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CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Bronson PG, Caillier S, Ramsay PP, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Sawcer SJ, Pericak-Vance MA, Haines JL; International Multiple Sclerosis Genetics Consortium; Hauser SL, Oksenberg JR, Barcellos LF. Bronson PG, et al. Hum Mol Genet. 2010 Jun 1;19(11):2331-40. doi: 10.1093/hmg/ddq101. Epub 2010 Mar 8. Hum Mol Genet. 2010. PMID: 20211854 Free PMC article.
Rare genetic variants impact muscle strength.
Huang Y, Bodnar D, Chen CY, Sanchez-Andrade G, Sanderson M; Biogen Biobank Team; Shi J, Meilleur KG, Hurles ME, Gerety SS, Tsai EA, Runz H. Huang Y, et al. Nat Commun. 2023 Jun 10;14(1):3449. doi: 10.1038/s41467-023-39247-1. Nat Commun. 2023. PMID: 37301943 Free PMC article.
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes.
Karczewski KJ, Solomonson M, Chao KR, Goodrich JK, Tiao G, Lu W, Riley-Gillis BM, Tsai EA, Kim HI, Zheng X, Rahimov F, Esmaeeli S, Grundstad AJ, Reppell M, Waring J, Jacob H, Sexton D, Bronson PG, Chen X, Hu X, Goldstein JI, King D, Vittal C, Poterba T, Palmer DS, Churchhouse C, Howrigan DP, Zhou W, Watts NA, Nguyen K, Nguyen H, Mason C, Farnham C, Tolonen C, Gauthier LD, Gupta N, MacArthur DG, Rehm HL, Seed C, Philippakis AA, Daly MJ, Davis JW, Runz H, Miller MR, Neale BM. Karczewski KJ, et al. Among authors: bronson pg. Cell Genom. 2022 Aug 15;2(9):100168. doi: 10.1016/j.xgen.2022.100168. eCollection 2022 Sep 14. Cell Genom. 2022. PMID: 36778668 Free PMC article.
Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease.
Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA. Martin ER, et al. Among authors: bronson pg. J Med Genet. 2005 Oct;42(10):787-92. doi: 10.1136/jmg.2004.029553. J Med Genet. 2005. PMID: 16199552 Free PMC article.
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.
Liang X, Schnetz-Boutaud N, Kenealy SJ, Jiang L, Bartlett J, Lynch B, Gaskell PC, Gwirtsman H, McFarland L, Bembe ML, Bronson P, Gilbert JR, Martin ER, Pericak-Vance MA, Haines JL. Liang X, et al. Mol Psychiatry. 2006 Mar;11(3):280-5. doi: 10.1038/sj.mp.4001766. Mol Psychiatry. 2006. PMID: 16222332
Lack of association between UBQLN1 and Alzheimer disease.
Slifer MA, Martin ER, Bronson PG, Browning-Large C, Doraiswamy PM, Welsh-Bohmer KA, Gilbert JR, Haines JL, Pericak-Vance MA. Slifer MA, et al. Among authors: bronson pg. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):208-13. doi: 10.1002/ajmg.b.30298. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16526030
Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.
Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Züchner S, et al. Among authors: bronson pg. Ann Hum Genet. 2008 Nov;72(Pt 6):725-31. doi: 10.1111/j.1469-1809.2008.00474.x. Epub 2008 Aug 28. Ann Hum Genet. 2008. PMID: 18761660 Free PMC article.
49 results