Celeste Bento

2.2k citations

46 papers · 777 indexed · h-index 16

Impact in

Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Genetics and Neurodevelopmental Disorders
- Myeloproliferative Neoplasms: Diagnosis and Treatment
Hematology top 5%
- Iron Metabolism and Disorders

Papers in ⓘ

Genetics 28
- Hemoglobinopathies and Related Disorders 25
- Myeloproliferative Neoplasms: Diagnosis and Treatment 8
- Genetics and Neurodevelopmental Disorders 5
Physiology 15
- Erythrocyte Function and Pathophysiology 15

Co-authors: Carla Marques (4 shared papers)Astrid M. Vicente (4 shared papers)Assunção Ataíde (4 shared papers)Letícia Ribeiro (17 shared papers)Teresa S. Miguel (3 shared papers)Guiomar Oliveira (3 shared papers)Catarina Correia (3 shared papers)Constantin Fesel (2 shared papers)
Journals: Blood Cells Molecules and Diseases (3 papers)British Journal of Haematology (2 papers)Haematologica (2 papers)European Journal Of Haematology (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)
Partner nations: Portugal United Kingdom Spain

In The Last Decade

Celeste Bento

45 papers receiving 763 citations

Peers

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-authors

The 25 scholars most cited alongside Celeste Bento, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Celeste Bento Line = papers co-authored together Celeste Bento links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels Human Genetics ·Ana M. Coutinho, Inês Sousa, Madalena Martins, Catarina Correia, Teresa Morgadinho, Celeste Bento, Carla Marques, Assunção Ataíde, Teresa S. Miguel, Jason H. Moore, Guiomar Oliveira, Astrid M. Vicente	2007	107
2	Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism Molecular Psychiatry ·Ana M. Coutinho, G. G. Oliveira, Teresa Morgadinho, Constantin Fesel, T.R.A. Macedo, Celeste Bento, Carla Marques, Assunção Ataíde, T Miguel, Luana Bolsoni Borges, Astrid M. Vicente	2004	101
3	Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations Haematologica ·Carlos Camps, Nayia Petousi, Celeste Bento, Holger Cario, Richard R. Copley, Mary Frances McMullin, Richard van Wijk, Peter J. Ratcliffe, Peter A. Robbins, Jenny C. Taylor	2016	64
4	Autoantibody repertoires to brain tissue in autism nuclear families Journal of Neuroimmunology ·Susana C Silva, Catarina Correia, Constantin Fesel, Marta Barreto, Ana M. Coutinho, Carla Marques, Teresa S. Miguel, Assunção Ataíde, Celeste Bento, Luís Borges, Guiomar Oliveira, Astrid M. Vicente	2004	61
5	MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ana Margarida Coutinho, Guiomar Oliveira, Cécile Katz, Jinong Feng, Yan Jin, Chunmei Yang, Carla Marques, Assunção Ataíde, Teresa S. Miguel, Luís Borges, Joana Almeida, Catarina Correia, António Currais, Celeste Bento, Luísa Mota‐Vieira, Teresa Temudo, Mònica Santos, Patrı́cia Maciel, Steve S. Sommer, Astrid M. Vicente	2007	46
6	The role of PHD2 mutations in the pathogenesis of erythrocytosis PubMed ·Betty Gardie, Melanie J. Percy, David Hoogewijs, Rasheduzzaman Chowdhury, Celeste Bento, Mary Frances McMullin, Christopher J. Schofield, Frank S. Lee, Richard J. Kahnoski, Patrick R. Arsenault, Helena Almeida, Joanne Ewing, Frédéric Lambert	2014	37
7	Genetic basis of congenital erythrocytosis International Journal of Laboratory Hematology ·Celeste Bento	2018	36
8	Diastolic Dysfunction in Liver Cirrhosis: Prognostic Predictor in Liver Transplantation? Transplantation Proceedings ·Frederico Carvalheiro, Cidália Rodrigues, T. Adrêgo, Joaquim Viana, Henrique Duarte Vieira, Carlos Seco, L.M. Pereira, Fausto J. Pinto, Ana Eufrásio, Celeste Bento, Erikson Felipe Furtado	2016	33
9	Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?) European Journal Of Haematology ·Celeste Bento, Helena Almeida, Tabita Maia, Luís Relvas, Ana Catarina Oliveira, Cédric Rossi, François Girodon, Carlos Fernández-Lago, Ascension Aguado‐Diaz, Cristina Fraga, Ricardo Marques da Costa, Ana Luiza Rosa de Araújo, João S. Silva, Helena Vitória, Natalina Miguel, Maria Pedro Silveira, Guillermo Martín–Núñez, Letícia Ribeiro	2013	32
10	Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next‐generation sequencing International Journal of Laboratory Hematology ·Rafael Del Orbe, Beatriz Arrizabalaga, Ana B. de la Hoz, África García‐Orad, María‐Isabel Tejada, Juan Carlos García‐Ruiz, Teresa Fidalgo, Celeste Bento, Licínio Manco, Letícia Ribeiro	2016	30
11	JAK2V617F allele burden is associated with thrombotic mechanisms activation in polycythemia vera and essential thrombocythemia patients International Journal of Hematology ·Margarida Coucelo, Gonçalo Caetano, Teresa Sevivas, Susana Santos, Teresa Fidalgo, Celeste Bento, Manuela Fortuna, Marta M.M.F. Duarte, Cristina Menezes, Letícia Ribeiro	2013	25
12	Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese origin Blood Cells Molecules and Diseases ·Clara Pereira, Luís Relvas, Celeste Bento, Augusto Abade, Letícia Ribeiro, Licínio Manco	2015	21
13	Evolutionary Constraints in the β-Globin Cluster: The Signature of Purifying Selection at the δ-Globin (HBD) Locus and Its Role in Developmental Gene Regulation Genome Biology and Evolution ·Ana Moleirinho, Susana Seixas, Alexandra M. Lopes, Celeste Bento, Maria João Prata, António Amorim	2013	19
14	High Prevalence of Hemoglobin Disorders and Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Republic of Guinea (West Africa) Hemoglobin ·Tamba S. Millimono, Kovana Marcel Loua, Silvia L. Rath, Luís Relvas, Celeste Bento, Mandiou Diakité, Martin Jarvis, Nathalie Daries, Leticia M. Ribeiro, Licínio Manco, Jaspal Kaeda	2011	17
15	Erythrocytosis in children and adolescents-classification, characterization, and consensus recommendations for the diagnostic approach Pediatric Blood & Cancer ·Holger Cario, Mary Frances McMullin, Celeste Bento, Dagmar Pospı́šilová, Melanie J. Percy, Kais Hussein, Jiřı́ Schwarz, Maria Åström, Sylvie Hermouet	2013	17
16	Genetic Heterogeneity of β-Thalassemia in Populations of the Iberian Peninsula Hemoglobin ·Letícia Ribeiro, P. Gonplves, E. Cunha, Celeste Bento, Helena Almeida, Janet Pereira, Guillermo Martín Núñez, G. P. Tamagnini	1997	15
17	Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel Human Mutation ·Petros Kountouris, Coralea Stephanou, Carsten W. Lederer, Joanne Traeger‐Synodinos, Celeste Bento, Cornelis L. Harteveld, Irene Fylaktou, Tamara T. Koopmann, Hashim Halim‐Fikri, Kyriaki Michailidou, Landry Nfonsam, John S. Waye, Bin Alwi Zilfalil, Marina Kleanthous, (unknown)	2021	15
18	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 ·Licínio Manco, Celeste Bento, Bruno L. Victor, Janet Pereira, Luís Relvas, Rui M. M. Brito, Carlos Seabra, Tabita Maia, Letícia Ribeiro	2016	14
19	Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older woman Blood Cells Molecules and Diseases ·Licínio Manco, Janet Pereira, Luís Relvas, Umbelina Rebelo, Ana Isabel Crisóstomo, Celeste Bento, Letícia Ribeiro	2011	11
20	Transient Neonatal Cyanosis Associated With a New Hb F Variant Journal of Pediatric Hematology/Oncology ·Celeste Bento, Tabita Maia, Inês Carvalhais, Filipa Moita, Gabriela de Azevedo Abreu, Luís Relvas, Alexandra Pereira, José Farela Neves, Maria Letícia Ribeiro	2013	10

About Celeste Bento

Celeste Bento is a scholar working on Genetics, Genetics, Physiology, Pediatrics, Perinatology and Child Health and Hematology, having authored 46 papers that have together received 777 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (25 papers), Erythrocyte Function and Pathophysiology (15 papers), Iron Metabolism and Disorders (10 papers), Neonatal Health and Biochemistry (9 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (8 papers), Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (291 citations), Hematology (183 citations), Cognitive Neuroscience (234 citations), Genetics (279 citations) and Physiology (173 citations). Celeste Bento has collaborated with scholars based in Portugal, United Kingdom and Spain. Frequent co-authors include Carla Marques, Astrid M. Vicente, Assunção Ataíde, Letícia Ribeiro, Teresa S. Miguel, Guiomar Oliveira, Catarina Correia, Constantin Fesel, Mary Frances McMullin and Licínio Manco. Their work appears in journals such as Blood Cells Molecules and Diseases, British Journal of Haematology, Haematologica, European Journal Of Haematology and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

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