A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.

Journal: American Journal of Human Genetics

Published: 2020-09-08

DOI: 10.1016/j.ajhg.2020.08.019

Affiliations: 11

Authors: 13

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Institutions Share
Icahn School of Medicine at Mount Sinai (ISMMS), MSHS, United States of America (USA) 0.31
University of California, Santa Cruz (UCSC), United States of America (USA) 0.23
Department of Genetics and Genomic Sciences, ISMMS, United States of America (USA) 0.15
University of Antwerp (UA), Belgium 0.15
University of California, Los Angeles (UCLA), United States of America (USA) 0.04
UCLA Health, United States of America (USA) 0.04
The University of Adelaide (Adelaide Uni), Australia 0.04
Women and Kids, SAHMRI, Australia 0.02
Women's and Children's Hospital (WCH), SA Health, Australia 0.02

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