English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Call for participation in the neurogenetics consortium within the Human Variome Project

Haworth, A., Bertram, L., Carrera, P., Elson, J. L., Braastad, C. D., Cox, D. W., et al. (2011). Call for participation in the neurogenetics consortium within the Human Variome Project. Neurogenetics, 12(3), 169-73. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/21630033 http://www.springerlink.com/content/660mkg1115r86328/fulltext.pdf.

Item is

Basic

show hide
Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-7806-2 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-7807-F
Genre: Journal Article

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Haworth, A., Author
Bertram, L.1, Author              
Carrera, P., Author
Elson, J. L., Author
Braastad, C. D., Author
Cox, D. W., Author
Cruts, M., Author
den Dunnen, J. T., Author
Farrer, M. J., Author
Fink, J. K., Author
Hamed, S. A., Author
Houlden, H., Author
Johnson, D. R., Author
Nuytemans, K., Author
Palau, F., Author
Rayan, D. L., Author
Robinson, P. N.2, Author              
Salas, A., Author
Schule, B., Author
Sweeney, M. G., Author
Woods, M. O., AuthorAmigo, J., AuthorCotton, R. G., AuthorSobrido, M. J., Author more..
Affiliations:
1Neuropsychiatric Genetics (Lars Bertram), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479655              
2Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              

Content

show
hide
Free keywords: Algorithms; Congresses as Topic; Databases, Genetic/*standards; *Genetic Variation/physiology; Genetics, Medical/*organization & administration/standards; Human Genome Project/organization & administration; Humans; *International Cooperation; Nervous System/*metabolism; Nervous System Diseases/genetics/metabolism; Research Report
 Abstract: 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.

Details

show
hide
Language(s):
 Dates: 2011
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: -
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Neurogenetics
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 12 (3) Sequence Number: - Start / End Page: 169 - 73 Identifier: ISSN: 1364-6753 (Electronic) 1364-6745 (Linking)