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Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Gharahkhani P, Jorgenson E, Hysi P, Khawaja AP, Pendergrass S, Han X, Ong JS, Hewitt AW, Segrè AV, Rouhana JM, Hamel AR, Igo RP Jr, Choquet H, Qassim A, Josyula NS, Cooke Bailey JN, Bonnemaijer PWM, Iglesias A, Siggs OM, Young TL, Vitart V, Thiadens AAHJ, Karjalainen J, Uebe S, Melles RB, Nair KS, Luben R, Simcoe M, Amersinghe N, Cree AJ, Hohn R, Poplawski A, Chen LJ, Rong SS, Aung T, Vithana EN; NEIGHBORHOOD consortium; ANZRAG consortium; Biobank Japan project; FinnGen study; UK Biobank Eye and Vision Consortium; GIGA study group; 23 and Me Research Team; Tamiya G, Shiga Y, Yamamoto M, Nakazawa T, Currant H, Birney E, Wang X, Auton A, Lupton MK, Martin NG, Ashaye A, Olawoye O, Williams SE, Akafo S, Ramsay M, Hashimoto K, Kamatani Y, Akiyama M, Momozawa Y, Foster PJ, Khaw PT, Morgan JE, Strouthidis NG, Kraft P, Kang JH, Pang CP, Pasutto F, Mitchell P, Lotery AJ, Palotie A, van Duijn C, Haines JL, Hammond C, Pasquale LR, Klaver CCW, Hauser M, Khor CC, Mackey DA, Kubo M, Cheng CY, Craig JE, MacGregor S, Wiggs JL. Gharahkhani P, et al. Among authors: haines jl. Nat Commun. 2021 Feb 24;12(1):1258. doi: 10.1038/s41467-020-20851-4. Nat Commun. 2021. PMID: 33627673 Free PMC article.
The genetic epidemiology of multiple sclerosis.
Kenealy SJ, Pericak-Vance MA, Haines JL. Kenealy SJ, et al. Among authors: haines jl. J Neuroimmunol. 2003 Oct;143(1-2):7-12. doi: 10.1016/j.jneuroim.2003.08.005. J Neuroimmunol. 2003. PMID: 14575907 Review.
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.
Barcellos LF, Begovich AB, Reynolds RL, Caillier SJ, Brassat D, Schmidt S, Grams SE, Walker K, Steiner LL, Cree BA, Stillman A, Lincoln RR, Pericak-Vance MA, Haines JL, Erlich HA, Hauser SL, Oksenberg JR. Barcellos LF, et al. Among authors: haines jl. Ann Neurol. 2004 Jun;55(6):793-800. doi: 10.1002/ana.20092. Ann Neurol. 2004. PMID: 15174013
Analysis of European mitochondrial haplogroups with Alzheimer disease risk.
van der Walt JM, Dementieva YA, Martin ER, Scott WK, Nicodemus KK, Kroner CC, Welsh-Bohmer KA, Saunders AM, Roses AD, Small GW, Schmechel DE, Murali Doraiswamy P, Gilbert JR, Haines JL, Vance JM, Pericak-Vance MA. van der Walt JM, et al. Among authors: haines jl. Neurosci Lett. 2004 Jul 15;365(1):28-32. doi: 10.1016/j.neulet.2004.04.051. Neurosci Lett. 2004. PMID: 15234467
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.
Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Rabionet R, et al. Among authors: haines jl. Neurosci Lett. 2004 Dec 6;372(3):209-14. doi: 10.1016/j.neulet.2004.09.037. Neurosci Lett. 2004. PMID: 15542242
Complement factor H variant increases the risk of age-related macular degeneration.
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA. Haines JL, et al. Science. 2005 Apr 15;308(5720):419-21. doi: 10.1126/science.1110359. Epub 2005 Mar 10. Science. 2005. PMID: 15761120
704 results