Bertha Molina

565 total citations
37 papers, 327 citations indexed

About

Bertha Molina is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Bertha Molina has authored 37 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Genetics and 11 papers in Plant Science. Recurrent topics in Bertha Molina's work include DNA Repair Mechanisms (18 papers), Genomic variations and chromosomal abnormalities (13 papers) and Prenatal Screening and Diagnostics (9 papers). Bertha Molina is often cited by papers focused on DNA Repair Mechanisms (18 papers), Genomic variations and chromosomal abnormalities (13 papers) and Prenatal Screening and Diagnostics (9 papers). Bertha Molina collaborates with scholars based in Mexico, Spain and United States. Bertha Molina's co-authors include Sara Frı́as, Alessandra Carnevale, Sílvia Sánchez, Emilio Rojas, Victoria del Castillo, Leda Torres, Carmen Esmer, Mario Altamirano‐Lozano, Alfredo Rodríguez and Mahara Valverde and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and International Journal of Molecular Sciences.

In The Last Decade

Bertha Molina

37 papers receiving 306 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bertha Molina Mexico 11 175 133 62 56 45 37 327
Н. П. Кулешов Russia 10 133 0.8× 129 1.0× 97 1.6× 71 1.3× 61 1.4× 17 337
Adrian Flores United States 6 177 1.0× 117 0.9× 237 3.8× 9 0.2× 16 0.4× 7 520
Christopher N. Greene United States 9 277 1.6× 94 0.7× 47 0.8× 6 0.1× 41 0.9× 13 384
Manuela Langbein Germany 5 208 1.2× 62 0.5× 56 0.9× 150 2.7× 72 1.6× 5 414
Andreas Plesch Germany 4 203 1.2× 140 1.1× 139 2.2× 41 0.7× 122 2.7× 7 384
Anna A. Pendina Russia 11 189 1.1× 61 0.5× 63 1.0× 147 2.6× 23 0.5× 40 400
Catherine S. Rodgers United Kingdom 9 145 0.8× 165 1.2× 152 2.5× 40 0.7× 67 1.5× 9 376
Hideaki Chiyo Japan 14 216 1.2× 196 1.5× 22 0.4× 101 1.8× 69 1.5× 24 430
Olga A. Efimova Russia 11 182 1.0× 51 0.4× 62 1.0× 129 2.3× 21 0.5× 39 402

Countries citing papers authored by Bertha Molina

Since Specialization
Citations

This map shows the geographic impact of Bertha Molina's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bertha Molina with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bertha Molina more than expected).

Fields of papers citing papers by Bertha Molina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bertha Molina. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bertha Molina. The network helps show where Bertha Molina may publish in the future.

Co-authorship network of co-authors of Bertha Molina

This figure shows the co-authorship network connecting the top 25 collaborators of Bertha Molina. A scholar is included among the top collaborators of Bertha Molina based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bertha Molina. Bertha Molina is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sánchez, Sílvia, Bertha Molina, Angélica Martínez‐Hernández, et al.. (2023). Frequent copy number variants in a cohort of Mexican-Mestizo individuals. Molecular Cytogenetics. 16(1). 2–2. 5 indexed citations
2.
Molina, Bertha, Sara Frı́as, & Sandra Ramos. (2022). Anemia de Fanconi, Parte 1. Diagnóstico citogenético.. Acta Pediátrica de México. 43(2). 102–102. 2 indexed citations
3.
Villarroel, Camilo E., et al.. (2020). Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review. Molecular Cytogenetics. 13(1). 42–42. 2 indexed citations
4.
Castillo, Victoria del, Sílvia Sánchez, Bertha Molina, et al.. (2018). Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics. Molecular Cytogenetics. 11(1). 30–30. 5 indexed citations
5.
Molina, Bertha, et al.. (2018). Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy. Environmental and Molecular Mutagenesis. 59(8). 755–768. 14 indexed citations
6.
Sánchez, Sílvia, Bertha Molina, Alfredo Rodríguez, et al.. (2017). 7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype. Molecular Cytogenetics. 10(1). 42–42. 3 indexed citations
7.
Aguinaga‐Ríos, Mónica, et al.. (2016). Heterogeneous Diagnoses Underlying Radial Ray Anomalies. The Indian Journal of Pediatrics. 84(3). 200–205. 3 indexed citations
8.
Córdova, Emilio J., Federico Centeno-Cruz, Angélica Martínez‐Hernández, et al.. (2015). NFE2L2Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model. Journal of Toxicology and Environmental Health. 78(10). 628–634. 4 indexed citations
9.
Molina, Bertha, Francesco Marchetti, Leda Torres, et al.. (2015). Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells. Environmental and Molecular Mutagenesis. 56(5). 457–467. 5 indexed citations
10.
Castillo, Victoria del, et al.. (2014). Diagnóstico clínico y de laboratorio de la anemia de Fanconi. Acta Pediátrica de México. 33(1). 38–43. 1 indexed citations
11.
Molina, Bertha, et al.. (2012). Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors. Environmental and Molecular Mutagenesis. 53(4). 271–280. 17 indexed citations
12.
Hinz, John M., et al.. (2008). Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 656(1-2). 1–7. 12 indexed citations
13.
Alcántara‐Ortigoza, Miguel Angel, et al.. (2007). Acrocentric cryptic translocation associated with nondisjunction of chromosome 21. American Journal of Medical Genetics Part A. 146A(1). 97–102. 3 indexed citations
14.
Cervera, M., Sílvia Sánchez, Bertha Molina, et al.. (2005). Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3). American Journal of Medical Genetics Part A. 136A(4). 381–385. 21 indexed citations
15.
Callén, Elsa, Marı́a José Ramı́rez, A. Creus, et al.. (2002). The clastogenic response of the 1q12 heterochromatic region to DNA cross-linking agents is independent of the Fanconi anaemia pathway. Carcinogenesis. 23(8). 1267–1271. 7 indexed citations
16.
Frı́as, Sara, et al.. (2002). Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 520(1-2). 25–37. 14 indexed citations
17.
Altamirano‐Lozano, Mario, et al.. (1999). Genotoxic studies of vanadium pentoxide (V2O5) in male mice. II. Effects in several mouse tissues. Teratogenesis Carcinogenesis and Mutagenesis. 19(4). 243–255. 36 indexed citations
18.
Angel, Ariadna González‐del, et al.. (1997). Chromosome instability with bleomycin and x-ray hypersensitivity in a boy with Nijmegen breakage syndrome. American Journal of Medical Genetics. 70(1). 24–27. 12 indexed citations
19.
Frı́as, Sara, et al.. (1996). Effect of hydroxyurea and normal plasma on DNA synthesis in lymphocytes from Fanconi anemia patients. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 357(1-2). 115–121. 10 indexed citations
20.
Carnevale, Alessandra, et al.. (1991). [Effect of gamma radiations on robertsonian translocations].. PubMed. 43(2). 151–6. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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