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Genetics

D-Index
78
Citations
37351
World Ranking
1665
National Ranking
71

Overview

Suzanne Lesage is affiliated with Université Paris Cité in France and works primarily in the fields of Medicine, Biochemistry, Genetics and Molecular Biology, and Neuroscience. Their research focuses notably on subfields such as Neurology, Genetics, Molecular Biology, Cellular and Molecular Neuroscience, and Physiology.

The main topics addressed in Suzanne Lesage's work include:

  • Parkinson's Disease Mechanisms and Treatments
  • Neurological diseases and metabolism
  • Nuclear Receptors and Signaling
  • Genetic Associations and Epidemiology
  • RNA regulation and disease
  • Lysosomal Storage Disorders Research
  • Alzheimer's disease research and treatments

Recent publications by Suzanne Lesage include:

  • "Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome" (2021) published in Nature Communications
  • "Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets" (2021) published in JAMA Neurology
  • "Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease" (2021) published in Nature Genetics
  • "RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses" (2024) published in The Lancet Neurology
  • "Identification of sixteen novel candidate genes for late onset Parkinson's disease" (2021) published in Molecular Neurodegeneration

The frequent coauthors collaborating with Suzanne Lesage are:

  • Alexis Brice (51 publications)
  • Jean-Christophe Corvol (42 publications)
  • Christelle Tesson (21 publications)
  • Graziella Mangone (18 publications)
  • Huw R. Morris (17 publications)

The most common venues where Suzanne Lesage has published work include:

  • bioRxiv (Cold Spring Harbor Laboratory) with 11 publications
  • Movement Disorders with 7 publications
  • Brain with 7 publications
  • Frontiers in Neurology with 5 publications
  • Annals of Neurology with 3 publications

Best Publications

  • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

    Jean-Pierre Hugot;Mathias Chamaillard;Mathias Chamaillard;Habib Zouali;Suzanne Lesage

  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz

  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Mike A Nalls;Cornelis Blauwendraat;Costanza L Vallerga;Karl Heilbron

  • Parkinson's disease: from monogenic forms to genetic susceptibility factors

    Suzanne Lesage;Alexis Brice

  • CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.

    Suzanne Lesage;Habib Zouali;Jean-Pierre Cézard;Jean-Frédéric Colombel

  • CARD15 mutations in Blau syndrome.

    Corinne Miceli-Richard;Suzanne Lesage;Michel Rybojad;Anne-Marie Prieur

  • Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes Mellitus

    Froguel P;Zouali H;Vionnet N;Velho G

  • Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

    Michael A Nalls;Vincent Plagnol;Dena G Hernandez

  • Close Linkage of Glucokinase Locus on Chromosome 7p to Early-Onset Non-Insulin-Dependent Diabetes Mellitus

    Ph. Froguel;M. Vaxillaire;F. Sun;G. Velho

  • G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome.

    Suzanne Lesage;Mathieu Anheim;Franck Letournel;Luc Bousset

  • Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus

    N. Vionnet;M. Stoffel;J. Takeda;K. Yasuda

  • What Genetics Tells us About the Causes and Mechanisms of Parkinson's Disease

    Olga Corti;Suzanne Lesage;Alexis Brice

  • LRRK2 G2019S as a Cause of Parkinson's Disease in North African Arabs

    Suzanne Lesage;Alexandra Dürr;Meriem Tazir;Ebba Lohmann

  • A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    Michael A. Nalls;Raquel Duran;Grisel Lopez;Marzena Kurzawa-Akanbi

  • Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease

    L.A. Robak;L.A. Robak;I.E. Jansen;I.E. Jansen;J van Rooij;A.G. Uitterlinden

  • Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

    Suzanne Lesage;Valérie Drouet;Elisa Majounie;Vincent Deramecourt

  • A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease

    V. Plagnol;M.A. Nalls;J.M. Bras;D.G. Hernandez;D.G. Hernandez

  • Infevers: an evolving mutation database for auto-inflammatory syndromes.

    Isabelle Touitou;Suzanne Lesage;Michael McDermott;Laurence Cuisset

  • Gene–environment interaction modulated by allelic heterogeneity in inflammatory diseases

    Mathias Chamaillard;Dana Philpott;Stephen E. Girardin;Habib Zouali

  • A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism.

    Simon Edvardson;Yuval Cinnamon;Asaf Ta-Shma;Avraham Shaag

Frequent Co-Authors

Alexis Brice
Alexis Brice Institut du Cerveau
Andrew B. Singleton
Andrew B. Singleton National Institutes of Health
Peter Heutink
Peter Heutink German Center for Neurodegenerative Diseases
Thomas Gasser
Thomas Gasser University of Tübingen
Dena G. Hernandez
Dena G. Hernandez National Institutes of Health
Ziv Gan-Or
Ziv Gan-Or McGill University
Alexandra Durr
Alexandra Durr Sorbonne University
Sonja W. Scholz
Sonja W. Scholz National Institutes of Health
Jose Bras
Jose Bras Van Andel Institute
Mike A. Nalls
Mike A. Nalls National Institutes of Health

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