Josée Dupuis
Nature Genetics · 2005–2020
A researcher in the Science corpus: 17 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Whom Josée Dupuis trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Josée Dupuis overall
- Hemant Ishwaran
- Heather J. Cordell
- Anne-Laure Boulesteix
- Paola Sebastiani
- X. Chen
- C. Herrera
- Carolin Strobl
- Miron Bartosz Kursa
Papers from Josée Dupuis's perspective
Ordered by how strongly the researchers Josée Dupuis trusts endorse each paper. Same corpus, a different order for every researcher.
- Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer.
- Prevalence of obesity and trends in the distribution of body mass index among US adults, 1999-2010. (Journal of the American Medical Association (JAMA))
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Nature Genetics)
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9 (Nature Genetics)
- Mutations in PCSK9 cause autosomal dominant hypercholesterolemia (Nature Genetics)
- Random Forests
- Defining the role of common variation in the genomic and biological architecture of adult human height
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Identifying SNPs predictive of phenotype using random forests (2005) — 388 citations
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) — 1,860 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- 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) — 1,485 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts (2013) — 1,061 citations
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) — 841 citations
- Common genetic determinants of vitamin D insufficiency: a genome-wide association study (2010) — 1,460 citations
- Common variants at 30 loci contribute to polygenic dyslipidemia (2008) — 1,471 citations
- Variants in MTNR1B influence fasting glucose levels (2008) — 723 citations
- Genotype Score in Addition to Common Risk Factors for Prediction of Type 2 Diabetes (2008) — 778 citations