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Author

René Ribacoba

Complex I Defect in muscle from patients with Huntington's disease
1998 · Joaquín Arenas, Yolanda Campos, et al. · Annals of Neurology · 173
Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population
2005 · Cecilia Huerta, Mónica G. Castro, et al. · Journal of the Neurological Sciences · 96
MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects
2014 · Lucía F. Cardo, Eliecer Coto, et al. · Journal of Molecular Neuroscience · 75
Mutational screening of the mortalin gene (HSPA9) in Parkinson’s disease
2009 · Lorena De Mena, Eliecer Coto, et al. · Journal of Neural Transmission · 75
Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease
2004 · Cecilia Huerta, Victoria Álvarez, et al. · Neuroscience Letters · 67
Analysis of the Micro‐RNA‐133 and PITX3 genes in Parkinson's disease
2010 · Lorena de Mena, Eliecer Coto, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 63
Clinical manifestations of intermediate allele carriers in Huntington disease
2016 · Esther Cubo, María A. Ramos-Arroyo, et al. · Neurology · 53
FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients
2010 · Lorena de Mena, Lucía F. Cardo, et al. · Neuroscience Letters · 49
A Search for SNCA 3′ UTR Variants Identified SNP rs356165 as a Determinant of Disease Risk and Onset Age in Parkinson’s Disease
2011 · Lucía F. Cardo, Eliecer Coto, et al. · Journal of Molecular Neuroscience · 48
Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms
2014 · Lucía F. Cardo, Eliecer Coto, et al. · Neuroscience Letters · 43
Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study
2018 · Paul McNulty, Richard Pilcher, et al. · Journal of Huntington s Disease · 35
Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease
2008 · Victoria Alvarez, Ana I. Corao, et al. · Neuroscience Letters · 32
No association between Parkinson's disease and three polymorphisms in the eNOS, nNOS, and iNOS genes
2006 · Cecilia Huerta, Elena Sánchez-Ferrero, et al. · Neuroscience Letters · 27
Single-nucleotide polymorphisms in the promoter region of the PARKIN gene and Parkinson's disease
2002 · Ignacio F Mata, Victoria Alvarez, et al. · Neuroscience Letters · 24
The screening of the 3′UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson’s disease
2014 · Lucía F Cardo, Eliecer Coto, et al. · Journal of Human Genetics · 19
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Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease
2012 · Lorena de Mena, LLuís Samaranch, et al. · Journal of Molecular Neuroscience · 10
Mutational screening of the Mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease
2008 · Elena Sánchez-Ferrero, Eliecer Coto, et al. · Parkinsonism & Related Disorders · 5
Works count: 19
Citation count: 894
H-index: 15
I10-index: 16
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