D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 51 Citations 22,219 117 World Ranking 3079 National Ranking 157

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Mutation
  • Genetics

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 most cited work include:

  • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (4710 citations)
  • Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease (1232 citations)
  • CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. (853 citations)

What are the main themes of her work throughout her whole career to date?

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

  • Family history and related Logistic regression and Candidate gene,
  • Genetic architecture which intersects with area such as Computational biology,
  • Frameshift mutation and Exome most often made with reference to Consanguinity. In her study, Allele frequency is inextricably linked to Phenotype, which falls within the broad field of Parkinson's disease. Her Internal medicine research focuses on Pathology and how it relates to Gene mutation.

She most often published in these fields:

  • Genetics (73.28%)
  • Disease (48.85%)
  • Parkinson's disease (43.51%)

What were the highlights of her more recent work (between 2017-2021)?

  • Disease (48.85%)
  • Parkinson's disease (43.51%)
  • Genetics (73.28%)

In recent papers she was focusing on the following fields of study:

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.

Between 2017 and 2021, her most popular works were:

  • Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. (108 citations)
  • Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study (105 citations)
  • Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk (83 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Genetics

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.

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.
Nature (2001)

6569 Citations

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)

1845 Citations

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)

1136 Citations

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

Suzanne Lesage;Alexis Brice.
Human Molecular Genetics (2009)

1135 Citations

CARD15 mutations in Blau syndrome.

Corinne Miceli-Richard;Suzanne Lesage;Michel Rybojad;Anne-Marie Prieur.
Nature Genetics (2001)

1028 Citations

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)

1013 Citations

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)

925 Citations

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)

874 Citations

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

N. Vionnet;M. Stoffel;J. Takeda;K. Yasuda.
Nature (1992)

836 Citations

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)

350 Citations

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