Detalles de la búsqueda
1.
Type 2 diabetes risks and determinants in second-generation migrants and mixed ethnicity people of South Asian and African Caribbean descent in the UK.
Diabetologia
; 65(1): 113-127, 2022 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34668055
2.
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference.
Nat Genet
; 56(2): 222-233, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38177345
3.
Genome-wide association studies and cross-population meta-analyses investigating short and long sleep duration.
Nat Commun
; 14(1): 6059, 2023 09 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37770476
4.
Genetics of myasthenia gravis: a case-control association study in the Hellenic population.
Clin Dev Immunol
; 2012: 484919, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23049601
5.
Genetic risk scores and dementia risk across different ethnic groups in UK Biobank.
PLoS One
; 17(12): e0277378, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36477264
6.
Adolescent Verbal Memory as a Psychosis Endophenotype: A Genome-Wide Association Study in an Ancestrally Diverse Sample.
Genes (Basel)
; 13(1)2022 01 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-35052446
7.
Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations.
Sci Rep
; 12(1): 1131, 2022 01 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-35064169
8.
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
Nat Genet
; 54(12): 1803-1815, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36474045
9.
The Influence of CYP2D6 and CYP2C19 Genetic Variation on Diabetes Mellitus Risk in People Taking Antidepressants and Antipsychotics.
Genes (Basel)
; 12(11)2021 11 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34828364
10.
Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers.
J Natl Cancer Inst
; 113(7): 893-899, 2021 07 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33372680
11.
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study.
JAMA Psychiatry
; 78(11): 1258-1269, 2021 11 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-34586374
12.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
; 52(12): 1314-1332, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33230300
13.
Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases.
J Am Coll Cardiol
; 73(23): 2932-2942, 2019 06 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-31196449
14.
Genetic data do not provide evidence that lower sclerostin is associated with increased risk of atherosclerosis: comment on the article by Zheng et al.
Arthritis Rheumatol
; 2023 Nov 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37942677
15.
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Nat Genet
; 49(9): 1385-1391, 2017 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-28714975
16.
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Nat Genet
; 53(5): 762, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-33727701
17.
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
Nat Genet
; 48(10): 1151-1161, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27618447
18.
Genomic variation in the MAP3K5 gene is associated with ß-thalassemia disease severity and hydroxyurea treatment efficacy.
Pharmacogenomics
; 14(5): 469-83, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23556445
19.
Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase.
Pharmacogenomics
; 12(1): 49-58, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-21174622
Resultados
1 -
19
de 19
1
Próxima >
>>