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 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.
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.
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.
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TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
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)
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)
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)
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)
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)
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
Juliane Neumann;Jose Bras;Jose Bras;Emma Deas;Sean S. O'Sullivan.
Brain (2009)
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)
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga;CM Karch;SC Jin;BA Benitez.
Nature (2014)
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)
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