Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromes.

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Bibliographic Details
Title: Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromes.
Authors: Buecking J; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Güler BE; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; These authors contributed equally., Eibl M; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; These authors contributed equally., Ali AS; Division of Proteomics of Stem Cell and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.; These authors contributed equally., Walczuch T; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Beschauner T; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; Research Institute of Molecular Pathology, Vienna, Austria., Theiss S; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Spanjaard M; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Hinderhofer K; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Herrmann-Sim F; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; Ludwig Maximilian University of Munich, Munich, Germany., de Esch CE; Center for Genomic Medicine, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA., Tai DJC; Center for Genomic Medicine, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA., Talkowski ME; Center for Genomic Medicine, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA., Krijgsveld J; Division of Proteomics of Stem Cell and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.; Medical Faculty, Heidelberg University, Heidelberg, Germany., Schaaf CP; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany., Laugsch M; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; Lead contact.
Source: BioRxiv : the preprint server for biology [bioRxiv] 2026 May 04. Date of Electronic Publication: 2026 May 04.
Publication Type: Journal Article; Preprint
Journal Info: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2692-8205
DOI:10.64898/2026.05.01.722223