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Human Heredity|October 6, 2012
Obtaining accurate p values from a dense SNP linkage scanWilliam C L Stewart, Ryan L SubaranHuman Mutation|October 8, 2020
FREQMAX provides an alternative approach for determining high-resolution allele frequency thresholds in carrier screeningRyan L Subaran, William C L StewartEpilepsia|December 10, 2014
Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestryRyan L Subaran, Juliette M Conte, William C L Stewart, et al.Eukaryotic Cell|October 14, 2003
Recapitulation of the sexual cycle of the primary fungal pathogen Cryptococcus neoformans var. gattii: implications for an outbreak on Vancouver Island, CanadaJames A Fraser, Ryan L Subaran, Connie B Nichols, et al.The American Journal of Psychiatry|August 3, 2012
Designing case-control studies: decisions about the controlsSusan E Hodge, Ryan L Subaran, Myrna M Weissman, et al.Genetic Epidemiology|April 20, 2007
Improving estimates of genetic maps: a meta-analysis-based approachWilliam C L StewartAmerican Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 30, 2016
Novel variants in ZNF34 and other brain-expressed transcription factors are shared among early-onset MDD relativesRyan L Subaran, Zagaa Odgerel, Rajeswari Swaminathan, et al.Frontiers in Genetics|December 7, 2013
Increasing the power of association studies with affected families, unrelated cases and controlsWilliam C L Stewart, Jane CeriseFrontiers in Genetics|May 25, 2017
A Pragmatic Test for Detecting Association between a Dichotomous Trait and the Genotypes of Affected Families, Controls and Independent CasesMeng Wang, William C L StewartAmerican Journal of Epidemiology|March 31, 2022
Revisiting the Wald Test in Small Case-Control Studies With a Skewed CovariateKomla M Gnona, William C L StewartPageof 4