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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.

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Title: Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
Authors: Bureau A; Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec and Département de Médecine Sociale et Préventive, Université Laval, Québec, QC G1V 0A6, Canada., Parker MM; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Ruczinski I; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Taub MA; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Marazita ML; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15219., Murray JC; Department of Pediatrics, School of Medicine, University of Iowa, Iowa City, Iowa 52242., Mangold E; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Noethen MM; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Ludwig KU; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111., Hetmanski JB; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205., Bailey-Wilson JE; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Cropp CD; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Li Q; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Szymczak S; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121., Albacha-Hejazi H; Hejazi Clinic, Clinic, Riyadh, Saudia Arabia 11461., Alqosayer K; Prime Health Clinic, Jeddah, Saudi Arabia 21511., Field LL; Department of Human Genetics, University of British Columbia, Vancouver, Canada V6T1Z3., Wu-Chou YH; Laboratory of Human Molecular Genetics, Chang Gung Memorial Hospital, Taipei, Taiwan 333., Doheny KF; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224., Ling H; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224., Scott AF; Institute of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland 21224., Beaty TH; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205 tbeaty1@jhu.edu.
Source: Genetics [Genetics] 2014 Jul; Vol. 197 (3), pp. 1039-44. Date of Electronic Publication: 2014 May 02.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Oxford University Press Country of Publication: United States NLM ID: 0374636 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1943-2631 (Electronic) Linking ISSN: 00166731 NLM ISO Abbreviation: Genetics Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts.
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  Data: <searchLink fieldCode="AU" term="%22Bureau+A%22">Bureau A</searchLink>; Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec and Département de Médecine Sociale et Préventive, Université Laval, Québec, QC G1V 0A6, Canada.<br /><searchLink fieldCode="AU" term="%22Parker+MM%22">Parker MM</searchLink>; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205.<br /><searchLink fieldCode="AU" term="%22Ruczinski+I%22">Ruczinski I</searchLink>; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205.<br /><searchLink fieldCode="AU" term="%22Taub+MA%22">Taub MA</searchLink>; Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205.<br /><searchLink fieldCode="AU" term="%22Marazita+ML%22">Marazita ML</searchLink>; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15219.<br /><searchLink fieldCode="AU" term="%22Murray+JC%22">Murray JC</searchLink>; Department of Pediatrics, School of Medicine, University of Iowa, Iowa City, Iowa 52242.<br /><searchLink fieldCode="AU" term="%22Mangold+E%22">Mangold E</searchLink>; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111.<br /><searchLink fieldCode="AU" term="%22Noethen+MM%22">Noethen MM</searchLink>; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111.<br /><searchLink fieldCode="AU" term="%22Ludwig+KU%22">Ludwig KU</searchLink>; Institute of Human Genetics, University of Bonn, Bonn, Germany D-53111.<br /><searchLink fieldCode="AU" term="%22Hetmanski+JB%22">Hetmanski JB</searchLink>; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205.<br /><searchLink fieldCode="AU" term="%22Bailey-Wilson+JE%22">Bailey-Wilson JE</searchLink>; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121.<br /><searchLink fieldCode="AU" term="%22Cropp+CD%22">Cropp CD</searchLink>; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121.<br /><searchLink fieldCode="AU" term="%22Li+Q%22">Li Q</searchLink>; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121.<br /><searchLink fieldCode="AU" term="%22Szymczak+S%22">Szymczak S</searchLink>; Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore Maryland 21121.<br /><searchLink fieldCode="AU" term="%22Albacha-Hejazi+H%22">Albacha-Hejazi H</searchLink>; Hejazi Clinic, Clinic, Riyadh, Saudia Arabia 11461.<br /><searchLink fieldCode="AU" term="%22Alqosayer+K%22">Alqosayer K</searchLink>; Prime Health Clinic, Jeddah, Saudi Arabia 21511.<br /><searchLink fieldCode="AU" term="%22Field+LL%22">Field LL</searchLink>; Department of Human Genetics, University of British Columbia, Vancouver, Canada V6T1Z3.<br /><searchLink fieldCode="AU" term="%22Wu-Chou+YH%22">Wu-Chou YH</searchLink>; Laboratory of Human Molecular Genetics, Chang Gung Memorial Hospital, Taipei, Taiwan 333.<br /><searchLink fieldCode="AU" term="%22Doheny+KF%22">Doheny KF</searchLink>; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224.<br /><searchLink fieldCode="AU" term="%22Ling+H%22">Ling H</searchLink>; Center for Inherited Disease Research, Johns Hopkins School of Medicine, Baltimore Maryland 21224.<br /><searchLink fieldCode="AU" term="%22Scott+AF%22">Scott AF</searchLink>; Institute of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland 21224.<br /><searchLink fieldCode="AU" term="%22Beaty+TH%22">Beaty TH</searchLink>; Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland 21205 tbeaty1@jhu.edu.
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  Data: <searchLink fieldCode="JN" term="%220374636%22">Genetics</searchLink> [Genetics] 2014 Jul; Vol. 197 (3), pp. 1039-44. <i>Date of Electronic Publication: </i>2014 May 02.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>0374636 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1943-2631 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200166731%22">00166731 </searchLink><i>NLM ISO Abbreviation: </i>Genetics <i>Subsets: </i>MEDLINE
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