Прати
Kristjan Moore
Kristjan Moore
Researcher, deCODE genetics
Верификована је имејл адреса на decode.is
Наслов
Навело
Навело
Година
The sequences of 150,119 genomes in the UK biobank
BV Halldorsson, HP Eggertsson, KHS Moore, H Hauswedell, O Eiriksson, ...
Nature 607 (7920), 732-740, 2022
3312022
Ancient genomes from Iceland reveal the making of a human population
SS Ebenesersdóttir, M Sandoval-Velasco, ED Gunnarsdóttir, ...
Science 360 (6392), 1028-1032, 2018
1252018
Associations of autozygosity with a broad range of human phenotypes
DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, ...
Nature communications 10 (1), 1-17, 2019
1182019
The Anglo-Saxon migration and the formation of the early English gene pool
J Gretzinger, D Sayer, P Justeau, E Altena, M Pala, K Dulias, CJ Edwards, ...
Nature 610 (7930), 112-119, 2022
842022
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
S Saevarsdottir, L Stefansdottir, P Sulem, G Thorleifsson, E Ferkingstad, ...
Annals of the Rheumatic Diseases, 2022
552022
Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events
H Helgason, T Eiriksdottir, MO Ulfarsson, A Choudhary, SH Lund, ...
JAMA 330 (8), 725-735, 2023
402023
HaploGrouper: A generalized approach to haplogroup classification
A Jagadeesan, SS Ebenesersdóttir, VB Guðmundsdóttir, EL Thordardottir, ...
Bioinformatics, 2020
352020
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
AT Skuladottir, G Bjornsdottir, MS Nawaz, H Petersen, S Rognvaldsson, ...
Communications Biology 4 (1), 1-9, 2021
302021
The genetic structure of Norway
M Mattingsdal, SS Ebenesersdóttir, KHS Moore, OA Andreassen, ...
European Journal of Human Genetics, 1-9, 2021
242021
Actionable Genotypes and Their Association with Life Span in Iceland
BO Jensson, GA Arnadottir, H Katrinardottir, R Fridriksdottir, H Helgason, ...
New England Journal of Medicine 389 (19), 1741-1752, 2023
232023
The population genomic legacy of the second plague pandemic
S Gopalakrishnan, SS Ebenesersdottir, IKC Lundstrøm, G Turner-Walker, ...
Current Biology 32 (21), 4743-4751. e6, 2022
232022
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
G Bjornsdottir, MA Chalmer, L Stefansdottir, AT Skuladottir, G Einarsson, ...
Nature Genetics, 1-11, 2023
222023
The genetic history of Scandinavia from the Roman Iron Age to the present
R Rodríguez-Varela, KHS Moore, SS Ebenesersdóttir, GM Kilinc, ...
Cell 186 (1), 32-46. e19, 2023
212023
A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy
AT Skuladottir, G Bjornsdottir, G Thorleifsson, GB Walters, MS Nawaz, ...
Scientific Reports 11 (1), 1-8, 2021
182021
The rate and nature of mitochondrial DNA mutations in human pedigrees
ER Árnadóttir, KHS Moore, VB Guðmundsdóttir, SS Ebenesersdóttir, ...
Cell, 2024
102024
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
A Oddsson, P Sulem, G Sveinbjornsson, GA Arnadottir, V Steinthorsdottir, ...
Nature Communications 14 (1), 3453, 2023
92023
Homozygosity for R47H in TREM2 and the Risk of Alzheimer’s Disease
H Stefansson, GB Walters, G Sveinbjornsson, V Tragante, G Einarsson, ...
New England Journal of Medicine 390 (23), 2217-2219, 2024
42024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency
A Oddsson, V Steinthorsdottir, GR Oskarsson, U Styrkarsdottir, ...
Nature Genetics, 1-7, 2024
12024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease
S Saevarsdottir, K Bjarnadottir, T Markusson, J Berglund, TA Olafsdottir, ...
Nature Communications 15 (1), 1-12, 2024
12024
Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga
MR Ellegaard, SS Ebenesersdóttir, KHS Moore, A Petersén, ÅJ Vågene, ...
iScience, 2024
2024
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