Tim Ripperger

2.3k total citations
46 papers, 756 citations indexed

About

Tim Ripperger is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Tim Ripperger has authored 46 papers receiving a total of 756 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Hematology. Recurrent topics in Tim Ripperger's work include Acute Myeloid Leukemia Research (10 papers), Genetic factors in colorectal cancer (9 papers) and Cancer Genomics and Diagnostics (7 papers). Tim Ripperger is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Genetic factors in colorectal cancer (9 papers) and Cancer Genomics and Diagnostics (7 papers). Tim Ripperger collaborates with scholars based in Germany, France and United States. Tim Ripperger's co-authors include Brigitte Schlegelberger, Dorothea Gadzicki, Alfons Meindl, Doris Steinemann, Christian P. Kratz, Ulrich Lehmann, Thomas Illig, H. Troger, Jörg Schmidtke and Katharina Wimmer and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and JNCI Journal of the National Cancer Institute.

In The Last Decade

Tim Ripperger

45 papers receiving 741 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tim Ripperger Germany 15 341 259 215 203 135 46 756
Chimene Kesserwan United States 14 240 0.7× 224 0.9× 118 0.5× 82 0.4× 179 1.3× 24 661
Nicolas Goardon France 16 470 1.4× 245 0.9× 223 1.0× 114 0.6× 160 1.2× 29 905
Marian Stevens‐Kroef Netherlands 14 366 1.1× 131 0.5× 133 0.6× 100 0.5× 153 1.1× 30 692
Catherine Dubois d’Enghien France 13 528 1.5× 177 0.7× 179 0.8× 71 0.3× 264 2.0× 19 870
Serena Masciari United States 13 320 0.9× 224 0.9× 245 1.1× 207 1.0× 445 3.3× 23 798
Beate Betz Germany 16 610 1.8× 243 0.9× 224 1.0× 167 0.8× 187 1.4× 25 928
Ilse Chudoba Germany 16 436 1.3× 410 1.6× 149 0.7× 86 0.4× 71 0.5× 36 858
Julie Tinat France 7 319 0.9× 281 1.1× 249 1.2× 157 0.8× 305 2.3× 13 703
Spyros Skoulakis United Kingdom 8 465 1.4× 149 0.6× 272 1.3× 76 0.4× 58 0.4× 10 770
Sabrina Tosi United Kingdom 20 550 1.6× 205 0.8× 125 0.6× 129 0.6× 151 1.1× 52 1.1k

Countries citing papers authored by Tim Ripperger

Since Specialization
Citations

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

Fields of papers citing papers by Tim Ripperger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tim Ripperger

This figure shows the co-authorship network connecting the top 25 collaborators of Tim Ripperger. A scholar is included among the top collaborators of Tim Ripperger 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 Tim Ripperger. Tim Ripperger 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.
Knops, Ruth, et al.. (2024). Acute myeloid leukemia associated RUNX1 variants induce aberrant expression of transcription factor TCF4. Leukemia. 39(2). 520–523. 1 indexed citations
2.
Lazić, Jelena, et al.. (2023). Perception and management of cancer predisposition in pediatric cancer centers: A European‐wide questionnaire‐based survey. Pediatric Blood & Cancer. 70(5). e30229–e30229.
3.
Kratz, Christian P., Robert J. Autry, Natalie Jäger, et al.. (2023). Reply to Li and Colleagues. JNCI Journal of the National Cancer Institute. 115(6). 760–761. 1 indexed citations
4.
Ripperger, Tim, Christian Vokuhl, Sebastian Bauer, et al.. (2023). Genetic susceptibility in children, adolescents, and young adults diagnosed with soft-tissue sarcomas. European Journal of Medical Genetics. 66(5). 104718–104718. 7 indexed citations
5.
Agarwal, Anupriya, Jane E. Churpek, Nicolas Duployez, et al.. (2022). Validation and clinical application of transactivation assays forRUNX1variant classification. Blood Advances. 6(11). 3195–3200. 4 indexed citations
6.
Ripperger, Tim, et al.. (2021). Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire. Familial Cancer. 20(4). 257–262. 11 indexed citations
7.
Penkert, Judith, Martin Seifert, Bernd Auber, et al.. (2021). Plasma Metabolome Signature Indicative of BRCA1 Germline Status Independent of Cancer Incidence. Frontiers in Oncology. 11. 627217–627217. 3 indexed citations
8.
Lammens, Tim, Alina Ferster, Miriam Erlacher, et al.. (2021). Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies. Leukemia. 35(11). 3304–3308. 10 indexed citations
9.
Morlot, Susanne, Gunnar Schmidt, Bernd Auber, et al.. (2020). De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia. Clinical Genetics. 98(4). 374–378. 5 indexed citations
10.
Sogkas, Georgios, Natalia Dubrowinskaja, Anke K. Bergmann, et al.. (2019). Progressive Immunodeficiency with Gradual Depletion of B and CD4+ T Cells in Immunodeficiency, Centromeric Instability and Facial Anomalies Syndrome 2 (ICF2). SHILAP Revista de lepidopterología. 7(2). 34–34. 16 indexed citations
11.
Golas, Monika M., Bernd Auber, Tim Ripperger, et al.. (2019). Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A. American Journal of Medical Genetics Part A. 179(7). 1383–1389. 9 indexed citations
12.
Penkert, Judith, Gunnar Schmidt, Winfried Hofmann, et al.. (2018). Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast Cancer Research. 20(1). 87–87. 6 indexed citations
13.
Ripperger, Tim & Brigitte Schlegelberger. (2018). Genetische Prädisposition für Krebserkrankungen im Kindesalter. Der Pathologe. 39(S2). 306–310. 4 indexed citations
14.
Maletzki, Claudia, Ingrid Bauer, Tim Ripperger, et al.. (2017). Frameshift mutational target gene analysis identifies similarities and differences in constitutional mismatch repair‐deficiency and Lynch syndrome. Molecular Carcinogenesis. 56(7). 1753–1764. 11 indexed citations
15.
Vogt, J., Tim Ripperger, Brigitte Pabst, et al.. (2016). PMS2 inactivation by a complex rearrangement involving an HERV retroelement and the inverted 100-kb duplicon on 7p22.1. European Journal of Human Genetics. 24(11). 1598–1604. 7 indexed citations
16.
Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations
17.
Ripperger, Tim, Marcel Tauscher, Kathrin Thomay, et al.. (2013). No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21–21q22. Leukemia Research. 37(6). 721–723. 2 indexed citations
18.
Ripperger, Tim, Marcel Tauscher, Brigitte Pabst, et al.. (2011). Constitutional trisomy 8p11.21‐q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia. British Journal of Haematology. 155(2). 209–217. 25 indexed citations
19.
Ripperger, Tim, Carmela Beger, Nils Rahner, et al.. (2009). Constitutional mismatch repair deficiency and childhood leukemia/lymphoma - report on a novel biallelic MSH6 mutation. Haematologica. 95(5). 841–844. 38 indexed citations
20.
Rudolph, Cornelia, Doris Steinemann, Nils von Neuhoff, et al.. (2004). Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genetics and Cytogenetics. 153(2). 144–150. 34 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 Chimene Kesserwan Breakdown of academic impact, for papers by Nicolas Goardon Breakdown of academic impact, for papers by Marian Stevens‐Kroef Breakdown of academic impact, for papers by Catherine Dubois d’Enghien Breakdown of academic impact, for papers by Serena Masciari Breakdown of academic impact, for papers by Beate Betz Breakdown of academic impact, for papers by Ilse Chudoba Breakdown of academic impact, for papers by Julie Tinat Breakdown of academic impact, for papers by Spyros Skoulakis Breakdown of academic impact, for papers by Sabrina Tosi
Rankless by CCL
2026