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                    Mutational analysis of the N-ras, p53, p16INK4a, CDK4, and MC1R genes in human congenital melanocytic naevi.J Med Genet. 1999 Aug;36(8):610-4.
                    
                        
                    
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                    Review: Vascular dementia: clinicopathologic and genetic considerations.Neuropathol Appl Neurobiol. 2018 Apr;44(3):247-266. doi: 10.1111/nan.12472. Epub 2018 Mar 1.
                    
                        
                    
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                    ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia.J Neurol Sci. 2012 Oct 15;321(1-2):100-2. doi: 10.1016/j.jns.2012.07.036. Epub 2012 Aug 3.
                    
                        
                    
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                    Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort.Psychiatr Genet. 2012 Aug;22(4):197-201. doi: 10.1097/YPG.0b013e32834c0cc8.
                    
                        
                    
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                    The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women.Breast Cancer Res. 2005;7(3):R353-6. doi: 10.1186/bcr1009. Epub 2005 Mar 4.
                    
                        
                    
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                    SCA2 family presenting as typical Parkinson's disease: 34 year follow up.Parkinsonism Relat Disord. 2017 Jul;40:69-72. doi: 10.1016/j.parkreldis.2017.04.003. Epub 2017 Apr 12.
                    
                        
                    
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                    Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.Sci Rep. 2015 Dec 1;5:17369. doi: 10.1038/srep17369.
                    
                        
                    
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                    Narrowing the critical region for congenital vertical talus in patients with interstitial 18q deletions.Am J Med Genet A. 2013 May;161A(5):1117-21. doi: 10.1002/ajmg.a.35791. Epub 2013 Mar 13.
                    
                        
                    
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                    Cerebral amyloid angiopathy-related cognitive impairment: The search for a specific neuropsychological pattern.Rev Neurol (Paris). 2017 Nov;173(9):562-565. doi: 10.1016/j.neurol.2017.09.006. Epub 2017 Oct 6.
                    
                        
                    
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                    The association between dilated cardiomyopathy and RTN4 3'UTR insertion/deletion polymorphisms.Clin Chim Acta. 2009 Feb;400(1-2):21-4. doi: 10.1016/j.cca.2008.09.028. Epub 2008 Oct 8.
                    
                        
                    
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                    Association of polymorphisms -1154G/A and -2578C/A in the vascular endothelial growth factor gene with decreased risk of endometriosis in Chinese women.Hum Reprod. 2009 Oct;24(10):2660-6. doi: 10.1093/humrep/dep208. Epub 2009 Jun 16.
                    
                        
                    
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                    Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.Nat Genet. 2018 Jul;50(7):928-936. doi: 10.1038/s41588-018-0142-8. Epub 2018 Jun 11.
                    
                        
                    
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                    Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.Acta Neuropathol. 2010 Feb;119(2):189-97. doi: 10.1007/s00401-009-0609-x. Epub 2009 Nov 13.
                    
                        
                    
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                    Genetic alterations in primary glioblastomas in Japan.J Neuropathol Exp Neurol. 2006 Jan;65(1):12-8. doi: 10.1097/01.jnen.0000196132.66464.96.
                    
                        
                    
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                    Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population.Int Immunopharmacol. 2015 Apr;25(2):425-31. doi: 10.1016/j.intimp.2015.02.020. Epub 2015 Feb 21.
                    
                        
                    
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                    Association of CAA and TATC Insertion/Deletion Genetic Polymorphisms in RTN4 3'-UTR with Hepatocellular Carcinoma Risk.Pathol Oncol Res. 2018 Jan;24(1):31-34. doi: 10.1007/s12253-017-0204-8. Epub 2017 Jan 31.
                    
                        
                    
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                    CAG Repeat Not Polyglutamine Length Determines Timing of Huntington's Disease Onset.Cell. 2019 Aug 8;178(4):887-900.e14. doi: 10.1016/j.cell.2019.06.036.
                    
                        
                    
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                    CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura.Haematologica. 2011 Dec;96(12):1883-5. doi: 10.3324/haematol.2011.045732. Epub 2011 Aug 9.
                    
                        
                    
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                    TSHZ1-dependent gene regulation is essential for olfactory bulb development and olfaction.J Clin Invest. 2014 Mar;124(3):1214-27. doi: 10.1172/JCI72466.
                    
                        
                    
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                    Mxi1 mutations in human neurofibrosarcomas.Jpn J Cancer Res. 1999 Jul;90(7):740-6. doi: 10.1111/j.1349-7006.1999.tb00809.x.
                    
                        
                    
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                    Frequency of UV-inducible NRAS mutations in melanomas of patients with germline CDKN2A mutations.J Natl Cancer Inst. 2003 Jun 4;95(11):790-8. doi: 10.1093/jnci/95.11.790.
                    
                        
                    
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                    Association study of 90 candidate gene polymorphisms in panic disorder.Psychiatr Genet. 2005 Mar;15(1):17-24. doi: 10.1097/00041444-200503000-00004.
                    
                        
                    
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                    The Pathogenic Role of Low Range Repeats in SCA17.PLoS One. 2015 Aug 12;10(8):e0135275. doi: 10.1371/journal.pone.0135275. eCollection 2015.
                    
                        
                    
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                    Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2).Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):524-531. doi: 10.1002/ajmg.b.31013.
                    
                        
                    
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                    N-ras mutation of thyroid tumor with special reference to the follicular type.Pathol Int. 1995 Jan;45(1):45-50. doi: 10.1111/j.1440-1827.1995.tb03378.x.
                    
                        
                    
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                    Gene expression profiling and identification of hub genes in Nellore cattle with different marbling score levels.Genomics. 2020 Jan;112(1):873-879. doi: 10.1016/j.ygeno.2019.06.001. Epub 2019 Jun 3.
                    
                        
                    
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                    Analysis of RTN4 3'UTR insertion/deletion polymorphisms in ventricular septal defect in a Chinese Han population.DNA Cell Biol. 2011 May;30(5):323-7. doi: 10.1089/dna.2010.1116. Epub 2010 Dec 17.
                    
                        
                    
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                    Two-step transplantation with adipose tissue-derived stem cells increases follicle survival by enhancing vascularization in xenografted frozen-thawed human ovarian tissue.Hum Reprod. 2018 Jun 1;33(6):1107-1116. doi: 10.1093/humrep/dey080.
                    
                        
                    
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                    CFH polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration.Acta Ophthalmol. 2015 Dec;93(8):e658-66. doi: 10.1111/aos.12790. Epub 2015 Jul 8.
                    
                        
                    
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                    Association of genetic variations in RTN4 3'-UTR with risk for clear cell renal cell carcinoma.Fam Cancer. 2018 Jan;17(1):129-134. doi: 10.1007/s10689-017-0005-y.
                    
                        
                    
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                    Prevalence and characterization of methicillin-resistant Staphylococcus aureus among healthy children in a city of Argentina.Infect Genet Evol. 2011 Jul;11(5):1066-71. doi: 10.1016/j.meegid.2011.03.019. Epub 2011 Apr 2.
                    
                        
                    
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                    Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen). Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6.
                    
                        
                    
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                    SLC44A2 single nucleotide polymorphisms, isoforms, and expression: Association with severity of Meniere's disease?.Genomics. 2016 Dec;108(5-6):201-208. doi: 10.1016/j.ygeno.2016.11.002. Epub 2016 Nov 6.
                    
                        
                    
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                    Genome-wide copy number profiling using a 100K SNP array reveals novel disease-related genes BORIS and TSHZ1 in juvenile angiofibroma.Int J Oncol. 2011 Nov;39(5):1143-51. doi: 10.3892/ijo.2011.1166. Epub 2011 Aug 18.
                    
                        
                    
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                    Tshz1 Regulates Pancreatic -Cell Maturation.Diabetes. 2015 Aug;64(8):2905-14. doi: 10.2337/db14-1443. Epub 2015 Apr 27.
                    
                        
                    
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                    SCA17 repeat expansion: mildly expanded CAG/CAA repeat alleles in neurological disorders and the functional implications.Clin Chim Acta. 2010 Mar;411(5-6):375-80. doi: 10.1016/j.cca.2009.12.002. Epub 2009 Dec 11.
                    
                        
                    
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                    Human embryonic stem cell-derived test systems for developmental neurotoxicity: a transcriptomics approach. Arch Toxicol. 2013 Jan;87(1):123-43.
                    
                        
                    
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                    Comparison of HepG2 and HepaRG by whole-genome gene expression analysis for the purpose of chemical hazard identification. Toxicol Sci. 2010 May;115(1):66-79.
                    
                        
                    
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                    Development of a neural teratogenicity test based on human embryonic stem cells: response to retinoic acid exposure. Toxicol Sci. 2011 Dec;124(2):370-7.
                    
                        
                    
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                    Bringing in vitro analysis closer to in vivo: studying doxorubicin toxicity and associated mechanisms in 3D human microtissues with PBPK-based dose modelling. Toxicol Lett. 2018 Sep 15;294:184-192.
                    
                        
                    
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                    Physiological and toxicological transcriptome changes in HepG2 cells exposed to copper. Physiol Genomics. 2009 Aug 7;38(3):386-401.
                    
                        
                    
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                    Activation of AIFM2 enhances apoptosis of human lung cancer cells undergoing toxicological stress. Toxicol Lett. 2016 Sep 6;258:227-236.
                    
                        
                    
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                    Prenatal arsenic exposure and the epigenome: identifying sites of 5-methylcytosine alterations that predict functional changes in gene expression in newborn cord blood and subsequent birth outcomes. Toxicol Sci. 2015 Jan;143(1):97-106. doi: 10.1093/toxsci/kfu210. Epub 2014 Oct 10.
                    
                        
                    
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                    The exosome-like vesicles derived from androgen exposed-prostate stromal cells promote epithelial cells proliferation and epithelial-mesenchymal transition. Toxicol Appl Pharmacol. 2021 Jan 15;411:115384. doi: 10.1016/j.taap.2020.115384. Epub 2020 Dec 25.
                    
                        
                    
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                    Gene Expression Regulation and Pathway Analysis After Valproic Acid and Carbamazepine Exposure in a Human Embryonic Stem Cell-Based Neurodevelopmental Toxicity Assay. Toxicol Sci. 2015 Aug;146(2):311-20. doi: 10.1093/toxsci/kfv094. Epub 2015 May 15.
                    
                        
                    
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                    Multi-level gene expression profiles affected by thymidylate synthase and 5-fluorouracil in colon cancer. BMC Genomics. 2006 Apr 3;7:68. doi: 10.1186/1471-2164-7-68.
                    
                        
                    
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                    Characterization of formaldehyde's genotoxic mode of action by gene expression analysis in TK6 cells. Arch Toxicol. 2013 Nov;87(11):1999-2012.
                    
                        
                    
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                    Keratinocyte-derived IL-36gama plays a role in hydroquinone-induced chemical leukoderma through inhibition of melanogenesis in human epidermal melanocytes. Arch Toxicol. 2019 Aug;93(8):2307-2320.
                    
                        
                    
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                    Transcriptional profiling of testosterone-regulated genes in the skeletal muscle of human immunodeficiency virus-infected men experiencing weight loss. J Clin Endocrinol Metab. 2007 Jul;92(7):2793-802. doi: 10.1210/jc.2006-2722. Epub 2007 Apr 17.
                    
                        
                    
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                    Ethyl carbamate induces cell death through its effects on multiple metabolic pathways. Chem Biol Interact. 2017 Nov 1;277:21-32.
                    
                        
                    
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                    New insights into BaP-induced toxicity: role of major metabolites in transcriptomics and contribution to hepatocarcinogenesis. Arch Toxicol. 2016 Jun;90(6):1449-58.
                    
                        
                    
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                    DNA methylome-wide alterations associated with estrogen receptor-dependent effects of bisphenols in breast cancer. Clin Epigenetics. 2019 Oct 10;11(1):138. doi: 10.1186/s13148-019-0725-y.
                    
                        
                    
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                    From transient transcriptome responses to disturbed neurodevelopment: role of histone acetylation and methylation as epigenetic switch between reversible and irreversible drug effects. Arch Toxicol. 2014 Jul;88(7):1451-68.
                    
                        
                    
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                    Gene expression changes in primary human nasal epithelial cells exposed to formaldehyde in vitro. Toxicol Lett. 2010 Oct 5;198(2):289-95.
                    
                        
                    
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                    Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach. BMC Genomics. 2006 Sep 29;7:246. doi: 10.1186/1471-2164-7-246.
                    
                        
                    
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