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The case for open science: rare diseases.
Rubinstein, Yaffa R; Robinson, Peter N; Gahl, William A; Avillach, Paul; Baynam, Gareth; Cederroth, Helene; Goodwin, Rebecca M; Groft, Stephen C; Hansson, Mats G; Harris, Nomi L; Huser, Vojtech; Mascalzoni, Deborah; McMurry, Julie A; Might, Matthew; Nellaker, Christoffer; Mons, Barend; Paltoo, Dina N; Pevsner, Jonathan; Posada, Manuel; Rockett-Frase, Alison P; Roos, Marco; Rubinstein, Tamar B; Taruscio, Domenica; van Enckevort, Esther; Haendel, Melissa A.
Afiliación
  • Rubinstein YR; Special Volunteer in the Office of Strategic Initiatives, National Library of Medicine, Bethesda, Maryland, USA.
  • Robinson PN; The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
  • Gahl WA; Undiagnosed Diseases Program and Office of the Clinical Director, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, Maryland, USA.
  • Avillach P; Department of Biomedical Informatics, Harvard Medical School, Boston, Massachusetts, USA.
  • Baynam G; Western Australian Register of Developmental Anomalies and Telethon Kids Institute, Perth, Australia.
  • Cederroth H; Wilhelm Foundation, Brottby, Sweden.
  • Goodwin RM; Department of Health and Human Services, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.
  • Groft SC; NCATS, National Institutes of Health, Bethesda, Maryland, USA.
  • Hansson MG; Center for Research Ethics and Bioethics, Uppsala Universitet, Uppsala, Sweden.
  • Harris NL; Department of Environmental Genomics & System Biology, Lawrence Berkeley National Laboratory, Berkeley, California, USA.
  • Huser V; Department of Health and Human Services, NCBI, National Institutes of Health, Bethesda, Maryland, USA.
  • Mascalzoni D; Center for Research Ethics and Bioethics, Uppsala University, Sweden and EURAC Research, Bolzano, Italy.
  • McMurry JA; Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA.
  • Might M; Hugh Kaul Precision Medicine Institute, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Nellaker C; Nuffield Department of Women's and Reproductive Health, Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, UK.
  • Mons B; Department of Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
  • Paltoo DN; Department of Health and Human Services, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.
  • Pevsner J; Department of Neurology, Kennedy Krieger Institute and Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Posada M; Rare Diseases Research Institute & CIBERER, Instituto de Salud Carlos III, Madrid, Spain.
  • Rockett-Frase AP; Joshua Frase Foundation, Ponte Vedra Beach, Florida, USA.
  • Roos M; Human Genetics, Leiden University Medical Center, Leiden, Netherlands.
  • Rubinstein TB; Children Hospital at Montefiore/Albert Einstein College of Medicine-Pediatrics, Bronx, New York, USA.
  • Taruscio D; National Centre for Rare Diseases, Istituto Superiore di Sanità, Rome, Italy.
  • van Enckevort E; Department of Genetics, University Medical Center Groningen, University of Groningen, Leiden, Netherlands.
  • Haendel MA; Linus Pauling Institute, Oregon State University, Corvallis, Oregon, USA.
JAMIA Open ; 3(3): 472-486, 2020 Oct.
Article en En | MEDLINE | ID: mdl-33426479
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: JAMIA Open Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: JAMIA Open Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos