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Genome Biology and Evolution|January 11, 2014
Genome degeneration and adaptation in a nascent stage of symbiosisKelly F Oakeson, Rosario Gil, Adam L Clayton, et al.Annals of Neurology|March 28, 2012
Evidence-based path to newborn screening for Duchenne muscular dystrophyJerry R Mendell, Chris Shilling, Nancy D Leslie, et al.Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 14, 2009
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypesTimothy B Baker, Robert B Weiss, Daniel Bolt, et al.Annals of Neurology|February 27, 2013
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophyKevin M Flanigan, Ermelinda Ceco, Kay-Marie Lamar, et al.American Journal of Human Genetics|October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular DystrophyLuca Bello, Kevin M Flanigan, Robert B Weiss, et al.Annals of Neurology|January 23, 2015
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45Andrew R Findlay, Nicolas Wein, Yuuki Kaminoh, et al.Plos Genetics|July 12, 2008
A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addictionRobert B Weiss, Timothy B Baker, Dale S Cannon, et al.Neurology. Genetics|May 2, 2019
Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>GAngela J Lee, Karra A Jones, Russell J Butterfield, et al.Human Mutation|October 6, 2011
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD geneKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.Pageof 10