I decided to put my activity on X “on hold” for the time being. Please follow me on Bluesky (@cpschaaf.bsky.social) or LinkedIn ( instead. See you there! 👋

RT @EthicsWinkler: "Bluttropfen kann Leben retten: Babyscreening auf Krankheiten" #NEW_LIVES @SZ @cpschaaf

RT @EACDtweet: The EACD / IAACD 2025 Registration for the main congress and the pre-congress sessions is now open! Benefit from the Early B…

RT @mackeithpress: #SchaafYang syndrome and its causal gene illustrates mechanistic understanding of complex neurogenetic disorders and how…

Die „genetische halbe Stunde“ 🧬 geht in die zweite Halbzeit ⚽️. Jetzt registrieren für das neue Jahr. Themen in 2025: Erkrankungen von Muskel, zentralem Nervensystem, Skelett, Haut, Nieren und Stoffwechsel. Wir freuen uns auf Euch!

I was interviewed by @SWRAktuellBW about the recent publication by @edwin_kirk in the @NEJM on couple-based genetic carrier screening.

- A collaborative and proactive team player, eager to contribute to a multidisciplinary research environment. Apply at

RT @MoritzMall: One of the most transformative days of my career: hosting with Maja Hempel Germany’s first #MYT1LSyndrome family meeting la…

RT @fpwr: 💗Leslie, a mom to Nathan who has Schaaf-Yang syndrome (SYS), will do whatever it takes to give him the best chance in life. "You…

RT @fpwr: ⚕️Our free fact sheet on Schaaf-Yang syndrome provides a quick overview of common SYS symptoms, including hypotonia and autism sp…