Literature DB >> 21610748

GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies.

Wei Yu1, Ajay Yesupriya, Anja Wulf, Lucia A Hindorff, Nicole Dowling, Muin J Khoury, Marta Gwinn.   

Abstract

Genome-wide association studies (GWAS) have successfully identified numerous genetic loci that are associated with phenotypic traits and diseases. GWAS Integrator is a bioinformatics tool that integrates information on these associations from the National Human Genome Research institute (NHGRI) Catalog, SNAP (SNP Annotation and Proxy Search), and the Human Genome Epidemiology (HuGE) Navigator literature database. This tool includes robust search and data mining functionalities that can be used to quickly identify relevant associations from GWAS, as well as proxy single-nucleotide polymorphisms (SNPs) and potential candidate genes. Query-based University of California Santa Cruz (UCSC) Genome Browser custom tracks are generated dynamically on the basis of users' selected GWAS hits or candidate genes from HuGE Navigator literature database (http://www.hugenavigator.net/HuGENavigator/gWAHitStartPage.do). The GWAS Integrator may help enhance inference on potential genetic associations identified from GWAS studies.

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Mesh:

Year:  2011        PMID: 21610748      PMCID: PMC3190251          DOI: 10.1038/ejhg.2011.91

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  6 in total

1.  A navigator for human genome epidemiology.

Authors:  Wei Yu; Marta Gwinn; Melinda Clyne; Ajay Yesupriya; Muin J Khoury
Journal:  Nat Genet       Date:  2008-02       Impact factor: 38.330

2.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

3.  Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations.

Authors:  W Yu; M Clyne; M J Khoury; M Gwinn
Journal:  Bioinformatics       Date:  2009-10-27       Impact factor: 6.937

Review 4.  Finding common susceptibility variants for complex disease: past, present and future.

Authors:  Kalliope Panoutsopoulou; Eleftheria Zeggini
Journal:  Brief Funct Genomic Proteomic       Date:  2009-07-01

5.  Genomewide association studies and human disease.

Authors:  John Hardy; Andrew Singleton
Journal:  N Engl J Med       Date:  2009-04-15       Impact factor: 91.245

6.  An open source infrastructure for managing knowledge and finding potential collaborators in a domain-specific subset of PubMed, with an example from human genome epidemiology.

Authors:  Wei Yu; Ajay Yesupriya; Anja Wulf; Junfeng Qu; Muin J Khoury; Marta Gwinn
Journal:  BMC Bioinformatics       Date:  2007-11-09       Impact factor: 3.169

  6 in total
  22 in total

Review 1.  Genetics of alcoholism.

Authors:  Priya A Iyer-Eimerbrink; John I Nurnberger
Journal:  Curr Psychiatry Rep       Date:  2014-12       Impact factor: 5.285

Review 2.  Cytokine gene polymorphisms and human autoimmune disease in the era of genome-wide association studies.

Authors:  Koen Vandenbroeck
Journal:  J Interferon Cytokine Res       Date:  2011-12-22       Impact factor: 2.607

3.  Epigenomic analysis of primary human T cells reveals enhancers associated with TH2 memory cell differentiation and asthma susceptibility.

Authors:  Grégory Seumois; Lukas Chavez; Anna Gerasimova; Matthias Lienhard; Nada Omran; Lukas Kalinke; Maria Vedanayagam; Asha Purnima V Ganesan; Ashu Chawla; Ratko Djukanović; K Mark Ansel; Bjoern Peters; Anjana Rao; Pandurangan Vijayanand
Journal:  Nat Immunol       Date:  2014-07-06       Impact factor: 25.606

Review 4.  How can polygenic inheritance be used in population screening for common diseases?

Authors:  Muin J Khoury; A Cecile J W Janssens; David F Ransohoff
Journal:  Genet Med       Date:  2013-02-14       Impact factor: 8.822

5.  DistiLD Database: diseases and traits in linkage disequilibrium blocks.

Authors:  Albert Pallejà; Heiko Horn; Sabrina Eliasson; Lars Juhl Jensen
Journal:  Nucleic Acids Res       Date:  2011-11-03       Impact factor: 16.971

6.  Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.

Authors:  Rui Li; Felix F Brockschmidt; Amy K Kiefer; Hreinn Stefansson; Dale R Nyholt; Kijoung Song; Sita H Vermeulen; Stavroula Kanoni; Daniel Glass; Sarah E Medland; Maria Dimitriou; Dawn Waterworth; Joyce Y Tung; Frank Geller; Stefanie Heilmann; Axel M Hillmer; Veronique Bataille; Sibylle Eigelshoven; Sandra Hanneken; Susanne Moebus; Christine Herold; Martin den Heijer; Grant W Montgomery; Panos Deloukas; Nicholas Eriksson; Andrew C Heath; Tim Becker; Patrick Sulem; Massimo Mangino; Peter Vollenweider; Tim D Spector; George Dedoussis; Nicholas G Martin; Lambertus A Kiemeney; Vincent Mooser; Kari Stefansson; David A Hinds; Markus M Nöthen; J Brent Richards
Journal:  PLoS Genet       Date:  2012-05-31       Impact factor: 5.917

7.  Expression and function of the protein tyrosine phosphatase receptor J (PTPRJ) in normal mammary epithelial cells and breast tumors.

Authors:  Chanel E Smart; Marjan E Askarian Amiri; Ania Wronski; Marcel E Dinger; Joanna Crawford; Dmitry A Ovchinnikov; Ana Cristina Vargas; Lynne Reid; Peter T Simpson; Sarah Song; Christiane Wiesner; Juliet D French; Richa K Dave; Leonard da Silva; Amy Purdon; Megan Andrew; John S Mattick; Sunil R Lakhani; Melissa A Brown; Stuart Kellie
Journal:  PLoS One       Date:  2012-07-17       Impact factor: 3.240

8.  Exome sequencing of only seven Qataris identifies potentially deleterious variants in the Qatari population.

Authors:  Juan L Rodriguez-Flores; Jennifer Fuller; Neil R Hackett; Jacqueline Salit; Joel A Malek; Eman Al-Dous; Lotfi Chouchane; Mahmoud Zirie; Amin Jayoussi; Mai A Mahmoud; Ronald G Crystal; Jason G Mezey
Journal:  PLoS One       Date:  2012-11-06       Impact factor: 3.240

9.  Predicting cell types and genetic variations contributing to disease by combining GWAS and epigenetic data.

Authors:  Anna Gerasimova; Lukas Chavez; Bin Li; Gregory Seumois; Jason Greenbaum; Anjana Rao; Pandurangan Vijayanand; Bjoern Peters
Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

10.  Functional relevance for associations between genetic variants and systemic lupus erythematosus.

Authors:  Fei-Yan Deng; Shu-Feng Lei; Yong-Hong Zhang; Zeng-Li Zhang; Yu-Fan Guo
Journal:  PLoS One       Date:  2013-01-14       Impact factor: 3.240

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