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Publication Details
AFRICAN RESEARCH NEXUS
SHINING A SPOTLIGHT ON AFRICAN RESEARCH
biochemistry, genetics and molecular biology
Call for participation in the neurogenetics consortium within the Human Variome Project
Neurogenetics, Volume 12, No. 3, Year 2011
Notification
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Description
The rate of DNA variation discovery has accelerated the need to collate, store and interpret the data in a standardised coherent way and is becoming a critical step in maximising the impact of discovery on the understanding and treatment of human disease. This particularly applies to the field of neurology as neurological function is impaired in many human disorders. Furthermore, the field of neurogenetics has been proven to show remarkably complex genotype-to-phenotype relationships. To facilitate the collection of DNA sequence variation pertaining to neurogenetic disorders, we have initiated the "Neurogenetics Consortium" under the umbrella of the Human Variome Project. The Consortium's founding group consisted of basic researchers, clinicians, informaticians and database creators. This report outlines the strategic aims established at the preliminary meetings of the Neurogenetics Consortium and calls for the involvement of the wider neurogenetic community in enabling the development of this important resource. © Springer-Verlag 2011.
Authors & Co-Authors
Haworth, Andrea
United Kingdom, London
National Hospital for Neurology and Neurosurgery
Bertram, Lars
Germany, Berlin
Max Planck Institute for Molecular Genetics
Carrera, Paola
Italy, Milan
Irccs Ospedale San Raffaele
Elson, Joanna L.
United Kingdom, Newcastle
University of Newcastle Upon Tyne, Faculty of Medical Sciences
Braastad, Corey D.
United States, Marlborough
Athena Diagnostics Inc.
Cox, Diane Wilson
Canada, Edmonton
University of Alberta
Cruts, Marc
Belgium, Antwerpen
Universiteit Antwerpen
den Dunnen, Johan T.
Netherlands, Leiden
Leids Universitair Medisch Centrum
Farrer, Matthew J.
Canada, Vancouver
Djavad Mowafaghian Centre for Brain Health
Fink, John K.
United States, Ann Arbor
University of Michigan, Ann Arbor
Hamed, Sherifa Ahmed
Egypt, Asyut
Assiut University
Houlden, Henry H.
United Kingdom, London
Ucl Queen Square Institute of Neurology
Johnson, Dennis R.
United States
Evidence Based Healthcare Consulting
Nuytemans, Karen
Belgium, Antwerpen
Universiteit Antwerpen
Palau, Francesc
Spain, Madrid
Centro de Investigación Biomédica en Red de Enfermedades Raras
Rayan, Dipa L.Raja
United Kingdom, London
Ucl Queen Square Institute of Neurology
Robinson, Peter Nicholas
Germany, Berlin
Charité – Universitätsmedizin Berlin
Salas, Antonio
Spain, Santiago de Compostela
Institute of Legal Medicine
Schüle, Birgitt
United States, Sunnyvale
Parkinson's Institute
Sweeney, Mary G.
United Kingdom, London
National Hospital for Neurology and Neurosurgery
Woods, Michael O.
Canada, St John's
Memorial University of Newfoundland
Amigo, Jorge
Spain, Santiago de Compostela
Universidad de Santiago de Compostela
Cotton, Richard G.H.
Australia, Melbourne
University of Melbourne
Sobrido, Maria Jesus
Spain, Santiago de Compostela
Fundación Pública Galega de Medicina Xenómica
Spain, Madrid
Instituto de Salud Carlos Iii
Statistics
Citations: 24
Authors: 24
Affiliations: 22
Identifiers
Doi:
10.1007/s10048-011-0287-4
ISSN:
13646745
e-ISSN:
13646753
Research Areas
Cancer
Genetics And Genomics