Josée Dupuis Canadian biostatistician
Dupuis, Josée
VIAF ID: 105927310 (Personal)
Permalink: http://viaf.org/viaf/105927310
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Dupuis, Josée
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Dupuis, Josée
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Josée Dupuis
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Canadian biostatistician
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Works
| Title | Sources |
|---|---|
| Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function |
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| Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels |
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| Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation |
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| Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility |
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| A low-frequency variant in MAPK14 provides mechanistic evidence of a link with myeloperoxidase: a prognostic cardiovascular risk marker |
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| Mapping complex traits using Random Forests |
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| Mapping quantitative traits in unselected families: algorithms and examples |
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| Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes |
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| Meta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohorts |
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| Meta-analysis of exome array data identifies six novel genetic loci for lung function |
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| Meta-analysis of gene-environment interaction: joint estimation of SNP and SNP × environment regression coefficients |
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| Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels |
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| Metabolic factors and genetic risk mediate familial type 2 diabetes risk in the Framingham Heart Study |
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| A method of moments estimator for random effect multivariate meta-analysis |
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| MicroRNA Signature of Cigarette Smoking and Evidence for a Putative Causal Role of MicroRNAs in Smoking-Related Inflammation and Target Organ Damage. |
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| Molecular Characterization of the NLRC4 Expression in Relation to Interleukin-18 Levels |
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| Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function |
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| Multipoint linkage analysis of the pseudoautosomal regions, using affected sibling pairs |
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| A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait |
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| Network-guided sparse regression modeling for detection of gene-by-gene interactions |
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| No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels |
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| Normal thymus in adults: appearance on CT and associations with age, sex, BMI and smoking |
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| La nouvelle vie de Kili, 2015: |
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| Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals |
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| Novel mutations in the gene encoding ATP-binding cassette 1 in four tangier disease kindreds |
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| NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium |
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| Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association |
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| Ordered stratification to reduce heterogeneity in linkage to diabetes-related quantitative traits |
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| Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis |
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| PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sample |
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| Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities |
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| Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults |
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| Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21 |
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| Performance of statistical methods on CHARGE targeted sequencing data |
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| Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations |
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| Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. |
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| Pleiotropic genes for metabolic syndrome and inflammation |
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| Pleural abnormalities in the Framingham Heart Study: prevalence and CT image features. |
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| Polygenic type 2 diabetes prediction at the limit of common variant detection |
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| Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans |
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| Poor performance of bootstrap confidence intervals for the location of a quantitative trait locus |
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| ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls |
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| Proximal hip geometry is linked to several chromosomal regions: genome-wide linkage results from the Framingham Osteoporosis Study |
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| Pulmonary cysts identified on chest CT: are they part of aging change or of clinical significance? |
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| Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis |
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| Racial/ethnic differences in association of fasting glucose-associated genomic loci with fasting glucose, HOMA-B, and impaired fasting glucose in the U.S. adult population |
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| Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease |
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| Rare genetic variant analysis on blood pressure in related samples |
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| Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project |
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| Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe |
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| Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes |
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| The relation of genetic and environmental factors to systemic inflammatory biomarker concentrations |
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| Revisiting heritability accounting for shared environmental effects and maternal inheritance |
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| Robust analysis of secondary phenotypes in case-control genetic association studies |
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| Selection of the most informative individuals from families with multiple siblings for association studies |
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| Sequence data and association statistics from 12,940 type 2 diabetes cases and controls |
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| Sequence kernel association test for survival traits. |
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| Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women. |
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| Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke |
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| Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose |
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| Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study |
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| Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases |
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| Structured mating: Patterns and implications |
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| Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis |
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| A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease |
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| TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study |
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| Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis |
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| Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations. |
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| Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin |
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| Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms |
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| Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource |
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| The type 2 deiodinase (DIO2) A/G polymorphism is not associated with glycemic traits: the Framingham Heart Study |
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| Type 2 Diabetes Genetic Predisposition, Obesity, and All-Cause Mortality Risk in the U.S.: A Multiethnic Analysis |
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| A unified framework for linkage and association analysis of quantitative traits |
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| United States Research Published in Major Surgical Journals Is Decreasing |
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| Using linkage analysis of large pedigrees to guide association analyses |
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| Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4 |
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| Variants at the endocannabinoid receptor CB1 gene (CNR1) and insulin sensitivity, type 2 diabetes, and coronary heart disease |
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| Variants in MTNR1B influence fasting glucose levels |
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| Variants in the CNR1 and the FAAH genes and adiposity traits in the community |
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| Whole blood gene expression and interleukin-6 levels |
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| Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation |
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| Whole genome sequence analyses of brain imaging measures in the Framingham Study |
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| Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants |
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