| 1 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Molina, Bertha, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 2 | Fanconi anemia, Part 1. Cytogenetic diagnosis | 1ᵉʳ autor: MOLINA, BERTHA, Ramos, Sandra, FRIAS, SARA | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000791750600005
Scopus-id: 2-s2.0-85130907534
| 3 | 3 |
| 3 | Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG | Coautor: Molina B., Reyes P., García-De Teresa B., Juárez U., et al. | 2022 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000971202400001
Scopus-id: 2-s2.0-85124879348
| 7 | 9 |
| 4 | MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia | Coautor: Molina B., Rodríguez A., Zhang K., Färkkilä A., et al. | 2021 | Cell Stem Cell | WoS-id: 000606536600009
Scopus-id: 2-s2.0-85092635441
| 39 | 41 |
| 5 | Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma | Coautor: Molina, Bertha, Frias, Sara, Ramos, Sandra, Salas, Consuelo, et al. | 2019 | GENES | WoS-id: 000459743800037
Scopus-id: 2-s2.0-85060618157
| 16 | 23 |
| 6 | Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes | Coautor: Molina, Bertha, Barrientos-Rios, Rehotbevely, Frias, Sara, Velazquez-Aragon, Jose A., et al. | 2019 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000461972100001
Scopus-id: 2-s2.0-85063099458
| 4 | 5 |
| 7 | FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México | Coautor: Molina B., García-de Teresa B., Frias S., Villarreal M.T., et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000476745400049
Scopus-id: 2-s2.0-85067281483
| 7 | 8 |
| 8 | Report of a patient with a de novo non-recurrent duplication of 17p11.2p12 and Yq11 deletion | Coautor: Molina-Álvarez B., Fernández-Hernández L., Navarro-Cobos M.J., Alcántara-Ortigoza M.A., et al. | 2019 | MOLECULAR CYTOGENETICS | WoS-id: 000478685400001
Scopus-id: 2-s2.0-85073890835
| 0 | 0 |
| 9 | Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples | Coautor: Molina, Bertha, Ramos, Sandra, Rodriguez, Rebeca, Castro, Oscar, et al. | 2019 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000498946100009
Scopus-id: 2-s2.0-85074168947
| 2 | 2 |
| 10 | Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics | Coautor: Molina B., Yokoyama E., Del Castillo V., Sánchez S., et al. | 2018 | MOLECULAR CYTOGENETICS | WoS-id: 000431897500002
Scopus-id: 2-s2.0-85046671603
| 5 | 6 |
| 11 | Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy | Coautor: Molina, Bertha, Ramos, Sandra, Navarrete-Meneses, Pilar, Cervantes-Barragan, David E., et al. | 2018 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000447275100008
Scopus-id: 2-s2.0-85052954475
| 12 | 15 |
ID's SCOPUS 