Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Media type: E-Article
Title: Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Contributor: Maury, Eduardo A. [Author]; Sherman, Maxwell A. [Author]; McCarroll, Steven A. [Author]; Webb, Bradley T. [Author]; Wolen, Aaron R. [Author]; Wormley, Brandon K. [Author]; Kendler, Kenneth S. [Author]; Riley, Brien P. [Author]; Kähler, Anna K. [Author]; Magnusson, Patrik K. E. [Author]; Hultman, Christina M. [Author]; Bertalan, Marcelo [Author]; Hansen, Thomas [Author]; Loh, Po-Ru [Author]; Olsen, Line [Author]; Rasmussen, Henrik B. [Author]; Werge, Thomas [Author]; Mattheisen, Manuel [Author]; Black, Donald W. [Author]; Bruggeman, Richard [Author]; Buccola, Nancy G. [Author]; Buckner, Randy L. [Author]; Roffman, Joshua L. [Author]; Byerley, William [Author]; [...]
imprint: Elsevier, 2023
Published in: Cell genomics 3(8), 100356 - (2023). doi:10.1016/j.xgen.2023.100356
Language: English
DOI: https://doi.org/10.1016/j.xgen.2023.100356; https://doi.org/10.34734/FZJ-2023-04285
ISSN: 2666-979X
Origination:
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Access State: Open Access

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