Thomas J. Borell

3.0k total citations · 1 hit paper
23 papers, 2.4k citations indexed

About

Thomas J. Borell is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Thomas J. Borell has authored 23 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Thomas J. Borell's work include Glioma Diagnosis and Treatment (10 papers), Cancer Genomics and Diagnostics (9 papers) and Renal cell carcinoma treatment (4 papers). Thomas J. Borell is often cited by papers focused on Glioma Diagnosis and Treatment (10 papers), Cancer Genomics and Diagnostics (9 papers) and Renal cell carcinoma treatment (4 papers). Thomas J. Borell collaborates with scholars based in United States, Germany and Netherlands. Thomas J. Borell's co-authors include Robert B. Jenkins, Judith R. OʼFallon, Justin S. Smith, Arie Perry, David W. Kimmel, Allan J. Yates, Bernd W. Scheithauer, Hyun K. Lee, Junqi Qian and B. W. Scheithauer and has published in prestigious journals such as Journal of Clinical Oncology, JNCI Journal of the National Cancer Institute and Oncogene.

In The Last Decade

Thomas J. Borell

23 papers receiving 2.3k citations

Hit Papers

Alterations of Chromosome Arms 1p and 19q as Predictors o... 2000 2026 2008 2017 2000 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas J. Borell United States 17 1.4k 1.1k 796 795 344 23 2.4k
L. Magnus Bäcklund Sweden 20 1.4k 1.0× 848 0.8× 658 0.8× 558 0.7× 473 1.4× 35 2.2k
Hendrik Witt Germany 23 1.9k 1.3× 1.9k 1.7× 626 0.8× 331 0.4× 421 1.2× 49 3.0k
Sylvia Kocialkowski United Kingdom 11 1.2k 0.9× 862 0.8× 518 0.7× 227 0.3× 235 0.7× 13 1.8k
Christian Koelsche Germany 24 1.1k 0.8× 594 0.5× 507 0.6× 757 1.0× 309 0.9× 46 2.0k
Emmanuelle Crinière France 20 1.3k 0.9× 697 0.6× 472 0.6× 392 0.5× 236 0.7× 29 1.7k
Nathalie Baeza France 17 887 0.6× 1.2k 1.0× 561 0.7× 226 0.3× 431 1.3× 28 2.2k
Ronald van Marion Netherlands 23 587 0.4× 745 0.7× 644 0.8× 571 0.7× 391 1.1× 54 1.8k
Blandine Boisselier France 22 2.2k 1.5× 1.2k 1.0× 1.1k 1.4× 571 0.7× 426 1.2× 47 2.9k
Sumihito Nobusawa Japan 24 2.2k 1.6× 1.3k 1.2× 1.1k 1.3× 575 0.7× 280 0.8× 115 3.1k
Dorine A. Bax United Kingdom 17 1.1k 0.8× 1.0k 0.9× 457 0.6× 270 0.3× 333 1.0× 28 1.9k

Countries citing papers authored by Thomas J. Borell

Since Specialization
Citations

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

Fields of papers citing papers by Thomas J. Borell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas J. Borell. 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 Thomas J. Borell. The network helps show where Thomas J. Borell may publish in the future.

Co-authorship network of co-authors of Thomas J. Borell

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas J. Borell. A scholar is included among the top collaborators of Thomas J. Borell 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 Thomas J. Borell. Thomas J. Borell 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.
Qian, Junqi, Kiyoshi Hirasawa, David G. Bostwick, et al.. (2002). Loss of p53 and c-myc Overrepresentation in Stage T2-3N1-3M0 Prostate Cancer are Potential Markers for Cancer Progression. Modern Pathology. 15(1). 35–44. 70 indexed citations
2.
Burger, Peter C., A. Yuriko Minn, Justin S. Smith, et al.. (2001). Losses of Chromosomal Arms 1p and 19q in the Diagnosis of Oligodendroglioma. A Study of Paraffin-Embedded Sections. Modern Pathology. 14(9). 842–853. 96 indexed citations
3.
Smith, Justin S., Issei Tachibana, Sandra Passe, et al.. (2001). PTEN Mutation, EGFR Amplification, and Outcome in Patients With Anaplastic Astrocytoma and Glioblastoma Multiforme. JNCI Journal of the National Cancer Institute. 93(16). 1246–1256. 493 indexed citations
4.
Smith, Justin S., Issei Tachibana, Hyun K. Lee, et al.. (2000). Mapping of the chromosome 19 q‐arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers. Genes Chromosomes and Cancer. 29(1). 16–25. 73 indexed citations
5.
Smith, Justin S., Issei Tachibana, Hyun K. Lee, et al.. (2000). Mapping of the chromosome 19 q-arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers. Genes Chromosomes and Cancer. 29(1). 16–25. 26 indexed citations
6.
Smith, Justin S., Arie Perry, Thomas J. Borell, et al.. (2000). Alterations of Chromosome Arms 1p and 19q as Predictors of Survival in Oligodendrogliomas, Astrocytomas, and Mixed Oligoastrocytomas. Journal of Clinical Oncology. 18(3). 636–636. 643 indexed citations breakdown →
7.
Smith, Justin S., Benjamin Alderete, Yuriko Minn, et al.. (1999). Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype. Oncogene. 18(28). 4144–4152. 309 indexed citations
8.
Perry, Arie, Thomas J. Borell, Judith R. OʼFallon, et al.. (1999). ALTERATIONS OF CHROMOSOME ARMS 1p AND 19q AS PREDICTORS OF SURVIVAL IN DIFFUSE GLIOMAS. Journal of Neuropathology & Experimental Neurology. 58(5). 512–512. 3 indexed citations
9.
Perry, Arie, Tsutomu Nobori, Ning Ru, et al.. (1997). Detection of p16 Gene Deletions in Gliomas. Journal of Neuropathology & Experimental Neurology. 56(9). 999–1008. 55 indexed citations
10.
Brown, James A., Kari L. Anderl, Thomas J. Borell, et al.. (1997). Simultaneous Chromosome 7 and 17 Gain and Sex Chromosome Loss Provide Evidence that Renal Metanephric Adenoma is Related to Papillary Renal Cell Carcinoma. The Journal of Urology. 370–374. 3 indexed citations
11.
Boerman, Rudolf H., Kari L. Anderl, John F. Herath, et al.. (1996). The Glial and Mesenchymal Elements of Gliosarcomas Share Similar Genetic Alterations. Journal of Neuropathology & Experimental Neurology. 55(9). 973–983. 98 indexed citations
12.
Persons, Diane L., Robert A. Robinson, Ping H. Hsu, et al.. (1996). Chromosome-specific aneusomy in carcinoma of the breast.. PubMed. 2(5). 883–8. 33 indexed citations
13.
Brown, James A., Satoru Takahashi, Antonio Alcaraz, et al.. (1996). Fluorescence In Situ Hybridization Analysis of Renal Oncocytoma Reveals Frequent Loss of Chromosomes Y and 1. The Journal of Urology. 31–35. 2 indexed citations
14.
Takahashi, Satoru, Antonio Alcaraz, James A. Brown, et al.. (1996). Aneusomies of chromosomes 8 and Y detected by fluorescence in situ hybridization are prognostic markers for pathological stage C (pt3N0M0) prostate carcinoma.. PubMed. 2(1). 137–45. 45 indexed citations
15.
Brown, James A., Satoru Takahashi, Antonio Alcaraz, et al.. (1996). Fluorescence In Situ Hybridization Analysis of Renal Oncocytoma Reveals Frequent Loss of Chromosomes Y and 1. The Journal of Urology. 156(1). 31–35. 43 indexed citations
16.
Qian, Junqi, David G. Bostwick, Satoru Takahashi, et al.. (1995). Chromosomal anomalies in prostatic intraepithelial neoplasia and carcinoma detected by fluorescence in situ hybridization.. PubMed. 55(22). 5408–14. 180 indexed citations
17.
Herath, John F., et al.. (1994). Correlation of Cytogenetic and FluorescenceIn SituHybridization (FISH) Studies in Normal and Gliotic Brain. Journal of Neuropathology & Experimental Neurology. 53(5). 448–456. 20 indexed citations
18.
Witzig, Thomas E., et al.. (1994). Detection of Trisomy 12 by FISH in Untreated B -Chronic Lymphocytic Leukemia: Correlation with Stage and CD20 Antigen Expression Intensity. Leukemia & lymphoma. 14(5-6). 447–451. 14 indexed citations
19.
Persons, Diane L., Lynn C. Hartmann, John F. Herath, et al.. (1993). Interphase molecular cytogenetic analysis of epithelial ovarian carcinomas.. PubMed. 142(3). 733–41. 40 indexed citations
20.
Borell, Thomas J., et al.. (1992). Fluorescent In Situ Hybridization: Use of Whole Chromosome Paint Probes to Identify Unbalanced Chromosome Translocations. Mayo Clinic Proceedings. 67(7). 658–662. 8 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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