C. Erikstrup

发表

Mapping the aetiological foundations of the heart failure spectrum using human genetics

J. Cook, D. Chasman, A. Helgadóttir, 2023, medRxiv.

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

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

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.

COVID-19 illness severity and 2-year prevalence of physical symptoms: an observational study in Iceland, Sweden, Norway and Denmark

T. Werge, T. Aspelund, A. Kähler, 2023, medRxiv.

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.

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

H. Stefánsson, B. Halldórsson, D. Gudbjartsson, 2024, Nature genetics.

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.

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

M. P. Concas, J. Murabito, S. Bandinelli, 2024, Nature genetics.