Author

Brynjolfur G. Jonsson

Icelandic Heart AssociationORCID 0000-0003-4730-5584Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Research Focus:GWAS / association mapping· 2 Assay:proteomics· 2 Approach:benchmark study· 1 Research Focus:database / resource· 1

Frequent Co-Authors

Elias Freyr GudmundssoniD· 3 shared John R. LambiD· 3 shared Lenore J. LauneriD· 3 shared Lori L. JenningsiD· 3 shared Thor AspelundiD· 3 shared Valborg GuðmundsdóttiriD· 3 shared Valur EmilssoniD· 3 shared Vilmundur G. GudnasoniD· 3 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Elias Freyr GudmundssonORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedJun 13, 2022

A Proteogenomic Signature of Age-related Macular Degeneration in Blood

Valur Emilsson, Elias Freyr Gudmundsson, Þórarinn Jónmundsson…·Tony E. Walshe

This study identifies a proteogenomic signature in blood associated with age-related macular degeneration, linking serum proteins to disease severity and progression.

42 citationstop 1%

humanproteomics

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GenomicsNature CommunicationsPeer-reviewedJan 25, 2022

A genome-wide association study of serum proteins reveals shared loci with common diseases

Alexander Guðjónsson, Valborg Guðmundsdóttir, Gisli Thor Axelsson…·Vilmundur G. Gudnason

This study identifies 4,113 genetic associations with serum proteins in 5,368 individuals, revealing shared loci between proteins and common diseases.

288 citationstop 1%

humanGWAS summary statistics

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GeneticsbioRxivPreprintMay 6, 2020

Coding and regulatory variants affect serum protein levels and common disease

Valur Emilsson, Valborg Guðmundsdóttir, Alexander Guðjónsson…·Vilmundur G. Gudnason

The paper identifies 2019 exome array variants affecting 2135 serum proteins and their association with hundreds of complex disease traits in the AGES Reykjavik cohort.

9 citations

humanproteomics

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