Celeste Bento

2.2k total citations
46 papers, 777 citations indexed

About

Celeste Bento is a scholar working on Genetics, Genetics and Physiology. According to data from OpenAlex, Celeste Bento has authored 46 papers receiving a total of 777 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 17 papers in Genetics and 15 papers in Physiology. Recurrent topics in Celeste Bento's work include Hemoglobinopathies and Related Disorders (25 papers), Erythrocyte Function and Pathophysiology (15 papers) and Iron Metabolism and Disorders (10 papers). Celeste Bento is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Erythrocyte Function and Pathophysiology (15 papers) and Iron Metabolism and Disorders (10 papers). Celeste Bento collaborates with scholars based in Portugal, United Kingdom and Spain. Celeste Bento's co-authors include Assunção Ataíde, Carla Marques, Astrid M. Vicente, Letícia Ribeiro, Catarina Correia, Guiomar Oliveira, Teresa S. Miguel, Constantin Fesel, Licínio Manco and Mary Frances McMullin and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Molecular Psychiatry.

In The Last Decade

Celeste Bento

45 papers receiving 763 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Celeste Bento Portugal 16 291 279 234 183 178 46 777
Chantal Thys Belgium 19 166 0.6× 194 0.7× 37 0.2× 501 2.7× 332 1.9× 45 1.1k
Richard Ziegler United States 14 124 0.4× 105 0.4× 46 0.2× 82 0.4× 664 3.7× 29 1.2k
June Allison United States 5 225 0.8× 71 0.3× 37 0.2× 223 1.2× 257 1.4× 9 832
Fabiola Quintero‐Rivera United States 16 96 0.3× 907 3.3× 83 0.4× 65 0.4× 634 3.6× 54 1.4k
F. George Otieno United States 12 96 0.3× 628 2.3× 37 0.2× 28 0.2× 307 1.7× 14 966
Hélène Bruyèrè Canada 17 164 0.6× 401 1.4× 44 0.2× 306 1.7× 462 2.6× 44 1.0k
Wang Ch Taiwan 9 57 0.2× 308 1.1× 232 1.0× 32 0.2× 420 2.4× 41 767
Zuo Luan China 15 161 0.6× 33 0.1× 28 0.1× 83 0.5× 192 1.1× 55 598
Rachel Kuperman United States 13 120 0.4× 106 0.4× 259 1.1× 11 0.1× 283 1.6× 21 1.3k
Keith Nykamp United States 18 75 0.3× 617 2.2× 60 0.3× 17 0.1× 582 3.3× 42 1.4k

Countries citing papers authored by Celeste Bento

Since Specialization
Citations

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

Fields of papers citing papers by Celeste Bento

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celeste Bento

This figure shows the co-authorship network connecting the top 25 collaborators of Celeste Bento. A scholar is included among the top collaborators of Celeste Bento 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 Celeste Bento. Celeste Bento 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.
Marcão, Ana, Teresa Faria, Ana Rita Coimbra Motta-Castro, et al.. (2025). Newborn Screening for Sickle Cell Disease: Results from a Pilot Study in the Portuguese Population. International Journal of Neonatal Screening. 11(1). 10–10. 1 indexed citations
2.
Manco, Licínio, et al.. (2024). Sickle cell trait in São Tomé e Príncipe: a population-based prevalence study in women of reproductive age. BMC Public Health. 24(1). 850–850. 2 indexed citations
3.
Bento, Celeste, Carsten W. Lederer, Petros Kountouris, et al.. (2024). Global Globin Network and adopting genomic variant database requirements for thalassemia. Database. 2024. 1 indexed citations
4.
Manco, Licínio, Celeste Bento, Tabita Maia, et al.. (2022). Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster. Hemoglobin. 46(3). 168–175. 3 indexed citations
5.
Tamana, Stella, Coralea Stephanou, Cornelis L. Harteveld, et al.. (2022). Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies. eLife. 11. 5 indexed citations
6.
Manco, Licínio, et al.. (2020). Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers. Hemoglobin. 44(2). 113–117. 2 indexed citations
7.
Bento, Celeste, et al.. (2018). Congenital erythrocytosis – discover of a new mutation in the EGLN1 gene. Clinical Case Reports. 6(6). 1109–1111. 5 indexed citations
8.
Camps, Carlos, Nayia Petousi, Celeste Bento, et al.. (2016). Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations. Haematologica. 101(11). 1306–1318. 64 indexed citations
9.
Manco, Licínio, Celeste Bento, Bruno L. Victor, et al.. (2016). Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study. Blood Cells Molecules and Diseases. 60. 18–23. 14 indexed citations
10.
Vagace, José Manuel, et al.. (2015). Clinical relevance of erythrocyte ferritin in microcytic anemias. Clinica Chimica Acta. 442. 1–5.
11.
Gardie, Betty, Melanie J. Percy, David Hoogewijs, et al.. (2014). The role of PHD2 mutations in the pathogenesis of erythrocytosis. PubMed. 2. 71–71. 37 indexed citations
12.
Bento, Celeste, Ana Oliveira, Joana B. Neves, et al.. (2013). Hb Plasencia [ α 125(H8)Leu→Arg ( α 2)] is a Frequent Cause of α + -Thalassemia in the Portuguese Population. Hemoglobin. 37(2). 183–187. 1 indexed citations
13.
Sevivas, Teresa, et al.. (2013). JAK2V617F allele burden is associated with thrombotic mechanisms activation in polycythemia vera and essential thrombocythemia patients. International Journal of Hematology. 99(1). 32–40. 25 indexed citations
14.
15.
Loua, Kovana Marcel, Celeste Bento, Mandiou Diakité, et al.. (2011). High Prevalence of Hemoglobin Disorders and Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Republic of Guinea (West Africa). Hemoglobin. 36(1). 25–37. 17 indexed citations
16.
Oliveira, Guiomar, Jinong Feng, Yan Jin, et al.. (2007). MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(4). 475–483. 46 indexed citations
17.
Sousa, Inês, Madalena Martins, Catarina Correia, et al.. (2007). Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. Human Genetics. 121(2). 243–256. 107 indexed citations
18.
Correia, Catarina, Constantin Fesel, Marta Barreto, et al.. (2004). Autoantibody repertoires to brain tissue in autism nuclear families. Journal of Neuroimmunology. 152(1-2). 176–182. 61 indexed citations
19.
Bento, Celeste, et al.. (2000). b-thalassemia intermedia resulting from compound heterozigosity for an IVSI-1 (G-A) and a silent 5' UTR +33 (C-G) mutations.. PubMed. 85(4). 443–4. 3 indexed citations
20.
Bento, Celeste, et al.. (2000). Hb Vila Real [β36(C2)Pro→His]: A Newly Discovered High Oxygen Affinity Variant. Hemoglobin. 24(1). 59–63. 4 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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