Ulrich Pannicke

7.5k total citations · 3 hit papers
40 papers, 4.5k citations indexed

About

Ulrich Pannicke is a scholar working on Immunology, Molecular Biology and Epidemiology. According to data from OpenAlex, Ulrich Pannicke has authored 40 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Immunology, 16 papers in Molecular Biology and 9 papers in Epidemiology. Recurrent topics in Ulrich Pannicke's work include Immunodeficiency and Autoimmune Disorders (15 papers), Immune Cell Function and Interaction (14 papers) and DNA Repair Mechanisms (12 papers). Ulrich Pannicke is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (15 papers), Immune Cell Function and Interaction (14 papers) and DNA Repair Mechanisms (12 papers). Ulrich Pannicke collaborates with scholars based in Germany, United States and Switzerland. Ulrich Pannicke's co-authors include Klaus Schwarz, Michael R. Lieber, Yunmei Ma, Wilhelm Friedrich, Manfred Hönig, Haihui Lu, Doris Niewolik, Stephan Ehl, Claus R. Bartram and Carl F. Ware and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Ulrich Pannicke

39 papers receiving 4.5k citations

Hit Papers

align trajectories

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.

Hairpin Opening and Overhang Processing by an Artemis/DNA-Dependent Protein Kinase Complex in Nonhomologous End Joining and V(D)J Recombination

2002 826 citations Yunmei Ma, Ulrich Pannicke et al. profile →
Mechanism and regulation of human non-homologous DNA end-joining

2003 769 citations Michael R. Lieber, Yunmei Ma et al. Nature Reviews Molecular Cell Biology profile →
Regulated Expression of Nuclear Receptor RORγt Confers Distinct Functional Fates to NK Cell Receptor-Expressing RORγt+ Innate Lymphocytes

2010 547 citations Cédric Vonarbourg, Arthur Mortha et al. Immunity profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ulrich Pannicke Germany	26	2.5k	1.9k	896	782	509	40	4.5k
Richard J. Bram United States	35	2.7k 1.1×	3.2k 1.6×	899 1.0×	775 1.0×	520 1.0×	76	6.2k
Galen H. Fisher United States	17	1.6k 0.7×	1.8k 0.9×	826 0.9×	393 0.5×	487 1.0×	30	3.7k
Akio Matsuzawa Japan	25	2.4k 1.0×	3.7k 1.9×	1.6k 1.8×	566 0.7×	455 0.9×	146	6.2k
Roberta Pelanda United States	35	1.5k 0.6×	3.2k 1.7×	774 0.9×	343 0.4×	409 0.8×	84	4.9k
Scott A. Ness United States	34	2.5k 1.0×	992 0.5×	982 1.1×	425 0.5×	635 1.2×	85	4.0k
Nobuo Sakaguchi Japan	37	1.9k 0.8×	2.7k 1.4×	537 0.6×	305 0.4×	267 0.5×	119	4.7k
Jayanta Chaudhuri United States	37	3.8k 1.5×	2.6k 1.3×	1.1k 1.2×	385 0.5×	497 1.0×	84	6.0k
Edward E. Max United States	40	2.7k 1.1×	2.7k 1.4×	608 0.7×	504 0.6×	359 0.7×	78	5.6k
Jens Dhein Germany	13	2.6k 1.1×	2.5k 1.3×	867 1.0×	213 0.3×	562 1.1×	24	4.8k

Countries citing papers authored by Ulrich Pannicke

Since Specialization

Citations

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

Fields of papers citing papers by Ulrich Pannicke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrich Pannicke

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

Baumann, Bernd, Francesca Ferrante, Eugen Tausch, et al.. (2025). A noncoding mutation in the NOTCH1 gene initiates oncogenic NOTCH signaling via wild-type NICD stabilization in CLL. Blood. 146(16). 1936–1949.

Bruyne, Marieke De, Ulrich Pannicke, Bart Vandekerckhove, et al.. (2021). A Novel Non-Coding Variant in DCLRE1C Results in Deregulated Splicing and Induces SCID Through the Generation of a Truncated ARTEMIS Protein That Fails to Support V(D)J Recombination and DNA Damage Repair. Frontiers in Immunology. 12. 674226–674226. 4 indexed citations

Schröder, Claudia, N.T. Baerlecken, Ulrich Pannicke, et al.. (2017). Evaluation of RAG1 mutations in an adult with combined immunodeficiency and progressive multifocal leukoencephalopathy. Clinical Immunology. 179. 1–7. 13 indexed citations

Fuchs, Sebastian, Anne Rensing‐Ehl, Ulrich Pannicke, et al.. (2015). Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency. Blood. 126(14). 1658–1669. 27 indexed citations

Pannicke, Ulrich, Bernd Baumann, Sebastian Fuchs, et al.. (2013). Deficiency of Innate and Acquired Immunity Caused by an IKBKB Mutation. New England Journal of Medicine. 369(26). 2504–2514. 121 indexed citations

Pannicke, Ulrich, Ellen D. Renner, Gundula Notheis, et al.. (2010). Successful Long-Term Correction of Autosomal Recessive Hyper-IgE Syndrome due to DOCK8 Deficiency by Hematopoietic Stem Cell Transplantation. Klinische Pädiatrie. 222(6). 351–355. 52 indexed citations

Gatz, Susanne A., Ulrike Benninghoff, Charlotte Schutz, et al.. (2010). Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation. Bone Marrow Transplantation. 46(4). 552–556. 59 indexed citations

Vonarbourg, Cédric, Arthur Mortha, Viet L. Bui, et al.. (2010). Regulated Expression of Nuclear Receptor RORγt Confers Distinct Functional Fates to NK Cell Receptor-Expressing RORγt+ Innate Lymphocytes. Immunity. 33(5). 736–751. 547 indexed citations breakdown →

Pannicke, Ulrich, Manfred Hönig, Ilka Schulze, et al.. (2009). The most frequentDCLRE1C(ARTEMIS) mutations are based on homologous recombination events. Human Mutation. 31(2). 197–207. 33 indexed citations

10.

Rohr, Jan, Ulrich Pannicke, Michaela Döring, et al.. (2009). Chronic Inflammatory Bowel Disease as Key Manifestation of Atypical ARTEMIS Deficiency. Journal of Clinical Immunology. 30(2). 314–320. 41 indexed citations

11.

Friesen, Claudia, et al.. (2008). DNA-Ligase IV and DNA-Protein Kinase Play a Critical Role in Deficient Caspases Activation in Apoptosis-resistant Cancer Cells by Using Doxorubicin. Molecular Biology of the Cell. 19(8). 3283–3289. 24 indexed citations

12.

Lu, Haihui, Ulrich Pannicke, Klaus Schwarz, & Michael R. Lieber. (2007). Length-dependent Binding of Human XLF to DNA and Stimulation of XRCC4·DNA Ligase IV Activity. Journal of Biological Chemistry. 282(15). 11155–11162. 85 indexed citations

13.

Enders, Anselm, Paul Fisch, Klaus Schwarz, et al.. (2006). A Severe Form of Human Combined Immunodeficiency Due to Mutations in DNA Ligase IV. The Journal of Immunology. 176(8). 5060–5068. 100 indexed citations

14.

Hirv, Kaimo, Ulrich Pannicke, Joannis Mytilineos, & Klaus Schwarz. (2006). Disulfide Bridge Disruption in the α2 Domain of the HLA Class I Molecule Leads to Low Expression of the Corresponding Antigen. Human Immunology. 67(8). 589–596. 8 indexed citations

15.

Hönig, Manfred, Michael H. Albert, Ansgar Schulz, et al.. (2006). Patients with adenosine deaminase deficiency surviving after hematopoietic stem cell transplantation are at high risk of CNS complications. Blood. 109(8). 3595–3602. 67 indexed citations

16.

Niewolik, Doris, Ulrich Pannicke, Haihui Lu, et al.. (2006). DNA-PKcs Dependence of Artemis Endonucleolytic Activity, Differences between Hairpins and 5′ or 3′ Overhangs. Journal of Biological Chemistry. 281(45). 33900–33909. 91 indexed citations

17.

Lieber, Michael R., Yunmei Ma, Ulrich Pannicke, & Klaus Schwarz. (2004). The mechanism of vertebrate nonhomologous DNA end joining and its role in V(D)J recombination. DNA repair. 3(8-9). 817–826. 185 indexed citations

18.

Lieber, Michael R., Yunmei Ma, Ulrich Pannicke, & Klaus Schwarz. (2003). Mechanism and regulation of human non-homologous DNA end-joining. Nature Reviews Molecular Cell Biology. 4(9). 712–720. 769 indexed citations breakdown →

19.

Linder, Stefan, Henry N. Higgs, Katharina Hüfner, et al.. (2000). The Polarization Defect of Wiskott-Aldrich Syndrome Macrophages Is Linked to Dislocalization of the Arp2/3 Complex. The Journal of Immunology. 165(1). 221–225. 131 indexed citations

20.

Pannicke, Ulrich, P. Tuchschmid, Wilhelm Friedrich, Claus R. Bartram, & Klaus Schwarz. (1996). Two novel missense and frameshift mutations in exons 5 and 6 of the purine nucleoside phosphorylase (PNP) gene in a severe combined immunodeficiency (SCID) patient. Human Genetics. 98(6). 706–709. 24 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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