Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Journal: Nature Communications

Published: 2020-01-14

DOI: 10.1038/s41467-019-13624-1

Affiliations: 16

Authors: 41

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Institutions Share
Center for Applied Genomics (CAG), CHOP, United States of America (USA) 0.69
Department of Pediatrics, Penn, United States of America (USA) 0.08
Department of Genome Sciences, UW, United States of America (USA) 0.04
Department of Biostatistics, Epidemiology and Informatics (DBEI), Penn, United States of America (USA) 0.03
Department of Computer Science (CS), NJIT, United States of America (USA) 0.02
Department of Biomedical and Health Informatics (DBHi), CHOP, United States of America (USA) 0.02
UCSF Department of Radiation Oncology, United States of America (USA) 0.02
UCSF Helen Diller Family Comprehensive Cancer Center, United States of America (USA) 0.02
Affiliated Cancer Hospital of Guangzhou Medical University, China 0.01
Division of Cardiology, CHOP, United States of America (USA) 0.01
Division of Oncology, CHOP, United States of America (USA) 0.01
University of Washington School of Medicine (UWSOM), United States of America (USA) 0.01
Department of Psychiatry, Penn, United States of America (USA) 0.01
Department of Child and Adolescent Psychiatry and Behavioral Sciences, CHOP, United States of America (USA) 0.01
Division of Human Genetics, CHOP, United States of America (USA) 0.01
Department of Experimental Medicine, Sapienza University of Rome, Italy 0.01

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