Henrik Ullum

Statens Serum Institut — Denmark

Immunology and Microbiology · Life Sciences

66h-index19.2kcitations515works8.42yr avg
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Research Topics

HIV Research and Treatment(79), Blood donation and transfusion practices(52), HIV-related health complications and treatments(50), Immune Cell Function and Interaction(48), SARS-CoV-2 and COVID-19 Research(39)

Publications507 total

Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Nature Genetics·2025· 2 citedOpen 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
Breast cancer risk prediction with a modified BOADICEA model in Danish women
British Journal of Cancer·2025Open Access
A structural deletion in the 3′ <scp>UTR</scp> of <i>SLC11A2</i> is associated with altered iron status: Evidence from two large Danish cohorts
British Journal of Haematology·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
The genetic architecture of fibromyalgia across 2.5 million individuals
2025Open Access
Subgrouping patients with ischemic heart disease by means of the Markov cluster algorithm
Communications Medicine·2025· 1 citedOpen Access
Genome-wide study of somatic symptom and related disorders identifies novel genomic loci and map genetic architecture
2025· 1 citedOpen Access
Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development
JHEP Reports·2025· 5 citedOpen Access
The burden of endometriosis on quality of life in Danish blood donors
2025Open Access
Cohort profile: Copenhagen Hospital Biobank-chronic inflammatory disease—inflammatory bowel disease (CHB-CID:IBD) genetic cohort
European Journal of Epidemiology·2025· 1 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
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum
Nature Genetics·2025· 12 citedOpen Access
Population-scale inheritance analysis of 858,635 individuals reveals North Sea migration from the Middle Ages to the Industrial Revolution
2025· 1 citedOpen Access
Psychometric properties and socio-demographic correlates of the Connor-Davidson Resilience Scale in three large population-based cohorts including Danish and Icelandic adults
Journal of Mood and Anxiety Disorders·2025· 2 citedOpen Access
The urgent need to protect WHO is also an opportunity
The Lancet·2025· 1 cited
Genome-wide associations spanning 194 in-hospital drug dosage change phenotypes highlight diverse genetic backgrounds in concurrent drug therapy
2025Open Access
Genome-Wide Association Study of Plasma Sodium Concentrations with and without Exposure to Thiazide Diuretics
Journal of the American Society of Nephrology·2025· 2 citedOpen Access
Genome-wide associations spanning 194 in-hospital drug dosage change phenotypes highlight diverse genetic backgrounds in concurrent drug therapy
Computational and Structural Biotechnology Journal·2025Open Access
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Frequent Co-authors

Christian Erikstrup(19), Ole Birger Pedersen(15), Erik Sørensen(11), Henrik Hjalgrim(11), Bente Klarlund Pedersen(10), Karina Banasik(8), Kristoffer Sølvsten Burgdorf(8), Thomas Folkmann Hansen(7), Daníel F. Guðbjartsson(7), Unnur Þorsteinsdóttir(7), Thomas Werge(7), Lise Wegner Thørner(7), Søren Brunak(7), Klaus Rostgaard(7), Hreinn Stefánsson(6), Kāri Stefánsson(6), Kasper Iversen(5), Sisse Rye Ostrowski(5), Guðmar Þorleifsson(5), Kaspar René Nielsen(5)