Author

Kerstin Welén-Schef

Danderyds sjukhusORCID 0000-0001-9852-9495Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Annica Ravn‐FischeriD· 1 shared Cecilia GunnarssoniD· 1 shared Christian DworeckiD· 1 shared Christos PagonisiD· 1 shared David ErlingeiD· 1 shared Erik Rydberg· 1 shared Eva SwahniD· 1 shared Jonas AnderssoniD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Annica Ravn‐FischerORCID

Mutual co-authors in cluster

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1 paper

Recent·Most cited

Comprehensive Exome Sequencing in Swedish Patients with Spontaneous Coronary Artery Dissection

Cecilia Gunnarsson, Rada Ellegård, Josefine Åhsberg, Sophia Huda, Jonas Andersson, Christian Dworeck, Natalie Glaser, David Erlinge, Loghman Henareh, Nina Johnston, Maria Nastase Mannila, Christos Pagonis, Annica Ravn‐Fischer, Erik Rydberg, Kerstin Welén-Schef, , Sofia Sederholm Lawesson

This study identifies rare genetic variants in Swedish SCAD patients, showing 4% with known SCAD-associated variants and 60% with potentially relevant variants in vascular-related genes.

medRxiv · Apr 24, 2026 · PreprintGenetic & Genomic Medicine