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Page 1
Genetic and functional association of FAM5C with myocardial infarction.
Connelly JJ, Shah SH, Doss JF, Gadson S, Nelson S, Crosslin DR, Hale AB, Lou X, Wang T, Haynes C, Seo D, Crossman DC, Mooser V, Granger CB, Jones CJ, Kraus WE, Hauser ER, Gregory SG. Connelly JJ, et al. Among authors: gregory sg. BMC Med Genet. 2008 Apr 22;9:33. doi: 10.1186/1471-2350-9-33. BMC Med Genet. 2008. PMID: 18430236 Free PMC article.
SNPselector: a web tool for selecting SNPs for genetic association studies.
Xu H, Gregory SG, Hauser ER, Stenger JE, Pericak-Vance MA, Vance JM, Züchner S, Hauser MA. Xu H, et al. Among authors: gregory sg. Bioinformatics. 2005 Nov 15;21(22):4181-6. doi: 10.1093/bioinformatics/bti682. Epub 2005 Sep 22. Bioinformatics. 2005. PMID: 16179360 Free PMC article.
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: gregory sg. 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. Among authors: gregory sg. 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.
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.
Gregory SG, Schmidt S, Seth P, Oksenberg JR, Hart J, Prokop A, Caillier SJ, Ban M, Goris A, Barcellos LF, Lincoln R, McCauley JL, Sawcer SJ, Compston DA, Dubois B, Hauser SL, Garcia-Blanco MA, Pericak-Vance MA, Haines JL; Multiple Sclerosis Genetics Group. Gregory SG, et al. Nat Genet. 2007 Sep;39(9):1083-91. doi: 10.1038/ng2103. Epub 2007 Jul 29. Nat Genet. 2007. PMID: 17660817
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
Sutton BS, Crosslin DR, Shah SH, Nelson SC, Bassil A, Hale AB, Haynes C, Goldschmidt-Clermont PJ, Vance JM, Seo D, Kraus WE, Gregory SG, Hauser ER. Sutton BS, et al. Among authors: gregory sg. Hum Mol Genet. 2008 May 1;17(9):1318-28. doi: 10.1093/hmg/ddn020. Epub 2008 Jan 18. Hum Mol Genet. 2008. PMID: 18204052 Free PMC article.
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.
Wang L, Hauser ER, Shah SH, Seo D, Sivashanmugam P, Exum ST, Gregory SG, Granger CB, Haines JL, Jones CJ, Crossman D, Haynes C, Kraus WE, Freedman NJ, Pericak-Vance MA, Goldschmidt-Clermont PJ, Vance JM. Wang L, et al. Among authors: gregory sg. Ann Hum Genet. 2008 Jul;72(Pt 4):443-53. doi: 10.1111/j.1469-1809.2008.00433.x. Epub 2008 Jul 3. Ann Hum Genet. 2008. PMID: 18318786 Free PMC article.
Refinement of 2q and 7p loci in a large multiplex NTD family.
Stamm DS, Siegel DG, Mehltretter L, Connelly JJ, Trott A, Ellis N, Zismann V, Stephan DA, George TM, Vekemans M, Ashley-Koch A, Gilbert JR, Gregory SG, Speer MC; NTD Collaborative Group. Stamm DS, et al. Among authors: gregory sg. Birth Defects Res A Clin Mol Teratol. 2008 Jun;82(6):441-52. doi: 10.1002/bdra.20462. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18452155
176 results