Josée Dupuis | Academic Influence

Josée Dupuis's AcademicInfluence.com Rankings

Josée Dupuis

Mathematics

#7134

World Rank

#9760

Historical Rank

Statistics

#790

World Rank

#878

Historical Rank

mathematics Degrees

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Mathematics

Josée Dupuis's Degrees

Masters Statistics University of British Columbia
Bachelors Mathematics McGill University

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Why Is Josée Dupuis Influential?

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According to Wikipedia, Josée Dupuis is a Canadian biostatistician. She is a professor in the Boston University School of Public Health, where she chairs the department of biostatistics. Her research interests include genome-wide association studies, gene–environment interaction, and applications to diabetes and cardiovascular disease.

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Josée Dupuis's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Common variants at 30 loci contribute to polygenic dyslipidemia (2009) (1380)
Common genetic determinants of vitamin D insufficiency: a genome-wide association study (2010) (1177)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (1028)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
The genetic architecture of type 2 diabetes (2016) (927)
Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts (2013) (892)
Genotype score in addition to common risk factors for prediction of type 2 diabetes. (2008) (761)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (2017) (693)
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge (2010) (648)
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels (2011) (476)
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals (2012) (459)
Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways (2010) (425)
A structural variation reference for medical and population genetics (2020) (394)
Identifying SNPs predictive of phenotype using random forests (2005) (384)
Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
Statistical methods for mapping quantitative trait loci from a dense set of markers. (1999) (320)
Association of vitamin D status with arterial blood pressure and hypertension risk: a mendelian randomisation study (2014) (318)
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis (2017) (308)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity (2014) (287)
NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium (2009) (281)
Association Between Interstitial Lung Abnormalities and All-Cause Mortality. (2016) (275)
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis (2017) (275)
MUC5B promoter polymorphism and interstitial lung abnormalities. (2013) (265)
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases (2012) (263)
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans (2010) (262)
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. (2010) (256)
Atrial Fibrillation: Current Knowledge and Future Directions in Epidemiology and Genomics (2011) (250)
Genome-wide association with bone mass and geometry in the Framingham Heart Study (2007) (249)
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels (2018) (246)
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports (2007) (227)
Genetic and non-genetic correlates of vitamins K and D (2009) (225)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. (2008) (219)
DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (215)
Sequence Kernel Association Test for Quantitative Traits in Family Samples (2013) (210)
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. (2010) (208)
Genome-Wide Association Scan Identifies Candidate Polymorphisms Associated with Differential Response to Anti-TNF Treatment in Rheumatoid Arthritis (2008) (204)
Poor Performance of Bootstrap Confidence Intervals for the Location of a Quantitative Trait Locus (2006) (203)
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (197)
Development and Progression of Interstitial Lung Abnormalities in the Framingham Heart Study. (2016) (187)
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. (2012) (187)
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility (2015) (185)
Genetic Risk Reclassification for Type 2 Diabetes by Age Below or Above 50 Years Using 40 Type 2 Diabetes Risk Single Nucleotide Polymorphisms (2010) (171)
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2018) (171)
A Method of Moments Estimator for Random Effect Multivariate Meta‐Analysis (2012) (168)
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. (2010) (168)
Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function (2012) (167)
A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels (2009) (164)
Common Variants in the Adiponectin Gene (ADIPOQ) Associated With Plasma Adiponectin Levels, Type 2 Diabetes, and Diabetes-Related Quantitative Traits (2008) (163)
Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project (2007) (161)
Meta‐analysis of gene‐environment interaction: joint estimation of SNP and SNP × environment regression coefficients (2011) (159)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (153)
Relations of Inflammatory Biomarkers and Common Genetic Variants With Arterial Stiffness and Wave Reflection (2008) (153)
The Trans-Ancestral Genomic Architecture of Glycemic Traits (2020) (151)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Genome-wide association analysis identifies six new loci associated with forced vital capacity (2014) (141)
Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies (2017) (133)
Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection (2014) (126)
Duffy antigen receptor for chemokines (Darc) polymorphism regulates circulating concentrations of monocyte chemoattractant protein-1 and other inflammatory mediators. (2010) (122)
Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
Pleiotropic genes for metabolic syndrome and inflammation. (2014) (118)
Genome-wide association with select biomarker traits in the Framingham Heart Study (2007) (114)
Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 Diabetes (2013) (113)
Genetic variation at the low-density lipoprotein receptor-related protein 5 (LRP5) locus modulates Wnt signaling and the relationship of physical activity with bone mineral density in men. (2007) (112)
A Screening Instrument for Chronic Fatigue Syndrome: Reliability and Validity (1997) (109)
Genome scan of systemic biomarkers of vascular inflammation in the Framingham Heart Study: evidence for susceptibility loci on 1q. (2005) (105)
Genome-wide association with diabetes-related traits in the Framingham Heart Study (2007) (103)
Association of Variants in RETN With Plasma Resistin Levels and Diabetes-Related Traits in the Framingham Offspring Study (2009) (101)
A 100K Genome-Wide Association Scan for Diabetes and Related Traits in the Framingham Heart Study (2007) (100)
Total Zinc Intake May Modify the Glucose-Raising Effect of a Zinc Transporter (SLC30A8) Variant (2011) (100)
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies. (2012) (99)
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus (2015) (98)
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease (2016) (92)
Transcript expression-aware annotation improves rare variant interpretation (2020) (89)
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. (2014) (88)
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation (2020) (88)
Genome-Wide Association Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci (2011) (87)
Evaluating drug targets through human loss-of-function genetic variation (2019) (86)
Metabolomics insights into early type 2 diabetes pathogenesis and detection in individuals with normal fasting glucose (2018) (84)
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. (2013) (83)
TCF7L2 variants are associated with increased proinsulin/insulin ratios but not obesity traits in the Framingham Heart Study (2009) (82)
Statistical methods for linkage analysis of complex traits from high-resolution maps of identity by descent. (1995) (80)
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) (78)
Association of Variation at the ABO Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin: A Meta-Analysis (2011) (72)
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (71)
Mapping complex traits using Random Forests (2003) (71)
The effect of LRRK2 loss-of-function variants in humans (2020) (69)
Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
Transferability and Fine Mapping of Type 2 Diabetes Loci in African Americans (2013) (63)
Epigenome-Wide Association Study of Incident Type 2 Diabetes in a British Population: EPIC-Norfolk Study (2019) (63)
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci (2016) (63)
Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. (2019) (61)
Heritability of Atrial Fibrillation (2017) (60)
The Relation of Genetic and Environmental Factors to Systemic Inflammatory Biomarker Concentrations (2009) (60)
Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function (2014) (59)
Sequence Kernel Association Test for Survival Traits (2014) (59)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Proximal hip geometry is linked to several chromosomal regions: genome-wide linkage results from the Framingham Osteoporosis Study. (2007) (57)
Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (55)
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin. (2016) (54)
Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD (2012) (54)
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
Galectin-3 Is Associated with Restrictive Lung Disease and Interstitial Lung Abnormalities. (2016) (54)
Peptidoglycan recognition proteins Pglyrp3 and Pglyrp4 are encoded from the epidermal differentiation complex and are candidate genes for the Psors4 locus on chromosome 1q21 (2006) (53)
Normal thymus in adults: appearance on CT and associations with age, sex, BMI and smoking (2015) (51)
The insulin gene variable number tandem repeat and risk of type 2 diabetes in a population-based sample of families and unrelated men and women. (2005) (50)
An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis (2019) (49)
Anterior mediastinal masses in the Framingham Heart Study: Prevalence and CT image characteristics (2015) (47)
Paraseptal emphysema: Prevalence and distribution on CT and association with interstitial lung abnormalities. (2015) (47)
Haplotype Structure of the ENPP1 Gene and Nominal Association of the K121Q Missense Single Nucleotide Polymorphism With Glycemic Traits in the Framingham Heart Study (2008) (46)
Genetic variants at 2 q 24 are associated with susceptibility to type 2 diabetes (2010) (46)
Genetically Driven Hyperglycemia Increases Risk of Coronary Artery Disease Separately From Type 2 Diabetes (2017) (45)
The type 2 deiodinase (DIO2) A/G polymorphism is not associated with glycemic traits: the Framingham Heart Study. (2007) (43)
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
Pulmonary cysts identified on chest CT: are they part of aging change or of clinical significance? (2015) (42)
Genome-Wide Association Study Evaluating Lipoprotein-Associated Phospholipase A2 Mass and Activity at Baseline and After Rosuvastatin Therapy (2012) (42)
Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies (2021) (41)
MUC5B Promoter Polymorphism and Interstitial Lung Abnormalities (2013) (41)
Association of exome sequences with plasma C-reactive protein levels in >9000 participants. (2015) (40)
MicroRNA Signature of Cigarette Smoking and Evidence for a Putative Causal Role of MicroRNAs in Smoking-Related Inflammation and Target Organ Damage (2017) (40)
Correction for multiple testing in a gene region (2013) (39)
Evidence for large-scale gene-by-smoking interaction effects on pulmonary function (2017) (38)
Clinical and genetic factors associated with lipoprotein-associated phospholipase A2 in the Framingham Heart Study. (2009) (38)
A comparison of visual and quantitative methods to identify interstitial lung abnormalities (2015) (36)
Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke (2016) (35)
Incorporating Gene-Environment Interaction in Testing for Association with Rare Genetic Variants (2014) (34)
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans (2014) (34)
Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III) (2012) (34)
Type 2 Diabetes Genetic Predisposition, Obesity, and All-Cause Mortality Risk in the U.S.: A Multiethnic Analysis (2016) (32)
Common genetic determinants of vitamin D insufficiency (2011) (32)
Clinical and genetic correlates of soluble P‐selectin in the community (2007) (31)
Meta-analysis of exome array data identifies six novel genetic loci for lung function (2017) (31)
Application of linear mixed-effect models for the analysis of exam scores: Online video associated with higher scores for undergraduate students with lower grades (2013) (30)
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations (2018) (30)
Variants in the CNR1 and the FAAH Genes and Adiposity Traits in the Community (2009) (30)
Bivariate Linkage Study of Proximal Hip Geometry and Body Size Indices: The Framingham Study (2007) (30)
Sex‐Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women (2017) (30)
No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels (2012) (29)
Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis (2019) (29)
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 (2018) (29)
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes (2020) (29)
Integrative Omics Approach to Identifying Genes Associated With Atrial Fibrillation (2019) (28)
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. (2013) (28)
Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits (2012) (28)
Integrative pathway genomics of lung function and airflow obstruction. (2015) (28)
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees (2017) (27)
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. (2019) (27)
Beverage Consumption and Longitudinal Changes in Lipoprotein Concentrations and Incident Dyslipidemia in US Adults: The Framingham Heart Study (2020) (26)
Whole genome sequence analyses of brain imaging measures in the Framingham Study (2018) (26)
Mendelian Randomization Analysis of Hemoglobin A1c as a Risk Factor for Coronary Artery Disease (2019) (26)
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer’s Disease Sequencing Project (2018) (25)
Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource (2012) (24)
Identification of Novel Type 2 Diabetes Candidate Genes Involved in the Crosstalk between the Mitochondrial and the Insulin Signaling Systems (2012) (24)
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 (2010) (24)
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose (2020) (24)
PAI‐1 Gene 4G/5G Polymorphism and Risk of Type 2 Diabetes in a Population‐based Sample (2006) (24)
Genome-wide association study of subclinical interstitial lung disease in MESA (2017) (23)
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms (2016) (23)
The Association of Aging Biomarkers, Interstitial Lung Abnormalities, and Mortality. (2020) (23)
Incident Type 2 Diabetes Risk is Influenced by Obesity and Diabetes in Social Contacts: a Social Network Analysis (2016) (23)
Association of Circulating Monocyte Chemoattractant Protein-1 Levels With Cardiovascular Mortality: A Meta-analysis of Population-Based Studies. (2020) (23)
Interpreting results of large-scale genetic association studies: separating gold from fool's gold. (2007) (23)
Whole Blood Gene Expression and Atrial Fibrillation: The Framingham Heart Study (2014) (23)
Structured mating: Patterns and implications (2017) (22)
Whole blood gene expression and interleukin-6 levels. (2014) (22)
ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls (2018) (22)
Molecular Characterization of the NLRC4 Expression in Relation to Interleukin-18 Levels (2015) (21)
Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe. (2010) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Strategies to Design and Analyze Targeted Sequencing Data: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study (2014) (20)
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease (2018) (20)
Comparison of methods for multivariate gene-based association tests for complex diseases using common variants (2019) (19)
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants (2020) (19)
Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults (2015) (18)
Variants at the Endocannabinoid Receptor CB1 Gene (CNR1) and Insulin Sensitivity, Type 2 Diabetes, and Coronary Heart Disease (2011) (18)
Evaluation of logistic regression models and effect of covariates for case–control study in RNA-Seq analysis (2017) (18)
Association of 25-Hydroxyvitamin D status and genetic variation in the vitamin D metabolic pathway with FEV1 in the Framingham Heart Study (2015) (18)
Gene expression markers of age-related inflammation in two human cohorts (2015) (17)
Peripheral Blood Transcriptomic Signatures of Fasting Glucose and Insulin Concentrations (2016) (17)
Revisiting heritability accounting for shared environmental effects and maternal inheritance (2015) (17)
Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans. (2008) (17)
Exo-proofreading, a versatile SNP scoring technology. (2003) (17)
Identification and Functional Characterization of G 6 PC 2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G 6 PC 2-ABCB 11 Locus (2015) (16)
Causal Relationship between Obesity and Vitamin D Status (2016) (16)
Metabolic factors and genetic risk mediate familial type 2 diabetes risk in the Framingham Heart Study (2015) (16)
Heritability and genome-wide association study of diffusing capacity of the lung (2018) (16)
META-ANALYSIS OF A RARE-VARIANT ASSOCIATION TEST. (2011) (16)
Increased Airway Wall Thickness in Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis (2019) (16)
A unified framework for linkage and association analysis of quantitative traits (2007) (15)
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project. (2019) (15)
Childhood Tobacco Smoke Exposure and Risk of Atrial Fibrillation in Adulthood. (2019) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Handling linkage disequilibrium in qualitative trait linkage analysis using dense SNPs: a two-step strategy (2009) (15)
Expectation Maximization Algorithm Based Haplotype Relative Risk (EM-HRR): Test of Linkage Disequilibrium Using Incomplete Case-Parents Trios (2005) (14)
Comparison of novel and existing methods for detecting differentially methylated regions (2018) (12)
Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study (2015) (12)
Potential Interplay between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome to Modulate Insulin Resistance and Diabetes Risk: Insights from a Meta‐Analysis of 19 005 Individuals (2019) (12)
Comparison of statistical approaches to rare variant analysis for quantitative traits (2011) (12)
Pleural abnormalities in the Framingham Heart Study: prevalence and CT image features (2017) (12)
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels. (2014) (11)
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts (2022) (11)
Association of Levels of Fasting Glucose and Insulin With Rare Variants at the Chromosome 11p11.2-MADD Locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study (2014) (11)
Evaluation of a Two‐Stage Approach in Trans‐Ethnic Meta‐Analysis in Genome‐Wide Association Studies (2016) (11)
Omega‐3 Fatty Acids and Genome‐Wide Interaction Analyses Reveal DPP10‐Pulmonary Function Association (2019) (11)
Clinical correlates, heritability, and genetic linkage of circulating CD40 ligand in the Framingham Offspring Study. (2008) (11)
Robust analysis of secondary phenotypes in case‐control genetic association studies (2016) (11)
Boundary crossing probabilities in linkage analysis (2000) (10)
Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study. (2013) (10)
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits (2021) (9)
Handling linkage disequilibrium in linkage analysis using dense single-nucleotide polymorphisms (2007) (9)
ADAM19 and HTR4 Variants and Pulmonary Function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study (2014) (9)
Using linkage analysis of large pedigrees to guide association analyses (2011) (9)
Associations of Omega-3 Fatty acids with Interstitial Lung Disease and Lung Imaging Abnormalities Among Adults. (2020) (9)
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci (2007) (9)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program (2019) (8)
Multipoint linkage analysis of the pseudoautosomal regions, using affected sibling pairs. (2000) (8)
Genetic associations with metabolic syndrome and its quantitative traits by race/ethnicity in the United States. (2011) (8)
Mapping quantitative traits in unselected families: algorithms and examples (2009) (8)
Epigenome-Wide Association Study of Soluble Tumor Necrosis Factor Receptor 2 Levels in the Framingham Heart Study (2018) (7)
Genetic Associations and Architecture of Asthma-COPD Overlap (2022) (7)
Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function (2018) (7)
Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfiler (2021) (7)
Identification of polymorphisms explaining a linkage signal: application to the GAW14 simulated data (2005) (7)
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project (2016) (7)
On the Detection of Linkage in Multiple Data Sets: A Comparison of Various Statistical Approaches (2001) (7)
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. (2019) (7)
A unified method for rare variant analysis of gene‐environment interactions (2019) (7)
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals (2019) (6)
Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries (2018) (6)
Haplotype Structure of the ENPP 1 Gene and Nominal Association of the K 121 Q Missense Single Nucleotide Polymorphism With Glycemic Traits in the Framingham Heart Study (2008) (6)
Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases (2015) (6)
Genome-Wide Meta-Analysis of Late-Onset Alzheimer's Disease Using Rare Variant Imputation in 324,809 Subjects Identifies Novel Rare Variant Locus NCK2: The International Genomics of Alzheimer's Project (IGAP) (2021) (6)
Rate Of FEV1 Decline In Healthy Adults: Defining The Upper Limit Of Normal In The Framingham Heart Study (2012) (6)
Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies (2017) (6)
Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratification (2021) (6)
A Low‐Frequency Variant in MAPK14 Provides Mechanistic Evidence of a Link With Myeloperoxidase: A Prognostic Cardiovascular Risk Marker (2014) (6)
Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease (2020) (5)
A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease. (2021) (5)
Evaluation of Approaches to Identify Associated SNPs That Explain the Linkage Evidence in Nuclear Families with Affected Siblings (2009) (5)
A Polygenic Risk Score and Age of Diagnosis of Chronic Obstructive Pulmonary Disease. (2022) (5)
Association Testing of the Mitochondrial Genome Using Pedigree Data (2013) (5)
Evaluation of a phenotype imputation approach using GAW20 simulated data (2018) (5)
Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol. (2021) (5)
Convex combination sequence kernel association test for rare‐variant studies (2020) (5)
Association of the IGF1 gene with fasting insulin levels (2016) (5)
A Comparison of Gene Region Simulation Methods (2012) (5)
Joint modeling of linkage and association using affected sib-pair data (2007) (5)
Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program (2020) (5)
Multiethnic meta-analysis identifies new loci for pulmonary function (2017) (5)
Detecting differentially methylated regions with multiple distinct associations. (2021) (5)
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. (2022) (5)
Anisocoria and Poor Pupil Reactivity by Quantitative Pupillometry in Patients With Intracranial Pathology (2021) (4)
Modeling gene-covariate interactions in sparse regression with group structure for genome-wide association studies (2015) (4)
Incorporating biological knowledge in the search for gene × gene interaction in genome-wide association studies (2009) (4)
A unified method for rare variant analysis of gene-environment interactions (2019) (4)
The importance of watching our weights: How the choice of weights for non‐independent sib pairs can dramatically alter results (1999) (4)
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation (2017) (4)
Evaluation of methods accounting for population structure with pedigree data and continuous outcomes (2011) (4)
Rare genetic variant analysis on blood pressure in related samples (2014) (4)
Network-guided sparse regression modeling for detection of gene-by-gene interactions (2013) (4)
Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis (2022) (4)
Ordered Stratification to Reduce Heterogeneity in Linkage to Diabetes‐related Quantitative Traits (2008) (4)
Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants. (2023) (4)
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
Approximate conditional phenotype analysis based on genome wide association summary statistics (2021) (3)
Joint association analysis of a binary and a quantitative trait in family samples (2016) (3)
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program (2021) (3)
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (3)
Epigenome-wide association study on diffusing capacity of the lung (2020) (3)
Multi-trait genome-wide association meta-analysis of dietary intake identifies new loci and genetic and functional links with metabolic traits (2019) (3)
Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic (2009) (3)
Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels (2018) (3)
Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations (2021) (3)
Interstitial lung abnormalities are associated with decreased mean telomere length (2022) (3)
Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions (2020) (3)
Abstract 18708: Novel DNA Methylation Loci Associated With Circulating Tumor Necrosis Factor-alpha, a Marker of Systemic Inflammation (2016) (3)
Beverage Consumption and Longitudinal Changes in Lipid Concentrations and Incident Dyslipidemia in U.S. Adults: The Framingham Heart Study (P18-017-19). (2019) (2)
Novel DNA methylation sites of glucose and insulin homeostasis: an integrative cross-omics analysis (2018) (2)
Adipocyte hyperplasia: the primary mechanism of supraspinatus intramuscular fat accumulation after a complete rotator cuff tendon tear: a study in the rabbit (2019) (2)
Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlap (2020) (2)
Evaluation of population stratification adjustment using genome‐wide or exonic variants (2020) (2)
Mapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis (2021) (2)
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2019) (2)
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits (2021) (2)
Sugar-sweetened Beverage Consumption May Modify Associations between Genetic Variants in the CHREBP Locus and HDL-C and TG Concentrations. (2021) (2)
Dexmedetomidine and Other Analgosedatives Alter Pupil Characteristics in Critically Ill Patients (2022) (2)
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (2023) (2)
Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airﬂow Obstruction (2012) (2)
Minutes of the 44th Genral Assembly of the European Association for the Study of Diabetes (2009) (2)
Large Meta-Analysis Provides Evidence for an Association of Serum Vitamin D with Pulmonary Function (2017) (2)
Clinical Correlates and Heritability of Vitamins K and D (2007) (2)
An Integrative Genomic Strategy Identifies sRAGE as a Causal and Protective Biomarker of Lung Function. (2021) (2)
Abstract MP58: Type 2 Diabetes Prediction with 17-, 40-, and 62-variant Genotype Risk Scores: The Framingham Offspring Study (2013) (1)
Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function (2021) (1)
Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer’s Disease Sequencing Project (2018) (1)
Effect of linkage disequilibrium between markers in linkage and association analyses (2007) (1)
Association of Levels of Fasting Glucose and Insulin with Rare Variants at the Chromosome 11 p 11 . 2-MADD Locus : the Cohorts for Heart and Aging Research in Genomic Epidemiology ( CHARGE ) Targeted Sequencing Study (2014) (1)
Impact of Type 2 Diabetes Susceptibility Loci on Variation in Physiologic Glycaemic Traits in Non-Diabetic Individuals (2012) (1)
Novel Genetic Loci Implicated in Fasting Glucose Homeostasis and Their Impact on Related Metabolic Traits (2009) (1)
Genetic association tests in family samples for multi-category phenotypes (2021) (1)
Transcript expression-aware annotation improves rare variant interpretation (2020) (1)
GENOME-WIDE META-ANALYSIS OF LATE-ONSET ALZHEIMER’S DISEASE USING RARE VARIANT IMPUTATION IN 64,859 SUBJECTS IDENTIFIES RISK LOCI WITH ROLES IN INNATE IMMUNITY AND CARDIOVASCULAR TRAITS: THE INTERNATIONAL GENOMICS OF ALZHEIMER’S PROJECT (IGAP) (2019) (1)
Statistical Aspect of Trait Mapping Using a Dense Set of Markers: A Partial Review (1996) (1)
ADAM19 and HTR4 Variants and Pulmonary Function: The Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study (2014) (1)
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function (2018) (1)
University of Groningen Genome-wide association studies identify CHRNA 5 / 3 and HTR 4 in the development of airflow obstruction (2017) (1)
Erratum. Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection. Diabetes 2014;63:2172–2182 (2018) (1)
Selection of the most informative individuals from families with multiple siblings for association studies (2009) (1)
The Proteomic Profile Associated with Lung Function and COPD in the Jackson Heart Study (2020) (1)
Sugar-sweetened Beverage Consumption and Plasma Lipoprotein Cholesterol, Apolipoprotein, and Lipoprotein Particle Size Concentrations in U.S. Adults. (2022) (1)
Positive Associations of Dietary Marine Omega-3 Polyunsaturated Fatty Acids with Lung Function: A Meta-analysis (P18-087-19). (2019) (1)
Leveraging family history in genetic association analyses of binary traits (2022) (1)
Comparison of multiple single-nucleotide variant association tests in a meta-analysis of Genetic Analysis Workshop 19 family and unrelated data (2016) (1)
A genome-wide association study of asthma-COPD overlap syndrome (ACOS) (2020) (1)
Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study. (2022) (1)
Genome-wide gene–environment interactions on quantitative traits using family data (2015) (1)
Comparisons of case-selection approaches based on allele sharing and/or disease severity index: application to the GAW14 simulated data (2005) (1)
Performance of statistical methods on CHARGE targeted sequencing data (2014) (1)
Exploiting Family History in Aggregation Unit-based Genetic Association Tests (2021) (1)
Genome‐wide meta‐analysis of late‐onset Alzheimer’s disease using rare variant imputation in 65,602 subjects identifies risk loci with roles in memory, neurodevelopment, and cardiometabolic traits: The international genomics of Alzheimer’s project (IGAP) (2020) (1)
Rare Variant Association Analysis: Beyond Collapsing Approaches (2015) (1)
RARE DELETERIOUS AND LOSS-OF-FUNCTION VARIANTS IN OPRL1 AND GAS2L2 CONTRIBUTE TO THE RISK OF LATE-ONSET ALZHEIMER’S DISEASE: ALZHEIMER’S DISEASE SEQUENCING PROJECT CASE-CONTROL STUDY (2016) (1)
The relationship between interstitial lung abnormalities, mortality, and multimorbidity: a cohort study (2022) (1)
A Large Genome-wide Association Study of Glycated Hemoglobin Identifies Ten Common Variants not Mediated Through BMI (2009) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
Meta-Analysis for Penalized Regression Methods with Multi-Cohort Genome-Wide Association Studies (2016) (1)
Search for novel type 2 diabetes susceptibility loci using genome-wide association studies imputed from a 1000 Genomes references panel (2012) (1)
Abstract 016: Artificially Sweetened Beverage Consumption, Plasma Metabolomics, And Risk Of Type 2 Diabetes Among US Adults (2022) (1)
Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2021) (1)
Comparative trans‐ethnic meta‐analysis of whole exome sequencing variation for Alzheimer’s disease (AD) in 18,402 individuals of the Alzheimer’s Disease Sequencing Project (ADSP) (2020) (1)
Genome-wide meta-analysis identifies novel genetic loci associated with OGTT-induced post-challenge glucose (2009) (1)
Meta-Analyses of Genome-Wide Association Studies for 2-Hour Glucose Levels during an Oral Glucose Tolerance Test Identify Novel Genetic Loci (2009) (0)
Abstract P100: Heritability of Atrial Fibrillation (2017) (0)
Lack of interaction of beta-cell-function-associated variants with hypertension on change in fasting glucose and diabetes risk: the Framingham Offspring Study (2013) (0)
Genome-wide association study imputed to 1000 Genomes Project reference panels reveals 17 novel associations with type 2 diabetes (2015) (0)
Whole Genome Sequence Analysis of Pulmonary Function and COPD for 44,403 Multi-Ethnic Participants from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program (2022) (0)
1655-P: Genetic Risk Factors for Incident Cardiovascular Disease in Type 2 Diabetes Patients (2020) (0)
IDENTIFICATION OF WHOLE EXOME SEQUENCING VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE IN THE COHORTS FOR HEART AND AGING RESEARCH IN GENOMIC EPIDEMIOLOGY (CHARGE) CONSORTIUM (2016) (0)
A Genome-Wide Association Study of > 250,000 Subjects Identifies Novel Risk Loci for COPD (2018) (0)
Performance of statistical methods on CHARGE targeted sequencing data (2014) (0)
Association of vitamin D status with arterial blood pressure and hypertension risk: A mendelian randomisation study (2014) (0)
Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2021) (0)
Whole genome sequencing analysis of cognitively Wellderly individuals identifies potential protective genetic variants for Alzheimer’s disease (2021) (0)
Abstract 48: A newly identified rare variant (chr11:47227430) with possible functional activity is associated with fasting insulin at the chromosome 11p11.2-NR1H3 locus in the Cohorts for Heart and Aging Research in Genetic Epidemiology Targeted Sequencing Study (CHARGE-TSS). (2014) (0)
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. (2023) (0)
Meta‐Analysis of the Association of Omega‐3 Fatty Acids Biomarkers with Pulmonary Function (2017) (0)
Frequency of familial Alzheimer’s disease gene mutations within the Alzheimer Disease Sequencing Project (ADSP) (2020) (0)
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2020) (0)
Rationale and Design of the Diet, CKD, and Apolipoprotein L1 Study in Low-Income and Middle-Income Countries. (2023) (0)
Edinburgh Research Explorer Causal Relationship between Obesity and Vitamin D Status (2018) (0)
A structural variation reference for medical and population genetics (2020) (0)
Whole genome sequence analysis of pulmonary function and COPD in 19,996 multiethnic participants. (2020) (0)
Fellowships, Grants, & Awards (2006) (0)
Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD (2012) (0)
Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease (2018) (0)
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans (2014) (0)
Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels (2018) (0)
Meta-analysis of the association of serum vitamin D with pulmonary function (2016) (0)
Abstract P215: Common Beta-cell-associated Genetic Variants and Hypertension or Anti-hypertensive Drugs do not Interact in Their Positive Associations With Risk for Rising Fasting Glucose or Incident Type 2 Diabetes in Framingham (2012) (0)
Author Correction: Evaluating drug targets through human loss-of-function genetic variation (2021) (0)
Sugar-Sweetened Beverage Consumption and Plasma Lipoprotein Cholesterol, Apolipoprotein, and Lipoprotein Particle Size Concentrations in US Adults (2022) (0)
Type 2 Diabetes Prediction (2016) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
Dissecting the genetic architecture of loci with established effects on multiple cardiometabolic phenotypes and type 2 diabetes (2014) (0)
Assisted clustering of gene expression data using regulatory data from partially overlapping sets of individuals (2022) (0)
Edinburgh Research Explorer Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes (2018) (0)
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications (2023) (0)
Meta‐Analysis of 19,005 Individuals Identifies Interplay Between Dietary Saturated Fats and Genetic Variants of the NLRP3 Inflammasome, to Modulate Insulin Resistance and Diabetes Risk (2017) (0)
Identifying important gene signatures of BMI using network structure‐aided nonparametric quantile regression (2023) (0)
Author Correction: Transcript expression-aware annotation improves rare variant interpretation (2021) (0)
RAREsim: A simulation method for very rare genetic variants (2021) (0)
TOPMED WHOLE GENOME SEQUENCE (WGS) ASSOCIATIONS WITH BRAIN MRI MEASURES IN THE FRAMINGHAM STUDY (2017) (0)
Revisiting heritability accounting for shared environmental effects and maternal inheritance (2014) (0)
Genome-Wide Association Study Evaluating Lp-PLA 2 Mass and Activity at Baseline and Following Rosuvastatin Therapy Running title : (2012) (0)
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps (2018) (0)
Functional Annotations‐Informed Whole Genome Sequence Analysis Identifies Novel Rare Variants for AD in the Alzheimer’s Disease Sequencing Project (2022) (0)
Genome-Wide Association Identi ﬁ es Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes (2011) (0)
General Framework for Meta‐Analysis of Haplotype Association Tests (2016) (0)
Genome-wide association analysis identifies six new loci associated with forced vital capacity | NOVA. The University of Newcastle's Digital Repository (2014) (0)
ABSTRACTS FROM THE TWENTY-SECOND ANNUAL MEETING OF THE INTERNATIONAL GENETIC EPIDEMIOLOGY SOCIETY (2013) (0)
UNCARBOXYLATED MATRIX G1A PROTEIN AS A PREDICTOR OF LUNG FUNCTION (2020) (0)
other inflammatory mediators circulating concentrations of monocyte chemoattractant protein-1 and Duffy antigen receptor for chemokines (Darc) polymorphism regulates (2014) (0)
Abstract P222: Consumption of Sugar-Sweetened Beverages, but Not 100% Fruit Juice, is Associated With Fasting High-density Lipoprotein and Triglyceride Concentrations in U.S. Adults (2018) (0)
Comparison of methods for multivariate gene-based association tests for complex diseases using common variants (2019) (0)
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans (2021) (0)
2256-PUB: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk (2020) (0)
Approximate conditional phenotype analysis based on genome wide association summary statistics (2021) (0)
Biomarkers of Aging, Interstitial Lung Abnormalities, and Mortality (2020) (0)
A network of pleiotropic genes for metabolic syndrome and inflammation (2013) (0)
Genetic Effect on Body Mass Index and Cardiovascular Disease Across Generations (2023) (0)
Abstract 291: Association of Single Nucleotide Polymorphisms in Inflammatory Candidate Genes with Circulating Inflammatory Biomarker Concentrations: The Framingham Heart Study (2007) (0)
The effect of LRRK2 loss-of-function variants in humans (2020) (0)
Systemic Biomarkers of Lung Function and FEV 1 Decline Across Multiple Cohorts (2020) (0)
Rare loss of function variants in candidate genes and risk of colorectal cancer (2018) (0)
A Comprehensive Type 1 Diabetes Genetic Risk Score Is Associated with Type 2 Diabetes in the Framingham Heart Study (2018) (0)
Genetic association tests in family samples for multi-category phenotypes (2021) (0)
ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES (2017) (0)
Comparison of novel and existing methods for detecting differentially methylated regions (2018) (0)
A genome-wide association study of bronchodilator response in participants of European and African ancestry from six independent cohorts (2022) (0)
Erratum (2020) (0)
Analysis of brain region-specific co-expression networks reveals clustering of established and novel genes associated with Alzheimer disease (2020) (0)
Abstract P002: Evidence For Smoking Dependent Genetic Effects on C-reactive Protein Levels in a Multi-ethnic Cohort Setting: The Care Consortium. (2012) (0)
Supplementary Material for: Meta-Analysis for Penalized Regression Methods with Multi-Cohort Genome-Wide Association Studies (2016) (0)
Searching for parent-of-origin effects on cardiometabolic traits in imprinted genomic regions (2020) (0)
Abstract MP59: Revisiting Heritability Accounting For Common Environmental Effects And Maternal Inheritance (2014) (0)
Erratum (1919) (0)
Meta-Analysis Of Genome-Wide Association Studies Of Longitudinal Decline In Lung Function (2012) (0)
Associations Between Genetic Variants near the CHREBP Locus and Lipoprotein Concentrations May Be Modified by Sugar-Sweetened Beverage Consumption (2020) (0)
The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk (2022) (0)
MAPPING GENE PATHWAYS ASSOCIATED WITH CORONARY ARTERY DISEASE THROUGH VERSATILE GENE-BASED ASSOCIATION STUDY: A CARDIOGRAM EXOME ANALYSIS (2021) (0)
Minutes of the 26th General Assembly of the European Association for the Study of Diabetes (2016) (0)
Abstract 13387: Genetic Variation in the NLRC4 Inflammasome Locus in Relation to Interleukin-18 Concentrations and Cardiovascular Disease (2010) (0)
DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases (2016) (0)
Genetic analysis of biobank data: Familial history aggregation‐based tests (FHAT) with application to Alzheimer's disease (2020) (0)
Variants in the DGKB Gene Influence Fasting Glucose Levels in Populations of European and East Asian Descent (2009) (0)
An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis (2019) (0)
Abstract 14977: Impact of Type 2 Diabetes Susceptibility Loci on Variation in Physiologic Glycaemic Traits in Non-Diabetic Individuals (2012) (0)
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg 1859, 2018) (2020) (0)
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels (2018) (0)
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls (2019) (0)
Dissecting the pleiotropic effects of established type 2 diabetes and other cardiometabolic trait loci to define pathways and gene networks involved in type 2 diabetes pathogenesis (2013) (0)
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data. (2020) (0)
The mutational constraint spectrum quantified from variation in 141,456 humans (2020) (0)
RARE DELETERIOUS AND LOSS-OF-FUNCTION VARIANTS IN OPRL1 AND GAS2L2 CONTRIBUTE TO THE RISK OF LATE-ONSET ALZHEIMER’S DISEASE: ALZHEIMER’S DISEASE SEQUENCING PROJECT CASE-CONTROL STUDY (2016) (0)
A polygenic risk score and age of diagnosis of COPD (2022) (0)
Interactions Between Sugar-Sweetened Beverage Consumption and Genetic Variants in the ChREBP Locus on Lipoprotein Concentrations in the UK Biobank: A Replication Study (2020) (0)
Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals (2019) (0)
Nutritional Epidemiology (2020) (0)
JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation (2020) (0)
Author Correction: A structural variation reference for medical and population genetics (2021) (0)
Abstract 66: Clonal Hematopoiesis of Indeterminate Potential and Incident Type 2 Diabetes Risk (2023) (0)
Evaluation of logistic regression models and effect of covariates for case–control study in RNA-Seq analysis (2017) (0)
Boston University to Hold Symposium on Statistics and Life Sciences (2019) (0)
Assessing whole genome sequencing variation for Alzheimer’s disease in 4707 individuals from the Alzheimer’s Disease Sequencing Project (ADSP) (2020) (0)
RAREsim: A simulation method for very rare genetic variants. (2022) (0)
73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk (2021) (0)
Evaluating drug targets through human loss-of-function genetic variation (2020) (0)
Errata (2011) (0)
Abstract 18874: A microRNA Signature of Tobacco Exposure (2014) (0)
Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) (0)
Epigenetic signatures of insulin resistance associated with Alzheimer’s Disease and related traits (2022) (0)

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