Egberto Reis Barbosa

Author

Also Known As

BARBOSA, Egberto Reis, Barbosa, E.R., Barbosa, ER, Barbosa, Egberto R., Barbosa, Egberto Reis, Cristina Sampaio, E Barbosa, E R Barbosa, E. Barbosa, E. R. Barbosa

408

Publications

11.7K

Citations

H-Index

163

Concepts

All Affiliations

Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Erasmus MC Erasmus University Rotterdam Universidade Federal de São Paulo

About

Egberto Reis Barbosa is an author at Universidade de São Paulo specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	58	3K
2	Social Sciences	13	15	544
3	Health Sciences	11	12	463
4	Allergy	2	2	45
5	Public Health	1	1	45

Egberto Reis Barbosa

134

Publications

9.3K

Citations

H-Index

Page 1

	Year	Citations
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease E. Sidransky, Mike A. Nalls, Jan Aasly, New England Journal of Medicine	2009	2.1K
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Alessio Di Fonzo, Christan F. Rohé, Joaquim J. Ferreira, The Lancet Molecular NeuroscienceMendelian DisorderAutosomal Dominant ParkinsonGenetic DisorderParkinson Disease	2005	529
Noninvasive cortical stimulation with transcranial direct current stimulation in Parkinson's disease Felipe Fregni, Paulo S. Boggio, M.C. Santos, Movement Disorders	2006	431
Early-onset parkinsonism associated with <i>PINK1</i> mutations Vincenzo Bonifati, Christan F. Rohé, Guido J. Breedveld, Neurology	2005	335
<i>ATP13A2</i> missense mutations in juvenile parkinsonism and young onset Parkinson disease Alessio Di Fonzo, Hsin Fen Chien, Mariana P. Socal, Neurology	2007	332
Mutation in the<i>SYNJ1</i>Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism Marialuisa Quadri, Mingyan Fang, Marina Picillo, Human Mutation Neurodegenerative DiseasesEarly-onset ParkinsonismMendelian DisorderGenetic DisorderExome Sequencing	2013	309
Neurological manifestations in Wilson's disease: Report of 119 cases Alexandre Alves Machado, Hsin Fen Chien, Marta Mitiko Deguti, Movement Disorders	2006	279
Effect of repetitive TMS and fluoxetine on cognitive function in patients with Parkinson's disease and concurrent depression Paulo S. Boggio, Felipe Fregni, Felix Bermpohl, Movement Disorders	2005	215
The G6055A (G2019S) mutation in <i>LRRK2</i> is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor Stefano Goldwurm, Alessio Di Fonzo, Erik Simons, Journal of Medical Genetics	2005	195
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska, The Lancet Neurology Neurodegenerative DiseasesGenetic DisorderGeneticsGenetic EpidemiologySequencing Study	2018	159

Page 1