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David-Alexandre Tregouet

Showing results (31-40 of 53) with videos related to

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Journal of Molecular Medicine (Berlin, Germany)|July 20, 2007
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approachSandrine Barbaux, David-Alexandre Tregouet, Viviane Nicaud, et al.
Environmental Health and Preventive Medicine|November 19, 2009
A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among CaucasiansWanyang Liu, Hirokuni Hashikata, Kayoko Inoue, et al.
The Journal of Experimental Medicine|June 25, 2014
Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleedingMatthias Canault, Dorsaf Ghalloussi, Charlotte Grosdidier, et al.
Diabetologia|December 6, 2014
SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetesMarine Germain, Marcus G Pezzolesi, Niina Sandholm, et al.
Diabetes Care|November 21, 2018
Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced NephropathyJan Skupien, Adam M Smiles, Erkka Valo, et al.
Blood Advances|June 24, 2025
Multi-population GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafishBrooke N Wolford, Queena Yakun Zhao, Kuan-Han H Wu, et al.
Diabetologia|December 15, 2018
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuriaTarunveer S Ahluwalia, Christina-Alexandra Schulz, Johannes Waage, et al.
Blood|May 13, 2025
A Multi-Omics Approach Reveals Novel Regulators of Plasma Factor V Levels: highlight on CLEC4M as a Clearance ReceptorGaëlle Munsch, Adarsh Mohapatra, Astrid van Hylckama Vlieg, et al.
Plos Genetics|December 7, 2011
Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humansMaxime Rotival, Tanja Zeller, Philipp S Wild, et al.
The New England Journal of Medicine|July 20, 2007
Genomewide association analysis of coronary artery diseaseNilesh J Samani, Jeanette Erdmann, Alistair S Hall, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Journal of Molecular Medicine (Berlin, Germany)|July 20, 2007
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approachSandrine Barbaux, David-Alexandre Tregouet, Viviane Nicaud, et al.
Environmental Health and Preventive Medicine|November 19, 2009
A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among CaucasiansWanyang Liu, Hirokuni Hashikata, Kayoko Inoue, et al.
The Journal of Experimental Medicine|June 25, 2014
Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleedingMatthias Canault, Dorsaf Ghalloussi, Charlotte Grosdidier, et al.
Diabetologia|December 6, 2014
SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetesMarine Germain, Marcus G Pezzolesi, Niina Sandholm, et al.
Diabetes Care|November 21, 2018
Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced NephropathyJan Skupien, Adam M Smiles, Erkka Valo, et al.
Blood Advances|June 24, 2025
Multi-population GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafishBrooke N Wolford, Queena Yakun Zhao, Kuan-Han H Wu, et al.
Diabetologia|December 15, 2018
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuriaTarunveer S Ahluwalia, Christina-Alexandra Schulz, Johannes Waage, et al.
Blood|May 13, 2025
A Multi-Omics Approach Reveals Novel Regulators of Plasma Factor V Levels: highlight on CLEC4M as a Clearance ReceptorGaëlle Munsch, Adarsh Mohapatra, Astrid van Hylckama Vlieg, et al.
Plos Genetics|December 7, 2011
Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humansMaxime Rotival, Tanja Zeller, Philipp S Wild, et al.
The New England Journal of Medicine|July 20, 2007
Genomewide association analysis of coronary artery diseaseNilesh J Samani, Jeanette Erdmann, Alistair S Hall, et al.
Pageof 6