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2023
Mark Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Oddsson, Asmundur ; Sulem, Patrick ; Sveinbjornsson, Gardar ; Arnadottir, Gudny A ; Steinthorsdottir, Valgerdur ; Halldorsson, Gisli H ; Atlason, Bjarni A ; Oskarsson, Gudjon R ; Helgason, Hannes and Nielsen, Henriette Svarre , et al. (2023) In Nature Communications 14(1). p.3453-3453
- Contribution to journal › Article
2019
Mark Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer, Alexander ; Li, Yong ; Ghasemi, Sahar ; Prins, Bram P. ; Wuttke, Matthias ; Hermle, Tobias ; Giri, Ayush ; Sieber, Karsten B. ; Qiu, Chengxiang and Kirsten, Holger , et al. (2019) In Nature Communications 10(1).
- Contribution to journal › Article
2017
Mark Identification of sequence variants influencing immunoglobulin levels
Jonsson, Stefan ; Sveinbjornsson, Gardar ; de Lapuente Portilla, Aitzkoa Lopez ^LU ; Swaminathan, Bhairavi ^LU ; Plomp, Rosina ; Dekkers, Gillian ; Ajore, Ram ^LU ; Ali, Mina ^LU ; Bentlage, Arthur E H and Elmér, Evelina ^LU , et al. (2017) In Nature Genetics 49(8). p.1182-1191
- Contribution to journal › Article
Mark Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Styrkarsdottir, Unnur ; Helgason, Hannes ; Sigurdsson, Asgeir ; Norddahl, Gudmundur L. ^LU ; Agustsdottir, Arna B. ; Reynard, Louise N. ; Villalvilla, Amanda ; Halldorsson, Gisli H. ; Jonasdottir, Aslaug and Magnusdottir, Audur , et al. (2017) In Nature Genetics 49(5). p.801-805
- Contribution to journal › Article

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