Author

Timothy Frayling

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Aaron McDaid· 1 shared Alan Kwong· 1 shared Aliki‐Eleni FarmakiiD· 1 shared Amit Joshi· 1 shared Andrea AngiusiD· 1 shared Andrew Tan ChaniD· 1 shared Andrew Tym HattersleyiD· 1 shared

Activity by Year

2016-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Aarno V. PalotieORCID

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2 papers

Recent·Most cited

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

Luke M. Evans, Rasool Tahmasbi, Matthew Jones, Scott I. Vrieze, Gonçalo R. Abecasis, Sayantan Das, Douglas W. Bjelland, Teresa R de Candia, David Altshuler, Carl A. Anderson, Andrea Angius, Jeffrey C. Barrett, Sonja I. Berndt, Michael Boehnke, Dorrett Boomsma, , George Davey Smith

This paper estimates narrow-sense heritability using identity-by-descent information in unrelated individuals and finds that IBD-based methods can capture rare variant contributions but are affected by stratification.

Heredity · Mar 28, 2018Peer-reviewedGenetics

Quantifying the extent to which index event biases influence large genetic association studies

Hanieh Yaghootkar, Michael Bancks, Sam Jones, Aaron McDaid, Robin Beaumont, Louise Donnelly, Andrew Wood, Archie Campbell, Jessica Tyrrell, Lynne Hocking, Marcus Tuke, Katherine Ruth, Ewan Pearson, Anna Murray, Rachel Freathy, , Zoltan Kutalik

This study quantifies index event bias in large genetic association studies and finds it can explain some associations between disease risk alleles and BMI.

bioRxiv · Sep 12, 2016Genetics