Her primary areas of study are Genetics, Genome-wide association study, Mutation, Internal medicine and Single-nucleotide polymorphism. Her Genetics research focuses on LRRK2, Mutation, Genetic variation, Gene and Leucine-rich repeat. Her studies examine the connections between Genetic variation and genetics, as well as such issues in Meta-analysis, with regards to Odds ratio.
Her studies deal with areas such as Blau syndrome and NOD2 as well as Mutation. Her work deals with themes such as Diabetes mellitus, Endocrinology, Glucokinase and MODY 2, which intersect with Internal medicine. Suzanne Lesage interconnects Genotyping, GPNMB, Haplotype and Candidate gene in the investigation of issues within Single-nucleotide polymorphism.
Her scientific interests lie mostly in Genetics, Disease, Parkinson's disease, Gene and Internal medicine. Her Genetics and LRRK2, Locus, Mutation, Genome-wide association study and Missense mutation investigations all form part of her Genetics research activities. Her LRRK2 research includes elements of Odds ratio, Glucocerebrosidase, Point mutation and Degenerative disease.
Her Disease research also works with subjects such as
Disease, Parkinson's disease, Genetics, Genome-wide association study and Gene are her primary areas of study. Her biological study spans a wide range of topics, including Odds ratio, Family history and Genetic architecture. A large part of her Parkinson's disease studies is devoted to LRRK2.
Her work deals with themes such as Alpha-synuclein and Age of onset, which intersect with Genetics. Her studies deal with areas such as Genetic variability, Dementia with Lewy bodies, Genetic association, Heritability and Genetic variation as well as Genome-wide association study. Her research in Gene intersects with topics in Cell biology and Proteasome.
Her primary areas of investigation include Disease, Parkinson's disease, Genetics, Genome-wide association study and LRRK2. The study incorporates disciplines such as Odds ratio, Single-nucleotide polymorphism, Gene and Genetic architecture in addition to Disease. Suzanne Lesage usually deals with Parkinson's disease and limits it to topics linked to Missense mutation and Penetrance.
Borrowing concepts from Context, Suzanne Lesage weaves in ideas under Genetics. Her Genome-wide association study study incorporates themes from Lewy body, Dementia and Age of onset. Her Internal medicine research includes themes of Oncology and Candidate gene.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Jean-Pierre Hugot;Mathias Chamaillard;Mathias Chamaillard;Habib Zouali;Suzanne Lesage.
Nature (2001)
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz.
The New England Journal of Medicine (2009)
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.
American Journal of Human Genetics (2002)
Parkinson's disease: from monogenic forms to genetic susceptibility factors
Suzanne Lesage;Alexis Brice.
Human Molecular Genetics (2009)
CARD15 mutations in Blau syndrome.
Corinne Miceli-Richard;Suzanne Lesage;Michel Rybojad;Anne-Marie Prieur.
Nature Genetics (2001)
Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes Mellitus
Froguel P;Zouali H;Vionnet N;Velho G.
The New England Journal of Medicine (1993)
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.
The Lancet (2011)
Close Linkage of Glucokinase Locus on Chromosome 7p to Early-Onset Non-Insulin-Dependent Diabetes Mellitus
Ph. Froguel;M. Vaxillaire;F. Sun;G. Velho.
Nature (1992)
Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus
N. Vionnet;M. Stoffel;J. Takeda;K. Yasuda.
Nature (1992)
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.
PLOS Genetics (2011)
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