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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.

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Title: Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
Authors: Fernandez TV; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, United States America., Williams ZP; Department of Psychiatry, Vanderbilt University School of Nursing, Nashville, TN, United States America., Kline T; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America., Rajendran S; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America., Augustine F; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America., Wright N; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America., Sullivan CAW; Department of Pediatrics, Yale University School of Medicine, New Haven, CT, United States America., Olfson E; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America., Abdallah SB; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America., Liu W; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America., Hoffman EJ; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America., Gupta AR; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.; Department of Pediatrics, Yale University School of Medicine, New Haven, CT, United States America., Singer HS; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.
Source: PloS one [PLoS One] 2023 Oct 03; Vol. 18 (10), pp. e0291978. Date of Electronic Publication: 2023 Oct 03 (Print Publication: 2023).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
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  Data: <searchLink fieldCode="AU" term="%22Fernandez+TV%22">Fernandez TV</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Williams+ZP%22">Williams ZP</searchLink>; Department of Psychiatry, Vanderbilt University School of Nursing, Nashville, TN, United States America.<br /><searchLink fieldCode="AU" term="%22Kline+T%22">Kline T</searchLink>; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.<br /><searchLink fieldCode="AU" term="%22Rajendran+S%22">Rajendran S</searchLink>; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.<br /><searchLink fieldCode="AU" term="%22Augustine+F%22">Augustine F</searchLink>; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.<br /><searchLink fieldCode="AU" term="%22Wright+N%22">Wright N</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Sullivan+CAW%22">Sullivan CAW</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Olfson+E%22">Olfson E</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Abdallah+SB%22">Abdallah SB</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Liu+W%22">Liu W</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Hoffman+EJ%22">Hoffman EJ</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Gupta+AR%22">Gupta AR</searchLink>; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.; Department of Pediatrics, Yale University School of Medicine, New Haven, CT, United States America.<br /><searchLink fieldCode="AU" term="%22Singer+HS%22">Singer HS</searchLink>; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.
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  Data: <searchLink fieldCode="JN" term="%22101285081%22">PloS one</searchLink> [PLoS One] 2023 Oct 03; Vol. 18 (10), pp. e0291978. <i>Date of Electronic Publication: </i>2023 Oct 03 (<i>Print Publication: </i>2023).
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