1) Rehotbevely Barrientos-Rios, Sara Frias, José A. Velázquez-Aragón, Camilo E. Villaroel, Silvia Sánchez, Bertha Molina, Angélica Martínez, Alessandra Carnevale, Benilde García-de- Teresa, Edmundo Bonilla, Christian David Alvarado-Araiza, Alejandro Valderrama-Hernández, Paul Tadeo Ríos-Gallardo, Raúl Calzada-León, Nelly Altamirano-Bustamante & Leda Torres (2019) Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes, Gynecological Endocrinology Marzo 2019. DOI: 10.1080/09513590.2019.1582626.(FI ) (Q2) (2 citas)

2) García-de Teresa B, Frias S, Molina B, Villarreal MT, Rodriguez A, Carnevale A, López- Hernández G, Vollbrechtshausen L, Olaya-Vargas A, Torres L. FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México. Mol Genet Genomic Med. 2019 May 1:e710. doi: 10.1002/mgg3.710.(FI)(Q3)(1 cita)

3) Alfredo Rodríguez, J. Jesús Naveja, Leda Torres, Benilde García de Teresa, Ulises Juárez Figueroa, Cecilia Ayala, Eugenio M. Azpeitia, Luis Mendoza, Sara Frías. WIP1 contributes to the adaptation of Fanconi anemia cells to DNA damage as determined by the regulatory network of the Fanconi anemia and checkpoint recovery pathways. Frontiers in Genetics. 2019;10 (411): 1-14. doi: 10.3389/fgene.2019.00411(FI)(Q2)(3 citas)

4) Alfredo Rodríguez, Kaiyang Zhang, Anniina Färkkilä, Jessica Filiatrault, Chunyu Yang, Martha Velázquez, Elissa Furutani, Devorah C. Goldman, Benilde García de Teresa, Gilda Garza-Mayen, Kelsey McQueen, Larissa A Sambel, Bertha Molina, Leda Torres, Marisol González, Eduardo Vadillo, Rosana Pelayo, William H. Fleming, Markus Grompe, Akiko Shimamura, Sampsa Hautaniemi, Joel Greenberger, Sara Frías, Kalindi Parmar, Alan D D’Andrea. MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia. Cell Stem Cell (2021) Volume 28, Issue 1, Pages 33 - 47.e87 https://doi.org/10.1016/j.stem.2020.09.004 (Q1)(21 citas).

5) Pedro Reyes, Benilde García-de Teresa, Ulises Juárez, Fernando Pérez-Villatoro, Moisés O. Fiesco-Roa, Alfredo Rodríguez, Bertha Molina , María Teresa Villarreal-Molina ,Jorge Meléndez-Zajgla, Alessandra Carnevale, Leda Torres and Sara Frias. Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG. Int. J. Mol. Sci. 2022, 23(4), 2334; https://doi.org/10.3390/ijms23042334.(Q1)

6) Torres Leda, Juárez Ulises, Reyes Pedro y Frías, Sara. Fanconi anemia, Part 2. Methodological strategy for molecular diagnosis in patients with Fanconi anemia. [Anemia de Fanconi, Parte 2. Estrategia metodológica para el diagnóstico molecular en pacientes con anemia de Fanconi] . Acta Pediatrica de Mexico (2023) Volume 44, Issue 1, Pages 29 – 55 ISSN 01862391. DOI 10.18233/APM44No1pp29-552548 (Q4)

7) Sánchez S, Juárez U, Domínguez J, Molina B, Barrientos R, Martínez‑Hernández A, Carnevale A, Grether‑González P, Mayen DG, Villarroel C, Lieberman E, Yokoyama E, Del Castillo V, Torres L and Frias S. Frequent copy number variants in a cohort of Mexican‑Mestizo individuals. Molecular Cytogenetics (2023) 16:2. https://doi.org/10.1186/s13039-022-00631-z
(FI)(Q3)(1 cita).

8) Ayala-Zambrano C, Yuste M, Frias S, Garcia-de-Teresa B, Mendoza L, Azpeitia E, Rodríguez A, Torres L. A Boolean network model of the double-strand break repair pathway choice. J Theor Biol. 2023 Aug 16;573:111608. doi: 10.1016/j.jtbi.2023.111608.

h index = 11

Circuito de Posgrado, Ciudad Universitaria
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