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GATA2 is associated with familial early-onset coronary artery disease.
Connelly JJ, Wang T, Cox JE, Haynes C, Wang L, Shah SH, Crosslin DR, Hale AB, Nelson S, Crossman DC, Granger CB, Haines JL, Jones CJ, Vance JM, Goldschmidt-Clermont PJ, Kraus WE, Hauser ER, Gregory SG. Connelly JJ, et al. Among authors: wang l, wang t. PLoS Genet. 2006 Aug 25;2(8):e139. doi: 10.1371/journal.pgen.0020139. Epub 2006 Jul 20. PLoS Genet. 2006. PMID: 16934006 Free PMC article.
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
Wang L, Hauser ER, Shah SH, Pericak-Vance MA, Haynes C, Crosslin D, Harris M, Nelson S, Hale AB, Granger CB, Haines JL, Jones CJ, Crossman D, Seo D, Gregory SG, Kraus WE, Goldschmidt-Clermont PJ, Vance JM. Wang L, et al. Am J Hum Genet. 2007 Apr;80(4):650-63. doi: 10.1086/512981. Epub 2007 Feb 8. Am J Hum Genet. 2007. PMID: 17357071 Free PMC article.
ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.
Shah SH, Hauser ER, Crosslin D, Wang L, Haynes C, Connelly J, Nelson S, Johnson J, Gadson S, Nelson CL, Seo D, Gregory S, Kraus WE, Granger CB, Goldschmidt-Clermont P, Newby LK. Shah SH, et al. Among authors: wang l. Atherosclerosis. 2008 Nov;201(1):148-54. doi: 10.1016/j.atherosclerosis.2008.01.011. Epub 2008 Feb 12. Atherosclerosis. 2008. PMID: 18374923 Free PMC article.
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.
Shah SH, Freedman NJ, Zhang L, Crosslin DR, Stone DH, Haynes C, Johnson J, Nelson S, Wang L, Connelly JJ, Muehlbauer M, Ginsburg GS, Crossman DC, Jones CJ, Vance J, Sketch MH, Granger CB, Newgard CB, Gregory SG, Goldschmidt-Clermont PJ, Kraus WE, Hauser ER. Shah SH, et al. Among authors: wang l. PLoS Genet. 2009 Jan;5(1):e1000318. doi: 10.1371/journal.pgen.1000318. Epub 2009 Jan 2. PLoS Genet. 2009. PMID: 19119412 Free PMC article.
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW, Wang L, Züchner S, Konidari I, Wang G, Singer C, Nahab F, Scott B, Stajich JM, Pericak-Vance M, Haines J, Vance JM, Martin ER. Edwards TL, et al. Among authors: wang g, wang l. Ann Hum Genet. 2010 Mar;74(2):97-109. doi: 10.1111/j.1469-1809.2009.00560.x. Epub 2010 Jan 8. Ann Hum Genet. 2010. PMID: 20070850 Free PMC article.
Vitamin D receptor gene as a candidate gene for Parkinson disease.
Butler MW, Burt A, Edwards TL, Zuchner S, Scott WK, Martin ER, Vance JM, Wang L. Butler MW, et al. Among authors: wang l. Ann Hum Genet. 2011 Mar;75(2):201-10. doi: 10.1111/j.1469-1809.2010.00631.x. Ann Hum Genet. 2011. PMID: 21309754 Free PMC article.
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.
Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, Frosch MP, Ghetti B, Foroud TM, Honig LS, Marder K, Vonsattel JP, Goldman SM, Vinters HV, Ross OA, Wszolek ZK, Wang L, Dykxhoorn DM, Pericak-Vance MA, Montine TJ, Leverenz JB, Dawson TM, Vance JM. Beecham GW, et al. Among authors: wang l. Neurology. 2015 Mar 10;84(10):972-80. doi: 10.1212/WNL.0000000000001332. Epub 2015 Feb 6. Neurology. 2015. PMID: 25663231 Free PMC article.
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