Detalhe da pesquisa
1.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature
; 627(8003): 347-357, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374256
2.
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.
Hum Mol Genet
; 31(19): 3377-3391, 2022 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35220425
3.
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies.
Kidney Int
; 102(3): 624-639, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35716955
4.
Fine-scale population structure in the UK Biobank: implications for genome-wide association studies.
Hum Mol Genet
; 29(16): 2803-2811, 2020 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32691046
5.
Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction.
PLoS Genet
; 10(5): e1004314, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24786987
6.
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
medRxiv
; 2023 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37034649
7.
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
; 13(1): 5144, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36050321
8.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Nat Genet
; 54(5): 560-572, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35551307
9.
The genomics of heart failure: design and rationale of the HERMES consortium.
ESC Heart Fail
; 8(6): 5531-5541, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34480422
10.
Education Level Predicts Appropriate Follow-Up of Incidental Findings From Lung Cancer Screening.
J Am Coll Radiol
; 17(5): 613-619, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31930985
11.
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Nat Commun
; 11(1): 2542, 2020 05 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32439900
12.
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nat Commun
; 11(1): 163, 2020 01 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31919418
13.
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
; 51(6): 1067, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31110354
14.
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Nat Commun
; 10(1): 4130, 2019 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31511532
15.
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
Nat Genet
; 51(1): 51-62, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30578418
16.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
; 51(3): 481-493, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30804560
17.
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Nat Genet
; 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641645
18.
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.
Nat Commun
; 10(1): 29, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30604766
19.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Nat Genet
; 50(4): 559-571, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29632382
20.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Nat Genet
; 50(11): 1505-1513, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30297969