🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

The Taiwan Precision Medicine Initiative enriches genomic resources with long-needed non-European data!🇹🇼🧬 👉N=500K 👉multiple novel risk variants 👉strongly predictive polygenic scores ❗️Summ stats freely available: tpmi.ibms.sinica.edu.tw/www/en/ 📜Preprint: medrxiv.org/content/10.110…

Very grateful to share my latest publication, which links metabolites and druggable proteins to AF and HF. Thanks to Connie Bezzina, Folkert Asselbergs, Jessica van Setten, and others from UCL Institute of Cardiovascular Science, The UCL Institute of Health Informatics, Circulatory Health UMC Utrecht, and Amsterdam UMC. Read the paper here: doi.org/10.1186/s13073…

Incredibly excited that my friend & colleague Patrick Ellinor is the new Executive Director of the Mass General Brigham Heart & Vascular Institute!! MassGeneral News Brigham and Women's Hospital

In Orli Bahcall, our international team delivers a GWAS of dilated cardiomyopathy (DCM) - major cause of heart failure/transplant - led by Sean Jurgens, Joel Rämö, et al., with key leadership from Patrick Ellinor, Mark Daly, Connie Bezzina, and others. nature.com/articles/s4158…

It turns out much needed huge international efforts on dilated cardiomyopathy are like buses... nature.com/articles/s4158… nature.com/articles/s4158… See threads: x.com/KrishnaAragam/… x.com/SeanLZheng/sta…

Cardiomyopathy —Genomic basis of dilated cardiomyopathy unravelled nature.com/articles/s4158… nature.com/articles/s4158… —Atrial cardiomyopathy of Athlete's heart nature.com/articles/s4432…

Eric Topol The study focuses on dilated cardiomyopathy (DCM), a serious heart disease that can lead to heart failure and other complications. Researchers wanted to better understand the genetic factors that contribute to DCM. The researchers identified 70 genetic regions associated with

What is the role of common genetic variation in dilated cardiomyopathy (DCM) 🧬 and what causal pathways underlie the disease? 🫀 Happy to share our GWAS for DCM, published last week in Nature Genetics nature.com/articles/s4158… Amsterdam UMC Broad Institute A detailed 🧵below:

Our latest paper on the contribution of individual comorbidities to diastolic dysfunction and HFpEF just been published Circ: Heart Failure ahajournals.org/doi/10.1161/CI… Congratulations and many thanks to all authors!! María Villalba Orero - Veterinaria Fatima Sanchez-Cabo Pablo Garcia-Pavia Domingo Pascual-Figal CNIC 👇🧵

A thread on some of the fascinating noncoding genetic discoveries from 2024. I've written long form posts and discussed on The Genetics Podcast about these stories. I'll share links to all below with a brief summary.

Onze polikliniek is op zoek naar een klinisch geneticus met aandachtsgebied cardiogenetica om ons team te komen versterken. Zie de vacature op de Amsterdam UMC website: lnkd.in/egXrKKag

For all passionate about cardiogenetics - go to your agendas and block the afternoons of March 20-21 and the morning of March 22nd 2025! This online course with free registration including such fantastic expert speakers will be an unmissable event! More details&link 1st comment.

#PulsDay #01MAR2025 #FeelThePulse! 📲 download the app for a free rhythm check! Amsterdam UMC EHRAPresident European Society of Cardiology Dominik Linz Julian Chun David Duncker Emma Svennberg Sanjiv Narayan

Skilled in bioinformatics? Join our cardiogenomics group Amsterdam UMC More about us and our approach 👉tinyurl.com/5brcsazv Full vacancy info 👉werkenbij.amsterdamumc.org/en/vacatures/r… Humane Genetica Amsterdam UMC NVHG MOLGENIS

🧵 I’m excited to share our latest preprint! We studied 252 SCN5A variants found in patients with Brugada Syndrome by automated patch clamp. [1/7]

📣New from Nicastro et al! 📄Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic #cardiomyopathy cell.com/ajhg/fulltext/…

RT Francisco Martínez: Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy #RareDisease #Genetics #morbidgene cell.com/ajhg/fulltext/…

Jiacheng Miao's PIGEON paper on GxE methodology is now published Nature Human Behaviour with a new title. In our view, this paper can reshape the study design for future complex trait GxE work. Paper📰doi.org/10.1038/s41562… Software🧑‍💻github.com/qlu-lab/GSUB

🗓️ 🧬 I am happy to announce that our next Bootcamp of Genetics for cardiologists will be an special edition in English. It will take place on May 8th 2026 in Barcelona just the day before ESC HFA congress so you can make the most of your trip!

Absolutely thrilled to be part of this ground breaking study with David R. Liu and so many others. One of the most important studies since discovery of the AHC gene in 2012.