Probably Genetic
We offer accessible, clinical-grade genetic sequencing for undiagnosed #chronicillness & #raredisease patients. Let’s end the diagnostic odyssey.
Starter Packs
Created by Probably Genetic (2)
@gbdownes.bsky.social
Dad of two, Professor of Biology @UMass, rare disease researcher and advocate, SPINES @MBL director, and runner. I use zebrafish to study the genetic control of locomotion and epilepsy genes. 🧪🧬🧠
@barbie4congress.bsky.social
Democratic candidate for Congress in Florida's 11th congressional district covering The Villages to Disney World Rare Disease Advocate and MLD Mom BarbieforCongress.com
@jaredwhitlock.bsky.social
features editor @endpts.com / fall 2021 fellow @ksjatmit.bsky.social Writing (and editing) stories on rare disease medicine, diagnostics and China Reach out privately on Signal: jaredwhitlock.73
@trish4democracy.bsky.social
Retired RN ER Trauma, 🚫Maga, former Republican no DMs Activist for abortion healthcare, Women, LGBTQ+, Indigenous people, Latino rights, Black rights, All people are equal. I have MDA5 Dermatomyositis, a rare autoimmune Disease for the past decade.
@varshneylab.social
Assoc. Prof. Interested in CRISPR, Zebrafish, Disease Modeling, Rare Diseases, and Neurodevelopmental Disorders. The opinions expressed here are my own.
@jxchong.bsky.social
Associate Professor. UW Center for Rare Disease Research, @MyGene2, Deputy Editor of @HGGAdvances. #raredisease genetics. CovidWA data
@srcamm.bsky.social
Just a dad of a disabled son, a deceased son and an amazing daughter with a rare disease. #DoBetter
@rdndlab.bsky.social
RDND Lab at King’s College London led by Cristina Dias. Clinical Geneticist and Rare Disease researcher. Rare Conditions, neurodevelopmental disorders of chromatin regulation and chromatin remodeller-TF interactions. https://tinyurl.com/rdndkcl
@ftdregistry.bsky.social
The FTD Disorders Registry is a powerful tool in the movement to create therapies and find a cure for frontotemporal degeneration. Numbers have power. Join the Registry. Advance the science. #EndFTD www.ftdregistry.org
@theaftd.bsky.social
AFTD envisions a world with compassionate care, effective support, and a future free of Frontotemporal Degeneration (FTD). #EndFTD https://www.theaftd.org/
@davidasimon.bsky.social
Associate Professor, Northeastern University School of Law www.davidasimon.us Co-Director, Amy J. Reed Collaborative for Medical Device Safety https://www.safemedicaldevices.org/ Researcher, the CLASSICA Project https://classicaproject.eu/team/
@nature.com
Research, news, and commentary from Nature, the international science journal. For daily science news, get Nature Briefing: https://go.nature.com/get-Nature-Briefing
@altnih4science.bsky.social
Facts & strategy, in an authoritarian takeover. Rightwing billionaires want to privatize NIH and use it to control universities. We work to cure diseases like cancer. Pers views. #science #medicine Signal: altnih4science.79
@erinmevans.bsky.social
Author of EMPIRE OF EXILES and RELICS OF RUIN (Orbit, out 4/24)| Brimstone Angels Saga | Dungeon Scrawlers DM and Concentration Check host | co-host of Writing About Dragons and Shit | she/her
@cnsdrughunter.bsky.social
🧠 🧬 Neuroscientist. Looking for new medicines for #CDKL5, #SCN1A, #SHANK3, #DHPS and other neurological #RareDiseases with #epilepsy
@schnorr.app
Seattle-based game marketing goon at Pokémon. Formerly Capcom & Six Foot. I also love writing, photography, and world travel. All views and opinions are both my own and likely based on a Simpsons quote.
@sdmagnolia.bsky.social
doing my best over here. mom, daughter, sister, advocate. progressive. prefers weirdos over normies. needs a vacation.
@thesumairafdn.bsky.social
TSF is a global nonprofit organization dedicated to raising awareness of rare neuroimmune conditions, building community, supporting research, advocating on behalf of patients. www.sumairafoundation.org
@anneotation.bsky.social
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
@avoidingpublic.bsky.social
Mom, wife, rare disease patient. Systemic Mastocytosis. Treading water till I find the right Dr.🦋🦓💙
@ctsa.bsky.social
Rare disease and cancer analysis models for sequencing data. Scientist at PacBio. Art school survivor. Views my own.
@profmarciniak.bsky.social
Professor of Respiratory Science University of Cambridge. Lung doctor. Fellow St Catharine’s College. Cell biology. Pleural medicine. Rare disease. Genetics. Lab webpage = https://www.cimr.cam.ac.uk/staff/professor-stefan-marciniak
@bsky.app
official Bluesky account (check username👆) Bugs, feature requests, feedback: support@bsky.app