| Rate of de novo mutations and the importance of father’s age to disease risk A Kong, ML Frigge, G Masson, S Besenbacher, P Sulem, G Magnusson, ... Nature 488 (7412), 471-475, 2012 | 2612 | 2012 |
| A high-resolution recombination map of the human genome A Kong, DF Gudbjartsson, J Sainz, GM Jonsdottir, SA Gudjonsson, ... Nature genetics 31 (3), 241-247, 2002 | 2053 | 2002 |
| Common variants conferring risk of schizophrenia H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ... Nature 460 (7256), 744-747, 2009 | 1999 | 2009 |
| A common variant on chromosome 9p21 affects the risk of myocardial infarction A Helgadottir, G Thorleifsson, A Manolescu, S Gretarsdottir, T Blondal, ... Science 316 (5830), 1491-1493, 2007 | 1980 | 2007 |
| Spread of SARS-CoV-2 in the Icelandic population DF Gudbjartsson, A Helgason, H Jonsson, OT Magnusson, P Melsted, ... New England Journal of Medicine 382 (24), 2302-2315, 2020 | 1669 | 2020 |
| Humoral immune response to SARS-CoV-2 in Iceland DF Gudbjartsson, GL Norddahl, P Melsted, K Gunnarsdottir, H Holm, ... New England Journal of Medicine 383 (18), 1724-1734, 2020 | 1145 | 2020 |
| A common inversion under selection in Europeans H Stefansson, A Helgason, G Thorleifsson, V Steinthorsdottir, G Masson, ... Nature genetics 37 (2), 129-137, 2005 | 959 | 2005 |
| Parental influence on human germline de novo mutations in 1,548 trios from Iceland H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ... Nature 549 (7673), 519-522, 2017 | 937 | 2017 |
| Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma G Thorleifsson, KP Magnusson, P Sulem, GB Walters, DF Gudbjartsson, ... Science 317 (5843), 1397-1400, 2007 | 936 | 2007 |
| The nature of nurture: Effects of parental genotypes A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ... Science 359 (6374), 424-428, 2018 | 911 | 2018 |
| Large-scale whole-genome sequencing of the Icelandic population DF Gudbjartsson, H Helgason, SA Gudjonsson, F Zink, A Oddson, ... Nature genetics 47 (5), 435-444, 2015 | 894 | 2015 |
| Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer SN Stacey, A Manolescu, P Sulem, T Rafnar, J Gudmundsson, ... Nature genetics 39 (7), 865-869, 2007 | 893 | 2007 |
| Large-scale integration of the plasma proteome with genetics and disease E Ferkingstad, P Sulem, BA Atlason, G Sveinbjornsson, MI Magnusson, ... Nature genetics 53 (12), 1712-1721, 2021 | 805 | 2021 |
| Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly F Zink, SN Stacey, GL Norddahl, ML Frigge, OT Magnusson, I Jonsdottir, ... Blood, The Journal of the American Society of Hematology 130 (6), 742-752, 2017 | 785 | 2017 |
| Sequence variants at the TERT-CLPTM1L locus associate with many cancer types T Rafnar, P Sulem, SN Stacey, F Geller, J Gudmundsson, A Sigurdsson, ... Nature genetics 41 (2), 221-227, 2009 | 720 | 2009 |
| Fine-scale recombination rate differences between sexes, populations and individuals A Kong, G Thorleifsson, DF Gudbjartsson, G Masson, A Sigurdsson, ... Nature 467 (7319), 1099-1103, 2010 | 697 | 2010 |
| Parental origin of sequence variants associated with complex diseases A Kong, V Steinthorsdottir, G Masson, G Thorleifsson, P Sulem, ... Nature 462 (7275), 868-874, 2009 | 673 | 2009 |
| Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche JRB Perry, F Day, CE Elks, P Sulem, DJ Thompson, T Ferreira, C He, ... Nature 514 (7520), 92-97, 2014 | 648 | 2014 |
| Detection of sharing by descent, long-range phasing and haplotype imputation A Kong, G Masson, ML Frigge, A Gylfason, P Zusmanovich, ... Nature genetics 40 (9), 1068-1075, 2008 | 598 | 2008 |
| Loss-of-function mutations in SLC30A8 protect against type 2 diabetes J Flannick, G Thorleifsson, NL Beer, SBR Jacobs, N Grarup, NP Burtt, ... Nature genetics 46 (4), 357-363, 2014 | 557 | 2014 |
Daniel GudbjartssonStatistician, Decode Geneticsdecode.is üzerinde doğrulanmış e-posta adresine sahip
