Maria José Rodríguez

Pedagogical and Technological University of Colombia — Colombia

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index617citations20works1.52yr avg
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Research Topics

Muscle Physiology and Disorders(8), Neurogenetic and Muscular Disorders Research(4), RNA Research and Splicing(2), Virus-based gene therapy research(2), Genetic Neurodegenerative Diseases(2)

Publications20 total

Infección por SARS-CoV-2 en niños menores de 15 años con glomerulopatías en Uruguay
Archivos de Pediatría del Uruguay·2024Open Access
Chromosomal Damage, Chromosome Instability, and Polymorphisms in GSTP1 and XRCC1 as Biomarkers of Effect and Susceptibility in Farmers Exposed to Pesticides
International Journal of Molecular Sciences·2024· 3 citedOpen Access
Anoctamin 5 (ANO5) muscular dystrophy—three different phenotypes and a new histological pattern
Neurological Sciences·2020· 7 cited
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain
Genes·2020· 48 citedOpen Access
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
Journal of Neurology Neurosurgery & Psychiatry·2018· 48 citedOpen Access
Erratum to “Characterization of strain of fowl adenoviruses circulating in Morocco”
Poultry Science·2018· 1 citedOpen Access
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement
Neuromuscular Disorders·2018· 30 cited
Characterization of strain of fowl adenoviruses circulating in Morocco
Poultry Science·2018· 23 citedOpen Access
SP253METFORMIN-ASOCIATED LACTIC ACIDOSIS AND ACUTE KIDNEY INJURY. AN UNDERESTIMATED DISEASE
Nephrology Dialysis Transplantation·2018· 1 cited
The Toll like receptor 4 ligand cold-inducible RNA-binding protein as vaccination platform against cancer
OncoImmunology·2017· 21 citedOpen Access
Development of biological tools to assess the role of TMPRSS4 and identification of novel tumor types with high expression of this prometastatic protein.
PubMed·2017· 5 cited
DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations
PLoS ONE·2015· 143 citedOpen Access
Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes
PLoS ONE·2013· 55 citedOpen Access
Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy
Orphanet Journal of Rare Diseases·2012· 53 citedOpen Access
Functional Analysis of<i>α</i>-DOX2, an Active<i>α</i>-Dioxygenase Critical for Normal Development in Tomato Plants
PLANT PHYSIOLOGY·2009· 41 citedOpen Access
LGMD2I in Spanish and Croatian Populations
Neuromuscular Disorders·2006
Isolation and identification of Streptomyces spp. from Venezuelan soils: Morphological and biochemical studies. I.
Microbiological Research·2005· 98 cited
Expression in <i>Escherichia coli</i> of a recombinant adenosine kinase from <i>Saccharomyces cerevisiae</i>: purification, kinetics and substrate analyses
Yeast·2003· 13 cited
Genética de las cardiopatías congénitas
Anales de Pediatría·2000· 3 cited
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the γ-sarcoglycan gene
European Journal of Human Genetics·1998· 24 citedOpen Access

Frequent Co-authors

P. Gallano(9), Lidia González‐Quereda(7), Montserrat Baiget(5), A. Nascimento(4), Jaume Colomer(4), Jordi Díaz‐Manera(4), Montse Olivé(4), Jonàs Juan‐Mateu(3), Edgard Verdura(3), Laura González(3), Eduard Gallardo(3), C. Ortez(2), Cristina Jou(2), C. Jimenez‐Mallebrera(2), Carmen Paradas(2), Adolfo López de Munaín(2), José C. Milisenda(2), Aurora Sánchez(2), Glòria Garrabou(2), Alicia Alonso‐Jiménez(2)