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Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.
Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. Poduri A, et al. Among authors: barker cummings c. Neurology. 2009 Oct 20;73(16):1264-72. doi: 10.1212/WNL.0b013e3181bd10d3. Neurology. 2009. PMID: 19841378 Free PMC article.
Localization of a gene for partial epilepsy to chromosome 10q.
Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS, Scheuer ML, et al. Ottman R, et al. Nat Genet. 1995 May;10(1):56-60. doi: 10.1038/ng0595-56. Nat Genet. 1995. PMID: 7647791 Free PMC article.
Familial risk of epilepsy: a population-based study.
Peljto AL, Barker-Cummings C, Vasoli VM, Leibson CL, Hauser WA, Buchhalter JR, Ottman R. Peljto AL, et al. Among authors: barker cummings c. Brain. 2014 Mar;137(Pt 3):795-805. doi: 10.1093/brain/awt368. Epub 2014 Jan 26. Brain. 2014. PMID: 24468822 Free PMC article.
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC. Kalachikov S, et al. Nat Genet. 2002 Mar;30(3):335-41. doi: 10.1038/ng832. Epub 2002 Jan 28. Nat Genet. 2002. PMID: 11810107 Free PMC article.
17 results