Author

Therese Johansson

Garvan Institute of Medical ResearchORCID 0000-0003-1043-7065Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:electronic health records· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexander NeumanniD· 1 shared Åsa JohanssoniD· 1 shared Clair A. EnthoveniD· 1 shared Fatemeh HadizadehiD· 1 shared Frances S. CheniD· 1 shared Julia HöglundiD· 1 shared Rosa H. MulderiD· 1 shared Valeria Lo FaroiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 12 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexander NeumannORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 7, 2026

Interactive effects of genetic variants and oral contraceptive use on depression in the UK Biobank

Clair A. Enthoven, Rosa H. Mulder, Alexander Neumann…·Frances S. Chen

The paper investigates genetic variants and oral contraceptive use interactions on depression risk in the UK Biobank, finding no genome-wide significant interactions.

DOI 10.64898/2026.08.05.26359775

humanelectronic health records

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Genetic & Genomic MedicinemedRxivPreprintApr 24, 2022

Using genotyping and whole-exome sequencing data to improve genetic risk prediction in deep venous thrombosis

Valeria Lo Faro, Therese Johansson, Julia Höglund…·Åsa Johansson

This study improves DVT risk prediction by combining polygenic risk scores with genotyping and whole-exome sequencing data in the UK Biobank cohort, identifying novel variants and demonstrating enhanced risk stratification.

1 citation

humanwhole-exome sequencing

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