H. Ullum

发表

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

H. Ullum, T. Werge, H. Hakonarson, 2020, Cell.

The healthy donor effect impacts self‐reported physical and mental health – results from the Danish Blood Donor Study (DBDS)

H. Ullum, K. Kyvik, A. Skytthe, 2019, Transfusion medicine.

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Jens K. Boldsen, Pall I. Olason, Bjarni V. Halldórsson, 2023, Nature Genetics.

An atlas of genetic determinants of forearm fracture

O. Mäkitie, T. Tuomi, S. Movérare-Skrtic, 2023, Nature Genetics.

Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth

T. Werge, R. Freathy, B. Shields, 2023, Nature Genetics.

Complex effects of sequence variants on lipid levels and coronary artery disease

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2023, Cell.

Development and validation of a neural network-based survival model for mortality in ischemic heart disease

H. Ullum, A. Helgadóttir, H. Hólm, 2023, medRxiv.

First cases of SARS-CoV-2 BA.2.86 in Denmark, 2023

N. B. Larsen, K. Ellegaard, C. Polacek, 2023, Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin.

Neutralisation of SARS-CoV-2 Omicron subvariants BA.2.86 and EG.5.1 by antibodies induced by earlier infection or vaccination

D. Planas, K. Ellegaard, C. Polacek, 2023, bioRxiv.

Variants at the Interleukin 1 Gene Locus and Pericarditis.

Brynja D. Sigurpálsdóttir, B. Halldórsson, A. Sigurdsson, 2023, JAMA cardiology.

Genome-wide association analysis reveals insights into the molecular aetiology underlying dilated cardiomyopathy

J. Cook, U. Thorsteinsdóttir, P. Ellinor, 2023, medRxiv.

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

J. Pankow, D. Gudbjartsson, U. Thorsteinsdóttir, 2023, Nature Genetics.

A second update on mapping the human genetic architecture of COVID-19

M. A. Hakim Newton, Jack D. Sanders, Jonathan H. Morgan, 2022, Nature.

Multi-ancestry GWAS deciphers genetic architecture of abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

J. Pankow, V. Zuber, G. Thorleifsson, 2022, medRxiv.

SMIM1 absence is associated with reduced energy expenditure and excess weight.

Tanya M. Teslovich, May E. Montasser, Nicholette D. Palmer, 2024, i Medicina.

Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors

K. Burgdorf, B. Winsvold, Jes Olesen, 2024, Communications biology.

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum

N. Timpson, T. Ferreira, I. Jónsdóttir, 2024, medRxiv.

Lifestyle and demographic associations with 47 inflammatory and vascular stress biomarkers in 9876 blood donors

Jens K. Boldsen, K. Burgdorf, N. Grarup, 2024, Communications medicine.

Blood donation and migraine relief: A national population cohort study in Denmark

K. Rostgaard, C. Erikstrup, E. Sørensen, 2024, Transfusion.

A genome-wide association study of social trust in 33,882 Danish blood donors

Jens K. Boldsen, H. Stefánsson, D. Gudbjartsson, 2024, Scientific reports.

Genetic prediction of 33 blood group phenotypes using an existing genotype dataset

C. Erikstrup, K. Banasik, J. Storry, 2023, Transfusion.

Blood donation and iron deficiency

H. Ullum, H. Hjalgrim, C. Erikstrup, 2017 .

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

C. Gieger, H. Stefánsson, M. Perola, 2024, Nature genetics.

Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus.

C. von Buchwald, S. Heilmann-Heimbach, P. Hallberg, 2024, The Journal of allergy and clinical immunology.

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

Jens K. Boldsen, H. Stefánsson, D. Gudbjartsson, 2024, Communications biology.

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

D. Gudbjartsson, P. Sulem, H. Hólm, 2024, Nature genetics.

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

Gardar Sveinbjornsson, P. Postema, H. Hólm, 2024, medRxiv.