10th i3S-Instituto de Investigação e Inovação em Saúde Annual Meeting it’s starting!!! Excited to know more about my colleagues work and their recent findings 😁

First Keynote Lecture of #SPGH 27th Annual Meeting with Alexander Hoischen! What a pleasure to host our peers from Solve-RD in my home country 😁

Don't miss this work from Público on the Hereditary diffuse gastric cancer syndrome, its impact on the lives of patients and the power of science. publico.pt/2024/06/19/cie… (in English) tinyurl.com/34zfuwvk (em PT) #i3Snews #i3Sresearch #cancer

Stay tuned this weekend 📣📣 for a journalistic piece on one Portuguese family carrying a CDH1 founder variant causing HDGC publico.pt/2024/08/17/cie…

BREAKING NEWS The 2024 #NobelPrize in Physiology or Medicine has been awarded to Victor Ambros and Gary Ruvkun for the discovery of microRNA and its role in post-transcriptional gene regulation.

Not all #Patients with #Cancer have smoked but for those who have, #SmokingCessation improves ⬆️survival (& the earlier the better). 🔥🚨OncoAlert Just published JAMA Oncology #Survival Outcomes of #Smoking #Cessation Treatment After Cancer Diagnosis. 👇🏼 jamanetwork.com/journals/jamao…

Thrilled to share that our paper is out!📢This marks my first co-second (wth Yaniv Eyal-Lubling) authorship collab during my PhD—couldn't be prouder of our team's work "Modeling TNBC drug responses with patient-derived xenografts opens doors to precision medicine strategies" Cancer Research 1/n

First ProgRET paper on dominant retinal disease with PhD fellows Stefanida Shliaga Radboudumc Nelson Martins UGent Geneeskunde & Gezondheidswetenschappen & PIs Susanne Roosing David Stanek CharlesUniversity Prague Susanne Kohl Universität Tübingen Miriam Bauwens Elfride De Baere INM_Montpellier Vision_INM Viki Kalatzis 🚀👏

First ProgRET paper on dominant retinal disease with PhD fellows Stefanida Shliaga Radboudumc Nelson Martins UGent Geneeskunde & Gezondheidswetenschappen & PIs Susanne Roosing David Stanek CharlesUniversity Prague S Kohl Universität Tübingen Miriam Bauwens Elfride De Baere INM_Montpellier Vision_INM Viki Kalatzis Sandro Banfi Lab 👇

At the beginning of the year we warmly welcome Mathys Weber and Nelson Martins Mathys will work on international relations 🌎and Nelson will contribute to the Social Media #Young #geneticists committees💻 #genetics #geneticists European Society of Human Genetics (ESHG) eshg_young

Autosomal dominant IRD accounts for 25-40% of cases, posing challenges due to variable phenotypes, milder forms, and later onset. Mutations are categorized as gain-of-function, dominant-negative, or haploinsufficiency. Stay tuned as we explore these mechanisms further!

Don’t miss this opportunity! ⬇️

Welcome to the ESHG-Young team, Maria Francesca, Nelson, Mathys and Ewelina! Together, they represent the diversity, collaboration, and innovation driving the future of human genetics! Get to know our four new members in these images! European Society of Human Genetics (ESHG) European Journal of Human Genetics #Genetics