Peter K. Rogan

5.9k total citations
121 papers, 3.8k citations indexed

About

Peter K. Rogan is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Peter K. Rogan has authored 121 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 50 papers in Genetics and 17 papers in Cancer Research. Recurrent topics in Peter K. Rogan's work include Genomic variations and chromosomal abnormalities (27 papers), Genetic Syndromes and Imprinting (24 papers) and RNA Research and Splicing (17 papers). Peter K. Rogan is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Genetic Syndromes and Imprinting (24 papers) and RNA Research and Splicing (17 papers). Peter K. Rogan collaborates with scholars based in United States, Canada and Germany. Peter K. Rogan's co-authors include Joan H.M. Knoll, Thomas D. Schneider, Robert D. Nicholls, Eliseos J. Mucaki, Brian M. Faux, Daniel J. Driscoll, Merlin G. Butler, Wayne Gottlieb, Roger L. Ladda and Maria J. Mascari and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Peter K. Rogan

117 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter K. Rogan United States 34 2.2k 1.7k 688 371 349 121 3.8k
Samuel S. Chong Singapore 35 2.1k 1.0× 1.2k 0.7× 820 1.2× 665 1.8× 422 1.2× 167 4.8k
Eric D. Wieben United States 40 2.9k 1.3× 780 0.5× 228 0.3× 741 2.0× 345 1.0× 109 5.4k
Eric W. Klee United States 34 2.1k 0.9× 1.0k 0.6× 201 0.3× 410 1.1× 652 1.9× 178 4.0k
Nicola Brunetti‐Pierri Italy 41 3.3k 1.5× 1.8k 1.0× 214 0.3× 530 1.4× 345 1.0× 191 5.7k
Jian-Bing Fan United States 25 4.8k 2.2× 1.3k 0.8× 702 1.0× 438 1.2× 951 2.7× 36 6.5k
Jeff Hall United States 23 1.5k 0.7× 2.0k 1.2× 226 0.3× 812 2.2× 709 2.0× 47 4.4k
Vivian G. Cheung United States 36 4.7k 2.1× 2.3k 1.3× 280 0.4× 389 1.0× 810 2.3× 74 6.5k
Andreas Braun Germany 39 2.9k 1.3× 1.2k 0.7× 161 0.2× 374 1.0× 234 0.7× 116 4.7k
Jin Yu United States 12 3.0k 1.4× 3.0k 1.8× 161 0.2× 243 0.7× 748 2.1× 17 5.9k
John D. Baxter United States 32 2.2k 1.0× 1.6k 0.9× 207 0.3× 259 0.7× 344 1.0× 49 4.7k

Countries citing papers authored by Peter K. Rogan

Since Specialization
Citations

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

Fields of papers citing papers by Peter K. Rogan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter K. Rogan. 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 K. Rogan. The network helps show where Peter K. Rogan may publish in the future.

Co-authorship network of co-authors of Peter K. Rogan

This figure shows the co-authorship network connecting the top 25 collaborators of Peter K. Rogan. A scholar is included among the top collaborators of Peter K. Rogan 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 K. Rogan. Peter K. Rogan 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
1.
Knoll, Joan H.M., et al.. (2020). Estimating partial-body ionizing radiation exposure by automated cytogenetic biodosimetry. International Journal of Radiation Biology. 96(11). 1492–1503. 13 indexed citations
2.
Rogan, Peter K., et al.. (2020). Meeting radiation dosimetry capacity requirements of population-scale exposures by geostatistical sampling. PLoS ONE. 15(4). e0232008–e0232008. 4 indexed citations
3.
Caputo, Sandrine M., Laurent Castéra, Adrien Briaux, et al.. (2017). Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predisposition. Breast Cancer Research and Treatment. 168(2). 311–325. 13 indexed citations
4.
Hannouf, Malek B., Eric Winquist, Salaheddin M. Mahmud, et al.. (2017). The Clinical Significance of Occult Gastrointestinal Primary Tumours in Metastatic Cancer: A Population Retrospective Cohort Study. Cancer Research and Treatment. 50(1). 183–194. 2 indexed citations
5.
Hannouf, Malek B., Eric Winquist, Salaheddin M. Mahmud, et al.. (2016). Cost-effectiveness of using a gene expression profiling test to aid in identifying the primary tumour in patients with cancer of unknown primary. The Pharmacogenomics Journal. 17(3). 286–300. 9 indexed citations
6.
Mucaki, Eliseos J., Natasha Caminsky, Ami M. Perri, et al.. (2016). A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer. BMC Medical Genomics. 9(1). 19–19. 14 indexed citations
7.
Rogan, Peter K., Yanxin Li, Ruth C. Wilkins, Farrah Flegal, & Joan H.M. Knoll. (2016). Radiation Dose Estimation by Automated Cytogenetic Biodosimetry. Radiation Protection Dosimetry. 172(1-3). 207–217. 18 indexed citations
8.
Kim, Chong S., Malek B. Hannouf, Sisira Sarma, et al.. (2015). Identification and survival outcomes of a cohort of patients with cancer of unknown primary in Ontario, Canada. Acta Oncologica. 54(10). 1781–1787. 8 indexed citations
9.
Mercer, Robert E., et al.. (2012). A Machine Learning Approach for Phenotype Name Recognition. Scholarship@Western (Western University). 1425–1440. 7 indexed citations
10.
Park, Nicole I., et al.. (2012). Structural and genic characterization of stable genomic regions in breast cancer: Relevance to chemotherapy. Molecular Oncology. 6(3). 347–359. 9 indexed citations
11.
Rogan, Peter K., et al.. (2005). Automated splicing mutation analysis by information theory. Human Mutation. 25(4). 334–342. 117 indexed citations
12.
Lamba, Vishal, Jatinder K. Lamba, Kazuto Yasuda, et al.. (2003). Hepatic CYP2B6 Expression: Gender and Ethnic Differences and Relationship to CYP2B6 Genotype and CAR (Constitutive Androstane Receptor) Expression. Journal of Pharmacology and Experimental Therapeutics. 307(3). 906–922. 320 indexed citations
13.
Knoll, Joan H.M. & Peter K. Rogan. (2003). Sequence‐Based, in situ detection of chromosomal abnormalities at high resolution. American Journal of Medical Genetics Part A. 121A(3). 245–257. 22 indexed citations
14.
Rogan, Peter K., Stan R. Svojanovsky, & J. Steven Leeder. (2003). Information theory-based analysis of CYP2C19, CYP2D6 and CYP3A5 splicing mutations. Pharmacogenetics. 13(4). 207–218. 46 indexed citations
15.
Belchis, Deborah, et al.. (1996). Loss of Heterozygosity and Microsatellite Instability at the Retinoblastoma Locus in Osteosarcomas. Diagnostic Molecular Pathology. 5(3). 214–219. 38 indexed citations
16.
Vgontzas, Alexandros N., Anthony Kales, James R. Seip, et al.. (1996). Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndrome. American Journal of Medical Genetics. 67(5). 478–482. 42 indexed citations
17.
Gabriel, James M., et al.. (1994). A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region. Human Molecular Genetics. 3(10). 1912–1912. 5 indexed citations
18.
Ladda, Roger L., Jonathan Zonana, Jeanette C. Ramer, Maria J. Mascari, & Peter K. Rogan. (1993). Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: A distinct syndrome. American Journal of Medical Genetics. 47(4). 550–555. 5 indexed citations
19.
Mowrey, Philip N., Michael J. Chorney, Charles P. Venditti, et al.. (1993). Clinical and molecular analyses of deletion 3p25‐pter syndrome. American Journal of Medical Genetics. 46(6). 623–629. 37 indexed citations
20.
Rogan, Peter K., et al.. (1991). Automatic detection of noisy spots in two-dimensional Southern blots. International Electrophoresis Society Meeting, Washington DC, March 16-19, 1991.. PubMed. 2(4-5). 141–9. 1 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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