Daniela Späth

6.1k citations
26 papers · 3.2k · 2 hit papers · h-index 12

Impact in

  • Hematology top 0.2%
    • Acute Myeloid Leukemia Research
    • Chronic Myeloid Leukemia Treatments
    • Hematopoietic Stem Cell Transplantation
  • Genetics top 1%
    • Myeloproliferative Neoplasms: Diagnosis and Treatment

Papers in

    • Acute Myeloid Leukemia Research 23
    • Chronic Myeloid Leukemia Treatments 9
    • Protein Degradation and Inhibitors 3
    • Histone Deacetylase Inhibitors Research 3
    • Epigenetics and DNA Methylation 1

Daniela Späth

26 papers receiving 3.1k citations

Daniela Späth's Hit Papers

IDH1andIDH2Mutations Are Frequent Genetic Alterations in Acute Myeloid Leukemia and Confer Adverse Prognosis in Cytogenetically Normal Acute Myeloid Leukemia WithNPM1Mutation WithoutFLT3Internal Tandem Duplication 2010 · 581 citations
5810+6+12Years since publication2505007501000

Peers

Daniela Späth
Comparison fields: 5 of 83
  • Hematology 2.6k
  • Genetics 844
  • Cancer Research 520
  • Public Health, Environmental and Occupational Health 537
  • Molecular Biology 1.4k
Replace Frédérik Damm with:
Frédérik Damm Germany
Pascual Bolufer Spain
Andrea Kuendgen Germany
Angelo Guerrasio Italy
Catherine C. Coombs United States
Erica Travaglino Italy
Yana Pikman United States
T Fujimoto Japan
Pinkal Desai United States
Christian Flotho Germany
Daniela Späth relative to Frédérik Damm Germany Frédérik Damm's profile →
Citations per field
00.5×1.5×2.1×
Frédérik Damm · 1×
Citations per year

Countries citing papers authored by Daniela Späth

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Späth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Daniela Späth, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniela Späth Line = papers co-authored together Daniela Späth links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations and Treatment Outcome in Cytogenetically Normal Acute Myeloid Leukemia
Hit paper breakdown →
20081112
2
IDH1andIDH2Mutations Are Frequent Genetic Alterations in Acute Myeloid Leukemia and Confer Adverse Prognosis in Cytogenetically Normal Acute Myeloid Leukemia WithNPM1Mutation WithoutFLT3Internal Tandem Duplication
Hit paper breakdown →
2010581
3 2011333
4 2010316
5 2009201
6 2013182
7 2008145
8 2012143
9 201242
10 200832
11 200027
12 200614
13 201210
14 20079
15 20076
16 20093
17 20113
18 20093
19 20112
20 20092

About Daniela Späth

Daniela Späth is a scholar working on Hematology, Molecular Biology, Genetics, Public Health, Environmental and Occupational Health and Infectious Diseases, having authored 26 papers that have together received 3.2k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (23 papers), Chronic Myeloid Leukemia Treatments (9 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (7 papers), Acute Lymphoblastic Leukemia research (3 papers), Protein Degradation and Inhibitors (3 papers), Histone Deacetylase Inhibitors Research (3 papers), Epigenetics and DNA Methylation (1 paper) and Cancer Risks and Factors (1 paper). The work is most often cited by research in Hematology (2.6k citations), Genetics (844 citations), Cancer Research (520 citations), Public Health, Environmental and Occupational Health (537 citations) and Molecular Biology (1.4k citations). Daniela Späth has collaborated with scholars based in Germany, Austria and United States. Frequent co-authors include Richard F. Schlenk, Hartmut Döhner, Konstanze Döhner, Lars Bullinger, Arnold Ganser, Jürgen Krauter, Marianne Habdank, Brigitte Schlegelberger, Andrea Corbacioglu and Katharina S. Götze. Their work appears in journals such as Blood, Journal of Clinical Oncology, Haematologica, Scandinavian Journal of Rheumatology and New England Journal of Medicine.

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