Edis Belini

433 total citations
22 papers, 330 citations indexed

About

Edis Belini is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Edis Belini has authored 22 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Hematology and 7 papers in Molecular Biology. Recurrent topics in Edis Belini's work include Hemoglobinopathies and Related Disorders (19 papers), Iron Metabolism and Disorders (15 papers) and Folate and B Vitamins Research (5 papers). Edis Belini is often cited by papers focused on Hemoglobinopathies and Related Disorders (19 papers), Iron Metabolism and Disorders (15 papers) and Folate and B Vitamins Research (5 papers). Edis Belini collaborates with scholars based in Brazil. Edis Belini's co-authors include Cláudia R. Bonini-Domingos, Danilo Grünig Humberto da Silva, Eduardo Alves de Almeida, Lidiane S. Torres, Clarisse Lopes de Castro Lobo, Rodolfo Delfini Cançado, Clarisse Lobo, Milton Artur Ruiz, Sônia Maria Oliani and Carlos Chiattone and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Free Radical Biology and Medicine.

In The Last Decade

Edis Belini

19 papers receiving 319 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edis Belini Brazil 10 246 181 95 70 47 22 330
H. P. Pati India 10 114 0.5× 165 0.9× 22 0.2× 43 0.6× 15 0.3× 44 249
Manit Nuinoon Thailand 9 168 0.7× 135 0.7× 70 0.7× 30 0.4× 7 0.1× 24 301
Julien Perrin France 9 44 0.2× 60 0.3× 66 0.7× 41 0.6× 15 0.3× 33 239
Reza Alibakhshi Iran 10 86 0.3× 75 0.4× 98 1.0× 14 0.2× 25 0.5× 47 326
Lisa Traeger Germany 9 61 0.2× 97 0.5× 71 0.7× 21 0.3× 19 0.4× 16 267
Terrence Tan Australia 8 63 0.3× 100 0.6× 37 0.4× 19 0.3× 18 0.4× 10 355
H. T. Hassan Germany 9 47 0.2× 155 0.9× 126 1.3× 23 0.3× 17 0.4× 26 344
Huisman Th Netherlands 8 351 1.4× 255 1.4× 72 0.8× 103 1.5× 16 0.3× 25 487
K. Sigvard Olsson Sweden 12 203 0.8× 336 1.9× 30 0.3× 18 0.3× 51 1.1× 20 434
Francesca Granata Italy 11 40 0.2× 43 0.2× 232 2.4× 29 0.4× 59 1.3× 32 320

Countries citing papers authored by Edis Belini

Since Specialization
Citations

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

Fields of papers citing papers by Edis Belini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edis Belini. 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 Edis Belini. The network helps show where Edis Belini may publish in the future.

Co-authorship network of co-authors of Edis Belini

This figure shows the co-authorship network connecting the top 25 collaborators of Edis Belini. A scholar is included among the top collaborators of Edis Belini 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 Edis Belini. Edis Belini 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.
Marquès, Bernard, et al.. (2025). Knowledge about globin genetics for precision diagnosis of hemoglobinopathies: A case Study. Clinical Biochemistry. 136. 110901–110901.
2.
Belini, Edis, et al.. (2023). Papel do profissional de enfermagem no teste do pezinho no Programa Nacional de Triagem Neonatal: uma revisão integrativa. Brazilian Journal of Health Review. 6(4). 15167–15184.
3.
Pereira‐Martins, Diego A., Edis Belini, Juan Luiz Coelho‐Silva, et al.. (2020). Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia. Hematology Transfusion and Cell Therapy. 43(3). 243–248. 3 indexed citations
4.
Silva, Danilo Grünig Humberto da, et al.. (2019). Atypical β-S haplotypes: classification and genetic modulation in patients with sickle cell anemia. Journal of Human Genetics. 64(3). 239–248. 7 indexed citations
5.
Belini, Edis, et al.. (2018). The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients. Archives of Endocrinology and Metabolism. 62(1). 21–26. 18 indexed citations
6.
Silva, Danilo Grünig Humberto da, Edis Belini, Lidiane S. Torres, et al.. (2017). Impact of genetic polymorphisms in key enzymes of homocysteine metabolism on the pathophysiology of sickle cell anemia. Free Radical Biology and Medicine. 106. 53–61. 6 indexed citations
7.
Torres, Lidiane S., et al.. (2016). Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein. PLoS ONE. 11(11). e0165833–e0165833. 22 indexed citations
8.
Torres, Lidiane S., et al.. (2016). Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab. Hemoglobin. 40(5). 356–358. 6 indexed citations
9.
Torres, Lidiane S., Danilo Grünig Humberto da Silva, Edis Belini, et al.. (2016). Plasma levels of TGF-β1 in homeostasis of the inflammation in sickle cell disease. Cytokine. 80. 18–25. 11 indexed citations
10.
Silva, Danilo Grünig Humberto da, et al.. (2016). Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide. Journal of Human Genetics. 61(7). 605–611. 6 indexed citations
11.
Silva, Danilo Grünig Humberto da, et al.. (2016). Hemoglobin (Hb) Val de Marne (Hb Footscray) in Brazil: the first case report. Genetics and Molecular Research. 15(2).
12.
Silva, Danilo Grünig Humberto da, Edis Belini, Lidiane S. Torres, et al.. (2013). Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia. BMC Medical Genetics. 14(1). 108–108. 20 indexed citations
13.
Torres, Lidiane S., Edis Belini, Danilo Grünig Humberto da Silva, et al.. (2013). Frequencies of -308G/A (TNFA) and -509C/T (TGFB1) polymorphisms in sickle cell anemia patients from Brazil. Genetics and Molecular Research. 12(4). 6762–6766. 3 indexed citations
14.
Silva, Danilo Grünig Humberto da, Edis Belini, Eduardo Alves de Almeida, & Cláudia R. Bonini-Domingos. (2013). Oxidative stress in sickle cell disease: An overview of erythrocyte redox metabolism and current antioxidant therapeutic strategies. Free Radical Biology and Medicine. 65. 1101–1109. 90 indexed citations
15.
Belini, Edis, et al.. (2012). Comet Assay as a technique to evaluate DNA damage in sickle cell anemia patients. SHILAP Revista de lepidopterología. 34(1). 68–68. 1 indexed citations
16.
Torres, Lidiane S., Danilo Grünig Humberto da Silva, Edis Belini, et al.. (2012). The influence of hydroxyurea on oxidative stress in sickle cell anemia. SHILAP Revista de lepidopterología. 34(6). 421–425. 27 indexed citations
17.
Silva, Danilo Grünig Humberto da, Edis Belini, Lidiane S. Torres, et al.. (2011). Relationship between oxidative stress, glutathione S-transferase polymorphisms and hydroxyurea treatment in sickle cell anemia. Blood Cells Molecules and Diseases. 47(1). 23–28. 43 indexed citations
18.
Belini, Edis, Danilo Grünig Humberto da Silva, Lidiane S. Torres, et al.. (2011). Oxidative stress and antioxidant capacity in sickle cell anaemia patients receiving different treatments and medications for different periods of time. Annals of Hematology. 91(4). 479–489. 24 indexed citations
19.
Silva, Danilo Grünig Humberto da, et al.. (2010). Serum melatonin level and oxidative stress in sickle cell anemia. Blood Cells Molecules and Diseases. 45(4). 297–301. 15 indexed citations
20.
Belini, Edis, Rodolfo Delfini Cançado, & Cláudia R. Bonini-Domingos. (2010). The XmnI polymorphic site 5’ to the gene Gγ in a Brazilian patient with sickle cell anaemia – fetal haemoglobin concentration, haematology and clinical features. Archives of Medical Science. 5(5). 822–825. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by H. P. Pati Breakdown of academic impact, for papers by Manit Nuinoon Breakdown of academic impact, for papers by Julien Perrin Breakdown of academic impact, for papers by Reza Alibakhshi Breakdown of academic impact, for papers by Lisa Traeger Breakdown of academic impact, for papers by Terrence Tan Breakdown of academic impact, for papers by H. T. Hassan Breakdown of academic impact, for papers by Huisman Th Breakdown of academic impact, for papers by K. Sigvard Olsson Breakdown of academic impact, for papers by Francesca Granata
Rankless by CCL
2026