Vincent Strehlow

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 3

Top Topics

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Bernt Popp, Melanie Brugger, Sibylle Poschmann, Bartolomaeus Tobias, Maximilian Radtke, Julia Hentschel, Nataliya Di Donato, Andreas Rump, Janina Gburek-Augustat, Elisabeth Graf, Matias Wagner, Ina Sorge, Johannes R Lemke, Thomas Meitinger, Rami Abou Jamra, Vincent Strehlow, Theresa Brunet
The constitutional gain-of-function variant p.Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical genetics (2022)
Vincent Strehlow, Claudine Rieubland, Sabina Gallati, Sukhan Kim, Scott J Myers, Vincent Peterson, Amy J Ramsey, Daniel D Teuscher, Stephen F Traynelis, Johannes R Lemke
Compound-heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy. Epilepsia 63 (10) (2022)
Franziska Roessler, Anita E Beck, Ball Susie, Bartolomaeus Tobias, Amber Begtrup, Saskia Biskup, Oana Caluseriu, Norman Delanty, Christine Fröhlich, Marie T Greally, Maike Karnstedt, Chiara Klöckner, Joanne Kurtzberg, Susanna Schubert, Martin Schulze, Michael Weidenbach, Dominik S Westphal, Maire White, Cordula M Wolf, Jacob Zyskind, Bernt Popp, Vincent Strehlow
Genetic and phenotypic spectrum in the NONO-associated syndromic disorder. American journal of medical genetics. Part A (2022)