Repositório Científico do Instituto Nacional de Saúde >
Departamento de Genética Humana >
DGH - Artigos em revistas internacionais >

Please use this identifier to cite or link to this item:

Título: Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Autor: Giardine, Belinda
Borg, Joseph
Higgs, Douglas R
Peterson, Kenneth
Philipsen, Sjaak
Maglott, Donna
Singleton, Belinda
Anstee, David J
Basak, Nazli
Clark, Barnaby
Costa, Flavia C
Faustino, Paula
Fedosyuk, Halyna
Felice, Alex E
Francina, Alain
Galanello, Renzo
Gallivan, Monica VE
Georgitsi, Marianthi
Gibbons, Richard J
Giordano, Piero C
Harteveld, Cornelis L
Hoyer, James D
Jarvis, Martin
Joly, Philippe
Kanavakis, Emmanuel
Kollia, Panagoula
Menzel, Stephan
Miller, Webb
Moradkhani, Kamran
Old, John
Papachatzopoulou, Adamantia
Papadakis, Manoussous N
Papadopoulos, Petros
Pavlovic, Sonja
Perseu, Lucia
Radmilovic, Milena
Riemer, Cathy
Satta, Stefania
Schrijver, Iris
Stojiljkovic, Maja
Thein, Swee Lay
Traeger-Synodinos, Jan
Tully, Ray
Wada, Takahito
Wayne, John S
Wiemann, Claudia
Zukic, Branda
Chui, David HK
Wajcman, Henri
Hardison, Ross C
Patrinos, George P
Palavras-chave: hemoglobinopathies
locus-specific databases
Doenças Genéticas
Issue Date: Apr-2011
Editora: Nature Publishing Group
Citação: Nat Genet. 2011 Mar 20;43(4):295-301
Resumo: We developed a series of interrelated locus-specific databases to store all published and unpublished genetic variation related to hemoglobinopathies and thalassemia and implemented microattribution to encourage submission of unpublished observations of genetic variation to these public repositories. A total of 1,941 unique genetic variants in 37 genes, encoding globins and other erythroid proteins, are currently documented in these databases, with reciprocal attribution of microcitations to data contributors. Our project provides the first example of implementing microattribution to incentivise submission of all known genetic variation in a defined system. It has demonstrably increased the reporting of human variants, leading to a comprehensive online resource for systematically describing human genetic variation in the globin genes and other genes contributing to hemoglobinopathies and thalassemias. The principles established here will serve as a model for other systems and for the analysis of other common and/or complex human genetic disease.
Arbitragem científica: yes
ISSN: 1061-4036
Appears in Collections:DGH - Artigos em revistas internacionais

Files in This Item:

File Description SizeFormat
Artigo Nature Genetics, final April 2011.pdf890,62 kBAdobe PDFView/Open
Restrict Access. You can request a copy!

Please give feedback about this item
FacebookTwitterDeliciousLinkedInDiggGoogle BookmarksMySpace
Formato BibTex MendeleyEndnote Logotipo do DeGóis 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.


  © 2010 - Todos os direitos reservados | Feedback Ministério da Saúde
Promotores do RCAAP   Financiadores do RCAAP

Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência PO Sociedade do Conhecimento (POSC) Portal oficial da União Europeia