Author

Samantha Welsh

UK BiobankORCID 0000-0003-1444-8765Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-genome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Adeolu Badi AdewoyeiD· 1 shared Adrián CortésiD· 1 shared Aimée M. DeatoniD· 1 shared Allan MotyeriD· 1 shared Alnylam Human Genetics· 1 shared Anders MälarstigiD· 1 shared Anil RajiD· 1 shared Anubha MahajaniD· 1 shared

Activity by Year

2017-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperGenetics

Adeolu Badi AdewoyeORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

GeneticsNaturePeer-reviewedOct 4, 2023

Genetic regulation of the human plasma proteome in 54,306 UK Biobank participants

Benjamin B. Sun, Joshua Chiou, Matthew Traylor…·Christopher D. Whelan

The paper maps genetic associations with plasma proteins in 54,306 UK Biobank participants, identifying 10,248 new protein quantitative trait loci (pQTLs) and expanding the genetic architecture of the plasma proteome.

1,831 citationstop 1%

humanproteomics

𝕏 PostBluesky

GeneticsWellcome Open ResearchPeer-reviewedFeb 21, 2018

Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function

Adeolu Badi Adewoye, Nick R. G. Shrine, Linda Odenthal-Hesse…·Louise V. Wain

The paper investigates the CCL3L1-CCR5 axis in lung function using genetic data, finding no association between CCL3L1 copy number or CCR5del32 genotype and lung function.

12 citations

humanDNA methylation

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GeneticsbioRxivPreprintJul 20, 2017

✦ In-depth digest

Genome-wide genetic data on ~500,000 UK Biobank participants

Clare Bycroft, Colin Freeman, Desislava Petkova…·Jonathan Marchini

Quality-controlled genotypes for 488,377 UK Biobank participants at 805,426 markers, imputed to ~96 million variants, plus ancestry PCs, kinship (30.3% have close relatives enrolled) and HLA calls.

623 citations

humanwhole-genome sequencing

𝕏 PostBluesky