Author

Per Tornvall

Karolinska InstitutetORCID 0000-0002-7529-1338Unclaimed 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

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 24, 2026

Comprehensive Exome Sequencing in Swedish Patients with Spontaneous Coronary Artery Dissection

Cecilia Gunnarsson, Rada Ellegård, Josefine Åhsberg…·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.

DOI 10.64898/2026.04.22.26351535

humanwhole-exome sequencing

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