Incredible experience at @epnsnews.bsky.social in Munich sharing our discovery of a novel #gene for #DEE. Grateful for the families, collaborators & Guarantors of Brain for the travel grant. Great science, discussions & new connections! @qs-neurogenetics.bsky.social
01.08.2025 20:05 โ ๐ 5 ๐ 1 ๐ฌ 0 ๐ 0
Neuroscientist. ๐ง
Professor at the University of Edinburgh
Current President of the British Neuroscience Association
FENS-Kavli Network Alumna
Mom to 2 teens, a cat, and a rescue dog. ๐โโฌ๐๐พ
SciFi/fantasy nut - book recommendations welcome! ๐ฝ๐๐ธ
UCL QS IoN Gene Therapy AAV ๐ง
Scientist studying molecular links between Alzheimer's, Ageing, microglia & diet @UCL @UKDRI @ARUKnews #Dementia Trained @BabrahamInst @Cambridge_uni @Stanford
Queen Square Neurologist, Huntingtonโs disease researcher, Associate Director UCL HD Centre, co-founder HDBuzz
Human Geneticist/Genomicist working on Mendelian & rare genetic disorders to enable Precision Medicine. Opinions are my own.
@cgonzagaj everywhere ๐ฆ๐ฆฃโ๏ธ๐งต
Postdoctoral Bioinformaticial in the Computational Rare Disease Genomics group (Nicky Whiffin). univ. Oxford ๐งฌ๐ป
Loves Evolution, regulation, cheese and cats. She/Her
Cardiovascular genetic scientist, crafter, mum.
Passionate about opening up cardiovascular research to more people - @thehearthive.bsky.social. Has too many hobbies. London, UK
Clinician Scientist. Cardiovascular genetics, genomics in healthcare, inherited cardiac conditions, open science, patient participation. He/him.
https://profiles.imperial.ac.uk/j.ware
Academic research scientist in human genetics and genomic medicine; pianist & composer; hiker & outdoors enthusiast.
PI of the Functional Genomics lab (https://fungenlab-ugent.be/) at Ghent University.
Elucidating the genetics of neurodevelopmental disorders.
Special interest in the role of the non-coding genome during neurodevelopment.
Molecular geneticist | Neurogenetics | repeat expansions | chromosome X | snRNAs | and more
Physician-scientist, Adult genetics, Human genetics research, Baylor College of Medicine. Thoughts expressed = my own.
Rare & neuromuscular disease researcher at UWA & the Harry Perkins Institute, Perth ๐ฆ๐บ
Passionate about #sciencefunding, #womeninSTEM, #EMCRs
Mum of ๐ฆ๐ง๐ถ
Posting about genomics, rare disease, PI life & wine
https://www.ravenscroftlab.com
rare disease neurogeneticist | epilepsy | epigenetics | iPSCs | mentor & genetics MedEd | here for the science, lab fun & occasionally my tiny hooman
https://sites.northwestern.edu/carvilllab/
postdoc @ http://debaerelab.com @ https://fungenlab-ugent.be | 3D genome, gene regulation, structural variation | retina, neurodev, space!
Group Leader in Human Genetics, Wellcome Sanger Institute
Rare disease program lead, Centre for Population Genomics.
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Clinical Geneticist, VCGS. Professor, University of Melbourne. Rare disease genomics. ๐งฌ๐ฆ๐บ
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
Happy European human geneticist enjoying life in the United Kingdom. Love everything genomics, even married a genomicist..;)
