Jose Bras

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Rita GuerreiroVan Andel Research InstituteVerificeret mail på vai.org
Andrew SingletonNational Institute on AgingVerificeret mail på mail.nih.gov
J Raphael GibbsLaboratory of Neurogenetics, NIA, NIHVerificeret mail på mail.nih.gov
Dena G. HernandezNational Institutes of Health, National Institute on AgingVerificeret mail på mail.nih.gov
Carlos CruchagaProfessor. NeuroGenomics and Informatics Center DirectorVerificeret mail på wustl.edu
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for AlzheimerVerificeret mail på mail.nih.gov
Javier Simón-SánchezHertie Institute for Clinical Brain Research (HIH)Verificeret mail på dzne.de
Kailash BhatiaProfessor of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG,Verificeret mail på ucl.ac.uk
Tammaryn LashleyInstitute of Neurology, UCL, LondonVerificeret mail på ucl.ac.uk
John KauwePresident, Brigham Young University–Hawaii; Professor of Biology, Brigham Young UniversityVerificeret mail på byu.edu
Ekaterina RogaevaTanz-CRND, University of TorontoVerificeret mail på utoronto.ca
Peter HeutinkAlectorVerificeret mail på alector.com
Michelle K LuptonGenetic Epidemiology, QIMR Berghofer Medical Research Institute, Queensland, Australia.Verificeret mail på QIMRberghofer.edu.au
Sara MoleUCLVerificeret mail på ucl.ac.uk
Professor Tamas ReveszEmeritus Professor of Neuropathology, UCL Queen Square Institute of Neurology, Univ Coll LondonVerificeret mail på ucl.ac.uk
Maria Stamelou (Μαρία Σταμέλου)Prof. of Neurology, Head of Movement Disorders Dept, Hygeia Hospital, Athens, Greece; EuropeanVerificeret mail på hygeia.gr
Jonathan RohrerUCL Institute of NeurologyVerificeret mail på ucl.ac.uk
Coro Paisán RuizAssociate Professor, Icahn School of Medicine at Mount SinaiVerificeret mail på mssm.edu
A SchapiraUniversity College London, Royal FreeVerificeret mail på ucl.ac.uk
Noah RosenbergStanford UniversityVerificeret mail på stanford.edu

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Jose Bras

Regeneron Genetics Center, Regeneron Pharmaceuticals

Verificeret mail på regeneron.com

Genomics Bioinformatics Neurodegenerative diseases Complex diseases


Titel Sortér efter henvisninger Sortér efter årstal Sortér efter titel	Citeret af Citeret af	År
Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium IG McKeith, BF Boeve, DW Dickson, G Halliday, JP Taylor, D Weintraub, ... Neurology 89 (1), 88-100, 2017	3787	2017
TREM2 variants in Alzheimer's disease R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ... New England Journal of Medicine 368 (2), 117-127, 2013	3254	2013
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ... Nature genetics 51 (3), 414-430, 2019	2470	2019
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ... New England Journal of Medicine 361 (17), 1651-1661, 2009	2352	2009
Genome-wide association study reveals genetic risk underlying Parkinson's disease J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ... Nature genetics 41 (12), 1308-1312, 2009	2244	2009
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ... Nature genetics 46 (9), 989-993, 2014	2066	2014
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019	1836	2019
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1462	2018
Genotype, haplotype and copy-number variation in worldwide human populations M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ... Nature 451 (7181), 998-1003, 2008	1033	2008
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies International Parkinson Disease Genomics Consortium The Lancet 377 (9766), 641-649, 2011	1021	2011
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ... Nature genetics 49 (9), 1373-1384, 2017	959	2017
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease J Neumann, J Bras, E Deas, SS O'Sullivan, L Parkkinen, RH Lachmann, ... Brain 132 (7), 1783-1794, 2009	807	2009
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ... Nature 505 (7484), 550-554, 2014	539	2014
A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies MA Nalls, R Duran, G Lopez, M Kurzawa-Akanbi, IG McKeith, ... JAMA neurology 70 (6), 727-735, 2013	501	2013
The age factor in Alzheimer’s disease R Guerreiro, J Bras Genome medicine 7, 1-3, 2015	484	2015
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016	435	2016
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ... Brain 140 (12), 3191-3203, 2017	414	2017
USing exome sequencing to reveal mutations in trem2 presenting as a frontotemporal dementia–like syndrome without bone involvement RJ Guerreiro, E Lohmann, JM Brás, JR Gibbs, JD Rohrer, N Gurunlian, ... JAMA neurology 70 (1), 78-84, 2013	411	2013
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014	388	2014
SNCA variants are associated with increased risk for multiple system atrophy SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ... Annals of Neurology: Official Journal of the American Neurological …, 2009	329	2009

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