Mário Campos - Concepedia

Author

Mário Campos

Universidade Federal do Rio de Janeiro ORCID

Also Known As

CamposJunior, M., Júnior, Mario Campos, M. Campos, M. Campos Júnior, Mario Campos, Mario Campos Junior, Mario Campos-Junior, Mario Campos Junior, Mário Campos, Mário Campos Junior

Publications

575

Citations

H-Index

Concepts

All Affiliations

Universidade Federal do Rio de Janeiro Universidade do Estado do Rio de Janeiro Fundação Oswaldo Cruz Hospital Universitário Clementino Fraga Filho Santa Casa de Misericórdia de Passos

About

Mário Campos is an author at Universidade Federal do Rio de Janeiro specializing in medicine, genetics, and parkinson disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	13	247
2	Diabetes	2	2	30
3	Public Health	1	1	16
4	Social Sciences	1	1	11
5	Biostatistics	1	1	16

Mário Campos

Publications

448

Citations

H-Index

Page 1

	Year	Citations
A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay Cíntia Barros Santos-Rebouças, Natalia Fintelman‐Rodrigues, Lars Riff Jensen, Neuroscience Letters	2011	55
A study of LRRK2 mutations and Parkinson's disease in Brazil Márcia Mattos Gonçalves Pimentel, Karla Cristina Vasconcelos Moura, Cláudia Bueno Abdalla, Neuroscience Letters Parkinson DiseaseGeneticsLrrk2 MutationsPathologyMedicine	2007	36
<p>The association of the fat mass and obesity-associated gene (FTO) rs9939609 polymorphism and the severe obesity in a Brazilian population</p> Ana Carolina Proença da Fonseca, Gabriella de Medeiros Abreu, Verônica Marques Zembrzuski, Diabetes Metabolic Syndrome and Obesity	2019	36
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation Márcia Mattos Gonçalves Pimentel, Fabíola C. Rodrigues, Marco Antônio Araújo Leite, Parkinsonism & Related Disorders Neurodegenerative DiseasesParkinson Diseaseα-Synuclein Mutational ScreeningDegenerative DiseaseP.e46k Mutation	2015	25
Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease Adriana Vaz dos Santos, Cristiane Pinheiro Pestana, Karen Rafaella da Silva Diniz, Neuroscience Letters Mutational AnalysisMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2010	23
Autosomal dominant Parkinson’s disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil Gabriella de Medeiros Abreu, D. Valença, Mário Campos, Neuroscience Letters Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2016	23
Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease Camilla P. da Silva, Gabriella de Medeiros Abreu, Pedro Hernán Cabello, Journal of the Neurological Sciences Gba MutationsParkinson DiseaseGeneticsPathologyNeurology	2017	23
Study of LEP, MRAP2 and POMC genes as potential causes of severe obesity in Brazilian patients Ana Carolina Proença da Fonseca, Gabriella de Medeiros Abreu, Verônica Marques Zembrzuski, Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity ObesityMetabolic SyndromeMetabolic DisorderGeneticsPomc Genes	2020	22
A Rare Potential Pathogenic Variant in the BDNF Gene is Found in a Brazilian Patient with Severe Childhood-Onset Obesity Ana Carolina Proença da Fonseca, Gabriella de Medeiros Abreu, Lohanna Palhinha, Diabetes Metabolic Syndrome and Obesity	2021	22
Genetic analysis of LRRK2 functional domains in Brazilian patients with Parkinson’s disease Cláudia Bueno Abdalla-Carvalho, Cíntia Barros Santos-Rebouças, Bonfim Guimarães, European Journal of Neurology	2010	18

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