| Nanoparticle technology for treatment of Parkinson's disease: the role of surface phenomena in reaching the brain G Leyva-Gomez, H Cortes, JJ Magana, N Leyva-García, ... Drug discovery today 20 (7), 824-837, 2015 | 111 | 2015 |
| Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect JJ Magaña, YS Tapia‐Guerrero, L Velázquez‐Pérez, ... Clinical genetics 85 (2), 159-165, 2014 | 49 | 2014 |
| A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7 L Velázquez-Pérez, CM Cerecedo-Zapata, O Hernández-Hernández, ... Neurogenetics 16, 11-21, 2015 | 38 | 2015 |
| Oxidative stress in spinocerebellar ataxia type 7 is associated with disease severity Y Torres-Ramos, A Montoya-Estrada, B Cisneros, K Tercero-Pérez, ... The Cerebellum 17, 601-609, 2018 | 34 | 2018 |
| Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population JJ Magaña, R Gómez, M Maldonado-Rodríguez, L Velázquez-Pérez, ... The Cerebellum 12, 902-905, 2013 | 33 | 2013 |
| Effects of physical rehabilitation in patients with spinocerebellar ataxia type 7 K Tercero-Pérez, H Cortés, Y Torres-Ramos, R Rodríguez-Labrada, ... The Cerebellum 18, 397-405, 2019 | 32 | 2019 |
| The relationship among IL-13, GSTP1, and CYP1A1 polymorphisms and environmental tobacco smoke in a population of children with asthma in Northern Mexico B Muñoz, JJ Magaña, I Romero-Toledo, E Juárez-Pérez, A López-Moya, ... Environmental toxicology and pharmacology 33 (2), 226-232, 2012 | 30 | 2012 |
| Distribution of CTG repeats at the DMPK gene in myotonic distrophy patients and healthy individuals from the Mexican population JJ Magaña, P Cortés-Reynosa, R Escobar-Cedillo, R Gómez, ... Molecular biology reports 38, 1341-1346, 2011 | 21 | 2011 |
| Congenital heart defect and conductive hypoacusia in a patient with the KBG syndrome. MR Rivera-Vega, SA Cuevas-Covarrubias, SH Kofman-Alfaro Clinical genetics 50 (4), 278-279, 1996 | 17 | 1996 |
| Transcriptome analysis reveals altered inflammatory pathway in an inducible glial cell model of myotonic dystrophy type 1 CN Azotla-Vilchis, D Sanchez-Celis, LE Agonizantes-Juárez, ... Biomolecules 11 (2), 159, 2021 | 16 | 2021 |
| Pathogenesis of myotonic dystrophy type 1 JJ Magana, N Leyva-Garcia, B Cisneros Gaceta Medica de Mexico 145 (4), 331-337, 2009 | 14 | 2009 |
| The molecular role of polyamines in age-related diseases: An update GE Jimenez Gutierrez, FV Borbolla Jiménez, LG Muñoz, ... International Journal of Molecular Sciences 24 (22), 16469, 2023 | 10 | 2023 |
| Association of TLR4 gene polymorphisms with sepsis after a burn injury: findings of the functional role of rs2737190 SNP CA Colín-Castro, R Franco-Cendejas, HI Rocha-González, ... Genes & Immunity 22 (1), 24-34, 2021 | 9 | 2021 |
| High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a … M González‐Del Carmen, S Montaño, OD Reyes‐Hernández, ... International Journal of Dermatology 59 (8), 969-977, 2020 | 9 | 2020 |
| Severity of dyskinesia and D3R signaling changes induced by L-DOPA treatment of hemiparkinsonian rats are features inherent to the treated subjects S Albarrán-Bravo, JA Ávalos-Fuentes, H Cortés, M Rodriguez-Sánchez, ... Biomolecules 9 (9), 431, 2019 | 8 | 2019 |
| Non-invasive methods for evaluation of skin manifestations in patients with ichthyosis H Cortés, G Figueroa-González, OD Reyes-Hernández, JJ Magaña, ... Archives of Dermatological Research 312, 231-236, 2020 | 7 | 2020 |
| Ataxia espinocerebelosa tipo 2 (parte A): epidemiología y características clínicas y genéticas L Velázquez-Pérez, O Hernández-Hernández, N Leyva-García, H Cortés, ... Investigación en Discapacidad 3 (3), 114-122, 2014 | 7 | 2014 |
| Strategies for clinical and molecular diagnosis of Charcot-Marie-Tooth 1A among Mexican patients E Hernández-Zamora, RE Escobar-Cedillo, NC González-Huerta, ... Gaceta Medica de Mexico 143 (5), 383-389, 2007 | 6 | 2007 |
| Myotonic Dystrophy Protein Kinase: Structure, Function and Its Possible Role in the Pathogenesis of Myotonic Dystrophy Type 1 JJ Magaña, R Suárez-Sánchez, N Leyva-García, B Cisneros, ... Advances in Protein Kinases, 213-42, 2012 | 4 | 2012 |
| RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7 R Suárez-Sánchez, RD Ávila-Avilés, JM Hernández-Hernández, ... Life 13 (1), 23, 2022 | 2 | 2022 |
