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Autosomal dominant midfrequency hearing impairment.
Kaksonen R, Widen E, Cormand B, Toppila E, Starck J, Pyykkö I, Kere J. Kaksonen R, et al. Among authors: widen e. Scand Audiol Suppl. 2001;(52):85-7. doi: 10.1080/010503901300007164. Scand Audiol Suppl. 2001. PMID: 11318494
A dominant gene for developmental dyslexia on chromosome 3.
Nopola-Hemmi J, Myllyluoma B, Haltia T, Taipale M, Ollikainen V, Ahonen T, Voutilainen A, Kere J, Widén E. Nopola-Hemmi J, et al. Among authors: widen e. J Med Genet. 2001 Oct;38(10):658-64. doi: 10.1136/jmg.38.10.658. J Med Genet. 2001. PMID: 11584043 Free PMC article.
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus.
Sigurdsson S, Nordmark G, Göring HH, Lindroos K, Wiman AC, Sturfelt G, Jönsen A, Rantapää-Dahlqvist S, Möller B, Kere J, Koskenmies S, Widén E, Eloranta ML, Julkunen H, Kristjansdottir H, Steinsson K, Alm G, Rönnblom L, Syvänen AC. Sigurdsson S, et al. Among authors: widen e. Am J Hum Genet. 2005 Mar;76(3):528-37. doi: 10.1086/428480. Epub 2005 Jan 18. Am J Hum Genet. 2005. PMID: 15657875 Free PMC article.
Consistently replicating locus linked to migraine on 10q22-q23.
Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A. Anttila V, et al. Among authors: widen e. Am J Hum Genet. 2008 May;82(5):1051-63. doi: 10.1016/j.ajhg.2008.03.003. Am J Hum Genet. 2008. PMID: 18423523 Free PMC article.
299 results