Sheila Pinto

1.3k total citations
20 papers, 1.0k citations indexed

About

Sheila Pinto is a scholar working on Immunology, Hematology and Nephrology. According to data from OpenAlex, Sheila Pinto has authored 20 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Immunology, 10 papers in Hematology and 9 papers in Nephrology. Recurrent topics in Sheila Pinto's work include Complement system in diseases (18 papers), Renal Diseases and Glomerulopathies (9 papers) and Blood groups and transfusion (7 papers). Sheila Pinto is often cited by papers focused on Complement system in diseases (18 papers), Renal Diseases and Glomerulopathies (9 papers) and Blood groups and transfusion (7 papers). Sheila Pinto collaborates with scholars based in Spain, United Kingdom and Italy. Sheila Pinto's co-authors include Santiago Rodrı́guez de Córdoba, Agustín Tortajada, Margarita López‐Trascasa, Pilar Sánchez‐Corral, Marina Noris, Véronique Frémeaux‐Bacchi, Timothy H.J. Goodship, Giuseppe Remuzzi, Marta R. Hidalgo and Marta Alberti and has published in prestigious journals such as Journal of Clinical Investigation, Blood and The Journal of Immunology.

In The Last Decade

Sheila Pinto

20 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sheila Pinto Spain 13 911 664 402 129 120 20 1.0k
Simona Brioschi Italy 5 863 0.9× 535 0.8× 401 1.0× 148 1.1× 181 1.5× 7 961
Elisabetta Valoti Italy 13 1.1k 1.2× 844 1.3× 429 1.1× 176 1.4× 157 1.3× 21 1.2k
Rossella Piras Italy 13 1.1k 1.2× 908 1.4× 418 1.0× 216 1.7× 147 1.2× 24 1.3k
Anthony Nicholls United Kingdom 5 423 0.5× 237 0.4× 200 0.5× 64 0.5× 80 0.7× 8 590
Manabu Yamashina Japan 7 404 0.4× 166 0.3× 204 0.5× 38 0.3× 75 0.6× 9 485
Fengqi An United States 6 734 0.8× 77 0.1× 77 0.2× 24 0.2× 42 0.3× 9 895
Caterina Pascariello Italy 5 220 0.2× 93 0.1× 150 0.4× 37 0.3× 78 0.7× 13 335
Pilar Nozal Spain 13 309 0.3× 189 0.3× 152 0.4× 13 0.1× 37 0.3× 40 433
Mohamed R. Daha Netherlands 8 466 0.5× 131 0.2× 70 0.2× 10 0.1× 30 0.3× 10 633
Margot Zielinska‐Skowronek Germany 11 357 0.4× 87 0.1× 96 0.2× 31 0.2× 39 0.3× 15 489

Countries citing papers authored by Sheila Pinto

Since Specialization
Citations

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

Fields of papers citing papers by Sheila Pinto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sheila Pinto

This figure shows the co-authorship network connecting the top 25 collaborators of Sheila Pinto. A scholar is included among the top collaborators of Sheila Pinto 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 Sheila Pinto. Sheila Pinto 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.
Córdoba, Santiago Rodrı́guez de, Daniel L. Sanchez, Sheila Pinto, et al.. (2025). Novel immunochromatographic test for rapid detection of anti-factor H autoantibodies with an assessment of its clinical relevance. Frontiers in Immunology. 15. 1527016–1527016. 3 indexed citations
2.
Bocanegra, Victoria, et al.. (2025). The role of the complement system in Shiga toxin-associated hemolytic uremic syndrome. Pediatric Nephrology. 40(5). 1711–1722. 2 indexed citations
3.
Breno, Matteo, Nicolò Ghiringhelli Borsa, Fengxiao Bu, et al.. (2018). Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. The Journal of Immunology. 200(7). 2464–2478. 119 indexed citations
4.
Tortajada, Agustín, Eduardo Gutiérrez, Elena Goicoechea de Jorge, et al.. (2017). Elevated factor H–related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy. Kidney International. 92(4). 953–963. 91 indexed citations
5.
Jiménez-Alcázar, Miguel, Jaouad Anter, Sheila Pinto, et al.. (2015). Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome. Molecular Immunology. 67(2). 276–286. 46 indexed citations
6.
Martínez-Barricarte, Rubén, Meike Heurich, Andrés López‐Perrote, et al.. (2015). The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome. Molecular Immunology. 66(2). 263–273. 46 indexed citations
7.
Recalde, Sergio, Agustín Tortajada, Marta Subías, et al.. (2015). Molecular Basis of Factor H R1210C Association with Ocular and Renal Diseases. Journal of the American Society of Nephrology. 27(5). 1305–1311. 25 indexed citations
8.
Nozal, Pilar, Sofía Garrido, Jorge Martínez-Ara, et al.. (2015). Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation. BMC Nephrology. 16(1). 40–40. 17 indexed citations
9.
10.
Pinto, Sheila, Bernd Höppe, Laura López, et al.. (2014). Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome. Clinical Journal of the American Society of Nephrology. 9(9). 1611–1619. 50 indexed citations
11.
Hidalgo, Marta R., Sheila Pinto, Agustín Tortajada, & Santiago Rodrı́guez de Córdoba. (2014). Genetics of Atypical Hemolytic Uremic Syndrome (aHUS). Seminars in Thrombosis and Hemostasis. 40(4). 422–430. 104 indexed citations
12.
Pinto, Sheila, et al.. (2013). Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene. Pediatric Nephrology. 29(1). 149–153. 32 indexed citations
13.
Bresin, Elena, Erica Rurali, Jessica Caprioli, et al.. (2013). Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype. Journal of the American Society of Nephrology. 24(3). 475–486. 263 indexed citations
14.
Tortajada, Agustín, Sheila Pinto, Jorge Martínez-Ara, et al.. (2011). Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance. Kidney International. 81(1). 56–63. 31 indexed citations
15.
Martínez-Barricarte, Rubén, Meike Heurich, Francisco Valdés-Cañedo, et al.. (2010). Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation. Journal of Clinical Investigation. 120(10). 3702–3712. 168 indexed citations
16.
Martínez‐Barricarte, Rubén, Meike Heurich, Eduardo Vázquez‐Martul, et al.. (2010). Human C3 mutation associated with Dense Deposit Disease unravels distinct structural requirements for factor H, MCP and DAF regulation. Molecular Immunology. 47(13). 2212–2212. 1 indexed citations
17.
Garcı́a-Garcı́a, Luis, et al.. (2009). Changes in NPY and POMC, but not serotonin transporter, following a restricted feeding/repletion protocol in rats. Brain Research. 1313. 103–112. 23 indexed citations
18.
Martínez-Barricarte, Rubén, Tamara Montes, Sheila Pinto, et al.. (2008). Novel C3 mutations associated with atypical haemolytic uraemic syndrome. Molecular Immunology. 45(16). 4130–4130. 1 indexed citations
19.
Jorge, Elena Goicoechea de, Agustín Tortajada, Tamara Montes, et al.. (2007). The Spanish atypical haemolytic uraemic syndrome registry: A genetic update. Molecular Immunology. 44(16). 3923–3923. 1 indexed citations
20.
Martínez-Barricarte, Rubén, Elena Goicoechea de Jorge, Sergio Recalde, et al.. (2007). Complement factor H haplotypes and copy number variations of the factor H-related genes in renal and ocular disorders. Molecular Immunology. 44(16). 3919–3920. 1 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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