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Studying the genetics of participation using footprints left on the ascertained genotypes.

Journal article

Benonisdottir S. and Kong A., (2023), Nat Genet

Deconstructing the sources of genotype-phenotype associations in humans.

Journal article

Young AI. et al, (2019), Science, 365, 1396 - 1400

Multiple transmissions of de novo mutations in families.

Journal article

Jónsson H. et al, (2018), Nat Genet, 50, 1674 - 1680

Relatedness disequilibrium regression estimates heritability without environmental bias.

Journal article

Young AI. et al, (2018), Nat Genet, 50, 1304 - 1310

The nature of nurture: Effects of parental genotypes.

Journal article

Kong A. et al, (2018), Science, 359, 424 - 428

Parental influence on human germline de novo mutations in 1,548 trios from Iceland.

Journal article

Jónsson H. et al, (2017), Nature, 549, 519 - 522

Whole genome characterization of sequence diversity of 15,220 Icelanders.

Journal article

Jónsson H. et al, (2017), Sci Data, 4

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

Journal article

Zink F. et al, (2017), Blood, 130, 742 - 752

Selection against variants in the genome associated with educational attainment.

Journal article

Kong A. et al, (2017), Proc Natl Acad Sci U S A, 114, E727 - E732

Genome-wide analysis identifies 12 loci influencing human reproductive behavior.

Journal article

Barban N. et al, (2016), Nat Genet, 48, 1462 - 1472

Genome-wide association study identifies 74 loci associated with educational attainment.

Journal article

Okbay A. et al, (2016), Nature, 533, 539 - 542