The sequences of 150,119 genomes in the UK Biobank

Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, +73

Nature

Characterizing mutagenic effects of recombination through a sequence-level genetic map

Bjarni V. Halldórsson, Gunnar Pálsson, Ólafur Andri Stefánsson, +17

Science

GeneticsMolecular BiologyMolecular GeneticsGenomicsMicroarray Genotype +14

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, +27

Nature Genetics

BioinformaticsStructural VariantsLong-read SequencingAllelic VariantHuman Diseases +9

Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, +26

Structural VariantsGeneticsGenetic EpidemiologyDisease Gene IdentificationGenomics +19

Actionable Genotypes and Their Association with Life Span in Iceland

Brynjar Ö. Jensson, Gudny A. Arnadottir, Hildigunnur Katrínardóttir, +37

New England Journal of Medicine

A Genetic Linkage Study of the D₂Dopamine Receptor Locus in Heavy Drinking and Alcoholism

Christopher C. H. Cook, Gunnar Pálsson, Adrian Turner, +5

The British Journal of Psychiatry

Sequence variants affecting the genome-wide rate of germline microsatellite mutations

Hákon Jónsson, Marteinn T. Hardarson, Gunnar Pálsson, +18

Nature Communications

Complete human recombination maps

Gunnar Pálsson, Marteinn T. Hardarson, Hákon Jónsson, +13

Nature

The sequences of 150,119 genomes in the UK biobank

Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, +50

GeneticsGenetic EpidemiologyGenomicsGenome-wide Association StudyGenotype-phenotype Association +18

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

Valgerður Steinthórsdóttir, Bjarni V. Halldórsson, Hákon Jónsson, +23

Nature Structural & Molecular Biology