Hafdis T Helgadottir
6PUBLICATIONS
25CO-AUTHORS
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Publications (6)
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|Aug 20, 2025
Induced somatic mutation accumulation during skeletal muscle regeneration reduces muscle strength.Peter Vrtačnik, Lara G Merino, Santhilal Subhash
|Jun 10, 2025
Recurrent somatic mutation and progerin expression in early vascular aging of chronic kidney disease.Gwladys Revêchon, Anna Witasp, Nikenza Viceconte
|Jan 05, 2025
Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 families.Meis Omran, Yaxuan Liu, Alexander Sun Zhang
|Nov 25, 2024
A Novel Type of Autosomal Dominant Episodic Nystagmus Segregating with a Variant in the FRMD5 Gene.Björn Hammar, Sofia Paulsson, Hafdis T Helgadottir
|Mar 10, 2022
A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16.Elin Barnekow, Wen Liu, Hafdis T Helgadottir
|Mar 17, 2021
Identification of known and novel familial cancer genes in Swedish colorectal cancer families.Hafdis T Helgadottir, Jessada Thutkawkorapin, Anna Rohlin
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Frequent Collaborators
2 joint publications
Maria Eriksson
2 joint publications
Gwladys Revêchon
1 joint publications
Elin Barnekow
1 joint publications
Kyriaki Michailidou
1 joint publications
Joe Dennis
1 joint publications
Per Hall
1 joint publications
Annika Lindblom
1 joint publications
Sofia Paulsson
1 joint publications
Irene Franco
1 joint publications
Meis Omran
