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Genes and Environmental Exposures in Veterans with Amyotrophic Lateral Sclerosis: the GENEVA study. Rationale, study design and demographic characteristics.
Schmidt S, Allen KD, Loiacono VT, Norman B, Stanwyck CL, Nord KM, Williams CD, Kasarskis EJ, Kamel F, McGuire V, Nelson LM, Oddone EZ. Schmidt S, et al. Version 2. Neuroepidemiology. 2008;30(3):191-204. doi: 10.1159/000126911. Epub 2008 Apr 18. Neuroepidemiology. 2008. PMID: 18421219 Free PMC article.
Myocilin mutations in black South Africans with POAG.
Whigham BT, Williams SE, Liu Y, Rautenbach RM, Carmichael TR, Wheeler J, Ziskind A, Qin X, Schmidt S, Ramsay M, Hauser MA, Allingham RR. Whigham BT, et al. Among authors: Schmidt S. Mol Vis. 2011 Apr 27;17:1064-9. Mol Vis. 2011. PMID: 21552496 Free PMC article.
Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma.
Challa P, Schmidt S, Liu Y, Qin X, Vann RR, Gonzalez P, Allingham RR, Hauser MA. Challa P, et al. Among authors: Schmidt S. Mol Vis. 2008 Jan 29;14:146-9. Mol Vis. 2008. PMID: 18334928 Free PMC article.
PURPOSE: To identify if recently described LOXL1 (lysyl oxidase-like 1) polymorphisms are associated with pseudoexfoliation glaucoma (XFG) in a United States (U.S.) ...
PURPOSE: To identify if recently described LOXL1 (lysyl oxidase-like 1) polymorphisms are associated with pseudoexfoliation glaucoma (XFG) i …
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations.
Liu Y, Schmidt S, Qin X, Gibson J, Hutchins K, Santiago-Turla C, Wiggs JL, Budenz DL, Akafo S, Challa P, Herndon LW, Hauser MA, Allingham RR. Liu Y, et al. Among authors: Schmidt S. Invest Ophthalmol Vis Sci. 2008 Aug;49(8):3465-8. doi: 10.1167/iovs.08-1850. Epub 2008 Apr 17. Invest Ophthalmol Vis Sci. 2008. PMID: 18421074 Free PMC article.
Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes.
Motsinger AA, Brassat D, Caillier SJ, Erlich HA, Walker K, Steiner LL, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD. Motsinger AA, et al. Among authors: Schmidt S. Neurogenetics. 2007 Jan;8(1):11-20. doi: 10.1007/s10048-006-0058-9. Epub 2006 Sep 22. Neurogenetics. 2007. PMID: 17024427
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis.
Chiò A, Schymick JC, Restagno G, Scholz SW, Lombardo F, Lai SL, Mora G, Fung HC, Britton A, Arepalli S, Gibbs JR, Nalls M, Berger S, Kwee LC, Oddone EZ, Ding J, Crews C, Rafferty I, Washecka N, Hernandez D, Ferrucci L, Bandinelli S, Guralnik J, Macciardi F, Torri F, Lupoli S, Chanock SJ, Thomas G, Hunter DJ, Gieger C, Wichmann HE, Calvo A, Mutani R, Battistini S, Giannini F, Caponnetto C, Mancardi GL, La Bella V, Valentino F, Monsurrò MR, Tedeschi G, Marinou K, Sabatelli M, Conte A, Mandrioli J, Sola P, Salvi F, Bartolomei I, Siciliano G, Carlesi C, Orrell RW, Talbot K, Simmons Z, Connor J, Pioro EP, Dunkley T, Stephan DA, Kasperaviciute D, Fisher EM, Jabonka S, Sendtner M, Beck M, Bruijn L, Rothstein J, Schmidt S, Singleton A, Hardy J, Traynor BJ. Chiò A, et al. Among authors: Schmidt S. Hum Mol Genet. 2009 Apr 15;18(8):1524-32. doi: 10.1093/hmg/ddp059. Epub 2009 Feb 4. Hum Mol Genet. 2009. PMID: 19193627 Free PMC article.
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