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972 results

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Page 1
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH Jr, Dawson G, Schellenberg GD, Battaglia A, Maestrini E; Autism Genome Project Consortium; Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB. Noor A, et al. Among authors: mcpherson r. Sci Transl Med. 2010 Sep 15;2(49):49ra68. doi: 10.1126/scitranslmed.3001267. Sci Transl Med. 2010. PMID: 20844286 Free PMC article.
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Lionel AC, Crosbie J, Barbosa N, Goodale T, Thiruvahindrapuram B, Rickaby J, Gazzellone M, Carson AR, Howe JL, Wang Z, Wei J, Stewart AF, Roberts R, McPherson R, Fiebig A, Franke A, Schreiber S, Zwaigenbaum L, Fernandez BA, Roberts W, Arnold PD, Szatmari P, Marshall CR, Schachar R, Scherer SW. Lionel AC, et al. Among authors: mcpherson r. Sci Transl Med. 2011 Aug 10;3(95):95ra75. doi: 10.1126/scitranslmed.3002464. Sci Transl Med. 2011. PMID: 21832240
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.
Davies RW, Dandona S, Stewart AF, Chen L, Ellis SG, Tang WH, Hazen SL, Roberts R, McPherson R, Wells GA. Davies RW, et al. Among authors: mcpherson r. Circ Cardiovasc Genet. 2010 Oct;3(5):468-74. doi: 10.1161/CIRCGENETICS.110.946269. Epub 2010 Aug 21. Circ Cardiovasc Genet. 2010. PMID: 20729558 Free PMC article.
Identifying genes for coronary artery disease: An idea whose time has come.
Roberts R, Stewart AF, Wells GA, Williams KA, Kavaslar N, McPherson R. Roberts R, et al. Among authors: mcpherson r. Can J Cardiol. 2007 Aug;23 Suppl A(Suppl A):7A-15A. doi: 10.1016/s0828-282x(07)71000-0. Can J Cardiol. 2007. PMID: 17668082 Free PMC article. Review.
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.
Jarinova O, Stewart AF, Roberts R, Wells G, Lau P, Naing T, Buerki C, McLean BW, Cook RC, Parker JS, McPherson R. Jarinova O, et al. Among authors: mcpherson r. Arterioscler Thromb Vasc Biol. 2009 Oct;29(10):1671-7. doi: 10.1161/ATVBAHA.109.189522. Epub 2009 Jul 10. Arterioscler Thromb Vasc Biol. 2009. PMID: 19592466
Comparative genome-wide association studies in mice and humans for trimethylamine N-oxide, a proatherogenic metabolite of choline and L-carnitine.
Hartiala J, Bennett BJ, Tang WH, Wang Z, Stewart AF, Roberts R, McPherson R, Lusis AJ, Hazen SL, Allayee H; CARDIoGRAM Consortium. Hartiala J, et al. Among authors: mcpherson r. Arterioscler Thromb Vasc Biol. 2014 Jun;34(6):1307-13. doi: 10.1161/ATVBAHA.114.303252. Epub 2014 Mar 27. Arterioscler Thromb Vasc Biol. 2014. PMID: 24675659 Free PMC article.
972 results