Svetlana Gorokhova
Svetlana Gorokhova, M.D., Ph.D., is working in Marseille Medical Genetics (@univamu) and @aphm-chu-marseille in Marseille, France, remote member of NNDCS @NIH @NINDSnews
@jdbux.bsky.social
Director, Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai. Shakuhachi student.
@fekrijeselimi.bsky.social
Neuroscientist, yoga aficionado, wish I could do more for equality and human rights all around the world
@carolinefwright.bsky.social
Academic research scientist in human genetics and genomic medicine; pianist & composer; hiker & outdoors enthusiast.
@anshulkundaje.bsky.social
Genomics, Machine Learning, Statistics, Big Data and Football (Soccer, GGMU)
@genomeresearch.bsky.social
A leading peer-reviewed genomics journal. https://genome.cshlp.org Submit: http://submit.genome.org
@francois-devred.bsky.social
Directeur UMR CNRS 7051, INP @inp-marseille.bsky.social @cnrsbiologie.bsky.social Équipe Interactions moléculaires & pharmacologie + plateforme PINT Vice Doyen @facpharmarseille.bsky.social @univ-amu.fr
@ewanbirney.bsky.social
Executive Director EMBL. I have an insatiable love of biology. Consultant to ONT and Cantata (Dovetail)
@ucscgenomics.bsky.social
Focusing the power of genomics to create a healthier world. Leader in pangenomics, conservation genomics, cancer genomics, pathogen genomics, and nanopore sequencing. Home of the UCSC Genome Browser, @ucscxena, UShER, Dockstore, and other high-power tools.
@gnomad-project.bsky.social
The world's largest open resource of human genetic variation. For help please use http://broad.io/gnomad_forum; feature requests/bug reports to http://broad.io/gnomad_github
@oligogirl.bsky.social
Translating science from bench to bedside and from jargon to lay language
@sambaxter.bsky.social
@anneotation.bsky.social
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
@ahoischen.bsky.social
Genomic technologies: WES/WGS, long-read sequencing, optical genome mapping, somatic mutations; Immuno-genomics: rare diseases; immunodeficiencies; inborn errors of immunity; clonal hematopoiesis https://shorturl.at/MxQ7O https://www.immuno-genomics.com
@ksamocha.bsky.social
Assistant Investigator @ MGH / Broad / HMS. Focus on human genomics and modeling rare variation. She/her
@aphm-chu-marseille.bsky.social
Bienvenue sur le compte officiel Bluesky des Hôpitaux Universitaires de Marseille, CHU de la 2ème ville de France. Notre ADN : prendre soin, innover, transmettre. #APHM
@sedlazeck.bsky.social
@khmiga.bsky.social
Associate Professor of Biomolecular Engineering at the University of California, Santa Cruz; Associate Director, UC Santa Cruz Genomics Institute
@mikeschatz.bsky.social
Bloomberg Distinguished Professor at Johns Hopkins University. http://schatz-lab.org
@aphillippy.bsky.social
Finished a human genome, working on a few more 👨💻 Lab: https://genomeinformatics.github.io Posts are my own
@jsantoyo.bsky.social
Molecular & Computational Biologist at the University of Edinburgh #Genomics #Bioinformatics #Sequencing Head of Edinburgh Genomics 🧬 🖥️ Opinions my own. He/Him Lab: https://genomics.ed.ac.uk/ LinkedIn: https://www.linkedin.com/in/javiersantoyolopez/
@ginaravenscroft.bsky.social
Rare & neuromuscular disease researcher at UWA & the Harry Perkins Institute, Perth 🇦🇺 Passionate about #sciencefunding, #womeninSTEM, #EMCRs Mum of 👦👧🐶 Posting about genomics, rare disease, PI life & wine https://www.ravenscroftlab.com
@broadinstitute.org
A multidisciplinary community of researchers with the mission to better understand the roots of disease and narrow the gap between new biological insights and impact for patients. Broadinstitute.org
@mehurles.bsky.social
Director, Wellcome Sanger Institute. Decipherer of developmental disorders. Co-founder Congenica. Dad, husband, cyclist, gardener. Views own.
@christeldepienne.bsky.social
Molecular geneticist | Neurogenetics | repeat expansions | chromosome X | snRNAs | and more
@zornitza.bsky.social
Clinical Lead, Australian Genomics. Clinical Geneticist, VCGS. Professor, University of Melbourne. Rare disease genomics. 🧬🇦🇺
@varianteffect.bsky.social
Advancing the promise of the Human Genome Project by interpreting the landscape of human genetic variation. https://www.varianteffect.org https://www.linkedin.com/company/atlas-of-variant-effects-alliance
@sbmontgom.bsky.social
Stephen Montgomery. Stanford Medicine Professor of Pathology, Genetics, Biomedical Data Science and, by courtesy, Computer Science.
@nicorobine.bsky.social
Director, Computational Biology. [nrobine]@nygenome[.org] RNA-Seq / Cancer Genomics / anything NYC / mostly in English, sometimes in French. #NoPasaran
@nygenome.org
An independent, nonprofit academic research institution at the forefront of transforming biomedical research to advance genomic science and precision medicine.
@euanashley.bsky.social
chair of stanford dept of medicine author of the genome odyssey founder of biotechnology companies
@aaronquinlan.bsky.social
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
@nickywhiffin.bsky.social
Associate Professor @ Big Data Institute, University of Oxford 2024 Lister Institute Fellow genomics | rare disease | gene regulation | genetic therapies https://rarediseasegenomics.org/ (field) hockey player | cyclist | hiker
@dgmacarthur.bsky.social
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.
@heidirehm.bsky.social
Genomic medicine researcher; chief genomics officer at MGH; clinical lab director at @broadinstitute