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Paper Details

VARPRISM: incorporating variant prioritization in tests of de novo mutation association.
Genome Med
6
2016
DLX3, KCND3, MYO1E, PDCD1, Patients, TSPAN4, autism, autism spectrum disorder, exonic mutation, genetic diseases, protein-coding genes
Author NameAffiliation
Hao HuThe University of Texas M.D. Anderson Cancer Center
Hilary CoonUniversity of Utah
Man LiDepartment of Human Genetics and USTAR Center for Genetic Discovery, University of Utah
Man LiDepartment of Human Genetics and USTAR Center for Genetic Discovery, University of Utah
Mark YandellDepartment of Human Genetics and USTAR Center for Genetic Discovery, University of Utah
Mark YandellDepartment of Human Genetics and USTAR Center for Genetic Discovery, University of Utah
Chad D HuffThe University of Texas M.D. Anderson Cancer Center
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