Irina Giurgea

3.5k total citations
74 papers, 2.0k citations indexed

About

Irina Giurgea is a scholar working on Molecular Biology, Surgery and Immunology. According to data from OpenAlex, Irina Giurgea has authored 74 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 22 papers in Surgery and 18 papers in Immunology. Recurrent topics in Irina Giurgea's work include Inflammasome and immune disorders (23 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (10 papers) and IL-33, ST2, and ILC Pathways (9 papers). Irina Giurgea is often cited by papers focused on Inflammasome and immune disorders (23 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (10 papers) and IL-33, ST2, and ILC Pathways (9 papers). Irina Giurgea collaborates with scholars based in France, United States and United Kingdom. Irina Giurgea's co-authors include Pascale de Lonlay, Serge Amselem, Arnold Münnich, Eman Assrawi, Fawaz Awad, Claire Jumeau, Agnès Rötig, Camille Louvrier, Sonia‐Athina Karabina and Gilles Grateau and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Irina Giurgea

68 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irina Giurgea France 25 1.2k 385 379 330 269 74 2.0k
Birgit Rathkolb Germany 27 880 0.7× 348 0.9× 400 1.1× 232 0.7× 137 0.5× 87 1.9k
Daniella Brasacchio Australia 11 1.0k 0.8× 270 0.7× 360 0.9× 396 1.2× 230 0.9× 16 1.9k
Yu Sun China 24 925 0.8× 419 1.1× 617 1.6× 196 0.6× 89 0.3× 103 1.9k
Julián Nevado Spain 26 892 0.7× 126 0.3× 621 1.6× 128 0.4× 132 0.5× 118 2.0k
M. Aguennouz Italy 27 1.4k 1.2× 145 0.4× 115 0.3× 110 0.3× 151 0.6× 85 2.2k
Fayez Dawood Canada 25 1.1k 0.9× 426 1.1× 125 0.3× 119 0.4× 380 1.4× 45 3.2k
Dennis L. Guberski United States 26 579 0.5× 613 1.6× 762 2.0× 522 1.6× 447 1.7× 39 2.1k
Junko Ono Japan 25 523 0.4× 717 1.9× 469 1.2× 447 1.4× 216 0.8× 96 1.6k
Naokazu Nagata Japan 26 1.3k 1.1× 180 0.5× 208 0.5× 188 0.6× 123 0.5× 95 2.4k
Fenfen Liu Taiwan 19 1.1k 0.9× 782 2.0× 368 1.0× 338 1.0× 103 0.4× 41 2.3k

Countries citing papers authored by Irina Giurgea

Since Specialization
Citations

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

Fields of papers citing papers by Irina Giurgea

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irina Giurgea

This figure shows the co-authorship network connecting the top 25 collaborators of Irina Giurgea. A scholar is included among the top collaborators of Irina Giurgea 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 Irina Giurgea. Irina Giurgea 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.
Piéroni, Laurence, Isabelle Kone-Paut, Linda Rossi‐Semerano, et al.. (2024). Performance of serum IL-18 levels for the follow-up of patients with familial Mediterranean fever. The Journal of Allergy and Clinical Immunology In Practice. 13(3). 695–697.e1.
2.
Khouri, Elma El, Camille Louvrier, Eman Assrawi, et al.. (2023). A critical region of A20 unveiled by missense TNFAIP3 variations that lead to autoinflammation. eLife. 12. 5 indexed citations
3.
Rodrigues, François, Laurence Cuisset, Irina Giurgea, et al.. (2022). AA amyloidosis complicating cryopyrin-associated periodic syndrome: a study of 86 cases including 23 French patients and systematic review. Lara D. Veeken. 61(12). 4827–4834. 10 indexed citations
4.
Assrawi, Eman, Camille Louvrier, Elma El Khouri, et al.. (2022). Mosaic variants in TNFRSF1A: an emerging cause of tumour necrosis factor receptor-associated periodic syndrome. Lara D. Veeken. 62(1). 473–479. 7 indexed citations
5.
Popp, Bernt, Thierry Bienvenu, Irina Giurgea, et al.. (2022). The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt‐Hopkins syndrome. Clinical Genetics. 102(6). 517–523. 4 indexed citations
6.
Khouri, Elma El, Jamal Ghoumid, Damien Haye, et al.. (2021). Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders. Molecular Psychiatry. 26(7). 3572–3585. 11 indexed citations
7.
Dumont, Anaël, Samuel Ardois, M. Le Besnerais, et al.. (2021). Association between familial Mediterranean fever and multiple sclerosis: A case series from the JIR cohort and systematic literature review. Multiple Sclerosis and Related Disorders. 50. 102834–102834. 9 indexed citations
8.
Talbot, Alexis, Camille Louvrier, Matthieu Mahévas, et al.. (2019). Monoclonal Gammopathy, Arthralgias, and Recurrent Fever Syndrome: A New Autoinflammatory Syndrome?. The Journal of Rheumatology. 46(11). 1535–1539. 4 indexed citations
9.
Assrawi, Eman, Camille Louvrier, C. Lepelletier, et al.. (2019). Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria. Journal of Investigative Dermatology. 140(4). 791–798.e2. 21 indexed citations
10.
Deshayes, Samuel, Soraya Fellahi, Jean‐Philippe Bastard, et al.. (2019). Specific changes in faecal microbiota are associated with familial Mediterranean fever. Annals of the Rheumatic Diseases. 78(10). 1398–1404. 16 indexed citations
11.
Awad, Fawaz, Eman Assrawi, Camille Louvrier, et al.. (2018). Photoaging and skin cancer: Is the inflammasome the missing link?. Mechanisms of Ageing and Development. 172. 131–137. 74 indexed citations
12.
Briand‐Suleau, Audrey, Jelena Martinović, Lucie Tosca, et al.. (2014). SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication. European Journal of Medical Genetics. 57(4). 174–180. 2 indexed citations
13.
Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations
14.
Costa, Cathérine, V. Prulière‐Escabasse, Alix de Becdelièvre, et al.. (2011). A recurrent deep-intronic splicing CF mutation emphasizes the importance of mRNA studies in clinical practice. Journal of Cystic Fibrosis. 10(6). 479–482. 17 indexed citations
15.
Coulet, Florence, Étienne Rouleau, Cédrick Lefol, et al.. (2010). A One-Step Prescreening for Point Mutations and Large Rearrangement in BRCA1 and BRCA2 Genes Using Quantitative Polymerase Chain Reaction and High-Resolution Melting Curve Analysis. Genetic Testing and Molecular Biomarkers. 14(5). 677–690. 16 indexed citations
16.
Becdelièvre, Alix de, Cathérine Costa, Jean‐Marie Jouannic, et al.. (2010). Comprehensive description of CFTR genotypes and ultrasound patterns in 694 cases of fetal bowel anomalies: a revised strategy. Human Genetics. 129(4). 387–396. 14 indexed citations
17.
Giurgea, Irina, Chantal Missirian, Pierre Cacciagli, et al.. (2008). TCF4Deletions in Pitt-Hopkins Syndrome. Human Mutation. 29(11). E242–E251. 45 indexed citations
18.
González‐Barroso, M. Mar, Irina Giurgea, Frédéric Bouillaud, et al.. (2008). Mutations in UCP2 in Congenital Hyperinsulinism Reveal a Role for Regulation of Insulin Secretion. PLoS ONE. 3(12). e3850–e3850. 91 indexed citations
19.
Ratbi, Ilham, et al.. (2007). Mowat-Wilson syndrome in a Moroccan consanguineous family. Indian journal of human genetics. 13(3). 122–122. 3 indexed citations
20.
Barnérias, Christine, Irina Giurgea, Lucie Hertz‐Pannier, et al.. (2006). Respiratory chain deficiency in a female with Aicardi-Goutières syndrome. Developmental Medicine & Child Neurology. 48(3). 227–230. 12 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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