Hans‐Peter Kiem

21.0k total citations · 3 hit papers
307 papers, 10.0k citations indexed

About

Hans‐Peter Kiem is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Hans‐Peter Kiem has authored 307 papers receiving a total of 10.0k indexed citations (citations by other indexed papers that have themselves been cited), including 172 papers in Genetics, 162 papers in Molecular Biology and 91 papers in Oncology. Recurrent topics in Hans‐Peter Kiem's work include Virus-based gene therapy research (170 papers), CRISPR and Genetic Engineering (85 papers) and CAR-T cell therapy research (77 papers). Hans‐Peter Kiem is often cited by papers focused on Virus-based gene therapy research (170 papers), CRISPR and Genetic Engineering (85 papers) and CAR-T cell therapy research (77 papers). Hans‐Peter Kiem collaborates with scholars based in United States, South Africa and Germany. Hans‐Peter Kiem's co-authors include Rainer Storb, Brian C. Beard, Grant D. Trobridge, Richard A. Nash, Jennifer E. Adair, H. Joachim Deeg, Julia Morris, Christopher W. Peterson, Paul J. Martin and KG Blume and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Hans‐Peter Kiem

296 papers receiving 9.9k citations

Hit Papers

Use of a SCID mouse/human lymphoma model to evaluate cyto... 1991 2026 2002 2014 1991 1997 2011 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans‐Peter Kiem United States 53 4.6k 3.8k 3.1k 2.9k 2.6k 307 10.0k
Boris Fehse Germany 54 5.1k 1.1× 2.8k 0.7× 2.0k 0.7× 2.7k 0.9× 1.5k 0.6× 252 9.2k
Robert E. Donahue United States 46 3.9k 0.8× 3.5k 0.9× 2.0k 0.7× 1.9k 0.7× 1.9k 0.7× 177 7.8k
Alessandro Aiuti Italy 50 4.3k 0.9× 3.4k 0.9× 1.3k 0.4× 3.6k 1.3× 3.8k 1.5× 193 10.1k
Kenneth I. Weinberg United States 51 3.9k 0.8× 1.7k 0.5× 2.1k 0.7× 2.2k 0.8× 4.1k 1.6× 180 10.8k
Fulvio Mavilio Italy 58 9.4k 2.0× 4.8k 1.3× 1.5k 0.5× 2.7k 0.9× 2.0k 0.8× 190 14.6k
Marina Cavazzana France 65 7.0k 1.5× 6.0k 1.6× 3.1k 1.0× 3.5k 1.2× 5.2k 2.0× 303 14.7k
Donald B. Kohn United States 69 9.8k 2.1× 7.8k 2.1× 1.5k 0.5× 3.6k 1.3× 3.1k 1.2× 361 16.0k
Claudio Bordignon Italy 58 5.9k 1.3× 4.7k 1.2× 2.0k 0.6× 5.9k 2.0× 5.0k 1.9× 222 14.1k
Kenneth Cornetta United States 46 3.3k 0.7× 3.1k 0.8× 1.3k 0.4× 2.4k 0.8× 1.3k 0.5× 171 7.1k
Megan Sykes United States 75 3.5k 0.8× 3.6k 1.0× 6.6k 2.1× 2.6k 0.9× 10.7k 4.1× 411 20.9k

Countries citing papers authored by Hans‐Peter Kiem

Since Specialization
Citations

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

Fields of papers citing papers by Hans‐Peter Kiem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans‐Peter Kiem. 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 Hans‐Peter Kiem. The network helps show where Hans‐Peter Kiem may publish in the future.

Co-authorship network of co-authors of Hans‐Peter Kiem

This figure shows the co-authorship network connecting the top 25 collaborators of Hans‐Peter Kiem. A scholar is included among the top collaborators of Hans‐Peter Kiem 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 Hans‐Peter Kiem. Hans‐Peter Kiem 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.
Petty, Nicholas, Stefan Radtke, Olivier Humbert, et al.. (2025). Protection of CD33-modified hematopoietic stem cell progeny from CD33-directed CAR T cells in rhesus macaques. Blood Advances. 9(10). 2367–2378.
2.
Bui, John, et al.. (2024). CD20 CAR T cells safely and reversibly ablate B cell follicles in a non-human primate model of HIV persistence. Molecular Therapy. 32(5). 1238–1251. 3 indexed citations
4.
Li, Chang, Peter Ruminski, Michael P. Rettig, et al.. (2024). A simplified G-CSF–free procedure allows for in vivo HSC gene therapy of sickle cell disease in a mouse model. Blood Advances. 8(15). 4089–4101. 7 indexed citations
5.
Li, Chang, Aphrodite Georgakopoulou, Gregory A. Newby, et al.. (2023). In vivo HSC prime editing rescues Sickle Cell Disease in a mouse model. Blood. 141(17). 2085–2099. 51 indexed citations
6.
Kiem, Hans‐Peter, et al.. (2023). Choosing the right mouse model: comparison of humanized NSG and NBSGW mice for in vivo HSC gene therapy. Blood Advances. 8(4). 916–926. 7 indexed citations
7.
Radtke, Stefan, Mark Enstrom, Dnyanada Pande, et al.. (2023). Stochastic fate decisions of HSCs after transplantation: early contribution, symmetric expansion, and pool formation. Blood. 142(1). 33–43. 10 indexed citations
8.
Galy, Anne, Ben Berkhout, Karine Breckpot, et al.. (2023). Recent Advances Using Genetic Therapies Against Infectious Diseases and for Vaccination. Human Gene Therapy. 34(17-18). 896–904. 2 indexed citations
9.
North, Khrystyna, Salima Benbarche, Bo Liu, et al.. (2022). Synthetic introns enable splicing factor mutation-dependent targeting of cancer cells. Nature Biotechnology. 40(7). 1103–1113. 38 indexed citations
10.
Humbert, Olivier, et al.. (2022). Efficient polymer nanoparticle-mediated delivery of gene editing reagents into human hematopoietic stem and progenitor cells. Molecular Therapy. 30(6). 2186–2198. 24 indexed citations
11.
Li, Chang, Aphrodite Georgakopoulou, Gregory A. Newby, et al.. (2022). In vivo base editing by a single i.v. vector injection for treatment of hemoglobinopathies. JCI Insight. 7(19). 24 indexed citations
12.
Singh, Swati, Chun‐Yu Chen, Chong Li, et al.. (2022). Intraosseous delivery of platelet-targeted factor VIII lentiviral vector in humanized NBSGW mice. Blood Advances. 6(19). 5556–5569. 5 indexed citations
13.
Sheih, Alyssa, Valentin Voillet, Laïla‐Aïcha Hanafi, et al.. (2020). Clonal kinetics and single-cell transcriptional profiling of CAR-T cells in patients undergoing CD19 CAR-T immunotherapy. Nature Communications. 11(1). 219–219. 177 indexed citations
14.
Humbert, Olivier, Stefan Radtke, Sowmya Reddy, et al.. (2019). Therapeutically relevant engraftment of a CRISPR-Cas9–edited HSC-enriched population with HbF reactivation in nonhuman primates. Science Translational Medicine. 11(503). 87 indexed citations
15.
Shahbazi, Reza, Sara Kubek, Kevin G. Haworth, et al.. (2019). Targeted homology-directed repair in blood stem and progenitor cells with CRISPR nanoformulations. Nature Materials. 18(10). 1124–1132. 135 indexed citations
16.
Radtke, Stefan, Jennifer E. Adair, Morgan A. Giese, et al.. (2017). A distinct hematopoietic stem cell population for rapid multilineage engraftment in nonhuman primates. Science Translational Medicine. 9(414). 75 indexed citations
17.
Richter, Maximilian, Kamola Saydaminova, Roma Yumul, et al.. (2016). In vivo transduction of primitive mobilized hematopoietic stem cells after intravenous injection of integrating adenovirus vectors. Blood. 128(18). 2206–2217. 84 indexed citations
18.
Flowers, Mary E.D., Yoshihiro Inamoto, Paul A. Carpenter, et al.. (2011). Comparative analysis of risk factors for acute graft-versus-host disease and for chronic graft-versus-host disease according to National Institutes of Health consensus criteria. Blood. 117(11). 3214–3219. 453 indexed citations breakdown →
19.
Purton, Louise E., Julia Morris, Irwin D. Bernstein, Steven Collins, & Hans‐Peter Kiem. (2001). All- trans Retinoic Acid Facilitates Oncoretrovirus-Mediated Transduction of Hematopoietic Repopulating Stem Cells. Journal of Hematotherapy & Stem Cell Research. 10(6). 815–825. 1 indexed citations
20.
Göerner, Martin, et al.. (2000). Expansion and Transduction of Nonenriched Human Cord Blood Cells Using HS-5 Conditioned Medium and FLT3-L. Journal of Hematotherapy & Stem Cell Research. 9(5). 759–765. 9 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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