Author

Karola Rehnström

University of Cambridge

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· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Abraham ReichenbergiD· 1 shared Adrian Park· 1 shared Albert KoulmaniD· 1 shared Alessandra CabassiiD· 1 shared Alicia R. MartiniD· 1 shared Amy J. FraryiD· 1 shared Anders Dupont BørglumiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Aarno V. PalotieORCID

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2 papers

Recent·Most cited

GenomicsClinical EpigeneticsPeer-reviewedMar 12, 2022

Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes.

Denis Seyres, Alessandra Cabassi, John J. Lambourne…·Mattia Frontini

The paper identifies molecular and metabolic signatures of cardiometabolic syndrome using extreme phenotype groups and shows changes after bariatric surgery.

13 citations

humanbulk RNA-seq

𝕏 PostBluesky

GeneticsNature GeneticsPeer-reviewedFeb 25, 2019

Common risk variants identified in autism spectrum disorder

Jakob Grove, BUPGEN, Stephan Ripke…·Anders Dupont Børglum

This study identifies five genome-wide significant loci and seven shared with other traits in a large ASD GWAS, highlighting polygenic heterogeneity and the value of large-scale GWAS in ASD.

2,421 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky