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Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.

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Title: Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.
Authors: Farlow JL; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America., Lin H; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America., Sauerbeck L; Department of Neurology and Rehabilitation Medicine, University of Cincinnati School of Medicine, Cincinnati, Ohio, United States of America., Lai D; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America., Koller DL; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America., Pugh E; Center for Inherited Disease Research, Johns Hopkins University; Baltimore, Maryland, United States of America., Hetrick K; Center for Inherited Disease Research, Johns Hopkins University; Baltimore, Maryland, United States of America., Ling H; Center for Inherited Disease Research, Johns Hopkins University; Baltimore, Maryland, United States of America., Kleinloog R; Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands., van der Vlies P; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Deelen P; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Swertz MA; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; Genomics Coordination Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Verweij BH; Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands., Regli L; Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands; Department of Neurosurgery, University Hospital Zurich, Zurich, Switzerland., Rinkel GJ; Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands., Ruigrok YM; Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands., Doheny K; Center for Inherited Disease Research, Johns Hopkins University; Baltimore, Maryland, United States of America., Liu Y; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America., Broderick J; Department of Neurology and Rehabilitation Medicine, University of Cincinnati School of Medicine, Cincinnati, Ohio, United States of America., Foroud T; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.
Corporate Authors: FIA Study Investigators
Source: PloS one [PLoS One] 2015 Mar 24; Vol. 10 (3), pp. e0121104. Date of Electronic Publication: 2015 Mar 24 (Print Publication: 2015).
Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; 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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