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Gísli Másson
Gísli Másson
VP of Informatics, deCODE Genetics
Verified email at decode.is
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
21592012
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
19242002
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
18402009
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
18402007
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
14532020
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
9122020
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
8802007
A common inversion under selection in Europeans
H Stefansson, A Helgason, G Thorleifsson, V Steinthorsdottir, G Masson, ...
Nature genetics 37 (2), 129-137, 2005
8602005
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
7962007
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
6942015
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
6632009
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
6062009
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
6012010
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
5882017
The nature of nurture: Effects of parental genotypes
A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ...
Science 359 (6374), 424-428, 2018
5702018
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
5372008
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
5142014
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
5032017
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
4922008
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
4752014
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