| Oxidative stress modulation in hepatitis C virus infected cells SA Lozano-Sepulveda, OL Bryan-Marrugo, C Cordova-Fletes, ... World journal of hepatology 7 (29), 2880, 2015 | 61 | 2015 |
| A de novo t(10;19)(q22.3;q13.33) leads to ZMIZ1/PRR12 reciprocal fusion transcripts in a girl with intellectual disability and neuropsychiatric alterations C Córdova-Fletes, MG Domínguez, I Delint-Ramirez, ... Neurogenetics 16, 287-298, 2015 | 33 | 2015 |
| Downregulation of inducible nitric oxide synthase (iNOS) expression is implicated in the antiviral activity of acetylsalicylic acid in HCV-expressing cells CP Ríos-Ibarra, S Lozano-Sepulveda, L Muñoz-Espinosa, ... Archives of virology 159, 3321-3328, 2014 | 28 | 2014 |
| Uncommon runs of homozygosity disclose homozygous missense mutations in two ciliopathy-related genes (SPAG17 and WDR35) in a patient with multiple brain and skeletal anomalies C Córdova-Fletes, LE Becerra-Solano, MM Rangel-Sosa, ... European Journal of Medical Genetics 61 (3), 161-167, 2018 | 19 | 2018 |
| Williams–Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH A Ramírez-Velazco, T Aguayo-Orozco, L Figuera, H Rivera, LJ Suárez, ... Journal of Genetics 98 (34), 1-7, 2019 | 12 | 2019 |
| CDKL5 truncation due to at (X; 2)(p22. 1; p25. 3) in a girl with X-linked infantile spasm syndrome. C Cordova-Fletes, N Rademacher, I Müller, JN Mundo-Ayala, ... Clinical Genetics 77 (1), 2010 | 12 | 2010 |
| Identification of NIPBL, a new ETV6 partner gene in t(5;12) (p13;p13)-associated acute megakaryoblastic leukemia E De Braekeleer, R Auffret, JRG García, JMS Padilla, CC Fletes, F Morel, ... Leukemia & lymphoma 54 (2), 423-424, 2013 | 10 | 2013 |
| Delineation of a de novo 7q21. 3q31. 1 deletion by CGH-SNP arrays in a girl with multiple congenital anomalies including severe glaucoma L Martínez-Jacobo, C Córdova-Fletes, R Ortiz-López, F Rivas, ... Molecular syndromology 4 (6), 285-291, 2013 | 9 | 2013 |
| Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion VA Neira, C Córdova‐Fletes, Y Grondin, A Ramirez‐Velazco, LE Figuera, ... American Journal of Medical Genetics-Part A 158 (6), 1498, 2012 | 8 | 2012 |
| Carbapenemase-Encoding Genes and Colistin Resistance in Gram-Negative Bacteria During the COVID-19 Pandemic in Mexico: Results from the Invifar Network U Garza-Ramos, J Silva-Sánchez, LE López-Jácome, ... Microbial Drug Resistance 29 (6), 239-248, 2023 | 7 | 2023 |
| Reduced SPAG17 expression in systemic sclerosis triggers myofibroblast transition and drives fibrosis P Sapao, EDO Roberson, B Shi, S Assassi, B Skaug, F Lee, A Naba, ... Journal of Investigative Dermatology 143 (2), 284-293, 2023 | 6 | 2023 |
| Exome sequencing reveals three homozygous missense variants in SNRPA in two sisters with syndromic intellectual disability MM Rangel‐Sosa, LE Figuera‐Villanueva, IA González‐Ramos, ... Clinical Genetics 93 (6), 1229-1233, 2018 | 5 | 2018 |
| De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features VA Neira, P Romero-Espinoza, A Rojas-Martínez, R Ortiz-López, ... Gene 524 (2), 381-385, 2013 | 5 | 2013 |
| Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis C Córdova-Fletes, MM Rangel-Sosa, LA Martínez-Jacobo, ... Autoimmunity 53 (6), 344-352, 2020 | 4 | 2020 |
| Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder JE García-Ortiz, AI Zarazúa-Niño, AA Hernández-Orozco, EA Reyes-Oliva, ... Journal of Autism and Developmental Disorders 50, 2247-2251, 2020 | 4 | 2020 |
| Complete genome sequence of houston virus, a newly discovered mosquito-specific virus isolated from Culex quinquefasciatus in Mexico N Cigarroa-Toledo, CM Baak-Baak, RC Cetina-Trejo, C Cordova-Fletes, ... Microbiology Resource Announcements 7 (10), 10.1128/mra. 00808-18, 2018 | 4 | 2018 |
| De novo dir dup/del of 18q characterized by SNP arrays and FISH in a girl child with mixed phenotypes C Córdova-Fletes, E Sáinz-González, RI Avendaño-Gálvez, ... Journal of genetics 93, 869-873, 2014 | 4 | 2014 |
| A de novo sSMC (22) characterized by high-resolution arrays in a Girl with Cat-Eye Syndrome without Coloboma C Córdova-Fletes, MG Domínguez, A Vázquez-Cárdenas, LE Figuera, ... Molecular Syndromology 3 (3), 131-135, 2012 | 4 | 2012 |
| A del (13)(q21. 32q31. 2) dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions C Córdova-Fletes, H Rivera, EA Garza-Villarreal, NA Vázquéz-Cárdenas, ... Clinical Dysmorphology 26 (1), 33-37, 2017 | 3 | 2017 |
| Transcriptomic analysis of biofilm formation in strains of Clostridioides difficile associated with recurrent and non-recurrent infection reveals potential candidate … D Rubio-Mendoza, C Córdova-Fletes, A Martínez-Meléndez, ... Plos one 18 (8), e0289593, 2023 | 2 | 2023 |
