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Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, Hofman A, Zwarts MJ, van Doormaal PT, Rujescu D, Strengman E, Giegling I, Muglia P, Tomik B, Slowik A, Uitterlinden AG, Hendrich C, Waibel S, Meyer T, Ludolph AC, Glass JD, Purcell S, Cichon S, Nöthen MM, Wichmann HE, Schreiber S, Vermeulen SH, Kiemeney LA, Wokke JH, Cronin S, McLaughlin RL, Hardiman O, Fumoto K, Pasterkamp RJ, Meininger V, Melki J, Leigh PN, Shaw CE, Landers JE, Al-Chalabi A, Brown RH Jr, Robberecht W, Andersen PM, Ophoff RA, van den Berg LH. van Es MA, et al. Among authors: nothen mm. Nat Genet. 2009 Oct;41(10):1083-7. doi: 10.1038/ng.442. Epub 2009 Sep 6. Nat Genet. 2009. PMID: 19734901
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.
Cichon S, Nöthen MM, Wolf HK, Propping P. Cichon S, et al. Among authors: nothen mm. Am J Med Genet. 1996 Apr 9;67(2):229-31. doi: 10.1002/(SICI)1096-8628(19960409)67:2<229::AID-AJMG17>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723054
Linking single nucleotide polymorphisms.
Nöthen MM, Cichon S. Nöthen MM, et al. Pharmacogenetics. 2002 Mar;12(2):89-90. doi: 10.1097/00008571-200203000-00001. Pharmacogenetics. 2002. PMID: 11875361 No abstract available.
1,027 results