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Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors.

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Title: Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors.
Authors: Willim J; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Woike D; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Greene D; Icahn School of Medicine at Mount Sinai, New York, NY, USA., Das S; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Pfeifer K; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Yuan W; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Lindsey A; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Itani O; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Böhme AL; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Tibbe D; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Hönck HH; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Hassani Nia F; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Zech M; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany.; Institute for Advanced Study, Technical University of Munich, Garching, Germany., Brunet T; Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Munich, Germany., Faivre L; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, CHU Dijon-Bourgogne, Dijon, France.; INSERM-Université de Bourgogne-UMR1231 GAD, Dijon, France., Sorlin A; INSERM-Université de Bourgogne-UMR1231 GAD, Dijon, France.; Laboratoire de Génomique médicale, Centre NEOMICS, CHU Dijon Bourgogne, Dijon, France., Vitobello A; INSERM-Université de Bourgogne-UMR1231 GAD, Dijon, France.; Laboratoire de Génomique médicale, Centre NEOMICS, CHU Dijon Bourgogne, Dijon, France., Smol T; Univ. Lille, CHU Lille, ULR7364 - RADEME, Lille, France., Colson C; Univ. Lille, CHU Lille, ULR7364 - RADEME, Lille, France., Baranano K; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Schatz K; Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA., Bayat A; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.; Department for Regional Health Research, University of Southern Denmark, Odense, Denmark.; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark., Schoch K; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA., Spillmann R; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA., Davis EE; Center for Human Disease Modeling, Duke University Medical Center, Durham, NC, USA.; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Departments of Pediatrics and Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA., Conboy E; Indiana University School of Medicine, Indianapolis, IN, USA., Vetrini F; Indiana University School of Medicine, Indianapolis, IN, USA., Platzer K; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany., Neuser S; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany., Gburek-Augustat J; Division of Neuropaediatrics, Hospital for Children and Adolescents, University of Leipzig Medical Center, Leipzig, Germany., Grace AN; Molecular and Human Genetics Department, Baylor College of Medicine, Houston, TX, USA., Mitchell B; Baylor College of Medicine in San Antonio, San Antonio, TX, USA., Stegmann A; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands., Sinnema M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands., Meeks N; Children's Hospital Colorado, Division of Clinical Genetics & Metabolism, Aurora, CO, USA., Saunders C; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, MO, USA.; School of Medicine, University of Missouri Kansas City, Kansas City, MO, USA.; Genomic Medicine Center, Children's Mercy Research Institute, Kansas City, MO, USA., Cadieux-Dion M; Department of Pathology and Laboratory Medicine, Children's Mercy Hospital, Kansas City, MO, USA., Hoyer J; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Van-Gils J; Genetics Lab, Centre Hospitalier Universitaire (CHU) de Bordeaux, Bordeaux, France., de Sainte-Agathe JM; Genetics Lab, Centre Hospitalier Universitaire (CHU) de Bordeaux, Bordeaux, France., Thompson ML; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA., Bebin EM; University of Alabama at Birmingham, Birmingham, AL, USA., Weisz-Hubshman M; Molecular and Human Genetics Department, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, Tx, USA., Tabet AC; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France., Verloes A; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France., Levy J; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France., Latypova X; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France., Harder S; Mass spectrometry and Proteome Analytics, Institute for Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Silverman GA; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Pak SC; Department of Pediatrics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Schedl T; Department of Genetics, Washington University in St Louis School of Medicine, St Louis, MO, USA., Freson K; Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium., Mumford A; School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK., Turro E; Icahn School of Medicine at Mount Sinai, New York, NY, USA., Schlein C; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Shashi V; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA., Kreienkamp HJ; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Kreienkamp@uke.de.
Corporate Authors: Undiagnosed Diseases Network
Source: Nature communications [Nat Commun] 2024 Sep 10; Vol. 15 (1), pp. 7909. Date of Electronic Publication: 2024 Sep 10.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:2041-1723
DOI:10.1038/s41467-024-52095-x