Author

Bjarni J. Vilhjálmsson

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 Assay:GWAS summary statistics· 2 Organism:human· 2 Research Focus:polygenic risk· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:fine-mapping· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Benjamin M Neale· 2 shared Bogdan Pasaniuc· 2 shared Gaurav Bhatia· 2 shared Mark Daly· 2 shared Noah A. Zaitlen· 2 shared Sang Hong Lee· 2 shared Schizophrenia Working Group of the Psychiatric Genomics Consortium· 2 shared Teresa R de Candia· 2 shared

Activity by Year

2015-2016 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetics

Benjamin M Neale

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintApr 13, 2016

Subtle stratification confounds estimates of heritability from rare variants

Gaurav Bhatia, Alexander Gusev, Po-Ru Loh…·Alkes L. Price

This study shows that subtle population stratification can confound heritability estimates from rare variants, even after standard corrections, suggesting the need for better stratification control in genetic studies.

DOI 10.1101/048181

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 12, 2015

Haplotypes of common SNPs can explain missing heritability of complex diseases

Gaurav Bhatia, Alexander Gusev, Po-Ru Loh…·Alkes L. Price

The paper shows that haplotypes of common SNPs explain more heritability of complex diseases than individual SNPs alone.

DOI 10.1101/022418

humanGWAS summary statistics

𝕏 PostBluesky