M. O. Ulfarsson

发表

Brain age prediction using deep learning uncovers associated sequence variants

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2019, Nature Communications.

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

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

Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition

H. Stefánsson, K. Stefánsson, L. Wilkinson, 2020, Biological Psychiatry.

Deep learning based brain age prediction uncovers associated sequence variants

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2019, bioRxiv.

Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

D. Gudbjartsson, T. Thorgeirsson, U. Thorsteinsdóttir, 2023, Nature Genetics.

Large-scale plasma proteomics comparisons through genetics and disease associations

Pall I. Olason, Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, 2023, Nature.

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Knut K. Kolskår, Dan J Stein, Lachlan T. Strike, 2018, Molecular Psychiatry.

MAP1B mutations cause intellectual disability and extensive white matter deficit

H. Stefánsson, A. Ingason, S. Steinberg, 2018, Nature Communications.

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

H. Stefánsson, K. Stefánsson, M. Owen, 2019, Biological Psychiatry.

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

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