Tabita Maia

434 total citations
13 papers, 159 citations indexed

About

Tabita Maia is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, Tabita Maia has authored 13 papers receiving a total of 159 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Physiology. Recurrent topics in Tabita Maia's work include Erythrocyte Function and Pathophysiology (6 papers), Hemoglobinopathies and Related Disorders (6 papers) and Neonatal Health and Biochemistry (5 papers). Tabita Maia is often cited by papers focused on Erythrocyte Function and Pathophysiology (6 papers), Hemoglobinopathies and Related Disorders (6 papers) and Neonatal Health and Biochemistry (5 papers). Tabita Maia collaborates with scholars based in Portugal, Spain and Austria. Tabita Maia's co-authors include Letícia Ribeiro, Celeste Bento, Licínio Manco, Eduard J. van Beers, Archana M. Agarwal, James D. Hoyer, Richard van Wijk, David J. Kuter, Stefan Eber and Patrick G. Gallagher and has published in prestigious journals such as SHILAP Revista de lepidopterología, Haematologica and American Journal of Hematology.

In The Last Decade

Tabita Maia

13 papers receiving 158 citations

Peers

Countries citing papers authored by Tabita Maia

Since Specialization

Citations

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

Fields of papers citing papers by Tabita Maia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tabita Maia

This figure shows the co-authorship network connecting the top 25 collaborators of Tabita Maia. A scholar is included among the top collaborators of Tabita Maia 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 Tabita Maia. Tabita Maia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Newborn Screening for Sickle Cell Disease: Results from a Pilot Study in the Portuguese Population 2025 ·International Journal of Neonatal Screening ·(unknown), Ana Marcão, (unknown), (unknown), Teresa Faria, (unknown), (unknown), (unknown), Ana Rita Coimbra Motta-Castro, (unknown), (unknown), Tabita Maia, (unknown), (unknown), (unknown), Fátima Ferreira, (unknown), Celeste Bento, Laura Vilarinho	1
2	Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster 2022 ·Hemoglobin ·Licínio Manco, (unknown), (unknown), (unknown), Celeste Bento, Tabita Maia, Verónica Gomes, António Amorim, Maria João Prata	3
3	Heterogeneidade Molecular da Deficiência em Glicose-6-Fosfato Desidrogenase (G6PD) na População Portuguesa 2022 ·Acta Médica Portuguesa ·Licínio Manco, Celeste Bento, (unknown), Tabita Maia, Letícia Ribeiro	1
4	Variants in the new E1ʹ cryptic exon of the VHL gene associated with congenital erythrocytosis—Description of three cases 2022 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Tabita Maia, (unknown), Celeste Bento	1
5	Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia Carriers 2020 ·Hemoglobin ·Licínio Manco, Celeste Bento, (unknown), (unknown), (unknown), (unknown), (unknown), Tabita Maia, Letícia Ribeiro	2
6	Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency 2018 ·American Journal of Hematology ·Paola Bianchi, Elisa Fermo, Bertil Glader, Hitoshi Kanno, Archana M. Agarwal, Wilma Barcellini, Stefan Eber, James D. Hoyer, David J. Kuter, Tabita Maia, María del Mar Mañú‐Pereira, Theodosia A. Kalfa, Serge Pissard, José C. Segovia, Eduard J. van Beers, Patrick G. Gallagher, David C. Rees, Richard van Wijk, (unknown)	57
7	Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing 2017 ·Research and Practice in Thrombosis and Haemostasis ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Licínio Manco, Tabita Maia, (unknown), (unknown), Irene Corrales, Francisco Vidal, Letícia Ribeiro	17
8	Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study 2016 ·Blood Cells Molecules and Diseases ·Licínio Manco, Celeste Bento, Bruno L. Victor, (unknown), (unknown), Rui M. M. Brito, (unknown), Tabita Maia, Letícia Ribeiro	14
9	Band 3 null^VIENNA, a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis 2016 ·Pediatric Blood & Cancer ·Leo Kager, Lesley J. Bruce, (unknown), Joanna F. Flatt, Tabita Maia, Letícia Ribeiro, Bernhard Fahrner, G. Fritsch, Kaan Boztuǧ, Oskar A. Haas	16
10	Hb Plasencia [ α 125(H8)Leu→Arg ( α 2)] is a Frequent Cause of α ⁺ -Thalassemia in the Portuguese Population 2013 ·Hemoglobin ·(unknown), Celeste Bento, Ana Oliveira, (unknown), Joana B. Neves, (unknown), (unknown), (unknown), (unknown), (unknown), Ricardo Costa, Tabita Maia, Letícia Ribeiro	1
11	Transient Neonatal Cyanosis Associated With a New Hb F Variant 2013 ·Journal of Pediatric Hematology/Oncology ·Celeste Bento, Tabita Maia, (unknown), (unknown), Gabriela de Azevedo Abreu, (unknown), (unknown), (unknown), Maria Letícia Ribeiro	10
12	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)?) 2013 ·European Journal Of Haematology ·Celeste Bento, (unknown), Tabita Maia, (unknown), (unknown), Cédric Rossi, François Girodon, (unknown), (unknown), Cristina Fraga, Ricardo Marques da Costa, (unknown), João S. Silva, (unknown), (unknown), (unknown), Guillermo Martín–Núñez, Letícia Ribeiro	32
13	thalassemia major due to acquired uniparental disomy in a previously healthy adolescent 2012 ·Haematologica ·Celeste Bento, Tabita Maia, Jelena D. Milosevic Feenstra, Isabel M. Carreira, Róbert Královics, Letícia Ribeiro	4

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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