Enabling global clinical collaborations on identifiable patient data: The Minerva initiative

Romano Corrado

Research output: Contribution to journalComment/debate

Original languageEnglish
Article number611
JournalFrontiers in Genetics
Volume10
Issue numberJUN
DOIs
Publication statusPublished - Jan 1 2019

Keywords

  • Consortium
  • Data protection
  • Data sharing
  • Facial features
  • Patient information
  • Phenotyping
  • Rare disease

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Genetics(clinical)

Cite this

Enabling global clinical collaborations on identifiable patient data : The Minerva initiative. / Romano Corrado.

In: Frontiers in Genetics, Vol. 10, No. JUN, 611, 01.01.2019.

Research output: Contribution to journalComment/debate

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AU - Romano Corrado

AU - Nellåker, Christoffer

AU - Alkuraya, Fowzan S.

AU - Baynam, Gareth

AU - Bernier, Raphael

AU - Bernier, Francois P.

AU - Boulanger, Vanessa

AU - Brudno, Michael

AU - Brunner, Han G.

AU - Clayton-Smith, Jill

AU - Cogné, Benjamin

AU - Dawkins, Hugh J.

AU - DeVries, Bert

AU - Douzgou, Sofia

AU - Dudding, Tracy

AU - Eichler, Evan E.

AU - Ferlaino, Michael

AU - Fieggen, Karen

AU - Firth, Helen V.

AU - FitzPatrick, David R.

AU - Gration, Dylan

AU - Groza, Tudor

AU - Haendel, Melissa A.

AU - Hallowell, Nina

AU - Hamosh, Ada

AU - Hehir-Kwa, Jayne

AU - Hitz, Marc Phillip

AU - Hughes, Mark

AU - Kini, Usha

AU - Kleefstra, Tjitske

AU - Kooy, R. Frank

AU - Krawitz, Peter M.

AU - Küry, Sébastien

AU - Lees, Melissa

AU - Lyon, Gholson J.

AU - Lyonnet, Stanislas

AU - Marcadier, Julien

AU - Meyn, Stephen

AU - Moslerová, Veronika

AU - Politei, Juan M.

AU - Poulton, Cathryn C.

AU - Raymond, F. Lucy

AU - Reijnders, Margot

AU - Robinson, Peter N.

AU - Romano, Corrado

AU - Rose, Catherine M.

AU - Sainsbury, David C.

AU - Schofield, Lyn

AU - Sutton, Vernon R.

AU - Turnovec, Marek

AU - Van Dijck, Anke

PY - 2019/1/1

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KW - Data protection

KW - Data sharing

KW - Facial features

KW - Patient information

KW - Phenotyping

KW - Rare disease

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