Peter Papenhausen
- Genetics top 10%
- Molecular Biology
- Plant Science
- Hematology
- Pediatrics, Perinatology and Child Health
- Co-authors
- Elisabeth PaiettaMichelle MachaBinquan HuangJohn A. CrollaSusan L. ChristianDavid H. LedbetterPeter H. WiernikE. Richard Stanley
- Topics
- Genomic variations and chromosomal abnormalities (5 papers)Acute Myeloid Leukemia Research (4 papers)Prenatal Screening and Diagnostics (3 papers)
- Cited by
- GeneticsHematologyPlant Science
- Journals
- SHILAP Revista de lepidopterologíaHuman GeneticsGenetics in Medicine
- Partner nations
- United StatesUnited KingdomQatar
In The Last Decade
Peter Papenhausen
14 papers receiving 336 citations
Peers
Comparison fields: 5 of 44
- Genetics 194
- Molecular Biology 154
- Plant Science 105
- Hematology 54
- Pediatrics, Perinatology and Child Health 49
Countries citing papers authored by Peter Papenhausen
This map shows the geographic impact of Peter Papenhausen'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 Peter Papenhausen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Papenhausen more than expected).
Fields of papers citing papers by Peter Papenhausen
This network shows the impact of papers produced by Peter Papenhausen. 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 Peter Papenhausen. The network helps show where Peter Papenhausen may publish in the future.
Co-authorship network of co-authors of Peter Papenhausen
This figure shows the co-authorship network connecting the top 25 collaborators of Peter Papenhausen. A scholar is included among the top collaborators of Peter Papenhausen 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 Peter Papenhausen. Peter Papenhausen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 8 | |
| 4 | 1 | |
| 5 | 9 | |
| 6 | 3 | |
| 7 | 4 | |
| 8 | 16 | |
| 9 | 129 | |
| 10 | 82 | |
| 11 | Expression of the macrophage growth factor, CSF-1 and its receptor c-fms by a Hodgkin's disease-derived cell line and its variants. | 51 |
| 12 | Distinct antigen expression related to DNA ploidy in a case of biphenotypic leukemia. | 4 |
| 13 | TdT+/nonlymphoid antigen+ acute leukemias: immunologic and karyotypic monitoring during therapy and at relapse suggests the transformation of a bipotential stem cell. | 8 |
| 14 | The 5q-- deletion: correlation of breakpoints with the immunophenotype of leukemic blast cells. | 9 |
| 15 | 16 |
About Peter Papenhausen
Peter Papenhausen is a scholar working on Hematology, Genetics and Pediatrics, Perinatology and Child Health, having authored 15 papers that have together received 341 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (194 citations), Hematology (54 citations) and Plant Science (105 citations). Peter Papenhausen has collaborated with scholars based in United States, United Kingdom and Qatar. Frequent co-authors include Elisabeth Paietta, Michelle Macha, Binquan Huang, John A. Crolla, Susan L. Christian, David H. Ledbetter, Peter H. Wiernik, E. Richard Stanley, Michael Andreeff and Janis Racevskis. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Genetics and Genetics in 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.