Publications by authors named "Xavier Hermant"

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The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects.
Erwan Lambert, Orthis Saha, Bruna Soares Landeira, Ana Raquel Melo de Farias, Xavier Hermant

Acta Neuropathol Commun· January 2022

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Identification of a functional FADS1 3'UTR variant associated with erythrocyte n-6 polyunsaturated fatty acids levels.
Xavier Hermant, Charlotte Delay, Amandine Flaig, Jimena Luque-Bedregal, Gilbert Briand

J Clin Lipidol· October 2019

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Associations of common SNPs in the SORT1, GCKR, LPL, APOA1, CETP, LDLR, APOE genes with lipid trait levels in an Algerian population sample.
Djabaria Naïma Meroufel, Sounnia Mediene-Benchekor, Sarah Aïcha Lardjam-Hetraf, Hadjira Ouhaïbi-Djellouli, Houssam Boulenouar, Xavier Hermant

Int J Clin Exp Pathol· May 2016

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Examination of the brain natriuretic peptide rs198389 single-nucleotide polymorphism on type 2 diabetes mellitus and related phenotypes in an Algerian population.
Djabaria Naïma Meroufel, Hadjira Ouhaïbi-Djellouli, Sounnia Mediene-Benchekor, Xavier Hermant, Benjamin Grenier-Boley

Gene· August 2015

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The TCF7L2 rs7903146 polymorphism, dietary intakes and type 2 diabetes risk in an Algerian population.
Hadjira Ouhaibi-Djellouli, Sounnia Mediene-Benchekor, Sarah Aïcha Lardjam-Hetraf, Imane Hamani-Medjaoui, Djabaria Naima Meroufel, Xavier Hermant

BMC Genet· December 2014

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Combined effect of established BMI loci on obesity-related traits in an Algerian population sample.
Manel Nassima Badsi, Sounnia Mediene-Benchekor, Hadjira Ouhaibi-Djellouli, Sarah Aicha Lardjam-Hetraf, Houssam Boulenouar, Xavier Hermant

BMC Genet· November 2014

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Impact of APOE gene polymorphisms on the lipid profile in an Algerian population.
Houssam Boulenouar, Sounnia Mediene Benchekor, Djabaria Naïma Meroufel, Sarah Aicha Lardjam Hetraf, Hadjira Ouhaibi Djellouli, Xavier Hermant

Lipids Health Dis· October 2013

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Genetic and molecular insights into the role of PROX1 in glucose metabolism.
Sophie Lecompte, Gianni Pasquetti, Xavier Hermant, Benjamin Grenier-Boley, Marcela Gonzalez-Gross

Diabetes· May 2013

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Impact of the matrix metalloproteinase MMP-3 on dementia.
Nicole Helbecque, Dominique Cottel, Xavier Hermant, Philippe Amouyel

Neurobiol Aging· August 2007

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The impact of the AMPD1 gene polymorphism on exercise capacity, other prognostic parameters, and survival in patients with stable congestive heart failure: a study in 686 consecutive patients.
Pascal de Groote, Nicolas Lamblin, Nicole Helbecque, Frédéric Mouquet, Xavier Hermant

Am Heart J· October 2006

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The impact of beta-adrenoreceptor gene polymorphisms on survival in patients with congestive heart failure.
Pascal de Groote, Nicolas Lamblin, Nicole Helbecque, Frédéric Mouquet, Eugène Mc Fadden, Xavier Hermant

Eur J Heart Fail· October 2005

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Association between beta-1 and beta-2 adrenergic receptor gene polymorphisms and the response to beta-blockade in patients with stable congestive heart failure.
Pascal de Groote, Nicole Helbecque, Nicolas Lamblin, Xavier Hermant, Eugène Mc Fadden

Pharmacogenet Genomics· March 2005

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Prognostic impact of matrix metalloproteinase gene polymorphisms in patients with heart failure according to the aetiology of left ventricular systolic dysfunction.
Frédérique Mizon-Gérard, Pascal de Groote, Nicolas Lamblin, Xavier Hermant, Jean Dallongeville

Eur Heart J· April 2004

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Beta-adrenergic receptor blockade and the angiotensin-converting enzyme deletion polymorphism in patients with chronic heart failure.
Pascal de Groote, Nicole Helbecque, Nicolas Lamblin, Xavier Hermant, Philippe Amouyel

Eur J Heart Fail· January 2004

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The role of matrix metalloproteinase-9 in dementia.
Nicole Helbecque, Xavier Hermant, Dominique Cottel, Philippe Amouyel

Neurosci Lett· October 2003

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Angiotensin Converting Enzyme and Angiotensin II Type 1 Receptor Polymorphisms in Patients with Coronary Aneurysms.
Nicolas Lamblin, Xavier Hermant, Jean-Marc Lablanche, Nicole Helbecque, Philippe Amouyel

Thromb J· August 2003

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Polymorphisms in the promoter regions of MMP-2, MMP-3, MMP-9 and MMP-12 genes as determinants of aneurysmal coronary artery disease.
Nicolas Lamblin, Christophe Bauters, Xavier Hermant, Jean-Marc Lablanche, Nicole Helbecque

J Am Coll Cardiol· July 2002

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