Author

Thea Bjørnland

Norwegian University of Science and TechnologyORCID 0000-0003-1054-5410Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Arthur GillyiD· 2 shared Dániel SüvegesiD· 2 shared Eleftheria ZegginiiD· 2 shared Emmanouil Tsafantakis· 2 shared George V. DedoussisiD· 2 shared Lorraine SouthamiD· 2 shared Nigel William RayneriD· 2 shared Adam S. ButterworthiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

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10 top collaborators · 43 mutual co-author links

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2 shared papersGenetics

Arthur GillyORCID

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2 papers

Recent·Most cited

GeneticsNature CommunicationsPeer-reviewedDec 10, 2020

Whole genome sequencing analysis of the cardiometabolic proteome

Arthur Gilly, Young‐Chan Park, Grace Png…·Eleftheria Zeggini

The paper uses whole-genome sequencing to analyze the genetic architecture of 257 cardiometabolic protein biomarkers, identifying 131 sequence variant associations and constructing polygenic scores that explain up to 45% of protein variation.

110 citationstop 3%

humanwhole-genome sequencing

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GeneticsNature CommunicationsPeer-reviewedNov 1, 2018

Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

Arthur Gilly, Dániel Süveges, Karoline B. Kuchenbaecker…·Eleftheria Zeggini

The paper performs deep whole genome sequencing on 1,457 individuals to investigate rare variant contributions to cardiometabolic traits, identifying new regulatory variants and gene-trait associations.

29 citations

humanwhole-genome sequencing

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