Marcos Bezerra

6.4k total citations
32 papers, 662 citations indexed

About

Marcos Bezerra is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Marcos Bezerra has authored 32 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 20 papers in Hematology and 11 papers in Molecular Biology. Recurrent topics in Marcos Bezerra's work include Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (15 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (5 papers). Marcos Bezerra is often cited by papers focused on Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (15 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (5 papers). Marcos Bezerra collaborates with scholars based in Brazil, United States and Netherlands. Marcos Bezerra's co-authors include Aderson S. Araújo, Fernando Ferreira Costa, Vijay G. Sankaran, David Schlessinger, Manuela Uda, Guillaume Lettre, Stuart H. Orkin, Antonio Cao, Serena Sanna and Joel N. Hirschhorn and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Molecules.

In The Last Decade

Marcos Bezerra

30 papers receiving 655 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marcos Bezerra Brazil	10	531	393	231	161	66	32	662
Helen Rooks United Kingdom	14	818 1.5×	615 1.6×	388 1.7×	313 1.9×	88 1.3×	20	995
M Patterson Canada	12	359 0.7×	262 0.7×	148 0.6×	90 0.6×	163 2.5×	27	505
Shi‐Ping Cai United States	11	614 1.2×	422 1.1×	287 1.2×	175 1.1×	89 1.3×	19	835
Mary Link United States	4	309 0.6×	232 0.6×	101 0.4×	178 1.1×	31 0.5×	8	445
Magnun Nueldo Nunes Santos Brazil	11	266 0.5×	192 0.5×	76 0.3×	66 0.4×	42 0.6×	41	341
Thongperm Munkongdee Thailand	16	582 1.1×	481 1.2×	126 0.5×	164 1.0×	81 1.2×	27	675
AE Kulozik United Kingdom	9	465 0.9×	367 0.9×	149 0.6×	100 0.6×	43 0.7×	12	566
Elizabeth R. Macari United States	8	174 0.3×	105 0.3×	217 0.9×	43 0.3×	83 1.3×	15	434
Rosalba Di Marzo Italy	10	251 0.5×	167 0.4×	146 0.6×	66 0.4×	34 0.5×	23	365
John G. Gilman United States	11	251 0.5×	151 0.4×	169 0.7×	64 0.4×	109 1.7×	21	464

Countries citing papers authored by Marcos Bezerra

Since Specialization

Citations

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

Fields of papers citing papers by Marcos Bezerra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcos Bezerra

This figure shows the co-authorship network connecting the top 25 collaborators of Marcos Bezerra. A scholar is included among the top collaborators of Marcos Bezerra 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 Marcos Bezerra. Marcos Bezerra 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

Pereira‐Martins, Diego A., et al.. (2025). Unraveling the multifaceted roles of peroxiredoxins in sickle cell anemia: implications in redox and inflammation adaptations. Annals of Hematology. 104(4). 2265–2277.

Lucena‐Araujo, Antonio R., et al.. (2023). Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia. Molecular Biology Reports. 50(4). 3341–3353. 3 indexed citations

Bezerra, Matheus Filgueira, Isabel Weinhäuser, Felipe Saldanha‐Araújo, et al.. (2023). Prognostic implications of the ID1 expression in acute myeloid leukemia patients treated in a resource-constrained setting. Hematology Transfusion and Cell Therapy. 46(3). 250–255.

Bezerra, Matheus Filgueira, Isabel Weinhäuser, Fernando Ferreira Costa, et al.. (2021). Screening for myeloid mutations in patients with myelodysplastic syndromes and AML with myelodysplasia-related changes. Hematology Transfusion and Cell Therapy. 44(3). 328–331. 2 indexed citations

Pereira‐Martins, Diego A., Juan Luiz Coelho‐Silva, Isabel Weinhäuser, et al.. (2021). The ratio of ATP11C/PLSCR1 mRNA transcripts has clinical significance in sickle cell anemia. Annals of Hematology. 101(2). 281–287. 2 indexed citations

Hounkpe, Bidossessi Wilfried, Antonio R. Lucena‐Araujo, Marcos Bezerra, et al.. (2021). Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients. Annals of Hematology. 100(11). 2669–2676. 6 indexed citations

Moura, Patrícia, et al.. (2020). LGALS3 +191A and +292C polymorphisms are associated with a reduction in serum gal-3 levels, but not with the clinical events of individuals with sickle cell anemia. Research Society and Development. 9(9). e442997314–e442997314. 2 indexed citations

Moura, Patrícia, et al.. (2020). MBL2 gene polymorphisms are not related to the occurrence of cerebrovascular disease in sickle cell anemia. Research Society and Development. 9(7). e439974240–e439974240. 1 indexed citations

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

10.

Pereira‐Martins, Diego A., John Brewin, Kate Gardner, et al.. (2020). Evaluation of oxidative stress-related genetic variants for predicting stroke in patients with sickle cell anemia. Journal of the Neurological Sciences. 414. 116839–116839. 8 indexed citations

11.

Albuquerque, Dulcinéia Martins de, Marcos Bezerra, Aderson S. Araújo, et al.. (2020). Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphisms and Markers of Hemolysis, Inflammation and Endothelial Dysfunction in Brazilian Sickle Cell Anemia Patients. Biochemical Genetics. 58(4). 580–594. 4 indexed citations

12.

Nagamatsu, Sheila T., Marcos Bezerra, Diego A. Pereira‐Martins, et al.. (2018). Global analysis of erythroid cells redox status reveals the involvement of Prdx1 and Prdx2 in the severity of beta thalassemia. PLoS ONE. 13(12). e0208316–e0208316. 21 indexed citations

13.

Vasconcelos, Luydson Richardson Silva, et al.. (2018). Association of the SOD2 polymorphism (Val6Ala) and SOD activity with vaso-occlusive crisis and acute splenic sequestration in children with sickle cell anemia. Mediterranean Journal of Hematology and Infectious Diseases. 10(1). e2018012–e2018012. 8 indexed citations

14.

Lucena‐Araujo, Antonio R., et al.. (2014). Mannose-binding lectin 2 (MBL2) gene polymorphisms do not influence frequency of infections in chronic lymphocytic leukemia patients. Revista Brasileira de Hematologia e Hemoterapia. 36(1). 29–34. 4 indexed citations

15.

Cunha, Anderson Ferreira da, Magnun Nueldo Nunes Santos, Dulcinéia Martins de Albuquerque, et al.. (2014). Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia. Annals of Hematology. 93(7). 1123–1129. 26 indexed citations

16.

Samico, Isabella, et al.. (2014). Follow-up of children with hemoglobinopathies diagnosed by the Brazilian Neonatal Screening Program in the State of Pernambuco. Revista Brasileira de Hematologia e Hemoterapia. 36(4). 250–255. 2 indexed citations

17.

Garrido, Vanessa T., Venina Marcela Dominical, Fabı́ola Traina, et al.. (2012). Elevated plasma levels and platelet‐associated expression of the pro‐thrombotic and pro‐inflammatory protein, T NFSF14 (LIGHT), in sickle cell disease. British Journal of Haematology. 158(6). 788–797. 25 indexed citations

18.

Lanaro, Carolina, Dulcinéia Martins de Albuquerque, Magnun Nueldo Nunes Santos, et al.. (2012). Expression profiles of phosphatidylinositol phosphate kinase genes during normal human in vitro erythropoiesis. Genetics and Molecular Research. 11(4). 3861–3868. 3 indexed citations

19.

Vasconcelos, Luydson Richardson Silva, Leila Maria Moreira Beltrão Pereira, Patrícia Moura, et al.. (2010). Association of variant alleles of MBL2 gene with vasoocclusive crisis in children with sickle cell anemia. Blood Cells Molecules and Diseases. 44(4). 224–228. 22 indexed citations

20.

Vasconcelos, Luydson Richardson Silva, Patrícia Moura, Marcos Bezerra, et al.. (2009). Association of the <i>MBL2</i> Gene EXON1 Polymorphism and Vasoocclusive Crisis in Patients with Sickle Cell Anemia. Acta Haematologica. 121(4). 212–215. 15 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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