Publications
] Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Brain 143, 2106-2118 (2020).
The Centers for Complex Disease Genomics are funded by
the National Human Genome Research Institute and the National Heart, Lung, and Blood Institute.
the National Human Genome Research Institute and the National Heart, Lung, and Blood Institute.
Baylor College of Medicine (UM1 HG008898), Broad Institute (UM1 HG008895),
New York Genome Center (UM1 HG008901), Washington University (UM1 HG008853)
New York Genome Center (UM1 HG008901), Washington University (UM1 HG008853)