-107. doi: 10.1016/j.gene.2017.07.070. Epub 2017 Jul 29.
429 Serum amyloid A induction of cytokines in monocytes/macrophages and lymphocytes.Atherosclerosis. 2009 Dec;207(2):374-83. doi: 10.1016/j.atherosclerosis.2009.05.007. Epub 2009 May 21.
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434 Novel genes in LDL metabolism--a comprehensive overview.Curr Opin Lipidol. 2015 Jun;26(3):179-87. doi: 10.1097/MOL.0000000000000175.
435 Genetic etiology of coronary artery disease considering NOS 3 gene variant rs1799983.Vascular. 2015 Jun;23(3):270-6. doi: 10.1177/1708538114544783. Epub 2014 Jul 23.
436 Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.Hum Mol Genet. 2012 Nov 1;21(21):4774-80. doi: 10.1093/hmg/dds300. Epub 2012 Jul 26.
437 p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP?"Gloria-Bottini F. Saccucci P
438 Long noncoding RNA NEXN-AS1 mitigates atherosclerosis by regulating the actin-binding protein NEXN.J Clin Invest. 2019 Mar 1;129(3):1115-1128. doi: 10.1172/JCI98230. Epub 2019 Feb 4.
439 Regulation of NADPH oxidase 5 by protein kinase C isoforms.PLoS One. 2014 Feb 5;9(2):e88405. doi: 10.1371/journal.pone.0088405. eCollection 2014.
440 Associations between plasma nesfatin-1 levels and the presence and severity of coronary artery disease.Heart Vessels. 2019 Jun;34(6):965-970. doi: 10.1007/s00380-018-01328-3. Epub 2019 Jan 1.
441 The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.Lipids Health Dis. 2015 Sep 29;14:120. doi: 10.1186/s12944-015-0102-6.
442 Platelet polymorphisms: frequency distribution and association with coronary artery disease in an Indian population.Platelets. 2011;22(2):85-91. doi: 10.3109/09537104.2010.522275. Epub 2010 Oct 29.
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445 Deciphering the Causal Role of sPLA2s and Lp-PLA2 in Coronary Heart Disease.Arterioscler Thromb Vasc Biol. 2015 Nov;35(11):2281-9. doi: 10.1161/ATVBAHA.115.305234. Epub 2015 Sep 3.
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447 Perilipin 2 levels are increased in patients with in-stent neoatherosclerosis: A clue to mechanisms of accelerated plaque formation after drug-eluting stent implantation.Int J Cardiol. 2018 May 1;258:55-58. doi: 10.1016/j.ijcard.2018.01.074.
448 Coronary Artery Disease Risk-Associated Plpp3 Gene and Its Product Lipid Phosphate Phosphatase 3 Regulate Experimental Atherosclerosis.Arterioscler Thromb Vasc Biol. 2019 Nov;39(11):2261-2272. doi: 10.1161/ATVBAHA.119.313056. Epub 2019 Sep 19.
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450 Cytochrome P450 genes in coronary artery diseases: Codon usage analysis reveals genomic GC adaptation.Gene. 2016 Sep 15;590(1):35-43. doi: 10.1016/j.gene.2016.06.011. Epub 2016 Jun 5.
451 Genome-wide association analysis of imputed rare variants: application to seven common complex diseases.Genet Epidemiol. 2012 Dec;36(8):785-96. doi: 10.1002/gepi.21675. Epub 2012 Sep 5.
452 Haplotypes encompassing the KIAA0391 and PSMA6 gene cluster confer a genetic link for myocardial infarction and coronary artery disease.Ann Hum Genet. 2009 Sep;73(Pt 5):475-83. doi: 10.1111/j.1469-1809.2009.00534.x. Epub 2009 Jun 16.
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455 Dysregulation of endothelial colony-forming cell function by a negative feedback loop of circulating miR-146a and -146b in cardiovascular disease patients.PLoS One. 2017 Jul 20;12(7):e0181562. doi: 10.1371/journal.pone.0181562. eCollection 2017.
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457 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.Respir Res. 2019 Apr 2;20(1):64. doi: 10.1186/s12931-019-1036-8.
458 Weighted gene co-expression network analysis identifies specific modules and hub genes related to coronary artery disease.BMC Cardiovasc Disord. 2016 Mar 5;16:54. doi: 10.1186/s12872-016-0217-3.
459 ScaI atrial natriuretic peptide gene polymorphisms and their possible association with postoperative atrial fibrillation - a preliminary report.Arch Med Sci. 2017 Apr 1;13(3):568-574. doi: 10.5114/aoms.2016.58270. Epub 2016 May 12.
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463 TIMD4 rs6882076 SNP Is Associated with Decreased Levels of Triglycerides and the Risk of Coronary Heart Disease and Ischemic Stroke.Int J Med Sci. 2019 Jun 2;16(6):864-871. doi: 10.7150/ijms.31729. eCollection 2019.
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465 Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.Circ Cardiovasc Genet. 2016 Jun;9(3):250-8. doi: 10.1161/CIRCGENETICS.115.001374. Epub 2016 Mar 24.
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468 SUGP1 is a novel regulator of cholesterol metabolism.Hum Mol Genet. 2016 Jul 15;25(14):3106-3116. doi: 10.1093/hmg/ddw151. Epub 2016 May 20.
469 SUMO4 Met55Val polymorphism is associated with coronary heart disease in Japanese type 2 diabetes individuals.Diabetes Res Clin Pract. 2009 Jul;85(1):85-9. doi: 10.1016/j.diabres.2009.04.001. Epub 2009 May 1.
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546 What determines do-not-resuscitate status in critically ill HIV-infected patients admitted to ICU?.J Crit Care. 2019 Oct;53:207-211. doi: 10.1016/j.jcrc.2019.06.010. Epub 2019 Jun 19.
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551 Predictors of Severe or Moderate Coronary Artery Disease in Asymptomatic Individuals with Extremely Low Coronary Calcium Scores.Yonsei Med J. 2019 Jul;60(7):619-625. doi: 10.3349/ymj.2019.60.7.619.
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558 Discrepancy between the European clinical guidelines and myocardial revascularization in patients with stable coronary artery disease in Russia.Int J Qual Health Care. 2019 May 1;31(4):269-275. doi: 10.1093/intqhc/mzy140.
559 Elevated methylation of cyclin dependent kinase inhibitor 2B contributes to the risk of coronary heart disease in women.Exp Ther Med. 2019 Jan;17(1):205-213. doi: 10.3892/etm.2018.6920. Epub 2018 Nov 2.
560 YKL-40 levels increase with declining ankle-brachial index and are associated with long-term cardiovascular mortality in peripheral arterial disease patients.Atherosclerosis. 2018 Jul;274:152-156. doi: 10.1016/j.atherosclerosis.2018.05.006. Epub 2018 May 9.
561 Association of Genetic Variation at AQP4 Locus with Vascular Depression.Biomolecules. 2018 Dec 5;8(4):164. doi: 10.3390/biom8040164.
562 Plasma soluble C-type lectin-like receptor-2 is associated with the risk of coronary artery disease.Front Med. 2020 Feb;14(1):81-90. doi: 10.1007/s11684-019-0692-x. Epub 2019 Jul 6.
563 RNA-sequencing reveals that STRN, ZNF484 and WNK1 add to the value of mitochondrial MT-COI and COX10 as markers of unstable coronary artery disease.PLoS One. 2019 Dec 10;14(12):e0225621. doi: 10.1371/journal.pone.0225621. eCollection 2019.
564 High factor VIII levels and arterial thrombosis: illustrative case and literature review.Ther Adv Hematol. 2019 Nov 20;10:2040620719886685. doi: 10.1177/2040620719886685. eCollection 2019.
565 Low CPNE3 expression is associated with risk of acute myocardial infarction: A feasible genetic marker of acute myocardial infarction in patients with stable coronary artery disease.Cardiol J. 2019;26(2):186-193. doi: 10.5603/CJ.a2017.0155. Epub 2018 Jan 3.
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567 Effects of 6 Months of Exercise-Based Cardiac Rehabilitation on Autonomic Function and Neuro-Cardiovascular Stress Reactivity in Coronary Artery Disease Patients.J Am Heart Assoc. 2019 Sep 3;8(17):e012257. doi: 10.1161/JAHA.119.012257. Epub 2019 Aug 23.
568 Clinical Evidence Supports a Protective Role for CXCL5 in Coronary Artery Disease.Am J Pathol. 2017 Dec;187(12):2895-2911. doi: 10.1016/j.ajpath.2017.08.006. Epub 2017 Nov 16.
569 Mechanisms underlying the J-curve for diastolic blood pressure: Subclinical myocardial injury and immune activation.Int J Cardiol. 2019 Feb 1;276:255-260. doi: 10.1016/j.ijcard.2018.09.028. Epub 2018 Sep 8.
570 A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients.Cardiovasc Diabetol. 2019 Aug 13;18(1):102. doi: 10.1186/s12933-019-0906-1.
571 DOCK7-ANGPTL3 SNPs and their haplotypes with serum lipid levels and the risk of coronary artery disease and ischemic stroke.Lipids Health Dis. 2018 Feb 17;17(1):30. doi: 10.1186/s12944-018-0677-9.
572 EBF1 gene polymorphism and its interaction with smoking and drinking on the risk of coronary artery disease for Chinese patients.Biosci Rep. 2018 Jun 21;38(3):BSR20180324. doi: 10.1042/BSR20180324. Print 2018 Jun 29.
573 Higher serum level of CTRP15 in patients with coronary artery disease is associated with disease severity, body mass index and insulin resistance.Arch Physiol Biochem. 2022 Feb;128(1):276-280. doi: 10.1080/13813455.2019.1675713. Epub 2019 Oct 12.
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576 Polymorphisms within vitamin D binding protein gene within a Preeclamptic South African population.Hypertens Pregnancy. 2019 Nov;38(4):260-267. doi: 10.1080/10641955.2019.1667383. Epub 2019 Sep 27.
577 Non-alcoholic fatty liver disease and cardiovascular disease: assessing the evidence for causality.Diabetologia. 2020 Feb;63(2):253-260. doi: 10.1007/s00125-019-05024-3. Epub 2019 Nov 11.
578 Association of G-protein beta3 subunit gene C825T polymorphism with cardiac and cerebrovascular events in Chinese hypertensive patients.Clin Exp Hypertens. 2017;39(1):80-84. doi: 10.1080/10641963.2016.1210621. Epub 2017 Jan 9.
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580 HHIPL1, a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis.Circulation. 2019 Aug 6;140(6):500-513. doi: 10.1161/CIRCULATIONAHA.119.041059. Epub 2019 Jun 5.
581 Association of heat shock protein70-2 (HSP70-2) gene polymorphism with coronary artery disease in an Iranian population.Gene. 2014 Oct 25;550(2):180-4. doi: 10.1016/j.gene.2014.08.012. Epub 2014 Aug 7.
582 Free IGF-1, Intact IGFBP-4, and PicoPAPP-A are Altered in Acute Myocardial Infarction Compared to Stable Coronary Artery Disease and Healthy Controls.Horm Metab Res. 2019 Feb;51(2):112-119. doi: 10.1055/a-0794-6163. Epub 2018 Nov 29.
583 Proteomic Biomarkers for Incident Aortic Stenosis Requiring Valvular Replacement.Circulation. 2018 Aug 7;138(6):590-599. doi: 10.1161/CIRCULATIONAHA.117.030414.
584 Evaluation of platelet reactivity during combined antiplatelet therapy in patients with stable coronary artery disease in relation to diabetes type 2 and the GPIIB/IIIA receptor gene polymorphism.J Physiol Pharmacol. 2019 Apr;70(2). doi: 10.26402/jpp.2019.2.01. Epub 2019 Jul 22.
585 Impaired HDL2-mediated cholesterol efflux is associated with metabolic syndrome in families with early onset coronary heart disease and low HDL-cholesterol level.PLoS One. 2017 Feb 16;12(2):e0171993. doi: 10.1371/journal.pone.0171993. eCollection 2017.
586 A Novel Y-Specific Long Non-Coding RNA Associated with Cellular Lipid Accumulation in HepG2 cells and Atherosclerosis-related Genes.Sci Rep. 2017 Dec 1;7(1):16710. doi: 10.1038/s41598-017-17165-9.
587 The Biological Role of Klotho Protein in the Development of Cardiovascular Diseases.Biomed Res Int. 2018 Dec 24;2018:5171945. doi: 10.1155/2018/5171945. eCollection 2018.
588 Krppel-like factor 14, a coronary artery disease associated transcription factor, inhibits endothelial inflammation via NF-B signaling pathway.Atherosclerosis. 2018 Nov;278:39-48. doi: 10.1016/j.atherosclerosis.2018.09.018. Epub 2018 Sep 15.
589 Genome-wide DNA methylation encodes cardiac transcriptional reprogramming in human ischemic heart failure.Lab Invest. 2019 Mar;99(3):371-386. doi: 10.1038/s41374-018-0104-x. Epub 2018 Aug 8.
590 Genetic variant at coronary artery disease and ischemic stroke locus 1p32.2 regulates endothelial responses to hemodynamics.Proc Natl Acad Sci U S A. 2018 Nov 27;115(48):E11349-E11358. doi: 10.1073/pnas.1810568115. Epub 2018 Nov 14.
591 Significant role and mechanism of microRNA-143-3p/KLLN axis in the development of coronary heart disease.Am J Transl Res. 2019 Jun 15;11(6):3610-3619. eCollection 2019.
592 Expression of Mac-2 binding protein in human carotid atheroma is associated with plaque instability and clinical manifestations.Biomed Pharmacother. 2019 Feb;110:465-472. doi: 10.1016/j.biopha.2018.12.015. Epub 2018 Dec 6.
593 A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.Circ Cardiovasc Genet. 2014 Aug;7(4):514-20. doi: 10.1161/CIRCGENETICS.113.000321. Epub 2014 May 27.
594 Risk factors for first-time acute myocardial infarction patients in Trinidad.BMC Public Health. 2018 Jan 19;18(1):161. doi: 10.1186/s12889-018-5080-y.
595 Efficacy and safety of the Shexiang Baoxin Pill for the treatment of coronary artery disease not amenable to revascularisation: study protocol for a randomised, placebo-controlled, double-blinded trial.BMJ Open. 2018 Feb 14;8(2):e018052. doi: 10.1136/bmjopen-2017-018052.
596 Lower serum levels of Meteorin-like/Subfatin in patients with coronary artery disease and type 2 diabetes mellitus are negatively associated with insulin resistance and inflammatory cytokines.PLoS One. 2018 Sep 13;13(9):e0204180. doi: 10.1371/journal.pone.0204180. eCollection 2018.
597 Analysis of necroptotic proteins in failing human hearts.J Transl Med. 2017 Apr 28;15(1):86. doi: 10.1186/s12967-017-1189-5.
598 C771G (His241Gln) polymorphism of MLXIPL gene, TG levels and coronary artery disease: a case control study.Anatol J Cardiol. 2015 Jan;15(1):8-12. doi: 10.5152/akd.2014.5135. Epub 2014 Feb 10.
599 Interleukin-18, matrix metalloproteinase-22 and -29 are independent risk factors of human coronary heart disease.J Zhejiang Univ Sci B. 2017 Aug.;18(8):685-695. doi: 10.1631/jzus.B1700073.
600 Common Variant in Glycoprotein Ia Increases Long-Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery.J Am Heart Assoc. 2016 Nov 23;5(12):e004496. doi: 10.1161/JAHA.116.004496.
601 Plasma levels of receptor interacting protein kinase-3 correlated with coronary artery disease.Chin Med J (Engl). 2019 Jun 20;132(12):1400-1405. doi: 10.1097/CM9.0000000000000225.
602 Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.PLoS One. 2014 Mar 11;9(3):e89029. doi: 10.1371/journal.pone.0089029. eCollection 2014.
603 Circulating autoantibodies against neuroblastoma suppressor of tumorigenicity 1 (NBL1): A potential biomarker for coronary artery disease in patients with obstructive sleep apnea.PLoS One. 2018 Mar 29;13(3):e0195015. doi: 10.1371/journal.pone.0195015. eCollection 2018.
604 Assessment of nociceptin/orphanin FQ and micro-opioid receptor mRNA in the human right atrium.Br J Anaesth. 2010 Jun;104(6):698-704. doi: 10.1093/bja/aeq089. Epub 2010 Apr 21.
605 The inflammasome NLRP12 is associated with both depression and coronary artery disease in Vietnam veterans.Psychiatry Res. 2018 Dec;270:775-779. doi: 10.1016/j.psychres.2018.10.051. Epub 2018 Oct 27.
606 A common NOS1AP genetic polymorphism, rs12567209 G>A, is associated with sudden cardiac death in patients with chronic heart failure in the Chinese Han population.J Card Fail. 2014 Apr;20(4):244-51. doi: 10.1016/j.cardfail.2014.01.006. Epub 2014 Jan 10.
607 Low Levels of Plasma Osteoglycin in Patients with Complex Coronary Lesions.J Atheroscler Thromb. 2018 Nov 1;25(11):1149-1155. doi: 10.5551/jat.43059. Epub 2018 Mar 5.
608 Treatment with triple combination of atorvastatin, perindopril, and amlodipine in patients with stable coronary artery disease: A subgroup analysis from the PAPA-CAD study.J Int Med Res. 2018 May;46(5):1902-1909. doi: 10.1177/0300060518760158. Epub 2018 Mar 20.
609 Variants of PEAR1 Are Associated With Outcome in Patients With ACS and Stable CAD Undergoing PCI.Front Pharmacol. 2018 May 15;9:490. doi: 10.3389/fphar.2018.00490. eCollection 2018.
610 PHACTR1 gene polymorphism with the risk of coronary artery disease in Chinese Han population.Postgrad Med J. 2019 Feb;95(1120):67-71. doi: 10.1136/postgradmedj-2018-136298. Epub 2019 Feb 18.
611 Low expression of PIK3C2A gene: A potential biomarker to predict the risk of acute myocardial infarction.Medicine (Baltimore). 2019 Apr;98(14):e15061. doi: 10.1097/MD.0000000000015061.
612 Alterations of protein expression of phospholamban, ZASP and plakoglobin in human atria in subgroups of seniors.Sci Rep. 2019 Apr 4;9(1):5610. doi: 10.1038/s41598-019-42141-w.
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615 Mechanisms of Myocardial Infarction inPatients With Nonobstructive Coronary Artery Disease: Results From the Optical Coherence Tomography Study.JACC Cardiovasc Imaging. 2019 Nov;12(11 Pt 1):2210-2221. doi: 10.1016/j.jcmg.2018.08.022. Epub 2018 Oct 17.
616 Association among PlA1/A2 gene polymorphism, laboratory aspirin resistance and clinical outcomes in patients with coronary artery disease: An updated meta-analysis.Sci Rep. 2019 Sep 11;9(1):13177. doi: 10.1038/s41598-019-49123-y.
617 In vitro and in vivo metabolite identification of a novel benzimidazole compound ZLN005 by liquid chromatography/tandem mass spectrometry.Rapid Commun Mass Spectrom. 2018 Mar 30;32(6):480-488. doi: 10.1002/rcm.8060.
618 High Serum Cyclophilin C levels as a risk factor marker for Coronary Artery Disease.Sci Rep. 2019 Jul 22;9(1):10576. doi: 10.1038/s41598-019-46988-x.
619 Systems Pharmacology Identifies an Arterial Wall Regulatory Gene Network Mediating Coronary Artery Disease Side Effects of Antiretroviral Therapy.Circ Genom Precis Med. 2019 Jun;12(6):e002390. doi: 10.1161/CIRCGEN.118.002390. Epub 2019 May 6.
620 Nutrient sensing pathway genes expression dysregulated in patients with T2DM and coronary artery disease.Diabetes Res Clin Pract. 2019 May;151:39-45. doi: 10.1016/j.diabres.2019.03.036. Epub 2019 Mar 30.
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622 Circulating Chemerin Levels, but not the RARRES2 Polymorphisms, Predict the Long-Term Outcome of Angiographically Confirmed Coronary Artery Disease.Int J Mol Sci. 2019 Mar 7;20(5):1174. doi: 10.3390/ijms20051174.
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625 Investigation of Renalase gene rs2576178 polymorphism in patients with coronary artery disease.Biosci Rep. 2018 Sep 13;38(5):BSR20180839. doi: 10.1042/BSR20180839. Print 2018 Oct 31.
626 Breast Arterial Calcification on screening mammography can predict significant Coronary Artery Disease in women.Clin Imaging. 2018 May-Jun;49:48-53. doi: 10.1016/j.clinimag.2017.10.021. Epub 2017 Nov 3.
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635 Emerging Roles of Tumor Necrosis Factor-Stimulated Gene-6 in the Pathophysiology and Treatment of Atherosclerosis.Int J Mol Sci. 2018 Feb 5;19(2):465. doi: 10.3390/ijms19020465.
636 Decoy receptor-3 regulates inflammation and apoptosis via PI3K/AKT signaling pathway in coronary heart disease.Exp Ther Med. 2019 Apr;17(4):2614-2622. doi: 10.3892/etm.2019.7222. Epub 2019 Jan 30.
637 Coronary artery disease-associated genetic variants and biomarkers of inflammation.PLoS One. 2017 Jul 7;12(7):e0180365. doi: 10.1371/journal.pone.0180365. eCollection 2017.
638 TREML4 mRNA Expression and Polymorphisms in Blood Leukocytes are Associated with Atherosclerotic Lesion Extension in Coronary Artery Disease.Sci Rep. 2019 May 10;9(1):7229. doi: 10.1038/s41598-019-43745-y.
639 TRIB1 and TRPS1 variants, GG and GE interactions on serum lipid levels, the risk of coronary heart disease and ischemic stroke.Sci Rep. 2019 Feb 20;9(1):2376. doi: 10.1038/s41598-019-38765-7.
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641 Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors.JAMA. 2018 Dec 25;320(24):2553-2563. doi: 10.1001/jama.2018.19329.
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643 Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults.Int J Epidemiol. 2017 Aug 1;46(4):1211-1222. doi: 10.1093/ije/dyw245.
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645 Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies.Circ Cardiovasc Genet. 2017 Apr;10(2):e001569. doi: 10.1161/CIRCGENETICS.116.001569.
646 CRISPLD1 rs12115090 polymorphisms alters antiplatelet potency of clopidogrel in coronary artery disease patients in Chinese Han.Gene. 2018 Dec 15;678:226-232. doi: 10.1016/j.gene.2018.08.027. Epub 2018 Aug 7.
647 PPBP and DEFA1/DEFA3 genes in hyperlipidaemia as feasible synergistic inflammatory biomarkers for coronary heart disease.Lipids Health Dis. 2017 Apr 19;16(1):80. doi: 10.1186/s12944-017-0471-0.
648 FAL1 regulates endothelial cell proliferation in diabetic arteriosclerosis through PTEN/AKT pathway.Eur Rev Med Pharmacol Sci. 2018 Oct;22(19):6492-6499. doi: 10.26355/eurrev_201810_16063.
649 Association of the FADS gene cluster with coronary artery disease and plasma lipid concentrations in the northern Chinese Han population.Prostaglandins Leukot Essent Fatty Acids. 2017 Feb;117:11-16. doi: 10.1016/j.plefa.2017.01.014. Epub 2017 Jan 26.
650 Insulin Resistance and Future Cognitive Performance and Cognitive Decline inElderly Patients with Cardiovascular Disease.J Alzheimers Dis. 2017;57(2):633-643. doi: 10.3233/JAD-161016.
651 Expression of the Marburg I Single Nucleotide Polymorphism (MI-SNP) and the Marburg II Single Nucleotide Polymorphism (MII-SNP) of the Factor VII-Activating Protease (FSAP) Gene and Risk of Coronary Artery Disease (CAD): A Pilot Study in a Single Population.Med Sci Monit. 2018 Jun 21;24:4271-4278. doi: 10.12659/MSM.906984.
652 Novel combined GPIHBP1 mutations in a patient with hypertriglyceridemia associated with CAD.J Atheroscler Thromb. 2013;20(10):777-84. doi: 10.5551/jat.18861. Epub 2013 Jul 8.
653 Novel protein biomarkers associated with coronary artery disease in statin-treated patients with familial hypercholesterolemia.J Clin Lipidol. 2017 May-Jun;11(3):682-693. doi: 10.1016/j.jacl.2017.03.014. Epub 2017 Apr 4.
654 How much for a broken heart? Costs of cardiovascular disease in Colombia using a person-based approach.PLoS One. 2018 Dec 19;13(12):e0208513. doi: 10.1371/journal.pone.0208513. eCollection 2018.
655 Circulating lncRNA IFNG-AS1 expression correlates with increased disease risk, higher disease severity and elevated inflammation in patients with coronary artery disease.J Clin Lab Anal. 2018 Sep;32(7):e22452. doi: 10.1002/jcla.22452. Epub 2018 May 9.
656 Rheumatoid Arthritis and Coronary Artery Disease: Genetic Analyses Do Not Support a Causal Relation.J Rheumatol. 2017 Jan;44(1):4-10. doi: 10.3899/jrheum.151444. Epub 2016 Oct 15.
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658 Oxidized phospholipids regulate amino acid metabolism through MTHFD2 to facilitate nucleotide release in endothelial cells.Nat Commun. 2018 Jun 12;9(1):2292. doi: 10.1038/s41467-018-04602-0.
659 Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease.PLoS One. 2017 Apr 17;12(4):e0175649. doi: 10.1371/journal.pone.0175649. eCollection 2017.
660 RPS3A positively regulates the mitochondrial function of human periaortic adipose tissue and is associated with coronary artery diseases.Cell Discov. 2018 Aug 21;4:52. doi: 10.1038/s41421-018-0041-2. eCollection 2018.
661 A robust method to estimate regional polygenic correlation under misspecified linkage disequilibrium structure.Genet Epidemiol. 2018 Oct;42(7):636-647. doi: 10.1002/gepi.22149. Epub 2018 Aug 29.
662 Effects of selenium supplementation on expression of SEPP1 in mRNA and protein levels in subjects with and without metabolic syndrome suffering from coronary artery disease: Selenegene study a double-blind randomized controlled trial.J Cell Biochem. 2018 Nov;119(10):8282-8289. doi: 10.1002/jcb.26844. Epub 2018 Jun 22.
663 Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci.Am J Hum Genet. 2018 Sep 6;103(3):377-388. doi: 10.1016/j.ajhg.2018.08.001. Epub 2018 Aug 23.
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665 Vinexin Ablation Inhibits Atherosclerosis in Apolipoprotein E-Deficient Mice by Inactivating the Akt-Nuclear Factor B Inflammatory Axis.J Am Heart Assoc. 2017 Feb 16;6(2):e004585. doi: 10.1161/JAHA.116.004585.