Peter Papenhausen

3.1k total citations
63 papers, 1.8k citations indexed

About

Peter Papenhausen is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Peter Papenhausen has authored 63 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 23 papers in Molecular Biology and 19 papers in Hematology. Recurrent topics in Peter Papenhausen's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (14 papers) and Acute Myeloid Leukemia Research (11 papers). Peter Papenhausen is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (14 papers) and Acute Myeloid Leukemia Research (11 papers). Peter Papenhausen collaborates with scholars based in United States, United Kingdom and Netherlands. Peter Papenhausen's co-authors include Haipeng Shao, James Tepperberg, Lynh Nguyen, Stuart Schwartz, Romela Pasion, Rachel D. Burnside, Sheila Shurtleff, Giuseppe Basso, Inder Gadi and Ken Mills and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Peter Papenhausen

60 papers receiving 1.7k citations

Peers

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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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical correlation and prognostic impact of cytogenetic clone size for myelodysplastic syndromes/neoplasm 2024 ·SHILAP Revista de lepidopterología ·Zhuoer Xie, (unknown), Ling Zhang, Peter Papenhausen, (unknown), Onyee Chan, Andrew Kuykendall, Seongseok Yun, Alison Walker, (unknown), Jeffrey E. Lancet, Eric Padron, David A. Sallman, Rami S. Komrokji	0
2	Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes 2024 ·Prenatal Diagnosis ·(unknown), Gloria Haskell, Alexandra Arreola, Christine M. Riordan, Inder Gadi, Andrea Penton, Peter Papenhausen, Stuart Schwartz	0
3	Clinical significance and mechanisms associated with segmental UPD 2021 ·Molecular Cytogenetics ·Peter Papenhausen, (unknown), (unknown), (unknown), Stuart Schwartz, Andrea Penton	6
4	Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms. 2018 ·PubMed ·Eduardo S. Cantú, Henry Y. Dong, (unknown), (unknown), Peter Papenhausen	2
5	Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia 2014 ·International Journal of Hematology ·Kendra Sweet, Najla H. Al Ali, Samir Dalia, Rami S. Komrokji, Robert M. Crescentini, Sara Tinsley, Jeffrey E. Lancet, Peter Papenhausen, Ling Zhang, Javier Pinilla‐Ibarz	1
6	Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency 2013 ·Molecular Genetics and Metabolism ·Graeme R. Frank, Joyce E. Fox, (unknown), (unknown), Elena G. Bochukova, Jeremiah Levine, Peter Papenhausen, Stephen O’Rahilly, I. Sadaf Farooqi	45
7	Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype 2013 ·American Journal of Medical Genetics Part A ·Rachel D. Burnside, John Pappas, Stephanie Sacharow, Carolyn Applegate, Ada Hamosh, Inder Gadi, Vikram Jaswaney, Elisabeth A. Keitges, Karen Phillips, (unknown), Hiba Risheg, Janice Smith, (unknown), Stuart Schwartz, Peter Papenhausen	30
8	FOXO1–FGFR1 fusion and amplification in a solid variant of alveolar rhabdomyosarcoma 2011 ·Modern Pathology ·Jinglan Liu, Miguel A. Guzmán, (unknown), (unknown), (unknown), (unknown), (unknown), Peter Papenhausen, (unknown), Hope H. Punnett, Gregory E. Halligan, Jean‐Pierre de Chadarévian	41
9	Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy 2007 ·Orphanet Journal of Rare Diseases ·E. Scott Sills, (unknown), (unknown), (unknown), (unknown), C.S. Dyer, Peter Papenhausen, Jessica G. Davis	8
10	Burkitt Lymphoma Arising in Organ Transplant Recipients 2003 ·The American Journal of Surgical Pathology ·Jerald Z. Gong, Timothy T. Stenzel, Ellen Bennett, Anand S. Lagoo, Cherie H. Dunphy, Joseph O. Moore, David A. Rizzieri, James Tepperberg, Peter Papenhausen, Patrick J. Buckley	39
11	Twin–twin transfusion syndrome in a dizygotic monochorionic–diamniotic twin pregnancy 2003 ·The Journal of Maternal-Fetal & Neonatal Medicine ·Rubén A. Quintero, O. Thomas Mueller, J. Martı́nez, Jorge Olmo Arroyo, Enid Gilbert‐Barness, Don R. Hilbelink, Peter Papenhausen, Maxine J. Sutcliffe	35
12	Epigenetic detection of human chromosome 14 uniparental disomy 2003 ·Human Mutation ·Susan K. Murphy, Andrew A. Wylie, Karen J. Coveler, Philip D. Cotter, Peter Papenhausen, V. Reid Sutton, Lisa G. Shaffer, Randy L. Jirtle	63
13	Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome 2000 ·Cytogenetic and Genome Research ·Brynn Levy, Peter Papenhausen, James Tepperberg, Teresa Dunn, Shari Fallet, (unknown), (unknown), Kurt Hirschhorn, Peter E. Warburton	25
14	Cytogenetic, morphologic and oncogene analysis of a cell line derived from a heterologous mixed mullerian tumor of the ovary 1997 ·In Vitro Cellular & Developmental Biology - Animal ·Jeanne L. Becker, Peter Papenhausen, Raymond H. Widen	16
15	Case report of spontaneous remission of cytogenetic relapse of chronic myelogenous leukemia suggestive of progression to blast crisis after allogeneic bone marrow transplantation 1995 ·Annals of Hematology ·(unknown), Peter Papenhausen, Lynn C. Moscinski, Gerald J. Elfenbein	3
16	Cleft palate and complex chromosome rearrangements 1992 ·Clinical Genetics ·Boris G. Kousseff, Peter Papenhausen, Richard L. Neu, (unknown), (unknown)	7
17	A primary encephalocele culture yields a pure population of human astrocytes 1991 ·Brain Research ·(unknown), Richard S. Morrison, James T. Goodrich, Peter Papenhausen, Joseph R. Moskal	1
18	Effect of maternal-fetal movement on concentration of cells obtained at genetic amniocentesis 1990 ·American Journal of Obstetrics and Gynecology ·S. J. Carlan, Peter Papenhausen, William F. O’Brien, Marcello Pietrantoni, Ronald A. Chez, (unknown)	1
19	Tissue limited mosaicism in a patient with tetrasomy 9p 1990 ·American Journal of Medical Genetics ·Peter Papenhausen, (unknown), Karen Miller, Boris G. Kousseff, Thomas A. Tedesco	19
20	Establishment of lymphoid cell lines in patients with common viral diseases. 1971 ·PubMed ·(unknown), Yashar Hirshaut, Peter Papenhausen, William Henley, Kurt Hirschhorn, (unknown)	1

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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