Author

Ute Moog

Heidelberg UniversityORCID 0000-0002-4580-7030Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam P. VogeliD· 1 shared Angela Tamsin MorganiD· 1 shared Angelika Rieß· 1 shared Brigitte VollmeriD· 1 shared Chirag PateliD· 1 shared Christiane ZweieriD· 1 shared Daisy G.Y. Thompson-LakeiD· 1 shared David A. KooleniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam P. VogelORCID

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1 paper

Recent·Most cited

Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

Lottie D. Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer, Katrin Schulze, Tracy Ann Briggs, Ruth O. Braden, Adam P. Vogel, Daisy G.Y. Thompson-Lake, Chirag Patel, Edward M. Blair, Himanshu Goel, Samantha J. Turner, Ute Moog, , Angela Tamsin Morgan

This study characterizes 29 individuals with FOXP2 variants, showing high prevalence of speech disorders and language impairments, with relatively specific phenotypes compared to other monogenic conditions.

medRxiv · Jun 1, 2022 · PreprintGenetic & Genomic Medicine