Susanne Schnittger

35.2k citations
435 papers · 17.5k indexed · 2 hit papers · h-index 71
Topics
Acute Myeloid Leukemia Research (300 papers)Chronic Myeloid Leukemia Treatments (122 papers)Chronic Lymphocytic Leukemia Research (96 papers)

In The Last Decade

Susanne Schnittger

419 papers receiving 17.2k citations

Hit Papers

Analysis of FLT3 length mutations in 1003 patients with a...200120262009201720022001200400600

Peers

Susanne Schnittger
Comparison fields: 5 of 123
  • Hematology 13.1k
  • Molecular Biology 7.7k
  • Genetics 6.2k
  • Public Health, Environmental and Occupational Health 3.8k
  • Cancer Research 2.1k
Replace D. Gary Gilliland with:
D. Gary Gilliland United States
Gordon W. Dewald United States
Rhett P. Ketterling United States
Cristina Mecucci Italy
Ghulam J. Mufti United Kingdom
Nicholas C.P. Cross United Kingdom
Marilyn L. Slovak United States
Bertil Johansson Sweden
H. R. Gralnick United States
Anne Hagemeijer Belgium
Susanne Schnittger relative to D. Gary Gilliland United States D. Gary Gilliland's profile →
Citations per field
00.5×1.7×
D. Gary Gilliland · 1×
Citations per year

Countries citing papers authored by Susanne Schnittger

Since Specialization
Citations

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

Fields of papers citing papers by Susanne Schnittger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanne Schnittger

This figure shows the co-authorship network connecting the top 25 collaborators of Susanne Schnittger. A scholar is included among the top collaborators of Susanne Schnittger 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 Susanne Schnittger. Susanne Schnittger 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
#WorkIndexed citations
1 28
2 0
3 15
4 219
5 8
6 21
7 248
8 41
9 6
10 23
11 12
12 59
13 3
14 232
15 161
16 32
17
Differentiation block in FLT3 mutant AML by inactivation of C/EBPalpha function by phosphorylation
1
18
Multi-genetic basis for prognostication in acute myeloid leukemia with aberrant and prognostically intermediate karyotypes as determined by gene expression profiling
1
19 49
20 0

About Susanne Schnittger

Susanne Schnittger is a scholar working on Hematology, Genetics and Pathology and Forensic Medicine, having authored 435 papers that have together received 17.5k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (300 papers), Chronic Myeloid Leukemia Treatments (122 papers) and Chronic Lymphocytic Leukemia Research (96 papers). The work is most often cited by research in Hematology (13.1k citations), Genetics (6.2k citations) and Cancer Research (2.1k citations). Susanne Schnittger has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Torsten Haferlach, Wolfgang Kern, Claudia Schoch, Claudia Haferlach, Wolfgang Hiddemann, Ulrike Bacher, Alexander Kohlmann, Frank Dicker, Tamara Alpermann and Martin Dugas. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

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

Rankless by CCL
2026