Jacinta Bustamante

36.6k total citations · 1 hit paper
162 papers, 4.7k citations indexed

About

Jacinta Bustamante is a scholar working on Immunology, Epidemiology and Infectious Diseases. According to data from OpenAlex, Jacinta Bustamante has authored 162 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 134 papers in Immunology, 65 papers in Epidemiology and 49 papers in Infectious Diseases. Recurrent topics in Jacinta Bustamante's work include Immunodeficiency and Autoimmune Disorders (106 papers), Mycobacterium research and diagnosis (46 papers) and Tuberculosis Research and Epidemiology (36 papers). Jacinta Bustamante is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (106 papers), Mycobacterium research and diagnosis (46 papers) and Tuberculosis Research and Epidemiology (36 papers). Jacinta Bustamante collaborates with scholars based in France, United States and United Kingdom. Jacinta Bustamante's co-authors include Jean‐Laurent Casanova, Stéphanie Boisson‐Dupuis, Laurent Abel, Capucine Pïcard, Anne Puel, Emmanuelle Jouanguy, Ariane Chapgier, Jacqueline Feinberg, Ludovic de Beaucoudrey and Orchidée Filipe‐Santos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Jacinta Bustamante

154 papers receiving 4.7k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mendelian susceptibility to mycobacterial disease: Genetic, immunological, and clinical features of inborn errors of IFN-γ immunity

2014 436 citations Jacinta Bustamante, Stéphanie Boisson‐Dupuis et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jacinta Bustamante France	35	3.5k	1.8k	1.5k	694	581	162	4.7k
Dinakantha Kumararatne United Kingdom	28	2.3k 0.7×	1.4k 0.8×	1.3k 0.9×	665 1.0×	560 1.0×	57	4.3k
Stéphanie Boisson‐Dupuis France	37	4.0k 1.1×	2.3k 1.3×	1.8k 1.3×	763 1.1×	695 1.2×	90	5.6k
Sergio D. Rosenzweig United States	34	2.9k 0.8×	1.0k 0.6×	918 0.6×	843 1.2×	709 1.2×	117	4.2k
Gülbû Uzel United States	41	3.3k 1.0×	1.1k 0.6×	686 0.5×	1.0k 1.5×	756 1.3×	99	5.2k
Claire Fieschi France	37	3.9k 1.1×	1.9k 1.1×	1.5k 1.0×	875 1.3×	408 0.7×	109	5.6k
Janine Reichenbach Switzerland	30	2.6k 0.7×	947 0.5×	643 0.4×	575 0.8×	1.4k 2.5×	73	4.2k
Esther van de Vosse Netherlands	32	1.5k 0.4×	1.4k 0.8×	1.5k 1.1×	294 0.4×	579 1.0×	89	3.2k
Peter Aichele Germany	39	4.1k 1.2×	958 0.5×	914 0.6×	601 0.9×	1.1k 1.9×	70	5.6k
Bernd H. Belohradsky Germany	38	2.4k 0.7×	1.0k 0.6×	740 0.5×	1.2k 1.7×	1.4k 2.4×	98	5.1k
Javier Rangel‐Moreno United States	41	4.8k 1.4×	2.1k 1.2×	2.3k 1.6×	257 0.4×	1.1k 1.8×	102	7.5k

Countries citing papers authored by Jacinta Bustamante

Since Specialization

Citations

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

Fields of papers citing papers by Jacinta Bustamante

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacinta Bustamante

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

All Works

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20 of 20 papers shown

Materna, Marie, Simin Seyedpour, Tom Le Voyer, et al.. (2025). Two different forms of inherited human TCRα chain deficiency. PubMed. 1(2).

Khavandegar, Armin, Seyed Alireza Mahdaviani, Majid Zaki‐Dizaji, et al.. (2024). Genetic, immunologic, and clinical features of 830 patients with Mendelian susceptibility to mycobacterial diseases (MSMD): A systematic review. Journal of Allergy and Clinical Immunology. 153(5). 1432–1444. 9 indexed citations

Baghdadi, Jamila El, Fatima Ailal, Ibtihal Benhsaien, et al.. (2023). Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds. Journal of Clinical Immunology. 43(4). 728–740. 6 indexed citations

Arango-Franco, Carlos A., Mélanie Migaud, Marcela Moncada‐Vélez, et al.. (2023). Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis. Journal of Clinical Immunology. 43(5). 921–932. 14 indexed citations

Rapaport, Franck, Bertrand Boisson, Anne Gregor, et al.. (2021). Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance. Proceedings of the National Academy of Sciences. 118(3). 18 indexed citations

Bigio, Benedetta, Yoann Seeleuthner, Gaspard Kerner, et al.. (2021). Detection of homozygous and hemizygous complete or partial exon deletions by whole-exome sequencing. NAR Genomics and Bioinformatics. 3(2). lqab037–lqab037. 5 indexed citations

Boisson‐Dupuis, Stéphanie & Jacinta Bustamante. (2021). Mycobacterial diseases in patients with inborn errors of immunity. Current Opinion in Immunology. 72. 262–271. 26 indexed citations

Singh, Preeti, Anastasia Resteu, Aneta Mikulášová, et al.. (2021). GATA2 deficiency phenotype associated with tandem duplication of GATA2 and overexpression of GATA2-AS1. Blood Advances. 5(24). 5631–5635. 5 indexed citations

Ogishi, Masato, Rui Yang, Conor Gruber, et al.. (2020). Multibatch Cytometry Data Integration for Optimal Immunophenotyping. The Journal of Immunology. 206(1). 206–213. 15 indexed citations

10.

Kerner, Gaspard, Matthieu Bouaziz, Aurélie Cobat, et al.. (2020). A genome-wide case-only test for the detection of digenic inheritance in human exomes. Proceedings of the National Academy of Sciences. 117(32). 19367–19375. 17 indexed citations

11.

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

12.

Bustamante, Jacinta. (2020). Mendelian susceptibility to mycobacterial disease: recent discoveries. Human Genetics. 139(6-7). 993–1000. 106 indexed citations

13.

Jobim, Mariana, et al.. (2019). Síndromes MonoMAC e Emberger em paciente com mutação no gene GATA2. 3(1). 89–92.

14.

Rosain, Jérémie, Xiao‐Fei Kong, Rubén Martínez‐Barricarte, et al.. (2018). Mendelian susceptibility to mycobacterial disease: 2014–2018 update. Immunology and Cell Biology. 97(4). 360–367. 130 indexed citations

15.

Boisson‐Dupuis, Stéphanie, et al.. (2017). Chronic Granulomatous Disease: An Unreported Mutation. 18(1). 45–53. 1 indexed citations

16.

Routes, John M., Mario Abinun, Waleed Al–Herz, et al.. (2014). ICON: The Early Diagnosis of Congenital Immunodeficiencies. Journal of Clinical Immunology. 34(4). 398–424. 30 indexed citations

17.

Schmitt, Nathalie, Jacinta Bustamante, Laure Bourdery, et al.. (2013). IL-12 receptor β1 deficiency alters in vivo T follicular helper cell response in humans. Blood. 121(17). 3375–3385. 124 indexed citations

18.

Kong, Xiao‐Fei, Aziz Bousfiha, Yuval Itan, et al.. (2013). A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease. PLoS ONE. 8(3). e58286–e58286. 27 indexed citations

19.

Kong, Xiao‐Fei, Guillaume Vogt, Ariane Chapgier, et al.. (2009). A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon. Human Molecular Genetics. 19(3). 434–444. 27 indexed citations

20.

Bustamante, Jacinta, Güzide Aksu, Guillaume Vogt, et al.. (2007). BCG-osis and tuberculosis in a child with chronic granulomatous disease. Journal of Allergy and Clinical Immunology. 120(1). 32–38. 91 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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