Carsten Speckmann

8.0k total citations
60 papers, 1.6k citations indexed

About

Carsten Speckmann is a scholar working on Immunology, Genetics and Hematology. According to data from OpenAlex, Carsten Speckmann has authored 60 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Immunology, 14 papers in Genetics and 11 papers in Hematology. Recurrent topics in Carsten Speckmann's work include Immunodeficiency and Autoimmune Disorders (29 papers), Immune Cell Function and Interaction (20 papers) and Blood disorders and treatments (10 papers). Carsten Speckmann is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (29 papers), Immune Cell Function and Interaction (20 papers) and Blood disorders and treatments (10 papers). Carsten Speckmann collaborates with scholars based in Germany, United Kingdom and United States. Carsten Speckmann's co-authors include Stephan Ehl, Klaus Schwarz, Jan Rohr, Thomas Vraetz, Ulrich Pannicke, Anne Rensing‐Ehl, Brigitte Strahm, Mads Gyrd‐Hansen, Annette Schmitt‐Graeff and Udo zur Stadt and has published in prestigious journals such as Nature Medicine, The Journal of Experimental Medicine and Blood.

In The Last Decade

Carsten Speckmann

56 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carsten Speckmann Germany 22 1.0k 410 408 360 214 60 1.6k
Hans‐Hartmut Peter Germany 25 1.5k 1.4× 359 0.9× 398 1.0× 272 0.8× 132 0.6× 58 2.3k
Hye Sun Kuehn United States 24 1.3k 1.3× 511 1.2× 243 0.6× 123 0.3× 89 0.4× 54 1.7k
Eyal Grunebaum Canada 25 888 0.9× 612 1.5× 517 1.3× 329 0.9× 136 0.6× 113 1.9k
Iván K. Chinn United States 20 1.1k 1.0× 498 1.2× 425 1.0× 269 0.7× 181 0.8× 55 1.9k
Daiichiro Hasegawa Japan 18 233 0.2× 366 0.9× 153 0.4× 364 1.0× 113 0.5× 105 1.2k
Nanette Solvason United States 16 979 1.0× 310 0.8× 232 0.6× 93 0.3× 22 0.1× 24 1.5k
Laurence Cuisset France 25 1.1k 1.1× 2.1k 5.0× 297 0.7× 510 1.4× 107 0.5× 62 2.5k
Yu Nee Lee United States 20 809 0.8× 479 1.2× 319 0.8× 75 0.2× 65 0.3× 35 1.3k
Yojiro Kawabe Japan 22 898 0.9× 520 1.3× 134 0.3× 105 0.3× 41 0.2× 51 1.8k
Julie Tellier Australia 18 1.1k 1.1× 351 0.9× 89 0.2× 167 0.5× 52 0.2× 28 1.6k

Countries citing papers authored by Carsten Speckmann

Since Specialization
Citations

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

Fields of papers citing papers by Carsten Speckmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carsten Speckmann

This figure shows the co-authorship network connecting the top 25 collaborators of Carsten Speckmann. A scholar is included among the top collaborators of Carsten Speckmann 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 Carsten Speckmann. Carsten Speckmann 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.
Kaiser‐Labusch, Petra, et al.. (2024). Variable Syndromic Immunodeficiency in Patients with Biallelic PRIM1 Mutations. Journal of Clinical Immunology. 44(6). 129–129. 2 indexed citations
2.
Strahm, Brigitte, et al.. (2024). The different faces of GATA2 deficiency: implications for therapy and surveillance. Frontiers in Oncology. 14. 1423856–1423856. 2 indexed citations
3.
Ghosh, Sujal, Michael H. Albert, Fabian Hauck, et al.. (2023). Neugeborenenscreening auf schwere kombinierte Immundefekte (SCID) in Deutschland. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 66(11). 1222–1231. 4 indexed citations
4.
Haeusler, Gabrielle M., Roland A. Ammann, Fabianne Carlesse, et al.. (2021). SARS-CoV-2 in children with cancer or after haematopoietic stem cell transplant: An analysis of 131 patients. European Journal of Cancer. 159. 78–86. 29 indexed citations
5.
Albert, Michael H., Nizar Mahlaoui, Fabian Hauck, et al.. (2020). Outcome of chronic granulomatous disease ‐ Conventional treatment vs stem cell transplantation. Pediatric Allergy and Immunology. 32(3). 576–585. 16 indexed citations
6.
Führer, Marita, Sebastian Fuchs, Myriam Ricarda Lorenz, et al.. (2020). Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development. EBioMedicine. 59. 102961–102961. 4 indexed citations
7.
Duppenthaler, Andrea, Matthias S. Dettmer, Urs C. Steiner, et al.. (2019). High Levels of IL-18 and IFN-γ in Chronically Inflamed Tissue in Chronic Granulomatous Disease. Frontiers in Immunology. 10. 2236–2236. 15 indexed citations
8.
König, Rainer, et al.. (2018). NBAS Gene Mutation Causes Insulin-Dependent Diabetes Mellitus in a Patient with a Multisystem Disorder Consisting Immunodeficiency and Extremely Short Stature.
9.
Ammann, Sandra, Kai Lehmberg, Udo zur Stadt, et al.. (2017). Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis. Journal of Clinical Immunology. 37(8). 770–780. 30 indexed citations
10.
Vogl, Christian, Natja Haag, Torben J. Hausrat, et al.. (2017). The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing. EMBO Reports. 18(11). 2015–2029. 16 indexed citations
11.
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
12.
Kunz, Joachim B., Margit Happich, Susanna Esposito, et al.. (2016). Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC). Clinical Immunology. 175. 51–55. 9 indexed citations
13.
Hauck, Fabian, Britta Blumenthal, Sebastian Fuchs, et al.. (2015). SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling. Clinical Immunology. 161(2). 103–109. 20 indexed citations
14.
Speckmann, Carsten. (2013). KRECs BUT NOT TRECs IDENTIFY PATIENTS WITH DELAYED-ONSET ADENOSINE DEAMINASE (ADA) DEFICIENCY IN NEONATAL SCREENING. 2 indexed citations
15.
Damgaard, Rune Busk, Berthe Katrine Fiil, Carsten Speckmann, et al.. (2013). Disease‐causing mutations in the XIAP BIR 2 domain impair NOD 2‐dependent immune signalling. EMBO Molecular Medicine. 5(8). 1278–1295. 108 indexed citations
16.
Felgentreff, Kerstin, Ruy Perez‐Becker, Carsten Speckmann, et al.. (2011). Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency. Clinical Immunology. 141(1). 73–82. 89 indexed citations
17.
Rohr, Jan, Karin Beutel, Andrea Maul‐Pavicic, et al.. (2010). Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases. Haematologica. 95(12). 2080–2087. 89 indexed citations
18.
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
19.
Schmidt, Manfred, Denise A. Carbonaro, Carsten Speckmann, et al.. (2003). Clonality analysis after retroviral-mediated gene transfer to CD34+ cells from the cord blood of ADA-deficient SCID neonates. Nature Medicine. 9(4). 463–468. 110 indexed citations
20.
Schmidt, Manfred, Hanno Glimm, Carsten Speckmann, et al.. (2001). A Model for the Detection of Clonality in Marked Hematopoietic Stem Cells. Annals of the New York Academy of Sciences. 938(1). 146–156. 25 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Hans‐Hartmut Peter Breakdown of academic impact, for papers by Hye Sun Kuehn Breakdown of academic impact, for papers by Eyal Grunebaum Breakdown of academic impact, for papers by Iván K. Chinn Breakdown of academic impact, for papers by Daiichiro Hasegawa Breakdown of academic impact, for papers by Nanette Solvason Breakdown of academic impact, for papers by Laurence Cuisset Breakdown of academic impact, for papers by Yu Nee Lee Breakdown of academic impact, for papers by Yojiro Kawabe Breakdown of academic impact, for papers by Julie Tellier
Rankless by CCL
2026