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Claire Perret

Showing results (31-40 of 43) with videos related to

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Clinical Genetics|June 28, 2019
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlationsFlavie Ader, Pascal De Groote, Patricia Réant, 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.
Circulation. Cardiovascular Genetics|January 14, 2015
PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease RiskMontse Guardiola, Holly J Exeter, Claire Perret, et al.
Plos One|October 8, 2011
Genetics of venous thrombosis: insights from a new genome wide association studyMarine Germain, Noémie Saut, Nicolas Greliche, et al.
Plos One|May 27, 2010
Genetics and beyond--the transcriptome of human monocytes and disease susceptibilityTanja Zeller, Philipp Wild, Silke Szymczak, 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.
Plos One|March 16, 2017
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
Plos One|February 15, 2020
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
Nature Genetics|February 10, 2009
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery diseaseDavid-Alexandre Trégouët, Inke R König, Jeanette Erdmann, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Clinical Genetics|June 28, 2019
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlationsFlavie Ader, Pascal De Groote, Patricia Réant, 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.
Circulation. Cardiovascular Genetics|January 14, 2015
PLA2G10 Gene Variants, sPLA2 Activity, and Coronary Heart Disease RiskMontse Guardiola, Holly J Exeter, Claire Perret, et al.
Plos One|October 8, 2011
Genetics of venous thrombosis: insights from a new genome wide association studyMarine Germain, Noémie Saut, Nicolas Greliche, et al.
Plos One|May 27, 2010
Genetics and beyond--the transcriptome of human monocytes and disease susceptibilityTanja Zeller, Philipp Wild, Silke Szymczak, 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.
Plos One|March 16, 2017
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
Plos One|February 15, 2020
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
Nature Genetics|February 10, 2009
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery diseaseDavid-Alexandre Trégouët, Inke R König, Jeanette Erdmann, et al.
Pageof 5