D-Index & Metrics Best Publications
Research.com 2022 Best Scientist Award Badge
Genetics and Molecular Biology
France
2022

D-Index & Metrics

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 and Molecular Biology D-index 137 Citations 83,543 557 World Ranking 98 National Ranking 2
Medicine D-index 115 Citations 54,189 470 World Ranking 1890 National Ranking 50
Best Scientists D-index 157 Citations 113,584 945 World Ranking 929 National Ranking 21

Research.com Recognitions

Awards & Achievements

2022 - Research.com Best Scientist Award

2022 - Research.com Genetics and Molecular Biology in France Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Genetics, Mutation, Pathology, Age of onset and Missense mutation are his primary areas of study. All of his Genetics and Locus, Genome-wide association study, Gene, Single-nucleotide polymorphism and Trinucleotide repeat expansion investigations are sub-components of the entire Genetics study. Within one scientific family, he focuses on topics pertaining to Parkin under Mutation, and may sometimes address concerns connected to Parkinsonism, Dystonia, Molecular biology and Ubiquitin.

The Pathology study combines topics in areas such as Central nervous system disease and Autosomal dominant cerebellar ataxia. His biological study spans a wide range of topics, including Apolipoprotein E and Degenerative disease. As a part of the same scientific study, Alexis Brice usually deals with the Missense mutation, concentrating on Proband and frequently concerns with Mutation.

His most cited work include:

  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2614 citations)
  • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2614 citations)
  • Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion (2181 citations)

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

Alexis Brice mainly investigates Genetics, Disease, Gene, Mutation and Pathology. His research related to Locus, Spinocerebellar ataxia, Haplotype, Allele and Missense mutation might be considered part of Genetics. His Spinocerebellar ataxia study incorporates themes from Ataxin 7, Autosomal dominant cerebellar ataxia, Trinucleotide repeat expansion and Cerebellar ataxia.

The study incorporates disciplines such as Genome-wide association study and Bioinformatics in addition to Disease. His research in Mutation tackles topics such as Parkin which are related to areas like Parkinsonism. His Internal medicine study integrates concerns from other disciplines, such as Gastroenterology, Endocrinology and Oncology.

He most often published in these fields:

  • Genetics (63.92%)
  • Disease (22.58%)
  • Gene (18.66%)

What were the highlights of his more recent work (between 2014-2021)?

  • Genetics (63.92%)
  • Disease (22.58%)
  • Internal medicine (17.94%)

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

Alexis Brice focuses on Genetics, Disease, Internal medicine, Parkinson's disease and Mutation. His study in Gene, Phenotype, Exome sequencing, Missense mutation and Spinocerebellar ataxia is carried out as part of his studies in Genetics. His Disease study combines topics from a wide range of disciplines, such as Odds ratio, Genome-wide association study and Bioinformatics.

His research integrates issues of Linkage disequilibrium, Genetic association, Locus and Age of onset in his study of Genome-wide association study. His Parkinson's disease research includes themes of Clinical trial, Family history and Parkinsonism. His work in Mutation tackles topics such as Ataxia which are related to areas like Pediatrics.

Between 2014 and 2021, his most popular works were:

  • Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (429 citations)
  • Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (429 citations)
  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies (353 citations)

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

  • Gene
  • Mutation
  • Internal medicine

His scientific interests lie mostly in Genetics, Disease, Genome-wide association study, Internal medicine and Mutation. His work in Genetics is not limited to one particular discipline; it also encompasses Parkinson's disease. His Disease research integrates issues from Allele, Cohort study, Bioinformatics and Confidence interval.

Alexis Brice has included themes like Alzheimer's disease, Linkage disequilibrium, Genetic association and Age of onset in his Genome-wide association study study. His Internal medicine research incorporates elements of Gerontology and Oncology. His studies in Mutation integrate themes in fields like Frontotemporal dementia, Parkin, Cerebellar ataxia, Mitochondrion and Mitophagy.

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

Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

Victoria Campuzano;Laura Montermini;Maria Dolores Moltò;Luigi Pianese.
Science (1996)

2873 Citations

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap.
Science (2003)

2801 Citations

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)

2605 Citations

Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

CB Lucking;A Durr;Bonifati;J Vaughan.
The New England Journal of Medicine (2000)

1714 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)

1592 Citations

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

Paul Hollingworth;Denise Harold;Rebecca Sims;Amy Gerrish.
Nature Genetics (2011)

1570 Citations

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

Anne Rovelet-Lecrux;Didier Hannequin;Gregory Raux;Nathalie Le Meur.
Nature Genetics (2006)

1338 Citations

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati.
Lancet Neurology (2008)

1268 Citations

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Andrew Escayg;Bryan T. MacDonald;Miriam H. Meisler;Stéphanie Baulac.
Nature Genetics (2000)

1148 Citations

Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease

P Ibáñez;A-M Bonnet;B Débarges;E Lohmann.
The Lancet (2004)

1120 Citations

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