Peter Papenhausen

447 total citations
15 papers, 341 citations indexed

About

Peter Papenhausen is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Peter Papenhausen has authored 15 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Hematology. Recurrent topics in Peter Papenhausen's work include Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Peter Papenhausen is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Peter Papenhausen collaborates with scholars based in United States, United Kingdom and Qatar. Peter Papenhausen's co-authors include Elisabeth Paietta, Susan L. Christian, David H. Ledbetter, Binquan Huang, Michelle Macha, John A. Crolla, Peter H. Wiernik, E. Richard Stanley, Janis Racevskis and Michael Andreeff and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Genetics and Genetics in Medicine.

In The Last Decade

Peter Papenhausen

14 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter Papenhausen United States	9	194	154	105	54	49	15	341
Anna Jauch Germany	10	137 0.7×	200 1.3×	91 0.9×	36 0.7×	33 0.7×	11	319
V. D. Marković Canada	8	183 0.9×	258 1.7×	80 0.8×	31 0.6×	76 1.6×	10	419
Eva Hilgenfeld Germany	10	92 0.5×	194 1.3×	51 0.5×	111 2.1×	11 0.2×	13	318
Detlef Trost France	10	124 0.6×	224 1.5×	23 0.2×	39 0.7×	48 1.0×	20	346
N B Spinner United States	7	186 1.0×	220 1.4×	73 0.7×	11 0.2×	74 1.5×	9	332
Robert Zori United States	9	106 0.5×	146 0.9×	41 0.4×	23 0.4×	23 0.5×	12	310
Marco Garieri Switzerland	10	156 0.8×	278 1.8×	29 0.3×	25 0.5×	52 1.1×	12	435
Chiara Perfumo Italy	11	211 1.1×	173 1.1×	75 0.7×	18 0.3×	95 1.9×	17	357
Hugo Vega Colombia	6	149 0.8×	477 3.1×	93 0.9×	11 0.2×	25 0.5×	10	583
T. M. Schroeder-Kurth Germany	7	143 0.7×	227 1.5×	135 1.3×	18 0.3×	47 1.0×	10	330

Countries citing papers authored by Peter Papenhausen

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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15 of 15 papers shown

Penton, Andrea, Peter Papenhausen, Stuart Schwartz, Tuan A. Vu, & Gloria Haskell. (2024). P140: A rare phenomenon: Double trisomy rescue detected during clinical SNP microarray testing*. SHILAP Revista de lepidopterología. 2. 101037–101037.

Penton, Andrea, Peter Papenhausen, Stuart Schwartz, & James Tepperberg. (2018). 35. Runs of homozygosity (ROH) reveal that segmental-UPD is associated with the repair of genomic imbalance. Cancer Genetics. 224-225. 64–64. 1 indexed citations

Burnside, Rachel D., Susan Sklower Brooks, Wendy K. Chung, et al.. (2018). Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN. American Journal of Medical Genetics Part A. 176(9). 1956–1963. 8 indexed citations

Schwartz, Stuart & Peter Papenhausen. (2017). Significance of Copy-Neutral Loss of Heterozygosity Detected in Oncology Samples: Insights and Mechanisms. Cancer Genetics. 214-215. 40–40. 1 indexed citations

Risheg, Hiba, Romela Pasion, Virginia K. Proud, et al.. (2013). Clinical Comparison of Overlapping Deletions of 19p13.3. American Journal of Medical Genetics Part A. 161(5). 1110–1116. 9 indexed citations

Choi, Sarah M., Peter Papenhausen, Gerald Wertheim, & Rebecca L. King. (2013). Near-haploid B lymphoblastic leukemia with an apparent hyperdiploid karyotype: the critical role of SNP analysis in establishing proper diagnosis. Journal of Hematopathology. 7(1). 27–32. 3 indexed citations

Qian, You‐Wen, et al.. (2012). Microarray, gene sequencing, and reverse transcriptase–polymerase chain reaction analyses of a cryptic PML-RARA translocation. Cancer Genetics. 205(10). 537–540. 16 indexed citations

Levy, Brynn, David Tegay, Peter Papenhausen, et al.. (2012). Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?. Genetics in Medicine. 14(9). 811–818. 4 indexed citations

Schröck, Evelin, Timothy Veldman, Hesed Padilla‐Nash, et al.. (1997). Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities. Human Genetics. 101(3). 255–262. 129 indexed citations

10.

Huang, Binquan, John A. Crolla, Susan L. Christian, et al.. (1996). Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes. Human Genetics. 99(1). 11–17. 82 indexed citations

11.

Paietta, Elisabeth, Janis Racevskis, E. Richard Stanley, et al.. (1990). Expression of the macrophage growth factor, CSF-1 and its receptor c-fms by a Hodgkin's disease-derived cell line and its variants.. PubMed. 50(7). 2049–55. 51 indexed citations

12.

Paietta, Elisabeth, Michael Andreeff, Peter Papenhausen, Rasim Gucalp, & Peter H. Wiernik. (1989). Distinct antigen expression related to DNA ploidy in a case of biphenotypic leukemia.. PubMed. 3(1). 76–8. 4 indexed citations

13.

Paietta, Elisabeth, et al.. (1989). TdT+/nonlymphoid antigen+ acute leukemias: immunologic and karyotypic monitoring during therapy and at relapse suggests the transformation of a bipotential stem cell.. PubMed. 3(7). 485–91. 8 indexed citations

14.

Paietta, Elisabeth, Peter Papenhausen, Rasim Gucalp, Jason W. Reed, & Wiernik Ph. (1987). The 5q-- deletion: correlation of breakpoints with the immunophenotype of leukemic blast cells.. PubMed. 1(12). 822–4. 9 indexed citations

15.

Hsu, Lillian Y. F., Peter Papenhausen, Michael Greenberg, & Kurt Hirschhorn. (1974). Trisomy D in Bone Marrow Cells in a Patient with Chronic Myelogenous Leukemia. Acta Haematologica. 52(1). 61–64. 16 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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