O. Marmontel

发表

PCSK9 post-transcriptional regulation: Role of a 3'UTR microRNA-binding site variant in linkage disequilibrium with c.1420G.

L. Dauchet, A. Meirhaeghe, P. Moulin, 2020, Atherosclerosis.

Alterations in plasma triglycerides lipolysis in patients with history of multifactorial chylomicronemia.

P. Moulin, Cyrielle Caussy, C. Marçais, 2017, Atherosclerosis.

Correction: Post-Heparin LPL Activity Measurement Using VLDL As a Substrate: A New Robust Method for Routine Assessment of Plasma Triglyceride Lipolysis Defects

M. Lagarde, P. Moulin, A. Sassolas, 2014, PloS one.

Post-Heparin LPL Activity Measurement Using VLDL As a Substrate: A New Robust Method for Routine Assessment of Plasma Triglyceride Lipolysis Defects

M. Lagarde, P. Moulin, A. Sassolas, 2014, PloS one.

Development of a new expanded next‐generation sequencing panel for genetic diseases involved in dyslipidemia

P. Moulin, N. Peretti, N. Chatron, 2020, Clinical genetics.

Normal serum ApoB48 and red cells vitamin E concentrations after supplementation in a novel compound heterozygous case of abetalipoproteinemia.

D. Bozon, Sujith Rajan, P. Moulin, 2019, Atherosclerosis.

APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia

J. Ferrières, A. Philippi, P. Giral, 2022, International journal of molecular sciences.

Pseudohyponatremia: interference of hyperglycemia on indirect potentiometry

R. Cartier, M. Di Filippo, O. Marmontel, 2022, Clinical chemistry and laboratory medicine.

Single, short in‐del, and copy number variations detection in monogenic dyslipidemia using a next‐generation sequencing strategy

D. Bozon, P. Moulin, N. Peretti, 2018, Clinical genetics.

A new 165-SNP low-density lipoprotein cholesterol polygenic risk score based on next generation sequencing outperforms previously published scores in routine diagnostics of familial hypercholesterolemia.

A. Meirhaeghe, P. Moulin, B. Cariou, 2022, Translational research : the journal of laboratory and clinical medicine.

APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants

J. Rieusset, P. Moulin, B. Cariou, 2022, International journal of molecular sciences.

Phenotypic Differences Between Polygenic and Monogenic Hypobetalipoproteinemia

R. Redon, E. Génin, J. Deleuze, 2020, Arteriosclerosis, thrombosis, and vascular biology.

Multiple microRNA regulation of lipoprotein lipase gene abolished by 3'UTR polymorphisms in a triglyceride-lowering haplotype harboring p.Ser474Ter.

M. Lagarde, J. Dallongeville, A. Meirhaeghe, 2016, Atherosclerosis.

Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia

P. Moulin, F. Paillard, B. Cariou, 2023, Arteriosclerosis, thrombosis, and vascular biology.

Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts

C. Zawadzki, C. Vinciguerra, P. Bouvagnet, 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

Post-Heparin LPL Activity Measurement Using VLDL As a Substrate: A New Robust Method for Routine Assessment of Plasma Triglyceride Lipolysis Defects

M. Lagarde, P. Moulin, A. Sassolas, 2014, PLoS ONE.

Assessment of three equations to calculate plasma LDL cholesterol concentration in fasting and non-fasting hypertriglyceridemic patients

M. Di Filippo, S. Charrière, O. Marmontel, 2023, Clinical chemistry and laboratory medicine.

Involvement of a homozygous exon 6 deletion of LMF1 gene in intermittent severe hypertriglyceridemia.

P. Moulin, T. Simonet, C. Marçais, 2020, Journal of clinical lipidology.

New rare genetic variants of LMF1 gene identified in severe hypertriglyceridemia.

M. Krempf, B. Vergès, P. Moulin, 2018, Journal of clinical lipidology.

Arteriosclerosis, Thrombosis, and Vascular Biology.

A. Inoue, M. Varret, T. Worgall, 2015, Arteriosclerosis, thrombosis, and vascular biology.

Arteriosclerosis, Thrombosis, and Vascular Biology.

M. Varret, Arterioscler Thromb, Vasc Biol, 2016, Arteriosclerosis, thrombosis, and vascular biology.