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Nature Genetics|May 23, 2017
Reevaluation of SNP heritability in complex human traitsDoug Speed, Na Cai, , et al.Genome Medicine|February 5, 2015
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicityDace Ruklisa, James S Ware, Roddy Walsh, et al.Proceedings of the National Academy of Sciences of the United States of America|November 5, 2003
Multipoint linkage-disequilibrium mapping narrows location interval and identifies mutation heterogeneityAndrew P Morris, John C Whittaker, Chun-Fang Xu, et al.Journal of Molecular Biology|July 9, 2004
Clustering of protein domains in the human genomeLianne R Mayor, Keiran P Fleming, Arne Müller, et al.Genetic Epidemiology|January 18, 2008
Genome-wide significance for dense SNP and resequencing dataClive J Hoggart, Taane G Clark, Maria De Iorio, et al.Genome Biology|September 6, 2007
Functional constraint and small insertions and deletions in the ENCODE regions of the human genomeTaane G Clark, Toby Andrew, Gregory M Cooper, et al.BMC Bioinformatics|September 10, 2008
Fregene: simulation of realistic sequence-level data in populations and ascertained samplesMarc Chadeau-Hyam, Clive J Hoggart, Paul F O'Reilly, et al.Brain : a Journal of Neurology|July 28, 2014
Describing the genetic architecture of epilepsy through heritability analysisDoug Speed, Terence J O'Brien, Aarno Palotie, et al.Genome Research|September 3, 2017
Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretationJoshua Traynelis, Michael Silk, Quanli Wang, et al.Nature|June 14, 2023
Mitotic tethering enables inheritance of shattered micronuclear chromosomesPrasad Trivedi, Christopher D Steele, Franco K C Au, et al.Pageof 11