Detalhe da pesquisa
1.
The power of genetic diversity in genome-wide association studies of lipids.
Nature
; 600(7890): 675-679, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34887591
2.
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Nature
; 586(7831): 749-756, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087929
3.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Am J Hum Genet
; 109(8): 1366-1387, 2022 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35931049
4.
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Am J Hum Genet
; 108(9): 1578-1589, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34265237
5.
Author Correction: The power of genetic diversity in genome-wide association studies of lipids.
Nature
; 618(7965): E19-E20, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37237109
6.
ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.
PLoS Genet
; 17(4): e1009501, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33909604
7.
Genetic, sociodemographic, lifestyle, and clinical risk factors of recurrent coronary artery disease events: a population-based cohort study.
Eur Heart J
; 44(36): 3456-3465, 2023 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37350734
8.
Genome-wide association study of cardiac troponin I in the general population.
Hum Mol Genet
; 30(21): 2027-2039, 2021 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33961016
9.
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.
Am J Hum Genet
; 106(3): 389-404, 2020 03 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32109421
10.
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland.
Am J Hum Genet
; 104(6): 1169-1181, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31155286
11.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Am J Hum Genet
; 102(1): 103-115, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29290336
12.
Translating genetic association of lipid levels for biological and clinical application.
Cardiovasc Drugs Ther
; 35(3): 617-626, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33604704
13.
Electronic health records: the next wave of complex disease genetics.
Hum Mol Genet
; 27(R1): R14-R21, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29547983
14.
Mitochondrial genome-wide association study of migraine - the HUNT Study.
Cephalalgia
; 40(6): 625-634, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32056457
15.
Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.
Addict Biol
; 24(3): 549-561, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29532581
16.
The Contribution of GWAS Loci in Familial Dyslipidemias.
PLoS Genet
; 12(5): e1006078, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27227539
17.
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.
PLoS Genet
; 11(7): e1005230, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26132169
18.
Integrative pathway genomics of lung function and airflow obstruction.
Hum Mol Genet
; 24(23): 6836-48, 2015 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26395457
19.
The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients.
Acta Derm Venereol
; 97(4): 456-463, 2017 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27840886
20.
Meta-analysis of 49â 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.
J Med Genet
; 53(7): 441-9, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27036123