Hanna IJspeert

2.1k total citations
42 papers, 1.2k citations indexed

About

Hanna IJspeert is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Hanna IJspeert has authored 42 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Immunology, 13 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Hanna IJspeert's work include Immunodeficiency and Autoimmune Disorders (22 papers), Immune Cell Function and Interaction (10 papers) and DNA Repair Mechanisms (7 papers). Hanna IJspeert is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (22 papers), Immune Cell Function and Interaction (10 papers) and DNA Repair Mechanisms (7 papers). Hanna IJspeert collaborates with scholars based in Netherlands, Germany and Czechia. Hanna IJspeert's co-authors include Mirjam van der Burg, Jacques J. M. van Dongen, Dik C. van Gent, Andrew Stubbs, Ingrid Pico‐Knijnenburg, Wouter W. Wiegant, Nicole S. Verkaik, Menno C. van Zelm, Pierre‐Olivier Mari and Tuba Turul and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Blood.

In The Last Decade

Hanna IJspeert

40 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hanna IJspeert Netherlands	20	637	530	206	184	162	42	1.2k
Nadine Taubenheim Australia	13	702 1.1×	836 1.6×	195 0.9×	140 0.8×	324 2.0×	14	1.6k
Sébastien Storck France	16	650 1.0×	504 1.0×	66 0.3×	101 0.5×	125 0.8×	19	1.2k
Nadia Catalan France	9	1.2k 1.9×	572 1.1×	228 1.1×	351 1.9×	144 0.9×	11	1.6k
Thach Mai United States	13	659 1.0×	572 1.1×	73 0.4×	122 0.7×	94 0.6×	16	1.2k
Carsten Wiethe Germany	11	699 1.1×	278 0.5×	93 0.5×	152 0.8×	162 1.0×	14	1.1k
Martina Minnich Austria	13	1.1k 1.8×	505 1.0×	129 0.6×	142 0.8×	210 1.3×	15	1.7k
Mark W. Brunvand United States	15	554 0.9×	375 0.7×	73 0.4×	86 0.5×	293 1.8×	22	1.2k
Agnès Moreau‐Aubry France	17	806 1.3×	448 0.8×	66 0.3×	131 0.7×	433 2.7×	30	1.3k
Catherine Sibille Belgium	18	577 0.9×	443 0.8×	154 0.7×	77 0.4×	280 1.7×	30	1.3k
Jason S. Mitchell United States	19	988 1.6×	293 0.6×	141 0.7×	98 0.5×	299 1.8×	36	1.4k

Countries citing papers authored by Hanna IJspeert

Since Specialization

Citations

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

Fields of papers citing papers by Hanna IJspeert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanna IJspeert

This figure shows the co-authorship network connecting the top 25 collaborators of Hanna IJspeert. A scholar is included among the top collaborators of Hanna IJspeert 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 Hanna IJspeert. Hanna IJspeert 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

Zhou, Zijun, Virgil A. S. H. Dalm, Fabian Kaiser, et al.. (2025). Novel STAT3 Y360C Gain-of-function Variant Underlies Immune Dysregulation and Aberrancy in Mitochondrial Dynamics. Immune Network. 25(2). e18–e18. 1 indexed citations

Zhou, Zijun, Tom Missotten, Mirjam E. J. van Velthoven, et al.. (2025). Gain-of-Function Variant in STAT3 and Retinal Macular Edema: Insights into the IL-6 R/JAK/ STAT3 Pathway in Retinal Pigment Epithelium. Ocular Immunology and Inflammation. 34(1). 11–25. 1 indexed citations

Putera, Ikhwanuliman, Benjamin Schrijver, Josianne C. ten Berge, et al.. (2024). A serum B-lymphocyte activation signature is a key distinguishing feature of the immune response in sarcoidosis compared to tuberculosis. Communications Biology. 7(1). 1114–1114. 4 indexed citations

Sharma, Hari S., Sigrid Swagemakers, Willem A. Dik, et al.. (2024). Bioinformatic meta-analysis reveals novel differentially expressed genes and pathways in sarcoidosis. Frontiers in Medicine. 11. 1381031–1381031. 2 indexed citations

Thüsen, Jan H. von der, Dana A. M. Mustafa, Thierry van den Bosch, et al.. (2024). Granulomas in Common Variable Immunodeficiency Display Different Histopathological Features Compared to Other Granulomatous Diseases. Journal of Clinical Immunology. 45(1). 22–22. 4 indexed citations

IJspeert, Hanna, Emily S.J. Edwards, Robyn E. O’Hehir, Virgil A. S. H. Dalm, & Menno C. van Zelm. (2024). Update on inborn errors of immunity. Journal of Allergy and Clinical Immunology. 155(3). 740–751. 5 indexed citations

Zhou, Zijun, Peter J. van der Spek, Sigrid Swagemakers, et al.. (2024). A patient-based murine model recapitulates human STAT3 gain-of-function syndrome. Clinical Immunology. 266. 110312–110312. 2 indexed citations

Kaiser, Fabian, Hanna IJspeert, P. Martin van Hagen, et al.. (2021). Activated PI3Kδ syndrome, an immunodeficiency disorder, leads to sensorimotor deficits recapitulated in a murine model. Brain Behavior & Immunity - Health. 18. 100377–100377. 9 indexed citations

Jong, Madelon M.E. de, Ingrid L. M. Wolvers‐Tettero, Cristina Teodósio, et al.. (2019). The presence of CLL-associated stereotypic B cell receptors in the normal BCR repertoire from healthy individuals increases with age. Immunity & Ageing. 16(1). 22–22. 20 indexed citations

10.

Bovenkamp, Fleur S. van de, Ninotska I. L. Derksen, Pleuni Ooijevaar‐de Heer, et al.. (2018). Adaptive antibody diversification through N -linked glycosylation of the immunoglobulin variable region. Proceedings of the National Academy of Sciences. 115(8). 1901–1906. 99 indexed citations

11.

Schouwenburg, Pauline A. van, Hanna IJspeert, Ingrid Pico‐Knijnenburg, et al.. (2018). Identification of CVID Patients With Defects in Immune Repertoire Formation or Specification. Frontiers in Immunology. 9. 2545–2545. 18 indexed citations

12.

Janda, Aleš, Klaus Schwarz, Mirjam van der Burg, et al.. (2016). Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome. Blood. 127(18). 2193–2202. 20 indexed citations

13.

IJspeert, Hanna, Marjolein Wentink, Gertjan J. Driessen, et al.. (2015). Strategies for B-Cell Receptor Repertoire Analysis in Primary Immunodeficiencies: From Severe Combined Immunodeficiency to Common Variable Immunodeficiency. Frontiers in Immunology. 6. 157–157. 16 indexed citations

14.

Wentink, Marjolein, Annechien J.A. Lambeck, Menno C. van Zelm, et al.. (2015). CD21 and CD19 deficiency: Two defects in the same complex leading to different disease modalities. Clinical Immunology. 161(2). 120–127. 24 indexed citations

15.

Janda, Aleš, Klaus Schwarz, Mirjam van der Burg, et al.. (2015). Disturbed B-lymphocytes selection in autoimmune lymphoproliferative syndrome. PubMed Central. 2(Suppl 1). A23–A23. 1 indexed citations

16.

Driessen, Gertjan J., Hanna IJspeert, Corry M.R. Weemaes, et al.. (2013). Antibody deficiency in patients with ataxia telangiectasia is caused by disturbed B- and T-cell homeostasis and reduced immune repertoire diversity. Journal of Allergy and Clinical Immunology. 131(5). 1367–1375.e9. 93 indexed citations

17.

IJspeert, Hanna, A Lankester, J. Merlijn van den Berg, et al.. (2011). Artemis splice defects cause atypical SCID and can be restored in vitro by an antisense oligonucleotide. Genes and Immunity. 12(6). 434–444. 25 indexed citations

18.

Horos, Rastislav, Hanna IJspeert, Dagmar Pospı́šilová, et al.. (2011). Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts. Blood. 119(1). 262–272. 128 indexed citations

19.

Wiegant, Wouter W., Nicole S. Verkaik, Mirjam van der Burg, et al.. (2010). A novel radiosensitive SCID patient with a pronounced G2/M sensitivity. DNA repair. 9(4). 365–373. 3 indexed citations

20.

Burg, Mirjam van der, Hanna IJspeert, Nicole S. Verkaik, et al.. (2008). A DNA-PKcs mutation in a radiosensitive T–B– SCID patient inhibits Artemis activation and nonhomologous end-joining. Journal of Clinical Investigation. 119(1). 91–8. 200 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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