Vicente Yepez

The ESHG is a non-profit organization. Its aims are to promote research in basic and applied human and medical genetics, to ensure high standards in clinical practice and to facilitate contacts between all persons who share these aims.

Medical geneticist studying rare neurodevelopmental and neurogenetic disorders. PhD student at University of Manchester

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

Clinical Geneticist, VCGS. Professor, University of Melbourne. Rare disease genomics. 🧬🇦🇺

🧬👨‍⚕️Academic Consultant in Clinical Genetics 💬 ESHG Social media chair. 🤖 @DiseaseGenes bot creator #Genetics #Genomics #RareDisease

Advancing prevention, diagnosis and treatment research for the 30 million people living with a rare disease in Europe. 🔗 erdera.org Co-funded by European Union's #HorizonEU Research & Innovation programme. Views expressed are of authors only.

Account for the BLACKSWAN Foundation and RE(ACT) Community #RAREvolution, stand up for research on #rarediseases blackswanfoundation.ch http://www.react-congress.org 🦓

News from the Gagneurlab@TUM -- To understand the genetic basis of gene regulation and its implication in diseases. https://www.cs.cit.tum.de/cmm

PhD student @gagneurlab.bsky.social (TU Munich and Helmholtz Munich). Interested in rare variant genetics. https://shubhankarlondhe.github.io/

Journalist. Lead Editor of the official NFL platform in Spanish. Also talk politics, soccer and day to day matters. Scientific, non toxic, data driven points of view.

official Bluesky account (check username👆) Bugs, feature requests, feedback: support@bsky.app