| 1 | Deciphering the etiology of undiagnosed ocular anomalies along with systemic alterations in pediatric patients through whole exome sequencing | 1ᵉʳ autor: Reyna-Fabián M.E., Fernández-Hernández L., Enríquez-Flores S., Apam-Garduño D., et al. | 2024 | SCIENTIFIC REPORTS | Scopus-id: 2-s2.0-85196640950
| 0 | 0 |
| 2 | Unusual Clinical Manifestations in a Mexican Patient with Sanfilippo B Syndrome | 2ᵒ autor: Reyna-Fabián M.E., Fernández-Hernández L., Alcántara-Ortigoza M.A., Aláez-Verson C., et al. | 2022 | Diagnostics | WoS-id: 000803365900001
Scopus-id: 2-s2.0-85130883933
| 1 | 1 |
| 3 | The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes | 2ᵒ autor: Reyna-Fabián M.E., Estandia-Ortega, Bernardette, Velázquez-Aragón J.A., Gonzalez-del Angel, Ariadna, et al. | 2022 | LIFE-BASEL | WoS-id: 000882101600001
Scopus-id: 2-s2.0-85141797854
| 0 | 2 |
| 4 | Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate | Coautor: Reyna-Fabián M.E., Velázquez-Aragón J.A., Angel A.G.-D., Alcántara-Ortigoza M.A., et al. | 2021 | CLEFT PALATE-CRAN J | Scopus-id: 2-s2.0-85097777693
| 0 | 3 |
| 5 | TSC2/PKD1 contiguous gene syndrome, with emphasis on a case with an atypical mild polycystic kidney phenotype and a novel genetic variant | 1ᵉʳ autor: Reyna-Fabian, Miriam E., Alcantara-Ortigoza, Miguel A., Hernandez-Martinez, Nancy L., Berumen, Jaime, et al. | 2020 | Nefrologia | WoS-id: 000507855500011
Scopus-id: 2-s2.0-85078574169
| 6 | 7 |
| 6 | First comprehensive TSC1/TSC2 mutational analysis in Mexican patients with Tuberous Sclerosis Complex reveals numerous novel pathogenic variants | 1ᵉʳ autor: Reyna-Fabian, Miriam E., Hernandez-Martinez, Nancy L., Alcantara-Ortigoza, Miguel A., Ayala-Sumuano, Jorge T., et al. | 2020 | SCIENTIFIC REPORTS | WoS-id: 000537155000019
Scopus-id: 2-s2.0-85083781910
| 10 | 15 |
| 7 | Predominance of dystrophinopathy genotypes in mexican male patients presenting as muscular dystrophy with a normal multiplex polymerase chain reaction DMD gene result: A study including targeted next-generation sequencing | 2ᵒ autor: Reyna-Fabián M.E., Alcántara-Ortigoza M.A., Gonzalez-del Angel, Ariadna, Estandia-Ortega, Bernardette, et al. | 2019 | GENES | WoS-id: 000502296000022
Scopus-id: 2-s2.0-85074443762
| 6 | 8 |
| 8 | Analysis of the Bacterial Diversity in Liver Abscess: Differences between Pyogenic and Amebic Abscesses | 1ᵉʳ autor: Reyna-Fabian, Miriam E., Zermeno, Valeria, Ximenez, Cecilia, Flores, Janin, et al. | 2016 | AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE | WoS-id: 000367705500026
Scopus-id: 2-s2.0-84954205513
| 14 | 20 |
| 9 | Gene interactions provide evidence for signaling pathways involved in cleft lip/palate in humans | Coautor: Reyna-Fabián, M.E., Velázquez-Aragón, J.A., Alcántara-Ortigoza, M.A., Estandia-Ortega, B., et al. | 2016 | JOURNAL OF DENTAL RESEARCH | WoS-id: 000384456800008
Scopus-id: 2-s2.0-84988470788
| 12 | 13 |
| 10 | Deletion of exon 1 of the SLC16A2 gene: A common occurrence in patients with allan-herndon-dudley syndrome | Coautor: Reyna-Fabián M.E., García-De Teresa B., González-Del Angel A., Ruiz-Reyes M.D.L.L., et al. | 2015 | Thyroid | WoS-id: 000350550400013
Scopus-id: 2-s2.0-84924408376
| 7 | 7 |
| 11 | Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects | Coautor: Reyna-Fabian M.E., Alcántara-Ortigoza M.A., De Rubens-Figueroa J., Estandía-Ortega B., et al. | 2015 | PEDIATRIC CARDIOLOGY | WoS-id: 000351553700014
Scopus-id: 2-s2.0-84925512114
| 9 | 8 |
| 12 | Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects [Pediatric Cardiology, 36, (2015), 802-808, DOI:10.1007/s00246-014-1091-3] | Coautor: Reyna-Fabian M.E., Alcántara-Ortigoza M.A., De Rubens-Figueroa J., Estandía-Ortega B., et al. | 2015 | PEDIATRIC CARDIOLOGY | WoS-id: 000361426700036
Scopus-id: 2-s2.0-84941942581
| 0 | 2 |
| 13 | 5,10-Methylenetetrahydrofolate reductase single nucleotide polymorphisms and gene-environment interaction analysis in non-syndromic cleft lip/palate | Coautor: Reyna-Fabian M.E., Estandia-Ortega B., Velázquez-Aragón J.A., Alcántara-Ortigoza M.A., et al. | 2014 | EUROPEAN JOURNAL OF ORAL SCIENCES | WoS-id: 000332589100003
Scopus-id: 2-s2.0-84897614967
| 18 | 19 |
| 14 | Association of Interactions Among the IRF6 Gene, the 8q24 Region, and Maternal Folic Acid Intake With Non-Syndromic Cleft Lip/Palate in Mexican Mestizos | Coautor: Reyna-Fabian, ME, Velazquez-Aragon, JA, Alcantara-Ortigoza, MA, Estandia-Ortega, B, et al. | 2012 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000311401800031
Scopus-id: 2-s2.0-84870240624
| 14 | 14 |
| 15 | Validating the systematic position of Plationus Segers, Murugan & Dumont, 1993 (Rotifera: Brachionidae) using sequences of the large subunit of the nuclear ribosomal DNA and of | 1ᵉʳ autor: Reyna-Fabián M.E., Laclette J.P., Cummings M.P., García-Varela M. | 2010 | Hydrobiologia | WoS-id: 000276071600026
Scopus-id: 2-s2.0-77950023599
| 7 | 8 |
| 16 | DETECTING A COMPLEX OF CRYPTIC SPECIES WITHIN NEOECHINORHYNCHUS GOLVANI (ACANTHOCEPHALA: NEOECHINORHYNCHIDAE) INFERRED FROM ITSs AND LSU rDNA GENE SEQUENCES | 2ᵒ autor: Reyna-Fabian, ME, Martinez-Aquino, A, Rosas-Valdez, R, Razo-Mendivil, U, et al. | 2009 | JOURNAL OF PARASITOLOGY | WoS-id: 000272015500002
Scopus-id: 2-s2.0-76849110758
| 62 | 61 |
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