Literature DB >> 32606005

LDtrait: An Online Tool for Identifying Published Phenotype Associations in Linkage Disequilibrium.

Shu-Hong Lin1, Derek W Brown1, Mitchell J Machiela2.   

Abstract

Genome-wide association studies (GWAS) have identified thousands of germline susceptibility loci associated with risk for cancer as well as a wide range of other traits and diseases. An interest of many investigators is identifying traits or diseases that share common susceptibility loci. We developed LDtrait (https://ldlink.nci.nih.gov/?tab=ldtrait) as an open access web tool for finding germline variation associated with multiple traits. LDtrait searches the NHGRI-EBI GWAS Catalog to identify susceptibility loci in linkage disequilibrium (LD) with a user-provided list of query variants. Options allow for modifying LD thresholds, calculating LD from a diverse set of reference populations, and downloading annotated variant lists. Results from example query searches highlight the utility of LDtrait in uncovering cross-trait associations for cancer risk and other traits. LDtrait accelerates etiologic understanding of cancer genetics by rapidly identifying genetic similarities with other traits or diseases. SIGNIFICANCE: The new GWAS search tool LDtrait will expedite discovery of shared genetic components underlying seemingly unrelated diseases and may offer novel insights into cancer research. ©2020 American Association for Cancer Research.

Entities:  

Year:  2020        PMID: 32606005      PMCID: PMC7442674          DOI: 10.1158/0008-5472.CAN-20-0985

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  23 in total

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2.  Principles for the post-GWAS functional characterization of cancer risk loci.

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Review 3.  Patterns of linkage disequilibrium in the human genome.

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Journal:  Nat Rev Genet       Date:  2002-04       Impact factor: 53.242

4.  Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.

Authors:  Tomas Tanskanen; Linda van den Berg; Niko Välimäki; Mervi Aavikko; Eivind Ness-Jensen; Kristian Hveem; Yvonne Wettergren; Elinor Bexe Lindskog; Neeme Tõnisson; Andres Metspalu; Kaisa Silander; Giulia Orlando; Philip J Law; Sari Tuupanen; Alexandra E Gylfe; Ulrika A Hänninen; Tatiana Cajuso; Johanna Kondelin; Antti-Pekka Sarin; Eero Pukkala; Pekka Jousilahti; Veikko Salomaa; Samuli Ripatti; Aarno Palotie; Heikki Järvinen; Laura Renkonen-Sinisalo; Anna Lepistö; Jan Böhm; Jukka-Pekka Mecklin; Nada A Al-Tassan; Claire Palles; Lynn Martin; Ella Barclay; Albert Tenesa; Susan M Farrington; Maria N Timofeeva; Brian F Meyer; Salma M Wakil; Harry Campbell; Christopher G Smith; Shelley Idziaszczyk; Tim S Maughan; Richard Kaplan; Rachel Kerr; David Kerr; Daniel D Buchanan; Aung K Win; John Hopper; Mark A Jenkins; Polly A Newcomb; Steve Gallinger; David Conti; Fredrick R Schumacher; Graham Casey; Jeremy P Cheadle; Malcolm G Dunlop; Ian P Tomlinson; Richard S Houlston; Kimmo Palin; Lauri A Aaltonen
Journal:  Int J Cancer       Date:  2017-10-12       Impact factor: 7.396

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

Authors:  Albert Pallejà; Heiko Horn; Sabrina Eliasson; Lars Juhl Jensen
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6.  A global reference for human genetic variation.

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Authors:  Zhaoming Wang; Katherine A McGlynn; Ewa Rajpert-De Meyts; D Timothy Bishop; Charles C Chung; Marlene D Dalgaard; Mark H Greene; Ramneek Gupta; Tom Grotmol; Trine B Haugen; Robert Karlsson; Kevin Litchfield; Nandita Mitra; Kasper Nielsen; Louise C Pyle; Stephen M Schwartz; Vésteinn Thorsson; Saran Vardhanabhuti; Fredrik Wiklund; Clare Turnbull; Stephen J Chanock; Peter A Kanetsky; Katherine L Nathanson
Journal:  Nat Genet       Date:  2017-06-12       Impact factor: 38.330

8.  The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.

Authors:  Annalisa Buniello; Jacqueline A L MacArthur; Maria Cerezo; Laura W Harris; James Hayhurst; Cinzia Malangone; Aoife McMahon; Joannella Morales; Edward Mountjoy; Elliot Sollis; Daniel Suveges; Olga Vrousgou; Patricia L Whetzel; Ridwan Amode; Jose A Guillen; Harpreet S Riat; Stephen J Trevanion; Peggy Hall; Heather Junkins; Paul Flicek; Tony Burdett; Lucia A Hindorff; Fiona Cunningham; Helen Parkinson
Journal:  Nucleic Acids Res       Date:  2019-01-08       Impact factor: 16.971

9.  Mosaic chromosome Y loss is associated with alterations in blood cell counts in UK Biobank men.

Authors:  Shu-Hong Lin; Erikka Loftfield; Josh N Sampson; Weiyin Zhou; Meredith Yeager; Neal D Freedman; Stephen J Chanock; Mitchell J Machiela
Journal:  Sci Rep       Date:  2020-02-27       Impact factor: 4.379

10.  Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women.

Authors:  Veron Ramsuran; Hemant Kulkarni; Weijing He; Koleka Mlisana; Edwina J Wright; Lise Werner; John Castiblanco; Rahul Dhanda; Tuan Le; Matthew J Dolan; Weihua Guan; Robin A Weiss; Robert A Clark; Salim S Abdool Karim; Sunil K Ahuja; Thumbi Ndung'u
Journal:  Clin Infect Dis       Date:  2011-05       Impact factor: 9.079

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2.  Common host variation drives malaria parasite fitness in healthy human red cells.

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3.  Genome-wide association study of posttraumatic stress disorder among childhood cancer survivors: results from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort.

Authors:  Donghao Lu; Yadav Sapkota; Unnur A Valdimarsdóttir; Karestan C Koenen; Nan Li; Wendy M Leisenring; Todd Gibson; Carmen L Wilson; Leslie L Robison; Melissa M Hudson; Gregory T Armstrong; Kevin R Krull; Yutaka Yasui; Smita Bhatia; Christopher J Recklitis
Journal:  Transl Psychiatry       Date:  2022-08-23       Impact factor: 7.989

  3 in total

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