Christian Flotho

4.6k total citations
62 papers, 1.6k citations indexed

About

Christian Flotho is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Christian Flotho has authored 62 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 40 papers in Hematology and 16 papers in Genetics. Recurrent topics in Christian Flotho's work include Acute Myeloid Leukemia Research (37 papers), Epigenetics and DNA Methylation (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Christian Flotho is often cited by papers focused on Acute Myeloid Leukemia Research (37 papers), Epigenetics and DNA Methylation (14 papers) and Chronic Lymphocytic Leukemia Research (12 papers). Christian Flotho collaborates with scholars based in Germany, United States and Italy. Christian Flotho's co-authors include Charlotte M. Niemeyer, Christoph Plass, Michael Lübbert, Christiane Batz, Rainer Claus, Inga Sandrock, James R. Downing, Henrik Hasle, Michaela Schneider and Christian P. Kratz and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and Blood.

In The Last Decade

Christian Flotho

58 papers receiving 1.5k citations

Peers

Christian Flotho
Sébastien Malinge United States
Zhaohui Gu United States
Sanne Lugthart Netherlands
Eva Barragán Spain
Manoj Raghavan United Kingdom
F Viguié France
Brenton G. Mar United States
Henrik Lilljebjörn Sweden
Eva Hellström‐Lindberg Sweden
Ulrike Schäkel Germany
Sébastien Malinge United States
Christian Flotho
Citations per year, relative to Christian Flotho Christian Flotho (= 1×) peers Sébastien Malinge

Countries citing papers authored by Christian Flotho

Since Specialization
Citations

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

Fields of papers citing papers by Christian Flotho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Flotho

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Flotho. A scholar is included among the top collaborators of Christian Flotho 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 Christian Flotho. Christian Flotho 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.
Flotho, Christian. (2024). Onkologische Erkrankungen beim Neugeborenen. 13(2). 151–164.
2.
Meng, Ke, Jun Wang, Alexandra Emilia Schlaak, et al.. (2024). CD39, CD73 and the Adenosine Pathway Mediate Immune Escape in Juvenile Myelomonocytic Leukemia (JMML). Blood. 144(Supplement 1). 4514–4514. 1 indexed citations
3.
Dvorak, Mai, Charlotte M. Niemeyer, Christian Flotho, et al.. (2023). Epigenetic Profiling of PTPN11 Mutant JMML Hematopoietic Stem and Progenitor Cells Reveals an Aberrant Histone Landscape. Cancers. 15(21). 5204–5204. 1 indexed citations
4.
Wu, Ying, Geoffroy Andrieux, Konrad Aumann, et al.. (2023). BH3 mimetics and azacitidine show synergistic effects on juvenile myelomonocytic leukemia. Leukemia. 38(1). 136–148. 3 indexed citations
5.
Saettini, Francesco, Tiziana Coliva, Francesca Vendemini, et al.. (2022). Abnormal B-Cell Maturation and Increased Transitional B Cells in CBL Syndrome. Frontiers in Pediatrics. 10. 935951–935951. 1 indexed citations
6.
Lammens, Tim, Ying Wu, Miriam Erlacher, et al.. (2021). Long non-coding RNAs as novel therapeutic targets in juvenile myelomonocytic leukemia. Scientific Reports. 11(1). 2801–2801. 13 indexed citations
7.
8.
Stieglitz, Elliot, Tali Mazor, Adam B. Olshen, et al.. (2017). Genome-wide DNA methylation is predictive of outcome in juvenile myelomonocytic leukemia. Nature Communications. 8(1). 2127–2127. 60 indexed citations
9.
Boerries, Melanie, Hauke Busch, Aikaterini Symeonidi, et al.. (2016). CREBBP is a target of epigenetic, but not genetic, modification in juvenile myelomonocytic leukemia. Clinical Epigenetics. 8(1). 50–50. 19 indexed citations
10.
Poetsch, Anna R., Daniel B. Lipka, Tania Witte, et al.. (2014). RASA4undergoes DNA hypermethylation in resistant juvenile myelomonocytic leukemia. Epigenetics. 9(9). 1252–1260. 29 indexed citations
11.
Sluis, I. van der, Anja Möricke, Arend von Stackelberg, et al.. (2013). Pediatric Acute Lymphoblastic Leukemia: Efficacy and safety of recombinant E. coli-asparaginase in infants (less than one year of age) with acute lymphoblastic leukemia. Haematologica. 98(11). 1697–1701. 14 indexed citations
12.
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
13.
Tauscher, Marcel, Gudrun Göhring, Stefanie Glaser, et al.. (2010). Clonal heterogeneity in childhood myelodysplastic syndromes—Challenge for the detection of chromosomal imbalances by array‐CGH. Genes Chromosomes and Cancer. 49(10). 885–900. 14 indexed citations
14.
Dührsen, Ulrich, Christian P. Kratz, Christian Flotho, et al.. (2010). Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 G208R mutation. Annals of Hematology. 90(3). 301–306. 5 indexed citations
15.
Yang, Zhenyun, Takako Kondo, Sarah C. Nabinger, et al.. (2009). Increased c-Jun Expression and Reduced GATA2 Expression Promote Aberrant Monocytic Differentiation Induced by Activating PTPN11 Mutants. Molecular and Cellular Biology. 29(16). 4376–4393. 20 indexed citations
16.
Steinemann, Doris, Larissa Arning, Manfred Stuhrmann, et al.. (2009). Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1. Haematologica. 95(2). 320–323. 48 indexed citations
17.
Flotho, Christian, Christian P. Kratz, & Charlotte M. Niemeyer. (2007). Targeting RAS Signaling Pathways in Juvenile Myelomonocytic Leukemia. Current Drug Targets. 8(6). 715–725. 31 indexed citations
18.
19.
Flotho, Christian, Sara Mach‐Pascual, Gerd E. Schmahl, et al.. (1999). RAS mutations and clonality analysis in children with juvenile myelomonocytic leukemia (JMML). Leukemia. 13(1). 32–37. 130 indexed citations
20.
Schmahl, Gerd E., et al.. (1997). Expression of the Evi‐1 gene in haemopoietic cells of children with juvenile myelomonocytic leukaemia and normal donors. British Journal of Haematology. 99(4). 882–887. 13 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 Sébastien Malinge Breakdown of academic impact, for papers by Zhaohui Gu Breakdown of academic impact, for papers by Sanne Lugthart Breakdown of academic impact, for papers by Eva Barragán Breakdown of academic impact, for papers by Manoj Raghavan Breakdown of academic impact, for papers by F Viguié Breakdown of academic impact, for papers by Brenton G. Mar Breakdown of academic impact, for papers by Henrik Lilljebjörn Breakdown of academic impact, for papers by Eva Hellström‐Lindberg Breakdown of academic impact, for papers by Ulrike Schäkel
Rankless by CCL
2026