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Paper Details

A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology.
Am J Hum Genet
39
2015
-BP5, 16p11, 600 kb BP4, ASDs, BBS7, BP4, BP5, CEP290, CNVs, Ciliary, Ciliary Dysfunction, Ciliary gene, KCTD13, abnormalities of head size, autism spectrum disorders, ciliary dysfunction, ciliopathies, ciliopathy, ciliopathy genes, ciliopathy-associated genes, genes, genetic lesions, kctd13, kctd13 morphants, mice, mouse, schizophrenia, zebrafish
Author NameAffiliation
Edwin C OhCenter for Human Disease Modeling and Department of Cell Biology, Duke University
Jack A KosmickiMassachusetts General Hospital and Harvard Medical School, USA Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT
Jack A KosmickiMassachusetts General Hospital and Harvard Medical School, USA Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT
James F GusellaCenter for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School
Mark J DalyMassachusetts General Hospital and Harvard Medical School, USA Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT
Mark J DalyMassachusetts General Hospital and Harvard Medical School, USA Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT
Jacques S BeckmannLausanne University Hospital (CHUV), University of Lausanne
Jacques S BeckmannLausanne University Hospital (CHUV), University of Lausanne
Nicholas KatsanisCenter for Human Disease Modeling and Department of Cell Biology, Duke University
Nicholas KatsanisCenter for Human Disease Modeling and Department of Cell Biology, Duke University
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne
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