Daníel F. Guðbjartsson

Reykjavík University — IS

Biochemistry, Genetics and Molecular Biology · Life Sciences

142h-index84.2kcitations523works10.52yr avg
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Research Topics

Genetic Associations and Epidemiology(145), RNA modifications and cancer(37), Genomics and Rare Diseases(37), Epigenetics and DNA Methylation(33), Genomic variations and chromosomal abnormalities(31)

Publications506 total

Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Nature Genetics·2025· 2 citedOpen Access
Variants Near <i>NOG</i> and <i>SOX9</i> Are Associated with Mandibular Retrognathia
Journal of Dental Research·2025Open Access
African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk
Nature Genetics·2025Open Access
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition
Human Molecular Genetics·2025
Genome-wide association study and polygenic risk prediction of hypothyroidism
Nature Genetics·2025Open Access
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication
Biological Psychiatry Global Open Science·2025Open Access
Genetic diversity fuels gene discovery for tobacco and alcohol use
UNC Libraries·2025Open Access
The burden of endometriosis on quality of life in Danish women: an analysis of the Danish Blood Donor Study
BMC Medicine·2025Open Access
Genomic analyses reveal new insights into Alzheimer’s disease
2025· 3 cited
Sequence Diversity Lost in Early Pregnancy
Obstetrical & Gynecological Survey·2025
The genetic architecture of fibromyalgia across 2.5 million individuals
2025Open Access
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
UNC Libraries·2025Open Access
Whole-genome sequencing of 490,640 UK Biobank participants
Nature·2025· 47 citedOpen Access
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development
JHEP Reports·2025· 5 citedOpen Access
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy
The American Journal of Human Genetics·2025· 1 citedOpen Access
Sequence diversity lost in early pregnancy
Nature·2025· 13 citedOpen Access
Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies
Genome Medicine·2025· 2 citedOpen Access
Missense variants in FRS3 affect body mass index in populations of diverse ancestries
Nature Communications·2025· 1 citedOpen Access
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder
Nature Genetics·2025· 7 citedOpen Access
Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis
The Journal of Headache and Pain·2025· 4 citedOpen Access
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Frequent Co-authors

Kāri Stefánsson(37), Augustine Kong(33), Unnur Þorsteinsdóttir(33), Patrick Sulem(28), Guðmar Þorleifsson(25), Jeffrey R. Gulcher(21), Gísli Másson(18), Agnar Helgason(18), Hreinn Stefánsson(15), Ásgeir Sigurðsson(14), Þórunn Rafnar(14), Michael L. Frigge(13), Arnaldur Gylfason(12), Áslaug Jónasdóttir(11), Valgerður Steinthórsdóttir(11), Lambertus A. Kiemeney(11), Simon Stacey(11), G. Bragi Walters(10), Jouke‐Jan Hottenga(10), Thorgeir E. Thorgeirsson(10)