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72 results

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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. 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.
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. BMC Med Genet. 2008 Apr 22;9:33. doi: 10.1186/1471-2350-9-33. BMC Med Genet. 2008. PMID: 18430236 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: connelly jj. 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
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: connelly jj. 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.
Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
Crosslin DR, Shah SH, Nelson SC, Haynes CS, Connelly JJ, Gadson S, Goldschmidt-Clermont PJ, Vance JM, Rose J, Granger CB, Seo D, Gregory SG, Kraus WE, Hauser ER. Crosslin DR, et al. Among authors: connelly jj. Hum Genet. 2009 Mar;125(2):217-29. doi: 10.1007/s00439-008-0619-0. Epub 2009 Jan 8. Hum Genet. 2009. PMID: 19130089 Free PMC article.
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.
Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, Lintas C, Abramson RK, Wright HH, Ellis P, Langford CF, Worley G, Delong GR, Murphy SK, Cuccaro ML, Persico A, Pericak-Vance MA. Gregory SG, et al. Among authors: connelly jj. BMC Med. 2009 Oct 22;7:62. doi: 10.1186/1741-7015-7-62. BMC Med. 2009. PMID: 19845972 Free PMC article.
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.
Zhang L, Connelly JJ, Peppel K, Brian L, Shah SH, Nelson S, Crosslin DR, Wang T, Allen A, Kraus WE, Gregory SG, Hauser ER, Freedman NJ. Zhang L, et al. Among authors: connelly jj. Hum Mol Genet. 2010 Jul 15;19(14):2754-66. doi: 10.1093/hmg/ddq172. Epub 2010 Apr 26. Hum Mol Genet. 2010. PMID: 20421368 Free PMC article.
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.
Minear MA, Crosslin DR, Sutton BS, Connelly JJ, Nelson SC, Gadson-Watson S, Wang T, Seo D, Vance JM, Sketch MH Jr, Haynes C, Goldschmidt-Clermont PJ, Shah SH, Kraus WE, Hauser ER, Gregory SG. Minear MA, et al. Among authors: connelly jj. Hum Genet. 2011 Jun;129(6):641-54. doi: 10.1007/s00439-011-0959-z. Epub 2011 Feb 5. Hum Genet. 2011. PMID: 21298289 Free PMC article.
72 results