Detalhe da pesquisa
1.
Large-scale plasma proteomics comparisons through genetics and disease associations.
Nature
; 622(7982): 348-358, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794188
2.
The sequences of 150,119 genomes in the UK Biobank.
Nature
; 607(7920): 732-740, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35859178
3.
Actionable Genotypes and Their Association with Life Span in Iceland.
N Engl J Med
; 389(19): 1741-1752, 2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37937776
4.
Genetic predisposition to mosaic Y chromosome loss in blood.
Nature
; 575(7784): 652-657, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31748747
5.
Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Nature
; 549(7673): 519-522, 2017 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28959963
6.
Selection against variants in the genome associated with educational attainment.
Proc Natl Acad Sci U S A
; 114(5): E727-E732, 2017 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28096410
7.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-28398513
8.
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.
Blood
; 130(6): 742-752, 2017 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28483762
9.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-26740556
10.
Genetics of gene expression and its effect on disease.
Nature
; 452(7186): 423-8, 2008 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-18344981
11.
A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes.
Genome Biol
; 25(1): 69, 2024 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38468278
12.
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.
Nat Genet
; 55(12): 2149-2159, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37932435
13.
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.
Nat Genet
; 55(11): 1843-1853, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37884687
14.
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Nat Commun
; 13(1): 634, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35110524
15.
Differences between germline genomes of monozygotic twins.
Nat Genet
; 53(1): 27-34, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33414551
16.
Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases.
BMJ Open
; 11(12): e049709, 2021 12 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36070241
17.
Large-scale integration of the plasma proteome with genetics and disease.
Nat Genet
; 53(12): 1712-1721, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34857953
18.
Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk.
Cancer Res
; 81(8): 1954-1964, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33602785
19.
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.
Commun Biol
; 3(1): 189, 2020 04 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32327693
20.
Characterizing mutagenic effects of recombination through a sequence-level genetic map.
Science
; 363(6425)2019 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30679340