Diverse Human References Drive Genomic Discoveries for Everyone
Our mission is to enable the promise of genomics to better human health by creating the world’s most advanced sequencing technologies.
The Precision Health Data Cloud
Learn more at dnanexus.com
https://www.cell.com/AJHG/home
MD, PhD; Neuromuscular Medicine at Brigham and Women’s Hospital; Rare disease research at Broad Institute
Join us in uniting the Genomics community! Our goal is to deliver the benefits of genomics to patients faster.
Stephen Montgomery. Stanford Medicine Professor of Pathology, Genetics, Biomedical Data Science and, by courtesy, Computer Science.
Sporadic on social media.
Genetics - Statistics - Psychiatry.
Depression pharmacogenetics.
SGDP Centre, King’s College London. Psychiatric Genomics Consortium.
The GREGoR Consortium (Genomics Research to Elucidate the Genetics of Rare diseases) seeks to develop and apply approaches to discover the cause of currently unexplained rare genetic disorders.
https://gregorconsortium.org/
Studying the genomics of Indian populations @CBR_IISc. Mental health in academia. Outreach. @Umich transplant.
Postdoctoral fellow at @sinaigenhealth.bsky.social
Genomics/Bioinformatics Assoc. Prof., University of Michigan
MsState, Duke, Stanford, Michigan
Genetic Variation, Silencers, RegulomeDB, Nanopore Tech
Faculty at Emory Human Genetics, periodically cool dad, typical Boston sports fan (sorry), big believer in Dunning-Kruger effect
Bioinformatician @ Center for Statistical Genetics, University of Michigan
https://github.com/welchr/
