James Pettay
About
James Pettay is a scholar working on Molecular Biology, Oncology and Radiology, Nuclear Medicine and Imaging.
According to data from OpenAlex, James Pettay has authored 43 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 20 papers in Oncology and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in James Pettay's work include HER2/EGFR in Cancer Research (14 papers), Monoclonal and Polyclonal Antibodies Research (12 papers) and Advanced Biosensing Techniques and Applications (12 papers). James Pettay is often cited by papers focused on HER2/EGFR in Cancer Research (14 papers), Monoclonal and Polyclonal Antibodies Research (12 papers) and Advanced Biosensing Techniques and Applications (12 papers). James Pettay collaborates with scholars based in United States, Japan and Germany. James Pettay's co-authors include Raymond R. Tubbs, Marek Skacel, Thomas M. Grogan, Patrick C. Roche, Mark H. Stoler, Robert B. Jenkins, Eric D. Hsi, Barbara P. Barna, Gene H. Barnett and Gary W. Procop and has published in prestigious journals such as Journal of Clinical Oncology, The Journal of Urology and American Journal Of Pathology.
In The Last Decade
James Pettay
43 papers receiving 1.7k citations
Peers
James Pettay
Allan Topham United States
P Bertheau France
Naoki Kanomata Japan
Sofia Haque United States
Deirdre Jill Cohen United States
Makiko Itami Japan
N R Lemoine United Kingdom
Friedrich Prall Germany
Lu Xu United States
Dan S. Gombos United States
Citations per year, relative to James Pettay James Pettay (= 1×)
peers
Allan Topham
Countries citing papers authored by James Pettay
Since
Specialization
Citations
This map shows the geographic impact of James Pettay'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 James Pettay with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James Pettay more than expected).
Fields of papers citing papers by James Pettay
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by James Pettay. 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 James Pettay. The network helps show where James Pettay may publish in the future.
Co-authorship network of co-authors of James Pettay
This figure shows the co-authorship network connecting the top 25 collaborators of James Pettay. A scholar is included among the top collaborators of James Pettay 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 James Pettay. James Pettay is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Nitta, Hiroaki, Beatrice Hauss‐Wegrzyniak, Fabien Gaire, et al.. (2008). Development of automated brightfield double In Situ hybridization (BDISH) application for HER2 gene and chromosome 17 centromere (CEN 17) for breast carcinomas and an assay performance comparison to manual dual color HER2 fluorescence In Situ hybridization (FISH). Diagnostic Pathology. 3(1). 41–41.
2.
Short, Sarah M., Brian J. Yoder, Shannon Tarr, et al.. (2007). The Expression of the Cytoskeletal Focal Adhesion Protein Paxillin in Breast Cancer Correlates with HER2 Overexpression and May Help Predict Response to Chemotherapy: A Retrospective Immunohistochemical Study. The Breast Journal. 13(2). 130–139.
3.
Tubbs, Raymond R., et al.. (2007). An approach to the validation of novel molecular markers of breast cancer via TMA-based FISH scanning. Journal of Molecular Histology. 38(2). 141–150.
4.
Tubbs, Raymond R., Kingshuk Das, James R. Cook, et al.. (2007). Genotyping of phenotypically defined cells in neoplasia: enhanced immunoFISH via tyramide signal amplification (TSA) segregates immunophenotypically—defined cell populations for gated genotyping. Journal of Molecular Histology. 38(2). 129–134.
5.
Tubbs, Raymond R., James Pettay, Todd Barry, et al.. (2006). The specificity of interphase FISH translocation probes in formalin fixed paraffin embedded tissue sections is readily assessed using automated staining and scoring of tissue microarrays constructed from murine xenografts. Journal of Molecular Histology. 38(2). 159–165.
6.
Tubbs, Raymond R., James Pettay, Patrick C. Roche, et al.. (2006). Automation of Manual Components and Image Quantification of Direct Dual Label Fluorescence In Situ Hybridization (FISH) for HER2 Gene Amplification. Applied immunohistochemistry & molecular morphology. 14(4). 436–440.
7.
Procop, Gary W., Rose Beck, James Pettay, et al.. (2006). JC Virus Chromogenic In Situ Hybridization in Brain Biopsies From Patients With and Without PML. Diagnostic Molecular Pathology. 15(2). 70–73.
8.
Cook, James R., et al.. (2006). Fluorescence in Situ Hybridization Analysis of Immunoglobulin Heavy Chain Translocations in Plasma Cell Myeloma Using Intact Paraffin Sections and Simultaneous CD138 Immunofluorescence. Journal of Molecular Diagnostics. 8(4). 459–465.
9.
Tubbs, Raymond, James Pettay, David G. Hicks, et al.. (2004). Novel bright field molecular morphology methods for detection of HER2 gene amplification. The Histochemical Journal. 35(6). 589–594.
10.
Beck, Rose, Raymond R. Tubbs, Mohamad A. Hussein, James Pettay, & Eric D. Hsi. (2003). Automated Colorimetric In Situ Hybridization (CISH) Detection of Immunoglobulin (Ig) Light Chain mRNA Expression in Plasma Cell (PC) Dyscrasias and Non-Hodgkin Lymphoma. Diagnostic Molecular Pathology. 12(1). 14–20.
11.
Tubbs, Raymond, James Pettay, Marek Skacel, et al.. (2002). Gold-Facilitated in Situ Hybridization. American Journal Of Pathology. 160(5). 1589–1595.
12.
Skacel, Marek, et al.. (2002). Tissue Microarrays: A Powerful Tool for High-Throughput Analysis of Clinical Specimens. Applied immunohistochemistry & molecular morphology. 10(1). 1–6.
13.
Ramalingam, Preetha, Lisa Rybicki, Marc D. Smith, et al.. (2002). Posttransplant Lymphoproliferative Disorders in Lung Transplant Patients: The Cleveland Clinic Experience. Modern Pathology. 15(6). 647–656.
14.
Skacel, Marek, Pamela L. Paris, James Pettay, et al.. (2002). Diffuse Large B-Cell Lymphoma of the Stomach: Assessment of Microsatellite Instability, Allelic Imbalance, and Trisomy of Chromosomes 3, 12, and 18. Diagnostic Molecular Pathology. 11(2). 75–82.
15.
Frater, John L., et al.. (2001). Use of Novel t(11;14) and t(14;18) Dual-Fusion Fluorescence In Situ Hybridization Probes in the Differential Diagnosis of Lymphomas of Small Lymphocytes. Diagnostic Molecular Pathology. 10(4). 214–222.
16.
Frater, John L., Jeffrey Hammel, Joël Shapiro, et al.. (2001). Typical and Atypical Chronic Lymphocytic Leukemia Differ Clinically and Immunophenotypically. American Journal of Clinical Pathology. 116(5). 655–664.
17.
Tubbs, Raymond R., et al.. (2000). Concomitant Oncoprotein Detection with Fluorescence in Situ Hybridization (CODFISH). Journal of Molecular Diagnostics. 2(2). 78–83.
18.
Yang, Bin, Raymond R. Tubbs, William G. Finn, et al.. (2000). Clinicopathologic Reassessment of Primary Cutaneous B-Cell Lymphomas With Immunophenotypic and Molecular Genetic Characterization. The American Journal of Surgical Pathology. 24(5). 694–702.
19.
Sreenan, Joseph J., James Pettay, Abdelghani Tbakhi, et al.. (1997). The Use of Amplified Variable Number of Tandem Repeats (VNTR) in the Detection of Chimerism Following Bone Marrow Transplantation: A Comparison With Restriction Fragment Length Polymorphism (RFLP) by Southern Blotting. American Journal of Clinical Pathology. 107(3). 292–298.
20.
Zhou, Ping, Mary Jane Thomassen, James Pettay, Sharad D. Deodhar, & Barbara P. Barna. (1995). Human Monocytes Produce Monocyte Chemoattractant Protein 1 (MCP-1) in Response to a Synthetic Peptide Derived from C-Reactive Protein. Clinical Immunology and Immunopathology. 74(1). 84–88.
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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