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 and Molecular Biology D-index 53 Citations 18,865 118 World Ranking 3251 National Ranking 1556

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Jose Bras mainly focuses on Genetics, Genome-wide association study, Parkinson's disease, Gene and Single-nucleotide polymorphism. His research on Genetics often connects related areas such as TREM2. His research integrates issues of Common disease-common variant, Allele frequency, Genetic association, Alzheimer's disease and Genetic heterogeneity in his study of Genome-wide association study.

Jose Bras combines subjects such as Neuroimaging, Dementia with Lewy bodies, REM sleep behavior disorder and Neurocognitive with his study of Alzheimer's disease. His studies in Parkinson's disease integrate themes in fields like Glucocerebrosidase and Meta-analysis. He has included themes like Odds ratio, Gene mutation, Ashkenazi jews, Genotyping and Dementia in his Glucocerebrosidase study.

His most cited work include:

  • TREM2 Variants in Alzheimer's Disease (1646 citations)
  • Genome-wide association study reveals genetic risk underlying Parkinson's disease (1433 citations)
  • Genome-wide association study reveals genetic risk underlying Parkinson's disease (1433 citations)

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

His primary scientific interests are in Genetics, Disease, Genome-wide association study, Parkinson's disease and Dementia. Jose Bras has researched Disease in several fields, including Allele and Bioinformatics. His research investigates the connection between Genome-wide association study and topics such as Heritability that intersect with problems in Genetic variation.

His work focuses on many connections between Genetic variation and other disciplines, such as Linkage disequilibrium, that overlap with his field of interest in Allele frequency. His Parkinson's disease research incorporates themes from Glucocerebrosidase, Case-control study, Genetic predisposition and Genotype. The study incorporates disciplines such as Common disease-common variant and TREM2 in addition to Alzheimer's disease.

He most often published in these fields:

  • Genetics (66.38%)
  • Disease (52.16%)
  • Genome-wide association study (29.74%)

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

  • Disease (52.16%)
  • Genetics (66.38%)
  • Genome-wide association study (29.74%)

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

His scientific interests lie mostly in Disease, Genetics, Genome-wide association study, Internal medicine and Frontotemporal dementia. His Disease study combines topics in areas such as Single-nucleotide polymorphism, Allele and Genetic architecture. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Parkinson's disease, Dementia with Lewy bodies, Genotyping, Genetic association and Heritability.

His Parkinson's disease research integrates issues from Meta-analysis and Mendelian inheritance. His Internal medicine study integrates concerns from other disciplines, such as Mutation, Polygenic risk score, Oncology and Genotype. His research investigates the link between Frontotemporal dementia and topics such as Gene mutation that cross with problems in Messenger RNA.

Between 2017 and 2021, his most popular works were:

  • Analysis of shared heritability in common disorders of the brain (726 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)
  • 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 primary areas of study are Disease, Genome-wide association study, Genetics, Single-nucleotide polymorphism and Dementia. The concepts of his Disease study are interwoven with issues in Odds ratio, Allele, Bioinformatics and Genetic architecture. As part of one scientific family, Jose Bras deals mainly with the area of Odds ratio, narrowing it down to issues related to the Case-control study, and often Loss function.

The various areas that he examines in his Genome-wide association study study include Dementia with Lewy bodies, Genetic heterogeneity, Genetic association and Risk factor. Specifically, his work in Genetics is concerned with the study of Gene. His research in Dementia focuses on subjects like Apolipoprotein E, which are connected to Cohort.

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

TREM2 Variants in Alzheimer's Disease

Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)

1821 Citations

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Javier Simón-Sánchez;Claudia Schulte;Jose M Bras;Jose M Bras;Manu Sharma.
Nature Genetics (2009)

1680 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

Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium

Ian G. McKeith;Bradley F. Boeve;Dennis W. DIckson;Glenda Halliday.
Neurology (2017)

1504 Citations

Genotype, haplotype and copy-number variation in worldwide human populations

Mattias Jakobsson;Sonja W. Scholz;Sonja W. Scholz;Paul A Scheet;J. Raphael Gibbs;J. Raphael Gibbs.
Nature (2008)

929 Citations

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease

Mike A. Nalls;Nathan Pankratz;Christina M. Lill;Chuong B. Do.
PMC (2014)

612 Citations

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

Juliane Neumann;Jose Bras;Jose Bras;Emma Deas;Sean S. O'Sullivan.
Brain (2009)

602 Citations

Analysis of shared heritability in common disorders of the brain

Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Science (2018)

547 Citations

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

C Cruchaga;CM Karch;SC Jin;BA Benitez.
Nature (2014)

415 Citations

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)

382 Citations

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