Hrefna S. Johannsdottir
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 20 publications
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Journal: Nature communications
Published: September 18, 2019
Identification of Lynch syndrome risk variants in the Romanian population.
Journal: Journal of cellular and molecular medicine
Published: May 03, 2018
Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin.
Journal: Journal of the National Cancer Institute
Published: August 22, 2017
Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
Journal: Nature genetics
Published: July 28, 2017
A genome-wide association study yields five novel thyroid cancer risk loci.
Journal: Nature communications
Published: August 08, 2016
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer.
Journal: Human molecular genetics
Published: September 03, 2015
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
Journal: European heart journal
Published: August 23, 2015
Loss-of-function variants in ATM confer risk of gastric cancer.
Journal: Nature genetics
Published: December 10, 2014
New basal cell carcinoma susceptibility loci.
Journal: Nature communications
Published: November 05, 2014
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease.
Journal: Nature genetics
Published: June 08, 2014
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.
Journal: Human molecular genetics
Published: May 28, 2014
Last Updated: 09/26/2026