Search details
1.
Large-scale plasma proteomics comparisons through genetics and disease associations.
Nature
; 622(7982): 348-358, 2023 Oct.
Article
in English
| MEDLINE | ID: mdl-37794188
2.
Actionable Genotypes and Their Association with Life Span in Iceland.
N Engl J Med
; 389(19): 1741-1752, 2023 Nov 09.
Article
in English
| MEDLINE | ID: mdl-37937776
3.
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease.
Nature
; 584(7822): 619-623, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32581359
4.
Spread of SARS-CoV-2 in the Icelandic Population.
N Engl J Med
; 382(24): 2302-2315, 2020 06 11.
Article
in English
| MEDLINE | ID: mdl-32289214
5.
Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Nature
; 549(7673): 519-522, 2017 09 28.
Article
in English
| MEDLINE | ID: mdl-28959963
6.
Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.
JAMA
; 330(8): 725-735, 2023 08 22.
Article
in English
| MEDLINE | ID: mdl-37606673
7.
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset.
Ann Rheum Dis
; 81(8): 1085-1095, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35470158
8.
Sequence variants associating with urinary biomarkers.
Hum Mol Genet
; 28(7): 1199-1211, 2019 04 01.
Article
in English
| MEDLINE | ID: mdl-30476138
9.
Selection against variants in the genome associated with educational attainment.
Proc Natl Acad Sci U S A
; 114(5): E727-E732, 2017 01 31.
Article
in English
| MEDLINE | ID: mdl-28096410
10.
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.
PLoS Genet
; 13(3): e1006659, 2017 03.
Article
in English
| MEDLINE | ID: mdl-28273074
11.
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.
Hum Mol Genet
; 26(12): 2364-2376, 2017 06 15.
Article
in English
| MEDLINE | ID: mdl-28398513
12.
Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.
N Engl J Med
; 374(22): 2131-41, 2016 Jun 02.
Article
in English
| MEDLINE | ID: mdl-27192541
13.
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.
Blood
; 130(6): 742-752, 2017 08 10.
Article
in English
| MEDLINE | ID: mdl-28483762
14.
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
Nature
; 497(7450): 517-20, 2013 May 23.
Article
in English
| MEDLINE | ID: mdl-23644456
15.
Multi-nucleotide de novo Mutations in Humans.
PLoS Genet
; 12(11): e1006315, 2016 Nov.
Article
in English
| MEDLINE | ID: mdl-27846220
16.
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer.
Hum Mol Genet
; 25(5): 1008-18, 2016 Mar 01.
Article
in English
| MEDLINE | ID: mdl-26740556
17.
Rate of de novo mutations and the importance of father's age to disease risk.
Nature
; 488(7412): 471-5, 2012 Aug 23.
Article
in English
| MEDLINE | ID: mdl-22914163
18.
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
Eur Heart J
; 38(1): 27-34, 2017 01 01.
Article
in English
| MEDLINE | ID: mdl-27742809
19.
BamHash: a checksum program for verifying the integrity of sequence data.
Bioinformatics
; 32(1): 140-1, 2016 Jan 01.
Article
in English
| MEDLINE | ID: mdl-26363028
20.
GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture.
Bioinformatics
; 32(20): 3081-3088, 2016 10 15.
Article
in English
| MEDLINE | ID: mdl-27339714