O. Pedersen

发表

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.

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.

Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

B. Halldórsson, D. Gudbjartsson, P. Sulem, 2024, Nature structural & molecular biology.

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

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

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.

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

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

An atlas of genetic determinants of forearm fracture

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

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

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

Evaluation of the HemoCue WBC DIFF in leukopenic patient samples

N. Holländer, L. Friis-Hansen, D. Kur, 2020, International journal of laboratory hematology.