Author

Gunnar Engström

Lund UniversityORCID 0000-0002-8618-9152Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Andrew P. MorrisiD· 2 shared Åsa JohanssoniD· 2 shared Åsa K. HedmaniD· 2 shared Cecilia M. LindgreniD· 2 shared Erik IngelssoniD· 2 shared Johan ÄrnlöviD· 2 shared Lars LindiD· 2 shared Marju Orho‐MelanderiD· 2 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Andrew P. MorrisORCID

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3 papers

Recent·Most cited

A national ecosystem for long-read genome sequencing: Integrating population genomics and rare disease diagnostics in Sweden

Adam Ameur, Fulya Taylan, Marlene Ek, Jesper Eisfeldt, Susana Häggqvist, Maria Pettersson, Ignas Bunikis, Joakim Klar, Ida Höijer, Maria Strandh, Rebecca Josefson, Michela Barbaro, Anna Beskow, Anders Blomberg, Marie-Louise Bondeson, , Hans Ehrencrona

This paper evaluates the clinical use of long-read genome sequencing in Sweden, showing it provides molecular diagnoses and reduces diagnostic costs.

medRxiv · Oct 13, 2026 · PreprintGenetic & Genomic Medicine

Genomic evaluation of circulating proteins for drug target characterisation and precision medicine

Lasse Folkersen, Stefan Gustafsson, Qin Wang, Daniel Hvidberg Hansen, Åsa K. Hedman, Andrew Joseph Schork, Karen M. Page, Daria V. Zhernakova, Yang Wu, James E. Peters, Niclas Ericsson, Sarah E. Bergen, Thibaud Boutin, Andrew D. Bretherick, Stefan Enroth, , Anders Mälarstig

The paper identifies pQTLs for cardiovascular proteins and uses them to evaluate drug targets and suggest new candidates for precision medicine.

bioRxiv · Apr 3, 2020 · PreprintGenetics

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

Sonia H Shah, Albert Henry, Carolina Roselli, Honghuang Lin, Garðar Sveinbjörnsson, Ghazaleh Fatemifar, Åsa K. Hedman, Jemma B. Wilk, Michael P. Morley, Mark D. Chaffin, Anna Helgadóttir, Niek Verweij, Abbas Dehghan, Peter Almgren, Charlotte Andersson, , 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.

bioRxiv · Jul 10, 2019 · PreprintGenetics