Literature DB >> 31427789

A global overview of pleiotropy and genetic architecture in complex traits.

Kyoko Watanabe1, Sven Stringer1, Oleksandr Frei2, Maša Umićević Mirkov1, Christiaan de Leeuw1, Tinca J C Polderman1, Sophie van der Sluis1,3, Ole A Andreassen2,4, Benjamin M Neale5,6,7, Danielle Posthuma8,9.   

Abstract

After a decade of genome-wide association studies (GWASs), fundamental questions in human genetics, such as the extent of pleiotropy across the genome and variation in genetic architecture across traits, are still unanswered. The current availability of hundreds of GWASs provides a unique opportunity to address these questions. We systematically analyzed 4,155 publicly available GWASs. For a subset of well-powered GWASs on 558 traits, we provide an extensive overview of pleiotropy and genetic architecture. We show that trait-associated loci cover more than half of the genome, and 90% of these overlap with loci from multiple traits. We find that potential causal variants are enriched in coding and flanking regions, as well as in regulatory elements, and show variation in polygenicity and discoverability of traits. Our results provide insights into how genetic variation contributes to trait variation. All GWAS results can be queried and visualized at the GWAS ATLAS resource ( https://atlas.ctglab.nl ).

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Mesh:

Year:  2019        PMID: 31427789     DOI: 10.1038/s41588-019-0481-0

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  237 in total

1.  Disentangling selection on genetically correlated polygenic traits via whole-genome genealogies.

Authors:  Aaron J Stern; Leo Speidel; Noah A Zaitlen; Rasmus Nielsen
Journal:  Am J Hum Genet       Date:  2021-01-12       Impact factor: 11.025

2.  Phosphoproteomic quantitation and causal analysis reveal pathways in GPVI/ITAM-mediated platelet activation programs.

Authors:  Özgün Babur; Alexander R Melrose; Jennifer M Cunliffe; John Klimek; Jiaqing Pang; Anna-Liisa I Sepp; Jevgenia Zilberman-Rudenko; Samuel Tassi Yunga; Tony Zheng; Iván Parra-Izquierdo; Jessica Minnier; Owen J T McCarty; Emek Demir; Ashok P Reddy; Phillip A Wilmarth; Larry L David; Joseph E Aslan
Journal:  Blood       Date:  2020-11-12       Impact factor: 22.113

3.  Statistical Impact of Sample Size and Imbalance on Multivariate Analysis in silico and A Case Study in the UK Biobank.

Authors:  Xinyuan Zhang; Ruowang Li; Marylyn D Ritchie
Journal:  AMIA Annu Symp Proc       Date:  2021-01-25

4.  Topologically associating domain boundaries that are stable across diverse cell types are evolutionarily constrained and enriched for heritability.

Authors:  Evonne McArthur; John A Capra
Journal:  Am J Hum Genet       Date:  2021-02-04       Impact factor: 11.025

5.  JASS: command line and web interface for the joint analysis of GWAS results.

Authors:  Hanna Julienne; Pierre Lechat; Vincent Guillemot; Carla Lasry; Chunzi Yao; Robinson Araud; Vincent Laville; Bjarni Vilhjalmsson; Hervé Ménager; Hugues Aschard
Journal:  NAR Genom Bioinform       Date:  2020-01-24

6.  Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.

Authors:  Jessica A Kaczorowski; Taylor F Smith; Amanda M Shrewsbury; Leah R Thomas; Valerie S Knopik; Maria T Acosta
Journal:  Behav Genet       Date:  2020-02-05       Impact factor: 2.805

7.  Convergent Evidence for Predispositional Effects of Brain Gray Matter Volume on Alcohol Consumption.

Authors:  David A A Baranger; Catherine H Demers; Nourhan M Elsayed; Annchen R Knodt; Spenser R Radtke; Aline Desmarais; Lauren R Few; Arpana Agrawal; Andrew C Heath; Deanna M Barch; Lindsay M Squeglia; Douglas E Williamson; Ahmad R Hariri; Ryan Bogdan
Journal:  Biol Psychiatry       Date:  2019-09-13       Impact factor: 13.382

Review 8.  Advancing the use of genome-wide association studies for drug repurposing.

Authors:  William R Reay; Murray J Cairns
Journal:  Nat Rev Genet       Date:  2021-07-23       Impact factor: 53.242

9.  Genomics at cellular resolution: insights into cognitive disorders and their evolution.

Authors:  Stefano Berto; Yuxiang Liu; Genevieve Konopka
Journal:  Hum Mol Genet       Date:  2020-09-30       Impact factor: 6.150

10.  snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets.

Authors:  Niccolo Tesi; Sven van der Lee; Marc Hulsman; Henne Holstege; Marcel J T Reinders
Journal:  Nucleic Acids Res       Date:  2021-07-02       Impact factor: 16.971

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