José Barbot

1.3k total citations
52 papers, 592 citations indexed

About

José Barbot is a scholar working on Physiology, Hematology and Genetics. According to data from OpenAlex, José Barbot has authored 52 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Physiology, 18 papers in Hematology and 17 papers in Genetics. Recurrent topics in José Barbot's work include Erythrocyte Function and Pathophysiology (21 papers), Hemoglobinopathies and Related Disorders (16 papers) and Neonatal Health and Biochemistry (12 papers). José Barbot is often cited by papers focused on Erythrocyte Function and Pathophysiology (21 papers), Hemoglobinopathies and Related Disorders (16 papers) and Neonatal Health and Biochemistry (12 papers). José Barbot collaborates with scholars based in Portugal, United Kingdom and Spain. José Barbot's co-authors include Elı́sio Costa, Susana Rocha, Alexandre Quintanilha, Luı́s Belo, Alice Santos‐Silva, Rodolfo Robles, Bernhard Lämmle, Marisol Guerra, Miha Furlan and Anna Demina and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

José Barbot

48 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José Barbot Portugal 14 236 211 153 150 126 52 592
Ayla Yalamanoglu United States 13 127 0.5× 126 0.6× 129 0.8× 43 0.3× 32 0.3× 20 442
Vicky Chaar France 10 197 0.8× 146 0.7× 210 1.4× 61 0.4× 166 1.3× 10 548
Julia E. Brittain United States 16 201 0.9× 399 1.9× 467 3.1× 57 0.4× 80 0.6× 26 721
Birol Güvenç Türkiye 13 79 0.3× 169 0.8× 173 1.1× 47 0.3× 25 0.2× 57 445
Patricia N. Konrad United States 12 260 1.1× 175 0.8× 90 0.6× 190 1.3× 48 0.4× 20 610
Maria Badaracco United States 10 117 0.5× 83 0.4× 45 0.3× 24 0.2× 95 0.8× 11 489
N. Gombakis Greece 15 108 0.5× 133 0.6× 104 0.7× 60 0.4× 27 0.2× 40 577
Constance Tom Noguchi United States 13 205 0.9× 420 2.0× 525 3.4× 97 0.6× 69 0.5× 18 759
Shinichiro Miyagawa Japan 12 75 0.3× 81 0.4× 38 0.2× 55 0.4× 31 0.2× 20 376
Sona Nair India 13 64 0.3× 382 1.8× 215 1.4× 45 0.3× 60 0.5× 32 544

Countries citing papers authored by José Barbot

Since Specialization
Citations

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

Fields of papers citing papers by José Barbot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of José Barbot

This figure shows the co-authorship network connecting the top 25 collaborators of José Barbot. A scholar is included among the top collaborators of José Barbot 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 José Barbot. José Barbot 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.
Morimoto, Marie, Elena‐Raluca Nicoli, Joseph C. Roney, et al.. (2023). Spectrum of LYST mutations in Chediak-Higashi syndrome: a report of novel variants and a comprehensive review of the literature. Journal of Medical Genetics. 61(3). 212–223. 8 indexed citations
2.
Gonçalves, Cristina, Ana Paula Fernandes, Joana Azevedo, et al.. (2016). Increased red cell distribution width in Fanconi anemia: a novel marker of stress erythropoiesis. Orphanet Journal of Rare Diseases. 11(1). 102–102. 17 indexed citations
3.
Vizcaíno, José R., et al.. (2013). Iron Deficiency Anemia Due to Lymphocytic Gastritis With Helicobacter pylori Infection in Childhood. Journal of Pediatric Hematology/Oncology. 35(4). 321–322. 4 indexed citations
4.
Ponte, Filipa, et al.. (2013). Fosfomycin increases chromosome instability in lymphocytes from Fanconi Anemia patients. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 754(1-2). 58–62. 1 indexed citations
5.
Faria, Maria, et al.. (2012). Atypical haemolytic-uraemic syndrome caused by factor H mutation: case report and new management strategies in children. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 26(1). 61–65. 2 indexed citations
6.
7.
Barbot, José, et al.. (2012). Infantile Pyknocytosis: An Under-Recognized Form of Neonatal Hemolytic Anemia?. PubMed. 18(4). 27–29. 2 indexed citations
8.
Rocha, Susana, Elı́sio Costa, Petronila Rocha‐Pereira, et al.. (2011). Erythropoiesis versus inflammation in Hereditary Spherocytosis clinical outcome. Clinical Biochemistry. 44(13). 1137–1143. 5 indexed citations
9.
Rocha, Susana, Elı́sio Costa, Petronila Rocha‐Pereira, et al.. (2010). Complementary markers for the clinical severity classification of hereditary spherocytosis in unsplenectomized patients. Blood Cells Molecules and Diseases. 46(2). 166–170. 15 indexed citations
10.
Barbot, José, et al.. (2009). Lúpus Eritematoso Neonatal. 18. 149–151. 1 indexed citations
11.
Barbot, José, et al.. (2008). Disqueratose congénita, uma doença enigmática. 80–82. 1 indexed citations
12.
Costa, Elı́sio, Jorge Saraiva, Miguel Costa, et al.. (2005). Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler–Najjar syndromes. Blood Cells Molecules and Diseases. 36(1). 91–97. 23 indexed citations
13.
Costa, Elı́sio, et al.. (2004). A NEW CASE OF (TA)8 ALLELE IN THE UGT1A1 GENE PROMOTER IN A CAUCASIAN GIRL WITH GILBERT’ SYNDROME. Pediatric Hematology and Oncology. 21(5). 371–374. 11 indexed citations
14.
Costa, Elı́sio, et al.. (2003). [Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome].. PubMed. 15(6). 409–12. 3 indexed citations
15.
Ferro, Anabela, Elı́sio Costa, Jorge Pinto‐Basto, et al.. (2003). Inherited and acquired risk factors and their combined effects in pediatric stroke. Pediatric Neurology. 28(2). 134–138. 58 indexed citations
16.
17.
Guerra, Marisol, et al.. (2000). Anemia de Fanconi - variabilidade fenotípica da doença em duas irmâs. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 31(3). 277–281. 1 indexed citations
18.
Manco, Licínio, Letícia Ribeiro, Valdemar Máximo, et al.. (2000). A new PKLR gene mutation in the R‐type promoter region affects the gene transcription causing pyruvate kinase deficiency. British Journal of Haematology. 110(4). 993–997. 38 indexed citations
19.
Morais, Lívia H., et al.. (2000). Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency. European Journal of Pediatrics. 159(7). 481–482. 39 indexed citations
20.
Vulliamy, Tom, Jaspal Kaeda, Rosa Mangerini, et al.. (1998). Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia. British Journal of Haematology. 101(4). 670–675. 31 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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