Grace Talbert
Rare disease advocate and mom to a child with Homocystinuria due to severe MTHFR deficiency
@cathsmstratton.bsky.social
Epidemiology PhD(c) @UofT; @CIHR_IRSC CGS-D & @fdnPETF Scholar; MPH @Yale; VP & Research Chair @moyamoyafoundation #KnowledgeTranslation #KnowledgeSynthesis #RareDisease #PainScience #Disability
@therddr.bsky.social
https://TheRDDR.org RDDR is an invaluable resource dedicated to the storage, organization, and dissemination of rare disease research datasets.
@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
@thecrid.bsky.social
https://TheCRID.org More data sharing, less data silos. CRID is a service that enables parents/patients create their own unique universal ID for clinical research.
@computingcaitie.bsky.social
I live in Switzerland now. @cellarchlab.com at the @biozentrum.bsky.social
@the-virosphere.bsky.social
Senior Scientist and facility manager for the NCI’s National Cryo-EM Facility. Will discuss at length: science, viruses, history, anime, sci-fi, and Star Trek. Views expressed are strictly my own.
@ievadr.bsky.social
Structural biologist | CryoCloud 🔬☁️ | Posts about #cryoEM, some running and cats | Views my own | She/her
@mikelove.bsky.social
Genetics, bioinformatics, comp bio, statistics, data science, open source, open science!
@allostericstate.bsky.social
Revealing the hidden world of shape shifting enzymes using Cryo-EM. Senior research associate at Newcastle University, UK. Currently working as part of Recon4IMD https://www.recon4imd.org Views are my own.
@raungar.bsky.social
Postdoc at @StanfordBioethx Genetics PhD @StanfordMed, BS @UArkansas elsi / rna-seq / rare disease / multi-omics / chronic illness / x-chromosome
@neurometabolism.bsky.social
Clinical-Translational Physician-Scientist 🧫🐭🔬🧬🧠 #MedicalGenetics, #Rare Disease, #Neuroscience #LCC #LabruneSyndrome #MPAN #Leukodystrophy #WomenInSTEM #WomenInMedicine #AcademicResearchMoms Likes/Posts ≠ Medical Advice
@varshneylab.social
Assoc. Prof. Interested in CRISPR, Zebrafish, Disease Modeling, Rare Diseases, and Neurodevelopmental Disorders. The opinions expressed here are my own.
@teresamastracci.bsky.social
Associate Professor, Department of Biology @ Indiana University Indianapolis @iuibiology.bsky.social My lab focuses on diabetes & rare disease research. Science enthusiast. Proudly 🇨🇦
@meberle.bsky.social
Head of CompBio at PacBio interested in rare disease, variant calling, population genetics and more
@anneotation.bsky.social
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
@sabucha.bsky.social
Genetic Counselor. Swiftie. Cat Lady. Ally. Traveler. VW Beetle owner. 36. Views are my own.
@juneanderson.bsky.social
💙💙💙Angry AF. Preparing for the inevitable collapse of our once great nation. Boomer grandma, who splits her time between FL and MS to be near the grands. Twitter refugee. DM's will be blocked. 🏳️🌈 🏳️⚧️ Awareness Homocystinuria due to SEVERE MTHFR Deficiency
@bsky.app
official Bluesky account (check username👆) Bugs, feature requests, feedback: support@bsky.app