Kamu erişimi zorunlu olan makaleler - Gísli MássonDaha fazla bilgi edinin
GenelNIHMRCSwedish Research CouncilWellcomeCancer Research UKNIHRDFFEuropean CommissionDFGBHFVillum FoundationKnut and Alice Wallenberg FoundationNordforskVersus Arthritis, UKRCNInnovation Fund DenmarkDCTIDSFINSERMRannisNWOMarianne and Marcus Wallenberg FoundationESRCDoris Duke Charitable FoundationGovernment of SpainBMBFUK Research & InnovationVinnova, Sweden
Hiçbir yerde sunulmuyor: 7
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
V Steinthorsdottir, G Thorleifsson, P Sulem, H Helgason, N Grarup, ...
Nature genetics 46 (3), 294-298, 2014
Zorunlu olanlar: Danish Council for Independent Research
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
U Styrkarsdottir, G Thorleifsson, P Sulem, DF Gudbjartsson, A Sigurdsson, ...
Nature 497 (7450), 517-520, 2013
Zorunlu olanlar: US National Institutes of Health
Weighting sequence variants based on their annotation increases power of whole-genome association studies
G Sveinbjornsson, A Albrechtsen, F Zink, SA Gudjonsson, A Oddson, ...
Nature genetics 48 (3), 314-317, 2016
Zorunlu olanlar: Villum Foundation
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
U Styrkarsdottir, SH Lund, G Thorleifsson, F Zink, OA Stefansson, ...
Nature genetics 50 (12), 1681-1687, 2018
Zorunlu olanlar: UK Medical Research Council
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ...
Nature genetics 51 (2), 267-276, 2019
Zorunlu olanlar: US National Institutes of Health, UK Medical Research Council
Identification of sequence variants influencing immunoglobulin levels
S Jonsson, G Sveinbjornsson, AL de Lapuente Portilla, B Swaminathan, ...
Nature genetics 49 (8), 1182-1191, 2017
Zorunlu olanlar: Knut and Alice Wallenberg Foundation, Marianne and Marcus Wallenberg …
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
U Styrkarsdottir, H Helgason, A Sigurdsson, GL Norddahl, AB Agustsdottir, ...
Nature genetics 49 (5), 801-805, 2017
Zorunlu olanlar: Versus Arthritis, UK, UK Medical Research Council
Bir yerde sunuluyor: 61
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
Zorunlu olanlar: US National Institutes of Health
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
Zorunlu olanlar: US National Institutes of Health
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
Zorunlu olanlar: British Heart Foundation
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
Zorunlu olanlar: US National Institutes of Health
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
Zorunlu olanlar: US National Institutes of Health, Cancer Research UK
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
Zorunlu olanlar: German Research Foundation
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
Zorunlu olanlar: US National Institutes of Health
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
Zorunlu olanlar: US National Institutes of Health, Cancer Research UK, UK Medical Research …
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
Zorunlu olanlar: US National Institutes of Health
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
Zorunlu olanlar: US National Institutes of Health, Danish Council for Independent Research …
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
Zorunlu olanlar: US National Institutes of Health
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ...
Nature genetics 42 (10), 906-909, 2010
Zorunlu olanlar: US National Institutes of Health, Swedish Research Council
A direct characterization of human mutation based on microsatellites
JX Sun, A Helgason, G Masson, SS Ebenesersdóttir, H Li, S Mallick, ...
Nature Genetics, 2012
Zorunlu olanlar: US National Institutes of Health
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