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  • Patrinos, George P. (author)

Human variome project country nodes: Documenting genetic information within a country

  • Article/chapterEnglish2012

Publisher, publication year, extent ...

  • 2012-07-18
  • Hindawi Limited,2012

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:178779e1-0972-433b-bcc1-81f08416a77f
  • https://lup.lub.lu.se/record/3284187URI
  • https://doi.org/10.1002/humu.22147DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • The Human Variome Project (http://www.humanvariomeproject.org) is an international effort aiming to systematically collect and share information on all human genetic variation. The two main pillars of this effort are gene/disease-specific databases and a network of Human Variome Project Country Nodes. The latter are nationwide efforts to document the genomic variation reported within a specific population. The development and successful operation of the Human Variome Project Country Nodes are of utmost importance to the success of Human Variome Project's aims and goals because they not only allow the genetic burden of disease to be quantified in different countries, but also provide diagnosticians and researchers access to an up-to-date resource that will assist them in their daily clinical practice and biomedical research, respectively. Here, we report the discussions and recommendations that resulted from the inaugural meeting of the International Confederation of Countries Advisory Council, held on 12th December 2011, during the 2011 Human Variome Project Beijing Meeting. We discuss the steps necessary to maximize the impact of the Country Node effort for developing regional and country-specific clinical genetics resources and summarize a few well-coordinated genetic data collection initiatives that would serve as paradigms for similar projects. Hum Mutat 33:15131519, 2012. (c) 2012 Wiley Periodicals, Inc.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Smith, Timothy D. (author)
  • Howard, Heather (author)
  • Al-Mulla, Fand (author)
  • Chouchane, Lotfi (author)
  • Hadjisavvas, Andreas (author)
  • Hamed, Sherifa A. (author)
  • Li, Xi-Tao (author)
  • Marafie, Makia (author)
  • Ramesar, Rajkumar S. (author)
  • Ramos, Feliciano J. (author)
  • de Rave, Thomy (author)
  • El-Ruby, Mona O. (author)
  • Shrestha, Tilak Ram (author)
  • Sobrido, Maria-Jess (author)
  • Tadmouri, Ghazi (author)
  • Witsch-Baumgartner, Martina (author)
  • Zilfali, Bin Alwi (author)
  • Auerbach, Arleen D. (author)
  • Carpenter, Kevin (author)
  • Cutting, Garry R. (author)
  • Chi Dung, Vu (author)
  • Grody, Wayne (author)
  • Hasler, Julia (author)
  • Jorde, Lynn (author)
  • Kaput, Jim (author)
  • Macek, Milan (author)
  • Matsubara, Yoichi (author)
  • Padilla, Carmancita (author)
  • Robinson, Helen (author)
  • Rojas-Martinez, Augusto (author)
  • Taylor, Graham R. (author)
  • Vihinen, MaunoLund University,Lunds universitet,Proteinbioinformatik,Forskargrupper vid Lunds universitet,Protein Bioinformatics,Lund University Research Groups(Swepub:lu)med-mnv (author)
  • Weber, Tom (author)
  • Burn, John (author)
  • Qi, Ming (author)
  • Cotton, Richard G. H. (author)
  • Rimoin, David (author)
  • ProteinbioinformatikForskargrupper vid Lunds universitet (creator_code:org_t)

Related titles

  • In:Human Mutation: Hindawi Limited33:11, s. 1513-15191059-7794

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