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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Glessner, Joseph T; Bick, Alexander G; Ito, Kaoru; Homsy, Jason; Rodriguez-Murillo, Laura; Fromer, Menachem; Mazaika, Erica; Vardarajan, Badri; Italia, Michael; Leipzig, Jeremy; DePalma, Steven R; Golhar, Ryan; Sanders, Stephan J; Yamrom, Boris; Ronemus, Michael; Iossifov, Ivan; Willsey, A Jeremy; State, Matthew W; Kaltman, Jonathan R; White, Peter S; Shen, Yufeng; Warburton, Dorothy; Brueckner, Martina; Seidman, Christine; Goldmuntz, Elizabeth; Gelb, Bruce D; Lifton, Richard; Seidman, Jonathan; Hakonarson, Hakon; Chung, Wendy K.
Afiliação
  • Glessner JT; The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Bick AG; Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
  • Ito K; Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Homsy J; Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Rodriguez-Murillo L; Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Fromer M; Mindich Child Health and Development Institute, Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Mazaika E; Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Vardarajan B; Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Italia M; Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Leipzig J; Psychiatric Genomics in the Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • DePalma SR; Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Golhar R; Systems Biology, Columbia University Medical Center, New York, NY 10032, USA.
  • Sanders SJ; Center for Biomedical Informatics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Yamrom B; Center for Biomedical Informatics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Ronemus M; Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Iossifov I; The Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Willsey AJ; Genetics, Yale University, New Haven, CT 06520, USA.
  • State MW; Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Kaltman JR; Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
  • White PS; Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
  • Shen Y; Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
  • Warburton D; Genetics, Yale University, New Haven, CT 06520, USA.
  • Brueckner M; Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Seidman C; Genetics, Yale University, New Haven, CT 06520, USA.
  • Goldmuntz E; Psychiatry, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Gelb BD; Cardiovascular Sciences, National Heart, Lung, and Blood Institute (NHLBI), NIH, Bethesda, MD 20892, USA.
  • Lifton R; Center for Biomedical Informatics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Seidman J; Systems Biology, Columbia University Medical Center, New York, NY 10032, USA.
  • Hakonarson H; Genetics and Development (in Medicine), Columbia University Medical Center, New York, NY 10032, USA.
  • Chung WK; Pediatrics, Yale University, New Haven, CT 06520, USA.
Circ Res ; 115(10): 884-896, 2014 Oct 24.
Article em En | MEDLINE | ID: mdl-25205790
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Variações do Número de Cópias de DNA / Exoma / Frequência do Gene / Cardiopatias Congênitas Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Variações do Número de Cópias de DNA / Exoma / Frequência do Gene / Cardiopatias Congênitas Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos