Artículos

• Fernandez-Figueroa EA, Espinosa-Martinez DV, Miranda-Ortiz H, Ruiz-Garcia E, Figueroa-Esquivel JM, Becerril-Moctezuma ML, Munoz-Rivas A, Rios-Munoz CA. Evidence of SARS-CoV-2 infection in companion animals from owners who tested positive for COVID-19 in the Valley of Mexico. Mol Biol Rep. 2024 Jan 25; 51(1):186.

• Garcia-Solorio J, Martinez-Villegas O, Rodriguez-Corona U, Molina-Garay C, Jimenez-Olivares M, Carrillo-Sanchez K, Mendoza-Caamal EC, Munoz-Rivas A, Villegas-Torres BE, Cervera A, Flores-Lagunes LL, Alaez-Verson C. Case report: A familial B-acute lymphoblastic leukemia associated with a new germline pathogenic variant in PAX5. The first report in Mexico. Front Oncol. 2024; 14:1355335.

• Molina Garay C, Carrillo Sanchez K, Jimenez Olivares M, Munoz Rivas A, Villegas Torres BE, Flores Aguilar H, Nunez Enriquez JC, Jimenez Hernandez E, Bekker Mendez VC, Torres Nava JR, Flores Lujano J, Martin Trejo JA, Mata Rocha M, Medina Sanson A, Espinoza Hernandez LE, Penaloza Gonzalez JG, Espinosa Elizondo RM, Flores Villegas LV, Amador Sanchez R, Perez Saldivar ML, Sepulveda Robles OA, Rosas Vargas H, Jimenez Morales S, Galindo Delgado P, Mejia Arangure JM, Alaez Verson C. Mutational Landscape of CEBPA in Mexican Pediatric Acute Myeloid Leukemia Patients: Prognostic Implications. Front Pediatr. 2022; 10:899742.

• Gonzalez-Dominguez CA, Fiesco-Roa MO, Gomez-Carmona S, Kleinert-Altamirano API, He M, Daniel EJP, Raymond KM, Abreu-Gonzalez M, Manrique-Hernandez S, Gonzalez-Jaimes A, Salinas-Marin R, Molina-Garay C, Carrillo-Sanchez K, Jimenez-Olivares M, Munoz-Rivas A, Cruz-Munoz ME, Ruiz-Garcia M, Freeze HH, Mora-Montes HM, Alaez-Verson C, Martinez-Duncker I. Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele. Front Genet. 2021; 12:777731.

En curso

• Abordaje genómico integral de la Leucemia Linfoblástica Aguda (LLA) en pacientes pediátricos”

Terminados

• Dengue y Dengue Hemorrágico: evaluación de la eficacia de un tratamiento
• “Determinación de las variantes en el patrón de impronta genómica en la región 11p15.5 en patologías pediátricas tipo síndrome de Silver Russell (SSR) o de Beckwith Wiedemann (SBW), Tumor de Wilms y hemihiperplasia”