Detalhe da pesquisa
1.
Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
Genet Epidemiol
; 46(1): 51-62, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34672391
2.
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
Hum Mol Genet
; 30(6): 500-513, 2021 04 30.
Artigo
Inglês
| MEDLINE | ID: mdl-33437986
3.
Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy.
J Med Genet
; 58(8): 556-564, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32732227
4.
Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease.
Bioinformatics
; 36(2): 552-557, 2020 01 15.
Artigo
Inglês
| MEDLINE | ID: mdl-31350884
5.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Nature
; 518(7537): 102-6, 2015 Feb 05.
Artigo
Inglês
| MEDLINE | ID: mdl-25487149
6.
Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.
PLoS Genet
; 13(5): e1006755, 2017 May.
Artigo
Inglês
| MEDLINE | ID: mdl-28459806
7.
Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers.
BMC Bioinformatics
; 20(1): 610, 2019 Nov 27.
Artigo
Inglês
| MEDLINE | ID: mdl-31775616
8.
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
N Engl J Med
; 374(12): 1134-44, 2016 03 24.
Artigo
Inglês
| MEDLINE | ID: mdl-26934567
9.
Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield.
Genet Med
; 21(7): 1576-1584, 2019 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30531895
10.
Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.
Circ Res
; 121(1): 81-88, 2017 Jun 23.
Artigo
Inglês
| MEDLINE | ID: mdl-28506971
11.
Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants.
Arterioscler Thromb Vasc Biol
; 38(11): 2718-2730, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30354237
12.
Genetically determined height and coronary artery disease.
N Engl J Med
; 372(17): 1608-18, 2015 Apr 23.
Artigo
Inglês
| MEDLINE | ID: mdl-25853659
13.
Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.
PLoS Med
; 14(5): e1002294, 2017 05.
Artigo
Inglês
| MEDLINE | ID: mdl-28486474
14.
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.
Am J Hum Genet
; 94(3): 349-60, 2014 Mar 06.
Artigo
Inglês
| MEDLINE | ID: mdl-24560520
15.
Inactivating mutations in NPC1L1 and protection from coronary heart disease.
N Engl J Med
; 371(22): 2072-82, 2014 Nov 27.
Artigo
Inglês
| MEDLINE | ID: mdl-25390462
16.
Loss-of-function mutations in APOC3, triglycerides, and coronary disease.
N Engl J Med
; 371(1): 22-31, 2014 Jul 03.
Artigo
Inglês
| MEDLINE | ID: mdl-24941081
17.
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Genet Med
; 19(2): 192-203, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27532257
18.
Distribution and medical impact of loss-of-function variants in the Finnish founder population.
PLoS Genet
; 10(7): e1004494, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25078778
19.
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.
JAMA
; 317(9): 937-946, 2017 03 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28267856
20.
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Hum Mol Genet
; 22(8): 1663-78, 2013 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23303523