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International Journal of Molecular Sciences|February 26, 2022
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCGPedro Reyes, Benilde García-de Teresa, Ulises Juárez, et al.
Rare Tumors|July 9, 2026
T-cell lymphoma of the breast and ovary presenting as a second malignant neoplasm in a pediatric leukemia survivor: A case report and literature reviewOscar Alvarez-Palacios, Luis Ojeda-Campos, Alfredo Rodríguez, et al.
Molecular Cytogenetics|January 11, 2023
Frequent copy number variants in a cohort of Mexican-Mestizo individualsSilvia Sánchez, Ulises Juárez, Julieta Domínguez, et al.
The Journal of Pathology. Clinical Research|August 5, 2026
Genomic profiling of Mexican patients with B-cell precursor acute lymphoblastic leukemia reveals clinically significant somatic and potential germline variantsDaniel Martínez Anaya, María Del Rocío Juárez-Velázquez, Ulises Juárez Figueroa, et al.
BMC Infectious Diseases|June 12, 2024
Detection of IgG antibodies against the receptor binding domain of the spike protein and nucleocapsid of SARS-CoV-2 at university students from Southern Mexico: a cross-sectional studyJesús Adolfo Bailón-Cuenca, Karen Cortés-Sarabia, José Legorreta-Soberanis, et al.
Frontiers in Aging|March 12, 2026
The tight bond between Fanconi anemia and agingMarco Antonio Mejía-Barrera, Enya Enara Martínez-Torres, Ulises Juárez-Figueroa, et al.
Plos Genetics|November 28, 2022
TGFβ pathway is required for viable gestation of Fanconi anemia embryosAlfredo Rodríguez, Michael Epperly, Jessica Filiatrault, et al.
International Journal of Molecular Sciences|September 9, 2022
Characterization of Philadelphia-like Pre-B Acute Lymphoblastic Leukemia: Experiences in Mexican Pediatric PatientsDaniel Martínez-Anaya, Dafné Moreno-Lorenzana, Adriana Reyes-León, et al.
NPJ Genomic Medicine|June 9, 2026
Dyskeratosis Congenita with Pigmentary Mosaicism and Hematopoietic Trisomy 9 in a Female Associated with a de novo DKC1 Variant and Markedly Skewed X Chromosome InactivationBenilde García-de-Teresa, Tianna Zhao, Consuelo Salas-Labadía, et al.
International Journal of Molecular Sciences|June 27, 2024
A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9-12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary CancerJulieta Dominguez-Ortiz, Rosa M Álvarez-Gómez, Rogelio Montiel-Manríquez, et al.
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