Author

Peter Almgren

Lund UniversityORCID 0000-0002-0473-0241Unclaimed 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· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Research Focus:fine-mapping· 2 Assay:whole-exome sequencing· 2

Frequent Co-Authors

Olle MelanderiD· 3 shared Allan R LinnebergiD· 2 shared Anna HelgadóttiriD· 2 shared Anubha MahajaniD· 2 shared Cramer Christensen· 2 shared Daniel Fannar GudbjartssoniD· 2 shared Emma AhlqvistiD· 2 shared Ivan BrandslundiD· 2 shared

Activity by Year

2018-2019 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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3 shared papersGenetics

Olle MelanderORCID

Mutual co-authors in cluster

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4 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 10, 2019

Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

Sonia H Shah, Albert Henry, Carolina Roselli…·David J. Stott

This study conducts a large GWAS on heart failure, identifying 12 genetic loci with associations to CAD, atrial fibrillation, and reduced left ventricular function, and provides causal evidence for several risk factors.

8 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsDiabetologiaPeer-reviewedDec 13, 2018

Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

Tarunveer S. Ahluwalia, Christina‐Alexandra Schulz, Johannes Waage…·Torben F. Hansen

35 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsNature GeneticsPeer-reviewedApr 1, 2018

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

Anubha Mahajan, Jennifer Wessel, Sara M. Willems…·Jun Liu

This study identifies 16 causal coding variants in type 2 diabetes using fine-mapping and shows that one third of signals are false leads.

441 citationstop 1%

humanwhole-exome sequencing

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedMar 1, 2018

Genome-wide analysis yields new loci associating with aortic valve stenosis

Anna Helgadóttir, Guðmar Þorleifsson, Sólveig Grétarsdóttir…·Kāri Stefánsson

This study identifies two new genetic loci associated with aortic valve stenosis through a large genome-wide association study.

125 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky