Thierry Levade

Centre National de la Recherche Scientifique — France

Biochemistry, Genetics and Molecular Biology · Life Sciences

72h-index16.3kcitations444works1.62yr avg
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Research Topics

Sphingolipid Metabolism and Signaling(167), Lysosomal Storage Disorders Research(127), Lipid Membrane Structure and Behavior(51), Cellular transport and secretion(39), Carbohydrate Chemistry and Synthesis(39)

Publications443 total

Correction: Advanced strategies for detecting acid sphingomyelinase deficiency type B with attenuated phenotypes
Orphanet Journal of Rare Diseases·2025Open Access
Hepatocyte FGF21 is not required for fasting-induced metabolic responses but guides protein appetite after energy depletion
2025Open Access
Advanced Strategies for Detecting Acid Sphingomyelinase Deficiency Type B with Attenuated Phenotypes
2025
Thermoneutral housing worsens MASLD and reveals defective brown adipose tissue response to β3-adrenergic stimulation
iScience·2025· 1 citedOpen Access
Neuraminidase 1 secondary deficiency contributes to CNS pathology in neurological mucopolysaccharidoses via brain protein hypersialylation
Journal of Clinical Investigation·2025· 1 citedOpen Access
Advanced strategies for detecting acid sphingomyelinase deficiency type B with attenuated phenotypes
Orphanet Journal of Rare Diseases·2025· 1 citedOpen Access
Liver gene expression and its rewiring in hepatic steatosis are controlled by PI3Kα-dependent hepatocyte signaling
PLoS Biology·2025· 1 citedOpen Access
Natural history of adult-onset metachromatic leukodystrophy
Journal of Neurology·2025· 1 citedOpen Access
Acid sphingomyelinase deficiency: Laboratory diagnosis, genetic and epidemiologic aspects of a 50-year French cohort
Molecular Genetics and Metabolism·2025· 2 cited
Acid Ceramidase Deficiency
Neurology Genetics·2025· 1 citedOpen Access
Acid Sphingomyelinase Deficiency: Laboratory Diagnosis, Genetic and Epidemiologic Aspects of a 50-Year French Cohort
SSRN Electronic Journal·2025Open Access
Cerebrotendinous xanthomatosis: a literature review and case study
Frontiers in Cardiovascular Medicine·2024· 2 citedOpen Access
Perspectives thérapeutiques pour les maladies lysosomales dues au déficit en céramidase acide
médecine/sciences·2024Open Access
Effect of thermoneutral housing on MASLD severity, hepatic gene expression, and BAT activation during β3-adrenergic stimulation in mice
2024Open Access
Targeting ceramide metabolism in melanoma to improve the efficacy of immune checkpoint inhibitor therapy: from basic mechanisms to the clinic.
SPIRE - Sciences Po Institutional REpository·2024
Acid sphingomyelinase deficiency in France: a retrospective survival study
Orphanet Journal of Rare Diseases·2024· 6 citedOpen Access
Ceramide metabolism alterations contribute to Tumor Necrosis Factor-induced melanoma dedifferentiation and predict resistance to immune checkpoint inhibitors in advanced melanoma patients
Frontiers in Immunology·2024· 3 citedOpen Access
Stratégie diagnostique à la recherche de mucopolysaccharidoses de phénotypes atténués à partir de signes d’appel rhumatologiques : étude rétrospective sur la base du PMSI
La Revue de Médecine Interne·2024
Human genetic defects of sphingolipid synthesis
Journal of Inherited Metabolic Disease·2024· 7 citedOpen Access
Secondary deficiency of neuraminidase 1 contributes to CNS pathology in neurological mucopolysaccharidoses via hypersialylation of brain glycoproteins
2024· 1 citedOpen Access
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Frequent Co-authors

Nathalie Andrieu‐Abadie(17), Robert Salvayre(10), Bruno Ségui(9), Stéphane Carpentier(8), Olivier Cuvillier(7), Patrice Codogno(6), Virginie Garcia(6), Anne Montfort(5), Céline Colacios(5), Nathalie Augè(5), Anne Nègre‐Salvayre(5), Philippe Rochaix(4), Nicolás Meyer(4), Jean‐Pierre Jaffrézou(4), Catherine Caillaud(3), Nicolas Maestre(3), Florie Bertrand(3), Thomas Filleron(3), Chantal Bauvy(3), Robert Jan Veldman(3)