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.
Student of life! Genome explorer
Stephen Montgomery. Stanford Medicine Professor of Pathology, Genetics, Biomedical Data Science and, by courtesy, Computer Science.
Sporadic on social media.
Director of Computational Biology, Data Sciences Platform at the Broad Institute.
Origins and consequences of genome mutation; software for genomic discovery.
Prof. and Chair of Human Genetics at U. of Utah.
https://www.genetics.utah.edu/
http://quinlanlab.org
Assistant Investigator @ MGH / Broad / HMS. Focus on human genomics and modeling rare variation. She/her
Postdoc at @StanfordBioethx
Genetics PhD @StanfordMed, BS @UArkansas
elsi / rna-seq / rare disease / multi-omics / chronic illness / x-chromosome
Postdoc in labs of @mwheelermd.bsky.social and @sbmontgom.bsky.social @Stanford - Exploring the 🧬 basis of rare diseases through multi-omic data integration 👨💻| ❤️ Computer Science best practices in biology | https://www.wiel.science
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.
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
Genetic Counselor, Clinical Assistant Professor @ Stanford Medicine
cardiovascular genetics | rare disease | all things genomics and multiomics | she/her | views my own
Scientist, Mom. Human Genetics, DNA Variation, Rare Genetic Diseases. Brasil&USA.
CS PhD Candidate at Stanford. Working at the intersection of Machine Learning, Regulatory Genomics, and Complex Disorders
Genomics, Machine Learning, Statistics, Big Data and Football (Soccer, GGMU)
genetics PhD candidate 👩🏻💻🔬 Stanford, CA 📍🌲
metabolomics & multi-omics for rare disease 🧫🧬🥼
MD, PhD; Neuromuscular Medicine at Brigham and Women’s Hospital; Rare disease research at Broad Institute
