Matías Oleastro

4.5k total citations
33 papers, 807 citations indexed

About

Matías Oleastro is a scholar working on Immunology, Epidemiology and Genetics. According to data from OpenAlex, Matías Oleastro has authored 33 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Immunology, 10 papers in Epidemiology and 10 papers in Genetics. Recurrent topics in Matías Oleastro's work include Immunodeficiency and Autoimmune Disorders (18 papers), Blood disorders and treatments (6 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Matías Oleastro is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (18 papers), Blood disorders and treatments (6 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Matías Oleastro collaborates with scholars based in Argentina, United States and Colombia. Matías Oleastro's co-authors include Marta Zelazko, Alain Fischer, Françoise Le Deist, Silvia Danielian, Andrea Bernasconi, Daniel Choquet, Carolin Thomas, Claire Hivroz, B. H. Belohradsky and Michel Partiseti and has published in prestigious journals such as Blood, PEDIATRICS and Journal of Allergy and Clinical Immunology.

In The Last Decade

Matías Oleastro

33 papers receiving 785 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matías Oleastro Argentina 14 521 187 136 113 91 33 807
Kerstin Kiefer United States 11 374 0.7× 181 1.0× 34 0.3× 47 0.4× 76 0.8× 17 653
Heidrun Ullrich Germany 12 249 0.5× 170 0.9× 46 0.3× 59 0.5× 126 1.4× 22 586
Marianna Boncristiano Italy 10 345 0.7× 152 0.8× 63 0.5× 43 0.4× 69 0.8× 12 601
P Hanke Germany 7 180 0.3× 172 0.9× 48 0.4× 54 0.5× 45 0.5× 23 628
Mark Tsang United States 11 197 0.4× 351 1.9× 117 0.9× 53 0.5× 124 1.4× 15 688
Donatella Buonfiglio Italy 12 429 0.8× 153 0.8× 41 0.3× 54 0.5× 112 1.2× 15 645
Jason Douangpanya United States 5 437 0.8× 357 1.9× 32 0.2× 52 0.5× 131 1.4× 5 784
Weiwei Chen China 14 558 1.1× 221 1.2× 40 0.3× 149 1.3× 114 1.3× 45 890
Roberto Caporale Italy 14 123 0.2× 243 1.3× 35 0.3× 76 0.7× 102 1.1× 23 633
Lucía Cabal‐Hierro United States 10 270 0.5× 316 1.7× 34 0.3× 107 0.9× 172 1.9× 16 796

Countries citing papers authored by Matías Oleastro

Since Specialization
Citations

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

Fields of papers citing papers by Matías Oleastro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matías Oleastro

This figure shows the co-authorship network connecting the top 25 collaborators of Matías Oleastro. A scholar is included among the top collaborators of Matías Oleastro 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 Matías Oleastro. Matías Oleastro 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.
Oleastro, Matías, et al.. (2024). A Clinical Neurological Approach to the Child With Adenosine Deaminase Deficiency. Pediatric Neurology. 158. 49–56. 1 indexed citations
2.
Rosain, Jérémie, Andrea Bernasconi, Tom Le Voyer, et al.. (2022). Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency. Journal of Clinical Immunology. 42(5). 975–985. 8 indexed citations
3.
Pérez, Laura, Fernando Messina, Ricardo Negroni, et al.. (2020). Inherited CARD9 Deficiency in a Patient with Both Exophiala spinifera and Aspergillus nomius Severe Infections. Journal of Clinical Immunology. 40(2). 359–366. 24 indexed citations
4.
Boogaard, Marlinde L. van den, Peter Thijssen, Caner Aytekin, et al.. (2017). Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2. Clinical Genetics. 92(4). 380–387. 36 indexed citations
5.
Almejún, María Belén, Virginia Patiño, Miguel Galicchio, et al.. (2016). Noninfectious complications in patients with pediatric-onset common variable immunodeficiency correlated with defects in somatic hypermutation but not in class-switch recombination. Journal of Allergy and Clinical Immunology. 139(3). 913–922. 8 indexed citations
6.
Valle, Solange Oliveira Rodrigues, Liliana Bezrodnik, Elma Nievas, et al.. (2014). Improving C1 inhibitor deficiency (type 1 and type 2 hereditary angioedema) in Latin America.. PubMed. 24(6). 445–7. 4 indexed citations
7.
Condino‐Neto, Antônio & Matías Oleastro. (2012). Phenotype and Genotype Spectrum of Chronic Granulomatous Disease in Latin American Patients: Results From the LASID Registry. Resumos. 1 indexed citations
8.
Condino‐Neto, Antônio, José Luis Franco, Francisco Espinosa‐Rosales, et al.. (2012). Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives. Allergologia et Immunopathologia. 40(3). 187–193. 7 indexed citations
9.
Yancoski, Judith, Carlos Rocco, Laura Pérez, et al.. (2012). A Missense Mutation in the Extracellular Domain of Fas: The Most Common Change in Argentinean Patients with Autoimmune Lymphoproliferative Syndrome Represents a Founder Effect. Journal of Clinical Immunology. 32(6). 1197–1203. 9 indexed citations
10.
Leiva, Lily E., Liliana Bezrodnik, Matías Oleastro, et al.. (2011). Primary immunodeficiency diseases in Latin America: Proceedings of the Second Latin American Society for Immunodeficiencies (LASID) Advisory Board. Allergologia et Immunopathologia. 39(2). 106–110. 16 indexed citations
11.
Almejún, María Belén, Elisa O. Sajaroff, Miguel Galicchio, et al.. (2011). Immunological Characteristics and Two Novel Mutations in TACI in a Cohort of 28 Pediatric Patients with Common Variable Immunodeficiency. Journal of Clinical Immunology. 32(1). 89–97. 11 indexed citations
12.
Condino‐Neto, Antônio, José Luis Franco, Claudia M. Trujillo‐Vargas, et al.. (2010). Critical issues and needs in management of primary immunodeficiency diseases in Latin America. Allergologia et Immunopathologia. 39(1). 45–51. 12 indexed citations
13.
Burgos, M. Eugenia, et al.. (2010). A vaccine derived poliovirus case in an immunocompromised argentinian child. International Journal of Infectious Diseases. 14. e450–e451. 1 indexed citations
14.
15.
Basile, Natalia, et al.. (2008). Clinical and Molecular Analysis of 49 Patients With X-linked Agammaglobulinemia From A Single Center in Argentina. Journal of Clinical Immunology. 29(1). 123–129. 27 indexed citations
16.
Oleastro, Matías, Sergio D. Rosenzweig, Laura Pérez, et al.. (2007). Efficacy and Tolerability of an Argentine Intravenous Immunoglobulin in Pediatric Patients with Primary Immunodeficiency Diseases. Journal of Clinical Immunology. 27(2). 227–232. 3 indexed citations
17.
Danielian, Silvia, et al.. (2007). Clinical Follow-Up of 11 Argentinian CD40L-Deficient Patients with 7 Unique Mutations Including the So-Called “Milder” Mutants. Journal of Clinical Immunology. 27(4). 455–459. 19 indexed citations
18.
Barese, Cecilia, et al.. (2004). X-Linked Chronic Granulomatous Disease. Journal of Pediatric Hematology/Oncology. 26(10). 656–660. 12 indexed citations
19.
Danielian, Silvia, Matías Oleastro, Sergio D. Rosenzweig, et al.. (2003). Bruton tyrosine kinase gene mutations in Argentina. Human Mutation. 21(4). 451–451. 8 indexed citations
20.
Rosenzweig, Sergio D., et al.. (2002). Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations. Human Mutation. 19(2). 186–187. 10 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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