Philipp A. Greif

5.1k total citations
59 papers, 1.4k citations indexed

About

Philipp A. Greif is a scholar working on Hematology, Molecular Biology and Cancer Research. According to data from OpenAlex, Philipp A. Greif has authored 59 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Hematology, 34 papers in Molecular Biology and 18 papers in Cancer Research. Recurrent topics in Philipp A. Greif's work include Acute Myeloid Leukemia Research (37 papers), Cancer Genomics and Diagnostics (16 papers) and Epigenetics and DNA Methylation (11 papers). Philipp A. Greif is often cited by papers focused on Acute Myeloid Leukemia Research (37 papers), Cancer Genomics and Diagnostics (16 papers) and Epigenetics and DNA Methylation (11 papers). Philipp A. Greif collaborates with scholars based in Germany, United States and New Zealand. Philipp A. Greif's co-authors include Sebastian Vosberg, Stefan K. Bohlander, Karsten Spiekermann, Klaus H. Metzeler, Helmut Blum, Martín Neumann, Cornelia Schlee, Claudia D. Baldus, Paul Kerbs and Tobias Herold and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Philipp A. Greif

55 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philipp A. Greif Germany 19 718 696 387 227 216 59 1.4k
Marc Delord France 20 699 1.0× 460 0.7× 325 0.8× 134 0.6× 212 1.0× 56 1.7k
Tinisha McDonald United States 12 753 1.0× 868 1.2× 543 1.4× 94 0.4× 372 1.7× 30 1.7k
Matthew Holt United States 16 581 0.8× 960 1.4× 467 1.2× 138 0.6× 160 0.7× 34 1.6k
Emmanuelle Clappier France 20 785 1.1× 807 1.2× 290 0.7× 712 3.1× 235 1.1× 46 1.7k
Regina Kunzmann Germany 20 496 0.7× 1.1k 1.5× 257 0.7× 183 0.8× 380 1.8× 33 1.5k
Violaine Havelange Belgium 17 769 1.1× 678 1.0× 558 1.4× 468 2.1× 206 1.0× 46 1.7k
Francesco Albano Italy 25 771 1.1× 1.0k 1.5× 236 0.6× 322 1.4× 597 2.8× 140 1.8k
Amy S. Duffield United States 22 570 0.8× 546 0.8× 343 0.9× 126 0.6× 211 1.0× 86 1.5k
Enkhtsetseg Purev United States 21 768 1.1× 551 0.8× 755 2.0× 75 0.3× 193 0.9× 55 1.6k
Luisa Anelli Italy 23 563 0.8× 693 1.0× 149 0.4× 237 1.0× 436 2.0× 87 1.3k

Countries citing papers authored by Philipp A. Greif

Since Specialization
Citations

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

Fields of papers citing papers by Philipp A. Greif

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philipp A. Greif. 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 Philipp A. Greif. The network helps show where Philipp A. Greif may publish in the future.

Co-authorship network of co-authors of Philipp A. Greif

This figure shows the co-authorship network connecting the top 25 collaborators of Philipp A. Greif. A scholar is included among the top collaborators of Philipp A. Greif 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 Philipp A. Greif. Philipp A. Greif 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.
Heinrich, Kathrin, Andreas Jung, C. Benedikt Westphalen, et al.. (2024). Genetics and beyond: Precision Medicine Real-World Data for Patients with Cervical, Vaginal or Vulvar Cancer in a Tertiary Cancer Center. International Journal of Molecular Sciences. 25(4). 2345–2345. 3 indexed citations
2.
Lange, Philipp, Dorit Di Gioia, M. Schmidt, et al.. (2023). Implementing precision oncology for sarcoma patients: the CCCLMUmolecular tumor board experience. Journal of Cancer Research and Clinical Oncology. 149(15). 13973–13983. 3 indexed citations
3.
Chang, Yun-Chien, Johannes Bagnoli, Paul Kerbs, et al.. (2023). UHMK1 is a novel splicing regulatory kinase. Journal of Biological Chemistry. 299(4). 103041–103041. 6 indexed citations
4.
Schmitz, Werner, Paul Kerbs, Monica Cusan, et al.. (2023). ZBTB7A Loss Promotes Synthesis of Lipids and Ketone Bodies in Myeloid Leukemia. Blood. 142(Supplement 1). 1390–1390. 1 indexed citations
5.
Barmettler, Sara, Svetlana Sharapova, Tomáš Milota, et al.. (2022). Genomics Driving Diagnosis and Treatment of Inborn Errors of Immunity With Cancer Predisposition. The Journal of Allergy and Clinical Immunology In Practice. 10(7). 1725–1736.e2. 3 indexed citations
6.
Kerbs, Paul, Sebastian Vosberg, Stefan Krebs, et al.. (2021). Fusion gene detection by RNA-sequencing complements diagnostics of acute myeloid leukemia and identifies recurring <i>NRIP1-MIR99AHG</i> rearrangements. Haematologica. 107(1). 100–111. 20 indexed citations
7.
Vosberg, Sebastian, Thomas Engleitner, Rupert Öllinger, et al.. (2021). Disease Modeling on Tumor Organoids Implicates AURKA as a Therapeutic Target in Liver Metastatic Colorectal Cancer. Cellular and Molecular Gastroenterology and Hepatology. 13(2). 517–540. 24 indexed citations
8.
Kerbs, Paul, Johannes Bagnoli, Luise Hartmann, et al.. (2020). ZBTB7A prevents RUNX1-RUNX1T1-dependent clonal expansion of human hematopoietic stem and progenitor cells. Oncogene. 39(15). 3195–3205. 14 indexed citations
9.
Westphalen, C. Benedikt, Andreas Jung, Joerg Kumbrink, et al.. (2020). NGS-guided precision oncology in metastatic breast and gynecological cancer: first experiences at the CCC Munich LMU. Archives of Gynecology and Obstetrics. 303(5). 1331–1345. 11 indexed citations
10.
Greif, Philipp A., et al.. (2019). GATA2 mutations in myeloid malignancies: Two zinc fingers in many pies. IUBMB Life. 72(1). 151–158. 12 indexed citations
11.
Chen-Wichmann, Linping, Colin Hockings, Karsten Spiekermann, et al.. (2018). Compatibility of RUNX1/ETO fusion protein modules driving CD34+ human progenitor cell expansion. Oncogene. 38(2). 261–272. 6 indexed citations
12.
Neumann, Martín, Sebastian Vosberg, Alva Rani James, et al.. (2016). Molecular alterations in bone marrow mesenchymal stromal cells derived from acute myeloid leukemia patients. Leukemia. 31(5). 1069–1078. 81 indexed citations
13.
Bauer, Julia, Katrin Reiter, Annika Dufour, et al.. (2016). The new and recurrent FLT3 juxtamembrane deletion mutation shows a dominant negative effect on the wild-type FLT3 receptor. Scientific Reports. 6(1). 28032–28032. 10 indexed citations
14.
Yang, Hui-Min, Michael Vieth, Lothar Veits, et al.. (2016). In-depth mutational analyses of colorectal neuroendocrine carcinomas with adenoma or adenocarcinoma components. Modern Pathology. 30(1). 95–103. 80 indexed citations
15.
Neumann, Martín, Sandra Heesch, Cornelia Schlee, et al.. (2013). Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations. Blood. 121(23). 4749–4752. 143 indexed citations
16.
Greif, Philipp A., Nikola P. Konstandin, Klaus H. Metzeler, et al.. (2012). RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes. Haematologica. 97(12). 1909–1915. 66 indexed citations
17.
Greif, Philipp A., Sebastian Eck, Nikola P. Konstandin, et al.. (2011). Identification of recurring tumor-specific somatic mutations in acute myeloid leukemia by transcriptome sequencing. Leukemia. 25(5). 821–827. 44 indexed citations
18.
Reindl, Carola, Hilmar Quentmeier, Konstantin Petropoulos, et al.. (2009). CBL Exon 8/9 Mutants Activate the FLT3 Pathway and Cluster in Core Binding Factor/11q Deletion Acute Myeloid Leukemia/Myelodysplastic Syndrome Subtypes. Clinical Cancer Research. 15(7). 2238–2247. 89 indexed citations
19.
Mohamed, Mahmoud, Philipp A. Greif, James J. Diamond, et al.. (2008). Changes in chromatin phenotype predict the response to hormonal deprivation therapy in patients with prostate cancer. British Journal of Urology. 103(3). 391–398. 4 indexed citations
20.
Greif, Philipp A., et al.. (2007). The leukemogenic CALM/AF10 fusion protein alters the subcellular localization of the lymphoid regulator Ikaros. Oncogene. 27(20). 2886–2896. 26 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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