Found: 31
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
- Published in:
- Nature Genetics, 2009, v. 41, n. 3, p. 334, doi. 10.1038/ng.327
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- Article
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.
- Published in:
- Nature Genetics, 2000, v. 24, n. 2, p. 120, doi. 10.1038/72769
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- Article
Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology.
- Published in:
- Scientific Reports, 2016, p. 30744, doi. 10.1038/srep30744
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- Article
Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study.
- Published in:
- Scientific Reports, 2016, p. 18672, doi. 10.1038/srep18672
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- Publication type:
- Article
Genetic Variants and Early Cigarette Smoking and Nicotine Dependence Phenotypes in Adolescents.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115716
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- Article
Correction of Population Stratification in Large Multi-Ethnic Association Studies.
- Published in:
- PLoS ONE, 2008, v. 3, n. 1, p. 1, doi. 10.1371/journal.pone.0001382
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- Article
Hypertension, brain imaging phenotypes, and cognitive impairment: lessons from Mendelian randomization.
- Published in:
- European Heart Journal, 2023, v. 44, n. 23, p. 2126, doi. 10.1093/eurheartj/ehad187
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- Article
Sortilin enhances fibrosis and calcification in aortic valve disease by inducing interstitial cell heterogeneity.
- Published in:
- European Heart Journal, 2023, v. 44, n. 10, p. 885, doi. 10.1093/eurheartj/ehac818
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- Publication type:
- Article
Periodontitis and hypertension: causally linked by immune mechanisms.
- Published in:
- European Heart Journal, 2019, v. 40, n. 42, p. 3471, doi. 10.1093/eurheartj/ehz729
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- Publication type:
- Article
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans.
- Published in:
- Human Genetics, 2009, v. 125, n. 3, p. 305, doi. 10.1007/s00439-009-0626-9
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- Article
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 342, doi. 10.1038/ejhg.2009.157
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- Publication type:
- Article
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 1, p. 105, doi. 10.1038/sj.ejhg.5201920
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- Article
Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease.
- Published in:
- JAMA: Journal of the American Medical Association, 2009, v. 302, n. 1, p. 37, doi. 10.1001/jama.2009.954
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- Publication type:
- Article
Interplay of Atherogenic Particle Number and Particle Size and the Risk of Coronary Heart Disease.
- Published in:
- Clinical Chemistry, 2023, v. 69, n. 1, p. 48, doi. 10.1093/clinchem/hvac172
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- Publication type:
- Article
The Genetics of Dilated Cardiomyopathy: A Prioritized Candidate Gene Study of LMNA, TNNT2, TCAP, and PLN.
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- Clinical Cardiology, 2013, v. 36, n. 10, p. 628, doi. 10.1002/clc.22193
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- Publication type:
- Article
Risks of Incident Cardiovascular Disease Associated With Concomitant Elevations in Lipoprotein(a) and Low-Density Lipoprotein Cholesterol-The Framingham Heart Study.
- Published in:
- 2020
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- Publication type:
- journal article
Lipoprotein(a) Interactions With Low-Density Lipoprotein Cholesterol and Other Cardiovascular Risk Factors in Premature Acute Coronary Syndrome (ACS).
- Published in:
- 2016
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- Publication type:
- journal article
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 12, p. 3582, doi. 10.1093/hmg/ddv097
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- Publication type:
- Article
Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study.
- Published in:
- Diabetes, 2008, v. 57, n. 4, p. 1147, doi. 10.2337/db07-1267
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- Publication type:
- Article
Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French-Canadian Population.
- Published in:
- Diabetes, 2006, v. 55, n. 10, p. 2896, doi. 10.2337/db06-0189
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- Publication type:
- Article
5' flanking variants of resistin are associated with obesity.
- Published in:
- 2002
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- Publication type:
- journal article
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design?
- Published in:
- PLoS Genetics, 2009, v. 5, n. 10, p. 1, doi. 10.1371/journal.pgen.1000694
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- Publication type:
- Article
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population.
- Published in:
- Human Mutation, 2008, v. 29, n. 5, p. 689, doi. 10.1002/humu.20702
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- Publication type:
- Article
Cohort Profile: The Nicotine Dependence in Teens (NDIT) Study.
- Published in:
- 2015
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- Publication type:
- journal article
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
- Published in:
- JAMA: Journal of the American Medical Association, 2014, v. 312, n. 17, p. 1764, doi. 10.1001/jama.2014.13959
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- Publication type:
- Article
Missing single nucleotide polymorphisms in Genetic Risk Scores: A simulation study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200630
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- Publication type:
- Article
Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population.
- Published in:
- Diabetes Care, 2013, v. 36, n. 9, p. 2836, doi. 10.2337/dc12-2553
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- Publication type:
- Article
Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study.
- Published in:
- 2013
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- Publication type:
- journal article
Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study.
- Published in:
- Diabetes Care, 2010, v. 33, n. 10, p. 2250, doi. 10.2337/dc10-0452
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- Publication type:
- Article
The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study.
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- PLoS Medicine, 2011, v. 8, n. 10, p. 1, doi. 10.1371/journal.pmed.1001106
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- Publication type:
- Article
Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants donot contribute to low levels of high-density lipoprotein cholesterol.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 79, doi. 10.1186/1471-2350-8-79
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- Publication type:
- Article