Christian Schaaf

@cpschaaf & his team developed two new mouse models of the Bosch-Boonstra-Schaad optic atrophy syndrome, carrying patient-specific Nr2f1 variants and capturing key aspects of the #BBSOAS, offering insights into genotype-phenotype links. #raredisease bit.ly/4rsjQVC

We look forward to welcoming you to the start of this comprehensive two-year journey in clinical genetics.

Online registration for Year 1 beginning in January 2026 is now open! gfhev.de/termine/k230-2…

Following the successful establishment of the seminar series with almost 500 participants from German-speaking countries, we are pleased to announce the international launch of the English edition of our course series: Genetic Half-Hour – Comprehensive Course in Clinical Genetics

Leitung des zytogenetischen Labors am Uniklinikum Heidelberg neu zu besetzen. karriere.klinikum.uni-heidelberg.de/index.php?ac=j…

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

"Bluttropfen kann Leben retten: Babyscreening auf Krankheiten" #NEW_LIVES @SZ @cpschaaf sueddeutsche.de/gesundheit/for…

The EACD / IAACD 2025 Registration for the main congress and the pre-congress sessions is now open! Benefit from the Early Bird rate until January 31st, 2025, and secure your spot in one of the pre-congress symposia. For more information, please visit: eacd-iaacd2025.org

#SchaafYang syndrome and its causal gene illustrates mechanistic understanding of complex neurogenetic disorders and how targeted therapies can be developed @cpschaaf buff.ly/4iAGzKx

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! gfhev.de/termine/k219-2…

swr.de/wissen/erbkran… 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 my-hbigs.uni-heidelberg.de/site/index.php…

- Exceptional communication and organizational skills, with the ability to manage multiple tasks and priorities effectively. - Self-motivated and capable of working independently while maintaining high standards of scientific rigor.

PhD position available at the Institute of Human Genetics @uniklinik_hd and @UniHeidelberg , start date February 2025.