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Suzanne Lesage
Affiliation : Centre National de la Recherche Scientifique · Inserm · Sorbonne Université · Institut des Sciences Moléculaires · Assistance Publique – Hôpitaux de Paris · Pitié-Salpêtrière Hospital · Institut du Cerveau
- 25Publications (affiliation in France)
- 313Total publications
- 35717Citations
- 75h-index
Research profile
Suzanne Lesage has 25 indexed publications (2005–2025). Their work appears mainly in “Revue Neurologique”, “The Lancet Neurology” and “SSRN Electronic Journal”. Their most cited article, “Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy” (2016), has been cited 438 times. 7 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in South Africa, Tunisia, Germany.
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Create my free profile Add my publicationsResearch areas
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Nuclear Receptors and Signaling
- Genetic Associations and Epidemiology
- Dementia and Cognitive Impairment Research
Publications (25)
- Subthalamic Nucleus Deep Brain Stimulation in Early-onset Parkinson’s Disease: Clinical Outcomes in LRRK2 Mutation Carriers Compared to Non-Carriers
- A PARK7 Mutation‐Induced Early‐Onset Parkinson's Disease in a Moroccan Family: Expanding the Geographic Spectrum
- RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses
- A Pathogenic Variant in Rab32 Causes Autosomal Dominant Parkinson's Disease and Activates LRRK2 Kinase
- Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
- An Overview of the Worldwide Distribution of LRRK2 Mutations in Parkinson’s Disease
- Identification of a DAGLB Mutation in a Non‐Chinese Patient with Parkinson's Disease
- PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability
- Clinical Variability of SYNJ1-Associated Early-Onset Parkinsonism
- Characterization of Recessive Parkinson Disease in a Large Multicenter Study
- Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease
- Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease
- Implication du gène GBA dans la maladie de Parkinson en Tunisie : fréquence et caractéristique clinique
- Genetic and Phenotypic Characterisation of Autosomal Recessive Parkinson's Disease in a Large Multicentre Cohort
- LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic
- Analyse génétique de patients consanguins Marocains atteints de la maladie de Parkinson combinant puce à ADN et panel de gènes
- Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel
- Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
- DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study
- Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers
- The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
- Diagnostic génétique de la forme PARK8 de la maladie de Parkinson en Algérie par recherche de la mutation c 6055G>A (p gly2019ser) dans le gène LRRK2
- LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort
- Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans
- G2019S LRRK2 mutation in French and North African families with Parkinson's disease
Publication venues
- Revue Neurologique × 3
- The Lancet Neurology × 2
- SSRN Electronic Journal × 2
- Movement Disorders × 2
- Frontiers in Neurology × 2
- Annals of Neurology × 2
Publications per year
- 20252
- 20242
- 20233
- 20221
- 20211
- 20203
- 20192
- 20182
- 20171
- 20163
Collaborations
Partner institutions : Université Pierre-et-Marie-Curie · Université d'Angers · CIC Pitié Neurosciences · Centre Hospitalier Universitaire de Grenoble · Physiopathologie des Comportements
Co-authors’ countries : South Africa · Tunisia · Germany
Co-authors
- Alexis Brice
- Christelle Tesson
- Jean‐Christophe Corvol
- François Viallet
- François Tison
- Marie Vidailhet
- Emmanuel Broussolle
- Alexandra Dürr
- Christine Tranchant
- Pierre Pollak
- Yves Agid
- Mathieu Anheim
Bibliographic data from OpenAlex (open database).
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