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Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity

PLoS genetics, 2021-01, Vol.17 (1), p.e1009325-e1009325

2021

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Insights into medical students' perceptions of work culture during the COVID-19 pandemic: a mixed method study

BMC medical education, 2024-01, Vol.24 (1), p.21-21, Article 21

2024

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Familial hypercholesterolemia: experience from France

Current opinion in lipidology, 2018-04, Vol.29 (2), p.65-71

2018

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Lessons from the Impact of COVID-19 on Medical Educational Continuity and Practices

Advances in physiology education, 2021-06, Vol.45 (2), p.390-398

2021

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Adrenocortical scavenger receptor class B type I deficiency exacerbates endotoxic shock and precipitates sepsis-induced mortality in mice

The Journal of immunology (1950), 2014-07, Vol.193 (2), p.817-826

2014

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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels

Journal of lipid research, 2014-07, Vol.55 (7), p.1189-1191

2014

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Association between a frequent allele of the gene encoding OATP1B1 and enhanced LDL-lowering response to fluvastatin therapy

Pharmacogenomics, 2008-09, Vol.9 (9), p.1217-1227

2008

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Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: Relevance to oxidative stress

Atherosclerosis, 2010-06, Vol.210 (2), p.607-613

2010

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Elevated gamma-glutamyltransferase activity and perturbed thiol profile are associated with features of metabolic syndrome

Arteriosclerosis, thrombosis, and vascular biology, 2008-03, Vol.28 (3), p.587-593

2008

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IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis

Human molecular genetics, 2003-06, Vol.12 (12), p.1415-1425

2003

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LDL-apheresis depletes apoE-HDL and pre-β1-HDL in familial hypercholesterolemia: relevance to atheroprotection

Journal of lipid research, 2011-12, Vol.52 (12), p.2304-2313

2011

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ClinVar database of global familial hypercholesterolemia‐associated DNA variants

Human mutation, 2018-11, Vol.39 (11), p.1631-1640

2018

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Evaluation of a semi-automatic isoelectric focusing method for apolipoprotein E phenotyping

Practical laboratory medicine, 2020-01, Vol.18, p.e00150-e00150, Article e00150

2020

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Clinical Genetic Testing for Familial Hypercholesterolemia

Journal of the American College of Cardiology, 2018-08, Vol.72 (6), p.662-680

2018

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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels1

Journal of lipid research, 2014-07, Vol.55 (7), p.1189-1191

2014

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A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

Cell, 1998-01, Vol.92 (1), p.51-61

1998

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Sitosterolemia: A new mutation in a Mediterranean patient

Journal of clinical lipidology, 2014-07, Vol.8 (4), p.451-454

2014

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Lysosomal acid lipase deficiency and familial hypercholesterolemia: A case report

Atherosclerosis, 2024-08, Vol.395

2024

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MECP2 mutations account for most cases of typical forms of Rett syndrome

Human molecular genetics, 2000-05, Vol.9 (9), p.1377-1384

2000

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LDL apheresis as an alternate method for plasma LPS purification in healthy volunteers and dyslipidemic and septic patients

Journal of lipid research, 2020-12, Vol.61 (12), p.1776-1783

2020

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APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia

International journal of molecular sciences, 2022-05, Vol.23 (10), p.5792

2022

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Free cholesterol transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis underlies the U-shape relationship between HDL-cholesterol and cardiovascular disease

European journal of preventive cardiology, 2020-10, Vol.27 (15), p.1606-1616

2020

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Effect of the LDL receptor mutation type on incident major adverse cardiovascular events in familial hypercholesterolaemia

European journal of preventive cardiology, 2022-11, Vol.29 (16), p.2125-2131

2022

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Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia

Atherosclerosis, 2012-08, Vol.223 (2), p.394-400

2012

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Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity

Insights into medical students' perceptions of work culture during the COVID-19 pandemic: a mixed method study

Familial hypercholesterolemia: experience from France

Lessons from the Impact of COVID-19 on Medical Educational Continuity and Practices

Adrenocortical scavenger receptor class B type I deficiency exacerbates endotoxic shock and precipitates sepsis-induced mortality in mice

Robust validation of methylation levels association at CPT1A locus with lipid plasma levels

Association between a frequent allele of the gene encoding OATP1B1 and enhanced LDL-lowering response to fluvastatin therapy

Plasma bilirubin and gamma-glutamyltransferase activity are inversely related in dyslipidemic patients with metabolic syndrome: Relevance to oxidative stress

Elevated gamma-glutamyltransferase activity and perturbed thiol profile are associated with features of metabolic syndrome

The Clinical Genome Resource (ClinGen) Familial Hypercholesterolemia Variant Curation Expert Panel consensus guidelines for LDLR variant classification

IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis

LDL-apheresis depletes apoE-HDL and pre-β1-HDL in familial hypercholesterolemia: relevance to atheroprotection

ClinVar database of global familial hypercholesterolemia‐associated DNA variants

Evaluation of a semi-automatic isoelectric focusing method for apolipoprotein E phenotyping

Clinical Genetic Testing for Familial Hypercholesterolemia

Robust validation of methylation levels association at CPT1A locus with lipid plasma levels1

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

Sitosterolemia: A new mutation in a Mediterranean patient

Lysosomal acid lipase deficiency and familial hypercholesterolemia: A case report

MECP2 mutations account for most cases of typical forms of Rett syndrome

LDL apheresis as an alternate method for plasma LPS purification in healthy volunteers and dyslipidemic and septic patients

APOE Molecular Spectrum in a French Cohort with Primary Dyslipidemia

Free cholesterol transfer to high-density lipoprotein (HDL) upon triglyceride lipolysis underlies the U-shape relationship between HDL-cholesterol and cardiovascular disease

Effect of the LDL receptor mutation type on incident major adverse cardiovascular events in familial hypercholesterolaemia

Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia

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