Year: 2018
Type: article
Study design: Observational Study
Authors: Simone Martinelli, Oliver H.F. Krumbach, Francesca Pantaleoni, Simona Coppola, Ehsan Amin, Luca Pannone, Kazem Nouri, Luciapia Farina, Radovan Dvorsky, Francesca Lepri, Marcel Buchholzer, Raphael Konopatzki, Laurence Walsh, Katelyn Payne, Mary Ella Pierpont, Samantha Schrier Vergano, Katherine G. Langley, Douglas Larsen, Kelly D. Farwell, Sha Tang, Cameron Mroske, Ivan Gallotta, Elia Di Schiavi, Matteo della Monica, Licia Lugli, Cesare Rossi, Marco Seri, Guido Cocchi, Lindsay Henderson, Berivan Baskin, Mariëlle Alders, Roberto Mendoza-Londono, Lucie Dupuis, Deborah A. Nickerson, Jessica X. Chong, Naomi Meeks, Kathleen Brown, Tahnee Causey, Megan T. Cho, Stephanie Demuth, Maria Cristina Digilio, Bruce D. Gelb, Michael J. Bamshad, Martin Zenker, Mohammad Reza Ahmadian, Raoul C. Hennekam, Marco Tartaglia, Ghayda M. Mirzaa
Institutions: Istituto Superiore di Sanità, Heinrich Heine University Düsseldorf, Bambino Gesù Children's Hospital, Riley Hospital for Children, University of Minnesota, Children's Minnesota, University of Minnesota Children's Hospital, Children's Hospital of The King's Daughters, Washington University in St. Louis, Ambry Genetics (United States), Institute of Biosciences and Bioresources, National Research Council, Meyer Children's Hospital, Azienda Ospedaliero-Universitaria di Modena, IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola, University of Bologna, Amsterdam UMC Location University of Amsterdam, University of Amsterdam, University of Toronto, Hospital for Sick Children, University of Washington, Children's Hospital Colorado, Virginia Commonwealth University, Icahn School of Medicine at Mount Sinai, University Hospital Magdeburg, Istituti di Ricovero e Cura a Carattere Scientifico, Seattle Children's Research Institute
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
Funders: University of Washington, E-Rare, Ministero della Salute, Heinrich-Heine-Universität Düsseldorf, Associazione Italiana per la Ricerca sul Cancro, Fondazione Bambino Gesù, National Institutes of Health, Center for Mendelian Genomics, University of Washington, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Office of Research Infrastructure Programs, National Institutes of Health
Awards: G1608136705, Genetics and genomics of congenital heart disease and associated neurodevelopmental abnormalities, The Genomic Basis of Congenital Heart Disease and Neurodevelopmental Outcomes, Genes and pathways underlying brain overgrowth and focal cortical malformations, G4576177769, UW Center for Mendelian Genomics, Genetics of Hypoplastic Left Heart Syndrome, Bridging the Gap between Genomics and Clinical Outcomes in CHD, G73439054, G7350793147, Administrative Coordinating Center: Bench to Bassinet Program, Genetics of conotruncal defects and associated neurodevelopmental outcomes, UW Center for Mendelian Genomics, Caenorhabditis Genetics Center
OpenAlex ID: W2784545598