Nóra Veszeli

817 total citations
35 papers, 466 citations indexed

About

Nóra Veszeli is a scholar working on Genetics, Hematology and Pathology and Forensic Medicine. According to data from OpenAlex, Nóra Veszeli has authored 35 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 13 papers in Hematology and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Nóra Veszeli's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (29 papers), Autoimmune Bullous Skin Diseases (9 papers) and Urticaria and Related Conditions (9 papers). Nóra Veszeli is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (29 papers), Autoimmune Bullous Skin Diseases (9 papers) and Urticaria and Related Conditions (9 papers). Nóra Veszeli collaborates with scholars based in Hungary, Italy and Israel. Nóra Veszeli's co-authors include Henriette Farkas, Lilian Varga, Kinga Viktória Kőhalmi, Dorottya Csuka, Zsuzsanna Zotter, Zoltán Prohászka, László Cervenak, Erika Kajdácsi, Batya Engel‐Yeger and Shmuel Kivity and has published in prestigious journals such as Journal of Allergy and Clinical Immunology, Frontiers in Immunology and Allergy.

In The Last Decade

Nóra Veszeli

33 papers receiving 457 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nóra Veszeli Hungary 14 355 167 147 141 107 35 466
György Temesszentandrási Hungary 8 325 0.9× 76 0.5× 113 0.8× 132 0.9× 91 0.9× 11 375
Beáta Visy Hungary 10 563 1.6× 100 0.6× 175 1.2× 235 1.7× 209 2.0× 22 604
Soken-Nakazawa J. Song Japan 5 133 0.4× 54 0.3× 212 1.4× 82 0.6× 22 0.2× 8 364
L. Bouillet France 9 611 1.7× 141 0.8× 181 1.2× 285 2.0× 241 2.3× 17 652
Donald McNeil United States 4 335 0.9× 106 0.6× 108 0.7× 153 1.1× 121 1.1× 14 415
Anders Lindholm Sørensen Denmark 12 351 1.0× 43 0.3× 244 1.7× 155 1.1× 12 0.1× 31 458
Yibin Jiang China 5 78 0.2× 180 1.1× 112 0.8× 102 0.7× 49 0.5× 8 443
Sara Mach‐Pascual Switzerland 9 161 0.5× 73 0.4× 218 1.5× 49 0.3× 29 0.3× 12 362
Yung Chyung United States 7 153 0.4× 85 0.5× 35 0.2× 54 0.4× 44 0.4× 19 359
Stephen R. Zeldenrust United States 10 201 0.6× 50 0.3× 302 2.1× 25 0.2× 94 0.9× 16 573

Countries citing papers authored by Nóra Veszeli

Since Specialization
Citations

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

Fields of papers citing papers by Nóra Veszeli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nóra Veszeli

This figure shows the co-authorship network connecting the top 25 collaborators of Nóra Veszeli. A scholar is included among the top collaborators of Nóra Veszeli 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 Nóra Veszeli. Nóra Veszeli 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.
Prohászka, Zoltán, et al.. (2025). Different patterns of complement activation markers are present in acute and chronic adult primary ITP patients. Immunobiology. 230(4). 153023–153023.
2.
Kajdácsi, Erika, Nóra Veszeli, Kinga Viktória Kőhalmi, et al.. (2021). Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency. Clinical Reviews in Allergy & Immunology. 60(3). 383–395. 7 indexed citations
3.
Nozal, Pilar, Emilia Arjona, A. Madrid, et al.. (2021). Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome. Frontiers in Immunology. 12. 641656–641656. 11 indexed citations
4.
Pollack, Shirley, Adi Mory, Tamar Paperna, et al.. (2021). A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report. Frontiers in Immunology. 12. 608604–608604. 1 indexed citations
5.
Kajdácsi, Erika, Nóra Veszeli, Veronika Makó, et al.. (2020). Patterns of C1-Inhibitor/Plasma Serine Protease Complexes in Healthy Humans and in Hereditary Angioedema Patients. Frontiers in Immunology. 11. 794–794. 34 indexed citations
6.
Veszeli, Nóra, et al.. (2020). Evaluation of the efficacy and safety of home treatment with the recombinant human C1-inhibitor in hereditary angioedema resulting from C1-inhibitor deficiency. International Immunopharmacology. 80. 106216–106216. 4 indexed citations
7.
Farkas, Henriette, Kinga Viktória Kőhalmi, Beáta Visy, Nóra Veszeli, & Lilian Varga. (2020). Clinical Characteristics and Safety of Plasma-Derived C1-Inhibitor Therapy in Children and Adolescents with Hereditary Angioedema—A Long-Term Survey. The Journal of Allergy and Clinical Immunology In Practice. 8(7). 2379–2383. 7 indexed citations
9.
Kőhalmi, Kinga Viktória, Nóra Veszeli, Szabolcs Benedek, et al.. (2020). Changes of coagulation parameters during erythema marginatum in patients with hereditary angioedema. International Immunopharmacology. 81. 106293–106293. 7 indexed citations
10.
Veszeli, Nóra, et al.. (2019). Serum fetuin-A, tumor necrosis factor alpha and C-reactive protein concentrations in patients with hereditary angioedema with C1-inhibitor deficiency. Orphanet Journal of Rare Diseases. 14(1). 67–67. 6 indexed citations
11.
Loffredo, Stefania, Anne Lise Ferrara, Maria Bova, et al.. (2018). Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency. Frontiers in Immunology. 9. 1721–1721. 22 indexed citations
12.
Veszeli, Nóra, Kinga Viktória Kőhalmi, Dorottya Csuka, et al.. (2018). Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema. The Journal of Allergy and Clinical Immunology In Practice. 6(4). 1205–1208. 11 indexed citations
13.
Veszeli, Nóra, Kinga Viktória Kőhalmi, Erika Kajdácsi, et al.. (2017). Complete kinetic follow‐up of symptoms and complement parameters during a hereditary angioedema attack. Allergy. 73(2). 516–520. 7 indexed citations
14.
Zotter, Zsuzsanna, Zsolt Nagy, Attila Patócs, et al.. (2017). Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency. Orphanet Journal of Rare Diseases. 12(1). 5–5. 6 indexed citations
15.
Kőhalmi, Kinga Viktória, Nóra Veszeli, László Cervenak, Lilian Varga, & Henriette Farkas. (2017). A novel prophylaxis with C1-inhibitor concentrate in hereditary angioedema during erythema marginatum. Immunology Letters. 189. 90–93. 9 indexed citations
16.
Farkas, Henriette, Nóra Veszeli, Erika Kajdácsi, László Cervenak, & Lilian Varga. (2016). “Nuts and Bolts” of Laboratory Evaluation of Angioedema. Clinical Reviews in Allergy & Immunology. 51(2). 140–151. 35 indexed citations
17.
Czaller, Ibolya, Dorottya Csuka, Zsuzsanna Zotter, et al.. (2016). Thyroid hormones and complement parameters in hereditary angioedema with C1-inhibitor deficiency. Annals of Allergy Asthma & Immunology. 117(2). 175–179. 1 indexed citations
18.
Farkas, Henriette, Kinga Viktória Kőhalmi, Nóra Veszeli, Ferenc Tóth, & Lilian Varga. (2016). First report of icatibant treatment in a pregnant patient with hereditary angioedema. Journal of obstetrics and gynaecology research. 42(8). 1026–1028. 16 indexed citations
19.
Csuka, Dorottya, Nóra Veszeli, Zsuzsanna Zotter, et al.. (2015). Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency. Orphanet Journal of Rare Diseases. 10(1). 132–132. 41 indexed citations
20.
Zotter, Zsuzsanna, Nóra Veszeli, Dorottya Csuka, Lilian Varga, & Henriette Farkas. (2014). Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema. Orphanet Journal of Rare Diseases. 9(1). 205–205. 23 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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