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Paper Details

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.
Genet Med
72
2016
genes, genetic disorders, genomic variation, medical disorder, pathogenic variants, patients
Author NameAffiliation
Jessica Ezzell HunterCenter for Health Research, Kaiser Permanente Northwest
Leslie G BieseckerNational Human Genome Research Institute, National Institutes of Health
Leslie G BieseckerNational Human Genome Research Institute, National Institutes of Health
Adam H BuchananGenomic Medicine Institute
Brian C JensenUniversity of North Carolina School of Medicine, McAllister Heart Institute
Kristy LeeUniversity of North Carolina
Christa Lese MartinAutism and Developmental Medicine Institute
Erin M RamosNational Human Genome Research Institute, National Institutes of Health
Sheri D SchullyNational Institutes of Health
Alan F ScottMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Anne SlavotinekUniversity of California san francisco
Anne SlavotinekUniversity of California san francisco
Nara SobreiraMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Natasha T StrandeUniversity of North Carolina
Marc S WilliamsGenomic Medicine Institute
Jonathan S BergUniversity of North Carolina
James P EvansUniversity of North Carolina
Katrina A B GoddardCenter for Health Research, Kaiser Permanente Northwest
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