Literature DB >> 32687429

Causal graphs for the analysis of genetic cohort data.

Oliver Hines1,2, Karla Diaz-Ordaz1, Stijn Vansteelandt1,3, Yalda Jamshidi2.   

Abstract

The increasing availability of genetic cohort data has led to many genome-wide association studies (GWAS) successfully identifying genetic associations with an ever-expanding list of phenotypic traits. Association, however, does not imply causation, and therefore methods have been developed to study the issue of causality. Under additional assumptions, Mendelian randomization (MR) studies have proved popular in identifying causal effects between two phenotypes, often using GWAS summary statistics. Given the widespread use of these methods, it is more important than ever to understand, and communicate, the causal assumptions upon which they are based, so that methods are transparent, and findings are clinically relevant. Causal graphs can be used to represent causal assumptions graphically and provide insights into the limitations associated with different analysis methods. Here we review GWAS and MR from a causal perspective, to build up intuition for causal diagrams in genetic problems. We also examine issues of confounding by ancestry and comment on approaches for dealing with such confounding, as well as discussing approaches for dealing with selection biases arising from study design.

Keywords:  GWAS; Mendelian randomisation; causal graphs

Mesh:

Year:  2020        PMID: 32687429      PMCID: PMC7509246          DOI: 10.1152/physiolgenomics.00115.2019

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  35 in total

1.  Many sequence variants affecting diversity of adult human height.

Authors:  Daniel F Gudbjartsson; G Bragi Walters; Gudmar Thorleifsson; Hreinn Stefansson; Bjarni V Halldorsson; Pasha Zusmanovich; Patrick Sulem; Steinunn Thorlacius; Arnaldur Gylfason; Stacy Steinberg; Anna Helgadottir; Andres Ingason; Valgerdur Steinthorsdottir; Elinborg J Olafsdottir; Gudridur H Olafsdottir; Thorvaldur Jonsson; Knut Borch-Johnsen; Torben Hansen; Gitte Andersen; Torben Jorgensen; Oluf Pedersen; Katja K Aben; J Alfred Witjes; Dorine W Swinkels; Martin den Heijer; Barbara Franke; Andre L M Verbeek; Diane M Becker; Lisa R Yanek; Lewis C Becker; Laufey Tryggvadottir; Thorunn Rafnar; Jeffrey Gulcher; Lambertus A Kiemeney; Augustine Kong; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nat Genet       Date:  2008-04-06       Impact factor: 38.330

2.  A General and Robust Framework for Secondary Traits Analysis.

Authors:  Xiaoyu Song; Iuliana Ionita-Laza; Mengling Liu; Joan Reibman; Ying We
Journal:  Genetics       Date:  2016-02-19       Impact factor: 4.562

3.  Survivor bias in Mendelian randomization analysis.

Authors:  Stijn Vansteelandt; Oliver Dukes; Torben Martinussen
Journal:  Biostatistics       Date:  2018-10-01       Impact factor: 5.899

Review 4.  BMI-associated gene variants in FTO and cardiometabolic and brain disease: obesity or pleiotropy?

Authors:  Ingeborg M M Ganeff; Maxime M Bos; Diana van Heemst; Raymond Noordam
Journal:  Physiol Genomics       Date:  2019-06-14       Impact factor: 3.107

5.  Instrumental variable estimation in a survival context.

Authors:  Eric J Tchetgen Tchetgen; Stefan Walter; Stijn Vansteelandt; Torben Martinussen; Maria Glymour
Journal:  Epidemiology       Date:  2015-05       Impact factor: 4.822

6.  Proper analysis of secondary phenotype data in case-control association studies.

Authors:  D Y Lin; D Zeng
Journal:  Genet Epidemiol       Date:  2009-04       Impact factor: 2.135

7.  Sex hormone-binding globulin and risk of type 2 diabetes in women and men.

Authors:  Eric L Ding; Yiqing Song; JoAnn E Manson; David J Hunter; Cathy C Lee; Nader Rifai; Julie E Buring; J Michael Gaziano; Simin Liu
Journal:  N Engl J Med       Date:  2009-08-05       Impact factor: 91.245

8.  The benefits of selecting phenotype-specific variants for applications of mixed models in genomics.

Authors:  Christoph Lippert; Gerald Quon; Eun Yong Kang; Carl M Kadie; Jennifer Listgarten; David Heckerman
Journal:  Sci Rep       Date:  2013       Impact factor: 4.379

9.  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

10.  Efficient multivariate linear mixed model algorithms for genome-wide association studies.

Authors:  Xiang Zhou; Matthew Stephens
Journal:  Nat Methods       Date:  2014-02-16       Impact factor: 28.547

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