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Gísli Másson
Gísli Másson
VP of Informatics, deCODE Genetics
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Title
Cited by
Cited by
Year
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
24292012
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
20032002
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
19362009
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
19272007
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
16422020
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
10882020
A common inversion under selection in Europeans
H Stefansson, A Helgason, G Thorleifsson, V Steinthorsdottir, G Masson, ...
Nature genetics 37 (2), 129-137, 2005
9412005
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
8982007
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
8812007
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
8332015
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
8292017
The nature of nurture: Effects of parental genotypes
A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ...
Science 359 (6374), 424-428, 2018
7942018
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
7032009
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
6882017
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
6612010
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
6562009
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
5952014
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
5682008
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
SN Stacey, A Manolescu, P Sulem, S Thorlacius, SA Gudjonsson, ...
Nature genetics 40 (6), 703-706, 2008
5482008
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
5322014
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