Michael Duyzend

Discover the Languages of Biology Build computational models to (help) solve biology? Join us! https://www.deboramarkslab.com DM or mail me!

My views are my own / My views do not reflect those of my institution.

All views and opinions expressed are my own.

GA4GH sets standards and frames policies to expand genomic and health data use within a human rights framework. https://www.ga4gh.org

Dictators are a cowardly and superstitious lot. | Head of Combating Kleptocracy Program at Human Rights Foundation | Author of AMERICAN KLEPTOCRACY and FOREIGN AGENTS | Posts in personal capacity

1. Writer (https://www.adamsharp.me/) 2. Obsessed with lists 3. COMMON PEOPLE 4. THE CORRECT ORDER OF BISCUITS 5. THE WHEEL IS SPINNING BUT THE HAMSTER IS DEAD (http://geni.us/yDxa)

Research, news, and commentary from Nature, the international science journal. For daily science news, get Nature Briefing: https://go.nature.com/get-Nature-Briefing

Genetic Counselor, Clinical Assistant Professor @ Stanford Medicine cardiovascular genetics | rare disease | all things genomics and multiomics | she/her | views my own

Physician-scientist @stanford medicine, AHFTC, genomics of rare disease, cardiovascular genetics, exercise multiomics, cardiomyopathy, novel therapeutics and data. #motrpac #UDN #Gregor #CFDE . Husband, kids and cats, mountains and snow. Resist hate.

Human genomicist 🧬 | Assistant Prof @ Institute for Genomic Health, Mount Sinai 🗽

Genomics, big data, open science, diversity. Director of the Centre for Population Genomics, focused on building a more equitable future for genomic medicine. Opinions my own.

Director, Wellcome Sanger Institute. Decipherer of developmental disorders. Co-founder Congenica. Dad, husband, cyclist, gardener. Views own.

Physician scientist @ St. Jude (neuro)genetics | genomics epilepsy | rare disease | precision medicine

MD-PhD candidate at the University of Sydney & Garvan Institute. Studying tandem repeats in single-cell contexts w/ @dgmacarthur.bsky.social

Genomic medicine researcher; chief genomics officer at MGH; clinical lab director at @broadinstitute

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/

CODA. Dad. Interested in genetics, long-read sequencing, and ultramarathon running. Assistant Professor at University of Washington. The command line is my happy place. https://millerlaboratory.com

Associate Professor. UW Center for Rare Disease Research, @MyGene2, Deputy Editor of @HGGAdvances. #raredisease genetics. CovidWA data

Assistant Professor @ Stanford