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Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes.
Yu, Mengyao; Aguirre, Matthew; Jia, Meiwen; Gjoni, Ketrin; Cordova-Palomera, Aldo; Munger, Chad; Amgalan, Dulguun; Rosa Ma, X; Pereira, Alexandre; Tcheandjieu, Catherine; Seidman, Christine; Seidman, Jonathan; Tristani-Firouzi, Martin; Chung, Wendy; Goldmuntz, Elizabeth; Srivastava, Deepak; Loos, Ruth J F; Chami, Nathalie; Cordell, Heather; Dreßen, Martina; Mueller-Myhsok, Bertram; Lahm, Harald; Krane, Markus; Pollard, Katherine S; Engreitz, Jesse M; Gagliano Taliun, Sarah A; Gelb, Bruce D; Priest, James R.
Afiliación
  • Yu M; Department of Pediatrics (M.Y., M.A., A.C.-P., C.T., J.R.P.), Stanford University School of Medicine.
  • Aguirre M; Fudan University, Shanghai, Chinia (M.Y.).
  • Jia M; Department of Pediatrics (M.Y., M.A., A.C.-P., C.T., J.R.P.), Stanford University School of Medicine.
  • Gjoni K; Department of Biomedical Data Science, Stanford University, CA (M.A.).
  • Cordova-Palomera A; Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry Munich, Germany (M.J., B.M.-M.).
  • Munger C; Gladstone Institutes; University of California San Francisco (K.G., C.T., D.S., K.S.P.).
  • Amgalan D; Department of Pediatrics (M.Y., M.A., A.C.-P., C.T., J.R.P.), Stanford University School of Medicine.
  • Rosa Ma X; Department of Genetics (C.M., D.A., X.R.M., J.M.E.), Stanford University School of Medicine.
  • Pereira A; Department of Genetics (C.M., D.A., X.R.M., J.M.E.), Stanford University School of Medicine.
  • Tcheandjieu C; Department of Genetics (C.M., D.A., X.R.M., J.M.E.), Stanford University School of Medicine.
  • Seidman C; Department of Genetics, Harvard University, Cambridge, MA (A.P., C.S., J.S.).
  • Seidman J; Department of Pediatrics (M.Y., M.A., A.C.-P., C.T., J.R.P.), Stanford University School of Medicine.
  • Tristani-Firouzi M; Gladstone Institutes; University of California San Francisco (K.G., C.T., D.S., K.S.P.).
  • Chung W; Department of Genetics, Harvard University, Cambridge, MA (A.P., C.S., J.S.).
  • Goldmuntz E; Department of Genetics, Harvard University, Cambridge, MA (A.P., C.S., J.S.).
  • Srivastava D; Department of Pediatrics, University of Utah, Salt Lake City (M.T.-F.).
  • Loos RJF; Department of Pediatrics, Columbia University, NY (W.C.).
  • Chami N; Department of Pediatrics, University of Pennsylvania, Philadelphia (E.G.).
  • Cordell H; Gladstone Institutes; University of California San Francisco (K.G., C.T., D.S., K.S.P.).
  • Dreßen M; Icahn School of Medicine at Mount Sinai, NY (R.J.F.L., N.C.).
  • Mueller-Myhsok B; Icahn School of Medicine at Mount Sinai, NY (R.J.F.L., N.C.).
  • Lahm H; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, United Kingdom (H.C.).
  • Krane M; Department of Cardiovascular Surgery, Division of Experimental Surgery, Institute Insure (Institute for Translational Cardiac Surgery), German Heart Center Munich & Technical University of Munich, School of Medicine & Health, Germany (M.D., H.L., M.K.).
  • Pollard KS; Department of Translational Research in Psychiatry, Max Planck Institute of Psychiatry Munich, Germany (M.J., B.M.-M.).
  • Engreitz JM; Department of Cardiovascular Surgery, Division of Experimental Surgery, Institute Insure (Institute for Translational Cardiac Surgery), German Heart Center Munich & Technical University of Munich, School of Medicine & Health, Germany (M.D., H.L., M.K.).
  • Gagliano Taliun SA; Department of Cardiovascular Surgery, Division of Experimental Surgery, Institute Insure (Institute for Translational Cardiac Surgery), German Heart Center Munich & Technical University of Munich, School of Medicine & Health, Germany (M.D., H.L., M.K.).
  • Gelb BD; Department of Cardiac Surgery, Yale School of Medicine, New Haven, CT (M.K.).
  • Priest JR; Gladstone Institutes; University of California San Francisco (K.G., C.T., D.S., K.S.P.).
Circ Genom Precis Med ; 16(3): 258-266, 2023 06.
Article en En | MEDLINE | ID: mdl-37026454
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Circ Genom Precis Med Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Circ Genom Precis Med Año: 2023 Tipo del documento: Article Pais de publicación: Estados Unidos