| Detecting a Complex of Cryptic Species within Neoechinorhynchus golvani (Acanthocephala: Neoechinorhynchidae) Inferred from ITSs and LSU rDNA Gene … A Martínez-Aquino, ME Reyna-Fabián, R Rosas-Valdez, U Razo-Mendivil, ... Journal of Parasitology 95 (5), 1040-1047, 2009 | 71 | 2009 |
| 5, 10‐Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene–environment interaction analysis in non‐syndromic cleft lip/palate B Estandia‐Ortega, JA Velázquez‐Aragón, MA Alcántara‐Ortigoza, ... European journal of oral sciences 122 (2), 109-113, 2014 | 30 | 2014 |
| First comprehensive TSC1/TSC2 mutational analysis in Mexican patients with Tuberous Sclerosis Complex reveals numerous novel pathogenic variants ME Reyna-Fabián, NL Hernández-Martínez, MA Alcántara-Ortigoza, ... Scientific reports 10 (1), 6589, 2020 | 23 | 2020 |
| Association of interactions among the IRF6 gene, the 8q24 region, and maternal folic acid intake with non‐syndromic cleft lip/palate in Mexican Mestizos JA Velázquez‐Aragón, MA Alcántara‐Ortigoza, B Estandia‐Ortega, ... American Journal of Medical Genetics-Part A 158 (12), 3207, 2012 | 22 | 2012 |
| Analysis of the Bacterial Diversity in Liver Abscess: Differences Between Pyogenic and Amebic Abscesses CR Reyna-Fabián ME, Zermeño V, Ximénez C, Flores J, Romero MF, Diaz D ... Am J Trop Med Hyg 94 (1), 147-155, 2016 | 21 | 2016 |
| Gene interactions provide evidence for signaling pathways involved in cleft lip/palate in humans JA Velázquez-Aragón, MA Alcántara-Ortigoza, B Estandia-Ortega, ... Journal of Dental Research 95 (11), 1257-1264, 2016 | 20 | 2016 |
| Deletion of Exon 1 of the SLC16A2 Gene: A Common Occurrence in Patients with Allan-Herndon-Dudley Syndrome B García-de Teresa, A González-del Angel, ME Reyna-Fabián, ... Thyroid 25 (3), 361-367, 2015 | 15 | 2015 |
| Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart … MA Alcántara-Ortigoza, J De Rubens-Figueroa, ME Reyna-Fabian, ... Pediatric cardiology 36, 802-808, 2015 | 14 | 2015 |
| Predominance of dystrophinopathy genotypes in mexican male patients presenting as muscular dystrophy with a normal multiplex polymerase chain reaction DMD gene result: a study … MA Alcántara-Ortigoza, ME Reyna-Fabián, A González-del Angel, ... Genes 10 (11), 856, 2019 | 13 | 2019 |
| Validating the systematic position of Plationus Segers, Murugan & Dumont, 1993 (Rotifera: Brachionidae) using sequences of the large subunit of the nuclear … ME Reyna-Fabián, JP Laclette, MP Cummings, M García-Varela Hydrobiologia 644, 361-370, 2010 | 12 | 2010 |
| TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant ME Reyna-Fabián, MA Alcántara-Ortigoza, NL Hernández-Martínez, ... nefrologia 40 (1), 91-98, 2020 | 8 | 2020 |
| The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes LFHMAAO Bernardette Estandia-Ortega, Miriam Erandi Reyna-Fabián, José ... Life 17 (1723), 2022 | 4* | 2022 |
| Clinical, pathological, and molecular correlation of folliculocystic and collagen hamartoma: A new potential diagnostic criterion for tuberous sclerosis complex? D Apam‐Garduño, J Cazarín‐Barrientos, NL Hernández‐Martínez, ... Journal of Cutaneous Pathology 50 (6), 481-486, 2023 | 3 | 2023 |
| Screening of IRF6 variants in patients subjected to genetic association studies for nonsyndromic cleft lip/palate JA Velázquez-Aragón, AG Angel, MA Alcántara-Ortigoza, ... The Cleft Palate-Craniofacial Journal 58 (9), 1128-1134, 2021 | 3 | 2021 |
| Unusual Clinical Manifestations in a Mexican Patient with Sanfilippo B Syndrome L Fernández-Hernández, ME Reyna-Fabián, MA Alcántara-Ortigoza, ... Diagnostics 12 (5), 1268, 2022 | 1 | 2022 |
| First Molecular Diagnosis of Oestrus ovis (Linnaeus, 1758) Larvae Causing Conjunctival Ophthalmomyiasis in Mexico City, Mexico CI Olivera-Pérez, O Lagunas-Calvo, V Cortés-González, ... Acta Parasitologica, 1-7, 2024 | | 2024 |
| Deciphering the etiology of undiagnosed ocular anomalies along with systemic alterations in pediatric patients through whole exome sequencing ME Reyna-Fabián, L Fernández-Hernández, S Enríquez-Flores, ... Scientific Reports 14 (1), 14380, 2024 | | 2024 |
| Whole exome sequencing provided a genetic diagnosis of unexplained ocular anomalies with systemic alterations in Mexican pediatric patients. V Cortes, ME Reyna-Fabian, L Fernández-Hernández, S Enríquez-Flores, ... Investigative Ophthalmology & Visual Science 64 (8), 4508-4508, 2023 | | 2023 |
| ECOLOGY-EPIDEMIOLOGY-BEHAVIOR-Detecting a Complex of Cryptic Species Within Neoechinorhynchus golvani (Acanthocephala: Neoechinorhynchidae) Inferred From ITSs and LSU rDNA Gene … A Martinez-Aquinio, ME Reyna-Fabian, R Rosas-Valdez, ... Journal of Parasitology 95 (5), 1040, 2009 | | 2009 |
José Velázquez-AragónInstituto Nacional de Pediatría Mexico在 comunidad.unam.mx 的电子邮件经过验证
