Melva Gutiérrez‐Angulo

616 total citations
46 papers, 392 citations indexed

About

Melva Gutiérrez‐Angulo is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Melva Gutiérrez‐Angulo has authored 46 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 17 papers in Pathology and Forensic Medicine and 12 papers in Genetics. Recurrent topics in Melva Gutiérrez‐Angulo's work include Genetic factors in colorectal cancer (14 papers), Genomic variations and chromosomal abnormalities (9 papers) and DNA Repair Mechanisms (8 papers). Melva Gutiérrez‐Angulo is often cited by papers focused on Genetic factors in colorectal cancer (14 papers), Genomic variations and chromosomal abnormalities (9 papers) and DNA Repair Mechanisms (8 papers). Melva Gutiérrez‐Angulo collaborates with scholars based in Mexico, United States and Spain. Melva Gutiérrez‐Angulo's co-authors include Jorge Peregrina-Sandoval, Jorge Durán-González, Juan Manuel Guzmán‐Flores, Fernando Martínez–Esquivias, Alejandro Pérez‐Larios, Jorge Alberto Sánchez-Burgos, Horacio Rivera, Patricio Barros‐Núñez, Christopher E. Mason and Matthew W. State and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of Clinical Pathology.

In The Last Decade

Melva Gutiérrez‐Angulo

44 papers receiving 391 citations

Peers

Melva Gutiérrez‐Angulo

ONCOL

GENET

PFM

Dangxiao Cheng Canada

Wojciech Barczak Poland

Xiaopeng Zhao China

Takamitsu Iwata Japan

Xiaoming Zeng China

Sang D. Park South Korea

R. Laherty Australia

Alberto Schanaider Brazil

Gang Yao China

Fabiana Vaccina Italy

Dangxiao Cheng Canada

Melva Gutiérrez‐Angulo

318 ×1.8

195 ×1.7

ONCOL

66 ×0.7

GENET

105 ×1.3

75 ×1.1

PFM

Citations per year, relative to Melva Gutiérrez‐Angulo Melva Gutiérrez‐Angulo (= 1×) peers Dangxiao Cheng

Countries citing papers authored by Melva Gutiérrez‐Angulo

Since Specialization

Citations

This map shows the geographic impact of Melva Gutiérrez‐Angulo'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 Melva Gutiérrez‐Angulo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melva Gutiérrez‐Angulo more than expected).

Fields of papers citing papers by Melva Gutiérrez‐Angulo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Melva Gutiérrez‐Angulo. 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 Melva Gutiérrez‐Angulo. The network helps show where Melva Gutiérrez‐Angulo may publish in the future.

Co-authorship network of co-authors of Melva Gutiérrez‐Angulo

This figure shows the co-authorship network connecting the top 25 collaborators of Melva Gutiérrez‐Angulo. A scholar is included among the top collaborators of Melva Gutiérrez‐Angulo 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 Melva Gutiérrez‐Angulo. Melva Gutiérrez‐Angulo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Gutiérrez‐Angulo, Melva, et al.. (2025). MLH1 Methylation Status and Microsatellite Instability in Patients with Colorectal Cancer. Genes. 16(2). 182–182. 4 indexed citations

Gutiérrez‐Angulo, Melva, et al.. (2024). In Silico Analysis of the Missense Variants of Uncertain Significance of CTNNB1 Gene Reported in GnomAD Database. Genes. 15(8). 972–972.

Gutiérrez‐Angulo, Melva, et al.. (2023). Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteria. Hereditary Cancer in Clinical Practice. 21(1). 21–21. 3 indexed citations

Gutiérrez‐Angulo, Melva, et al.. (2023). Microbiota composition and its impact on DNA methylation in colorectal cancer. Frontiers in Genetics. 14. 1037406–1037406. 20 indexed citations

Ramírez‐García, Sergio A., et al.. (2023). Epidemiology of environmental factors related to beta-catenin pathway and its impact on the development and progression of colorectal cancer. Gaceta Médica de México. 159(3). 240–246. 1 indexed citations

Martínez–Esquivias, Fernando, et al.. (2022). Bioinformatic Analysis of the Effect of Silver Nanoparticles on Colorectal Cancer Cell Line. BioMed Research International. 2022(1). 6828837–6828837. 10 indexed citations

Martínez–Esquivias, Fernando, et al.. (2021). Anticancer Activity of Selenium Nanoparticles In Vitro Studies. Anti-Cancer Agents in Medicinal Chemistry. 22(9). 1658–1673. 36 indexed citations

Gutiérrez‐Angulo, Melva, et al.. (2019). ADIPOQ rs2241766 SNP as protective marker against DIBC development in Mexican population. PLoS ONE. 14(3). e0214080–e0214080. 11 indexed citations

Gutiérrez‐Angulo, Melva, et al.. (2015). Analysis of ERCC1 and ERCC2 gene variants in osteosarcoma, colorectal and breast cancer. Oncology Letters. 9(4). 1657–1661. 12 indexed citations

10.

Peregrina-Sandoval, Jorge, et al.. (2015). RUNX3 gene polymorphisms and haplotypes in Mexican patients with colorectal cancer. Genetics and Molecular Research. 14(4). 15505–15510. 4 indexed citations

11.

Gutiérrez‐Angulo, Melva, et al.. (2015). Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population. Familial Cancer. 14(3). 349–354. 16 indexed citations

12.

Gutiérrez‐Angulo, Melva, et al.. (2014). Association of MMP7-181A/G and MMP13-77A/G polymorphisms with colorectal cancer in a Mexican population. Genetics and Molecular Research. 13(2). 3537–3544. 13 indexed citations

13.

Gutiérrez‐Angulo, Melva, et al.. (2012). 46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report. Journal of Medical Case Reports. 6(1). 301–301. 4 indexed citations

14.

Gutiérrez‐Angulo, Melva, et al.. (2009). XRCC1 polymorphisms and haplotypes in Mexican patients with acute lymphoblastic leukemia. Genetics and Molecular Research. 8(4). 1451–1458. 29 indexed citations

15.

Gutiérrez‐Angulo, Melva, et al.. (2008). MDR1 C3435T Polymorphism in Mexican Children with Acute Lymphoblastic Leukemia and in Healthy Individuals. Human Biology. 80(4). 449–455. 21 indexed citations

16.

Durán-González, Jorge, et al.. (2007). Ade novo interstitial 6q deletion in a boy with a split hand malformation. Journal of Applied Genetics. 48(4). 405–407. 8 indexed citations

17.

Gutiérrez‐Angulo, Melva, et al.. (2005). A complex translocation (9;22;16)(q34;q11.2;p13) in chronic myelocytic leukemia. Cancer Genetics and Cytogenetics. 157(2). 175–177. 8 indexed citations

18.

Bohlander, Stefan K., et al.. (2004). A t(1;9)(q23.3∼q25;q34) affecting the ABL1 gene in a biphenotypic leukemia. Cancer Genetics and Cytogenetics. 152(1). 81–83. 3 indexed citations

19.

Gutiérrez‐Angulo, Melva, et al.. (2002). del(X)(p22.1)/r(X)(p22.1q28) dynamic mosaicism in a Turner syndrome patient. Annales de Génétique. 45(1). 17–20. 3 indexed citations

20.

Gutiérrez‐Angulo, Melva, et al.. (1999). An extra idic(21)(q22.1) in a child with some features of Down’s syndrome. Clinical Genetics. 55(3). 203–206. 7 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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