Studying the genetics of participation using footprints left on the ascertained genotypes.
Benonisdottir S. and Kong A., (2023), Nature genetics
Mendelian imputation of parental genotypes improves estimates of direct genetic effects.
Young AI. et al, (2022), Nature genetics
Deconstructing the sources of genotype-phenotype associations in humans.
Young AI. et al, (2019), Science (New York, N.Y.), 365, 1396 - 1400
Multiple transmissions of de novo mutations in families.
Jónsson H. et al, (2018), Nature genetics, 50, 1674 - 1680
Relatedness disequilibrium regression estimates heritability without environmental bias
Young AI. et al, (2018), Nature Genetics, 50, 1304 - 1310
Whole genome characterization of sequence diversity of 15,220 Icelanders.
Jónsson H. et al, (2017), Scientific data, 4
Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Jónsson H. et al, (2017), Nature, 549, 519 - 522
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly
Zink F. et al, (2017), Blood, 130, 742 - 752
Selection against variants in the genome associated with educational attainment
Kong A. et al, (2017), Proceedings of the National Academy of Sciences, 114, E727 - E732
A sequence variant associating with educational attainment also affects childhood cognition
Gunnarsson B. et al, (2016), Scientific Reports, 6
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N. et al, (2016), Nature Genetics, 48, 1462 - 1472
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A. et al, (2016), Nature, 533, 539 - 542