Marco A. Zago

10.6k total citations
208 papers, 6.9k citations indexed

About

Marco A. Zago is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Marco A. Zago has authored 208 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Hematology, 69 papers in Molecular Biology and 55 papers in Genetics. Recurrent topics in Marco A. Zago's work include Hemoglobinopathies and Related Disorders (32 papers), Forensic and Genetic Research (30 papers) and Iron Metabolism and Disorders (28 papers). Marco A. Zago is often cited by papers focused on Hemoglobinopathies and Related Disorders (32 papers), Forensic and Genetic Research (30 papers) and Iron Metabolism and Disorders (28 papers). Marco A. Zago collaborates with scholars based in Brazil, United States and France. Marco A. Zago's co-authors include Wilson A. Silva, Rodrigo Alexandre Panepucci, Dimas Tadeu Covas, Rendrik F. Franco, Roberto Passetto Falcão, Ândrea Ribeiro‐dos‐Santos, Rodrigo Proto‐Siqueira, Sidney Emanuel Batista dos Santos, Luciano Neder and Maristela Delgado Orellana and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Marco A. Zago

202 papers receiving 6.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marco A. Zago Brazil 43 2.3k 1.8k 1.6k 1.4k 1.1k 208 6.9k
Lambert Busque Canada 35 2.0k 0.9× 1.8k 1.0× 2.9k 1.8× 930 0.7× 927 0.9× 149 5.8k
Leanne M. Wiedemann United Kingdom 41 4.4k 1.9× 2.0k 1.1× 3.3k 2.0× 884 0.7× 1.4k 1.3× 81 8.8k
Esmail D. Zanjani United States 47 3.1k 1.3× 3.1k 1.7× 3.2k 2.0× 1.2k 0.9× 1.6k 1.5× 186 8.7k
Annelies de Klein Netherlands 52 5.2k 2.2× 2.5k 1.4× 3.3k 2.1× 1.3k 0.9× 1.2k 1.1× 219 11.5k
Andreas E. Kulozik Germany 54 6.4k 2.8× 2.0k 1.1× 1.5k 0.9× 772 0.6× 659 0.6× 230 10.2k
Claude Férec France 55 3.9k 1.7× 1.8k 1.0× 2.1k 1.3× 2.8k 2.1× 558 0.5× 445 11.8k
Wilson A. Silva Brazil 41 2.8k 1.2× 1.1k 0.6× 487 0.3× 929 0.7× 953 0.9× 273 6.4k
Charles E. Hart United States 40 2.7k 1.2× 544 0.3× 946 0.6× 469 0.3× 973 0.9× 71 6.9k
Warren G. Sanger United States 40 1.4k 0.6× 1.3k 0.7× 501 0.3× 679 0.5× 892 0.8× 196 5.7k
Kenneth I. Weinberg United States 51 3.9k 1.7× 1.2k 0.7× 2.1k 1.3× 1.7k 1.3× 4.1k 3.9× 180 10.8k

Countries citing papers authored by Marco A. Zago

Since Specialization
Citations

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

Fields of papers citing papers by Marco A. Zago

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marco A. Zago. 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 Marco A. Zago. The network helps show where Marco A. Zago may publish in the future.

Co-authorship network of co-authors of Marco A. Zago

This figure shows the co-authorship network connecting the top 25 collaborators of Marco A. Zago. A scholar is included among the top collaborators of Marco A. Zago 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 Marco A. Zago. Marco A. Zago 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.
Mascarello, Giulia, et al.. (2025). Integrating ethical assessment and media content analysis to explore social conflicts over large carnivores. Biological Conservation. 310. 111342–111342.
2.
Fontes, Aparecida Maria, K. Abraham, Maristela Delgado Orellana, et al.. (2017). Expression differences of genes in the PI3K/AKT, WNT/b-catenin, SHH, NOTCH and MAPK signaling pathways in CD34+ hematopoietic cells obtained from chronic phase patients with chronic myeloid leukemia and from healthy controls. Clinical & Translational Oncology. 20(4). 542–549. 15 indexed citations
3.
Toledo, Sílvia Regina Caminada de, Reynaldo Jesús-García, Antônio Sérgio Petrilli, et al.. (2011). Insights on PRAME and osteosarcoma by means of gene expression profiling. Journal of Orthopaedic Science. 16(4). 458–466. 14 indexed citations
4.
Panepucci, Rodrigo Alexandre, Felipe Saldanha‐Araújo, Wilson A. Silva, et al.. (2011). Association study between SNPS in genes related to adenosine signaling and distinct clinical manifestations in sickle cell disease. Haematologica. 96. 173. 1 indexed citations
5.
Calado, Rodrigo T., Joshua A. Regal, Mark Hills, et al.. (2009). Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proceedings of the National Academy of Sciences. 106(4). 1187–1192. 125 indexed citations
6.
Peria, Fernanda Maris, Luciano Neder, Suely Kazue Nagahashi Marie, et al.. (2007). Pleiotrophin expression in astrocytic and oligodendroglial tumors and it’s correlation with histological diagnosis, microvascular density, cellular proliferation and overall survival. Journal of Neuro-Oncology. 84(3). 255–261. 17 indexed citations
7.
Petrilli, Antônio Sérgio, et al.. (2007). TNF-alpha, TNF-beta, IL-6, IL-10, PECAM-1 and the MPO Inflammatory Gene Polymorphisms in Osteosarcoma. Journal of Pediatric Hematology/Oncology. 29(5). 293–297. 24 indexed citations
8.
Pintão, Maria Carolina Tostes, Amélia G. Araújo, Vânia M. Morelli, et al.. (2003). Factor XIII gene variation and the risk of venous thrombosis.. Blood. 102(11). 1 indexed citations
9.
Araújo, Aderson S., et al.. (2003). A Different Molecular Pattern of β‐Thalassemia Mutations in Northeast Brazil. Hemoglobin. 27(4). 211–217. 22 indexed citations
10.
Tsuneto, Luiza Tamie, Christian Probst, Mara Helena Hutz, et al.. (2003). HLA class II diversity in seven Amerindian populations. Clues about the origins of the Aché. Tissue Antigens. 62(6). 512–526. 82 indexed citations
11.
Franco, Rendrik F., et al.. (2002). The prevalence of the MTHFR C677T polymorphism in patients with preeclampsia. The Hematology Journal. 3.
12.
Silva, Wilson A., Sandro L. Bonatto, Ândrea Ribeiro‐dos‐Santos, et al.. (2002). Mitochondrial Genome Diversity of Native Americans Supports a Single Early Entry of Founder Populations into America. The American Journal of Human Genetics. 71(1). 187–192. 81 indexed citations
13.
Zago, Marco A., Wilson A. Silva, & Rendrik F. Franco. (1999). Hemoglobinopathies and other hereditary hematological diseases in the Brazilian population. Ciência e Cultura. 51. 226–234. 7 indexed citations
14.
Vallinoto, Antônio Carlos Rosário, et al.. (1998). D1S80 polymorphism in Amerindians from the Amazon region of Brazil.. PubMed. 70(3). 507–16. 10 indexed citations
15.
Franco, Rendrik F., et al.. (1996). Factor viii gene polymorphisms in amerindians from the brazilian amazon region. 19(2). 351–354. 5 indexed citations
16.
Zago, Marco A., et al.. (1993). Molecular genetics and anthropology: genes, races and diseases. Ciencia e cultura. 45. 249–257. 5 indexed citations
17.
Bernardi, Francesco, et al.. (1992). A novel deletion of FVIII gene associated with variable levels of FVIII inhibitor*. European Journal Of Haematology. 48(3). 152–154. 5 indexed citations
18.
Zago, Marco A.. (1987). [Hemoglobinopathies: prevalence and variability].. PubMed. 104(6). 300–4. 3 indexed citations
19.
Zago, Marco A.. (1986). Hemoglobinopatias: prevalencia e variabilidade. 104. 4 indexed citations
20.
Zago, Marco A., Fernando Ferreira Costa, Luíz Gonzaga Tone, & C Bottura. (1983). Hereditary Hemoglobin Disorders in a Brazilian Population. Human Heredity. 33(2). 125–129. 30 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 Lambert Busque Breakdown of academic impact, for papers by Leanne M. Wiedemann Breakdown of academic impact, for papers by Esmail D. Zanjani Breakdown of academic impact, for papers by Annelies de Klein Breakdown of academic impact, for papers by Andreas E. Kulozik Breakdown of academic impact, for papers by Claude Férec Breakdown of academic impact, for papers by Wilson A. Silva Breakdown of academic impact, for papers by Charles E. Hart Breakdown of academic impact, for papers by Warren G. Sanger Breakdown of academic impact, for papers by Kenneth I. Weinberg
Rankless by CCL
2026