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Bertha Molina

DEB test for Fanconi anemia detection in patients with atypical phenotypes
2003 · Carmen Esmer, Silvia Sánchez, et al. · American Journal of Medical Genetics Part A · 128
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia
2020 · Alfredo Rodríguez, Kaiyang Zhang, et al. · Cell stem cell · 65
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A Boolean network model of the FA/BRCA pathway
2012 · Alfredo Rodríguez, David Sosa, et al. · Bioinformatics · 49
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Genotoxic studies of vanadium pentoxide (V2O5) in male mice. II. Effects in several mouse tissues
1999 · Mario Altamirano-Lozano, Mahara Valverde, et al. · Teratogenesis Carcinogenesis and Mutagenesis · 48
Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma
2019 · Sara Frias, Sandra Ramos, et al. · Genes · 29
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Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3)
2005 · M. Cervera, S. Sánchez, et al. · American Journal of Medical Genetics Part A · 26
Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors
2012 · C. Salas, A. Niembro, et al. · Environmental and Molecular Mutagenesis · 22
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Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy
2018 · Sandra Ramos, Pilar Navarrete‐Meneses, et al. · Environmental and Molecular Mutagenesis · 20
Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring
2002 · Sara Frias, Sandra Ramos, et al. · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · 16
Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment
2008 · Angélica Martinez, John M. Hinz, et al. · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · 15
Trisomy 9 mosaicism in a girl with multiple malformations.
1990 · L Diaz-Mares, B Molina, et al. · PubMed · 14
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG
2022 · Pedro Reyes, Benilde García-deTeresa, et al. · International Journal of Molecular Sciences · 13
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Chromosome instability with bleomycin and x-ray hypersensitivity in a boy with Nijmegen breakage syndrome
1997 · Patricia Pérez-Vera, Ariadna González-del Angel, et al. · American Journal of Medical Genetics · 13
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México
2019 · Benilde García‐de Teresa, Sara Frias, et al. · Molecular Genetics & Genomic Medicine · 11
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Effect of hydroxyurea and normal plasma on DNA synthesis in lymphocytes from Fanconi anemia patients
1996 · Sara Frias, Laura Gómez, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 11
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes
2019 · Rehotbevely Barrientos-Rios, Sara Frias, et al. · Gynecological Endocrinology · 8
Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in F anconi anemia cells
2015 · Bertha Molina, Francesco Marchetti, et al. · Environmental and Molecular Mutagenesis · 8
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Detection of short-term chromosomal damage due to therapeutic 131I exposure in patients with thyroid cancer.
2010 · Angélica Hernández-Jardines, Bertha Molina, et al. · PubMed · 8
Acrocentric cryptic translocation associated with nondisjunction of chromosome 21
2007 · Sandra Ramos, Miguel Angel Alcántara, et al. · American Journal of Medical Genetics Part A · 8
The clastogenic response of the 1q12 heterochromatic region to DNA cross-linking agents is independent of the Fanconi anaemia pathway
2002 · E. Callén, M.J. Ramírez, et al. · Carcinogenesis · 8
Frequent copy number variants in a cohort of Mexican-Mestizo individuals
2023 · Silvia Sánchez, Ulises Juárez, et al. · Molecular Cytogenetics · 6
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Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics
2018 · Emiy Yokoyama, Victoria Del Castillo, et al. · Molecular Cytogenetics · 6
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Anemia de Fanconi, Parte 1. Diagnóstico citogenético.
2022 · Bertha Molina, Sara Frías, et al. · Acta Pediátrica de México · 5
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Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples
2019 · Sandra Ramos, Rebeca Rodríguez, et al. · International Journal of Molecular Sciences · 5
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Heterogeneous Diagnoses Underlying Radial Ray Anomalies
2016 · Rosalba Sevilla-Montoya, Mónica Aguinaga, et al. · The Indian Journal of Pediatrics · 5
Works count: 53
Citation count: 581
H-index: 13
I10-index: 15
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