Jesse S. Voss

3.2k total citations
70 papers, 2.0k citations indexed

About

Jesse S. Voss is a scholar working on Pulmonary and Respiratory Medicine, Oncology and Surgery. According to data from OpenAlex, Jesse S. Voss has authored 70 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pulmonary and Respiratory Medicine, 23 papers in Oncology and 20 papers in Surgery. Recurrent topics in Jesse S. Voss's work include Cancer Genomics and Diagnostics (14 papers), Lung Cancer Treatments and Mutations (9 papers) and Pancreatic and Hepatic Oncology Research (8 papers). Jesse S. Voss is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Lung Cancer Treatments and Mutations (9 papers) and Pancreatic and Hepatic Oncology Research (8 papers). Jesse S. Voss collaborates with scholars based in United States, United Kingdom and Switzerland. Jesse S. Voss's co-authors include Benjamin R. Kipp, Kevin C. Halling, Sarah E. Kerr, Emily G. Barr Fritcher, Gregory J. Gores, Amy C. Clayton, Lewis R. Roberts, Michael B. Campion, Michael Henry and W. Edward Highsmith and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and PLoS ONE.

In The Last Decade

Jesse S. Voss

65 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jesse S. Voss United States	24	852	787	700	478	395	70	2.0k
Sherri Z. Millis United States	25	1.1k 1.3×	435 0.6×	852 1.2×	421 0.9×	772 2.0×	93	2.3k
Udo Rudloff United States	23	787 0.9×	736 0.9×	592 0.8×	419 0.9×	561 1.4×	75	2.1k
Paxton V. Dickson United States	24	756 0.9×	835 1.1×	431 0.6×	443 0.9×	540 1.4×	101	2.0k
Yoshitaka Honma Japan	22	952 1.1×	591 0.8×	776 1.1×	674 1.4×	878 2.2×	170	2.3k
Takushi Monden Japan	28	1.1k 1.3×	686 0.9×	537 0.8×	309 0.6×	1.1k 2.7×	146	2.6k
Léonor Benhaïm France	20	745 0.9×	677 0.9×	438 0.6×	400 0.8×	377 1.0×	71	1.7k
Emanuela Bonoldi Italy	23	738 0.9×	218 0.3×	292 0.4×	499 1.0×	801 2.0×	80	1.9k
Willeke Ros Netherlands	14	1.6k 1.9×	666 0.8×	436 0.6×	194 0.4×	293 0.7×	22	2.2k
Sasinya N. Scott United States	19	904 1.1×	554 0.7×	586 0.8×	689 1.4×	1.0k 2.6×	29	2.2k

Countries citing papers authored by Jesse S. Voss

Since Specialization

Citations

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

Fields of papers citing papers by Jesse S. Voss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jesse S. Voss. 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 Jesse S. Voss. The network helps show where Jesse S. Voss may publish in the future.

Co-authorship network of co-authors of Jesse S. Voss

This figure shows the co-authorship network connecting the top 25 collaborators of Jesse S. Voss. A scholar is included among the top collaborators of Jesse S. Voss 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 Jesse S. Voss. Jesse S. Voss 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

Jenkinson, Garrett, Asha Nair, Jesse S. Voss, et al.. (2021). SeekFusion - A Clinically Validated Fusion Transcript Detection Pipeline for PCR-Based Next-Generation Sequencing of RNA. Frontiers in Genetics. 12. 739054–739054. 11 indexed citations

Boland, Jennifer M., Hee Eun Lee, Emily G. Barr Fritcher, et al.. (2020). Molecular Genetic Landscape of Sclerosing Pneumocytomas. American Journal of Clinical Pathology. 155(3). 397–404. 7 indexed citations

Murphy, Stephen J., James B. Smadbeck, Bruce W. Eckloff, et al.. (2020). Chromosomal Junction Detection from Whole-Genome Sequencing on Formalin-Fixed, Paraffin-Embedded Tumors. Journal of Molecular Diagnostics. 23(4). 375–388. 2 indexed citations

DeLeon, Thomas, Daniel Almquist, Benjamin R. Kipp, et al.. (2020). Assessment of clinical outcomes with immune checkpoint inhibitor therapy in melanoma patients with CDKN2A and TP53 pathogenic mutations. PLoS ONE. 15(3). e0230306–e0230306. 23 indexed citations

Gupta, Sounak, Chad Vanderbilt, Bradley C. Leibovich, et al.. (2020). Secondary renal neoplasia following chemotherapy or radiation in pediatric patients. Human Pathology. 103. 1–13. 11 indexed citations

Zarei, Shabnam, Jesse S. Voss, Alan H. Bryce, et al.. (2019). Mutational Profile in Vulvar, Vaginal, and Urethral Melanomas: Review of 37 Cases With Focus on Primary Tumor Site. International Journal of Gynecological Pathology. 39(6). 587–594. 21 indexed citations

Levy, Michael J., Benjamin R. Kipp, Dragana Milosevic, et al.. (2018). Analysis of Cell-Free DNA to Assess Risk of Tumoremia Following Endoscopic Ultrasound Fine-Needle Aspiration of Pancreatic Adenocarcinomas. Clinical Gastroenterology and Hepatology. 16(10). 1632–1640.e1. 14 indexed citations

Vaubel, Rachael A., Thomas M. Kollmeyer, Alissa Caron, et al.. (2017). Synchronous gemistocytic astrocytoma IDH-mutant and oligodendroglioma IDH-mutant and 1p/19q-codeleted in a patient with CCDC26 polymorphism. Acta Neuropathologica. 134(2). 317–319. 3 indexed citations

Boland, Jennifer M., Joseph J. Maleszewski, Jason A. Wampfler, et al.. (2017). Pulmonary invasive mucinous adenocarcinoma and mixed invasive mucinous/nonmucinous adenocarcinoma—a clinicopathological and molecular genetic study with survival analysis. Human Pathology. 71. 8–19. 48 indexed citations

10.

Kipp, Benjamin R., Michael J. Levy, Jesse S. Voss, et al.. (2015). Somatic STK11 and Concomitant STK11/KRAS Mutational Frequency in Stage IV Lung Adenocarcinoma Adrenal Metastases. Journal of Thoracic Oncology. 10(3). 531–534. 15 indexed citations

11.

Fritcher, Emily G. Barr, Jesse S. Voss, Shannon M. Brankley, et al.. (2015). An Optimized Set of Fluorescence In Situ Hybridization Probes for Detection of Pancreatobiliary Tract Cancer in Cytology Brush Samples. Gastroenterology. 149(7). 1813–1824.e1. 98 indexed citations

12.

Kizilbash, Sani H., Caterina Giannini, Jesse S. Voss, et al.. (2014). The impact of concurrent temozolomide with adjuvant radiation and IDH mutation status among patients with anaplastic astrocytoma. Journal of Neuro-Oncology. 120(1). 85–93. 30 indexed citations

13.

Voss, Jesse S., Leonard M. Holtegaard, Sarah E. Kerr, et al.. (2013). Molecular profiling of cholangiocarcinoma shows potential for targeted therapy treatment decisions. Human Pathology. 44(7). 1216–1222. 109 indexed citations

14.

Voss, Jesse S., Sarah M. Jenkins, Michael Henry, et al.. (2013). Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation. Human Pathology. 45(1). 41–47. 2 indexed citations

15.

Kipp, Benjamin R., Jesse S. Voss, Amy C. Clayton, et al.. (2011). Primary Sclerosing Cholangitis Patients With Serial Polysomy Fluorescence In Situ Hybridization Results Are at Increased Risk of Cholangiocarcinoma. The American Journal of Gastroenterology. 106(11). 2023–2028. 83 indexed citations

16.

Voss, Jesse S., Benjamin R. Kipp, Kevin C. Halling, et al.. (2009). Fluorescence in Situ Hybridization Testing Algorithm Improves Lung Cancer Detection in Bronchial Brushing Specimens. American Journal of Respiratory and Critical Care Medicine. 181(5). 478–485. 19 indexed citations

17.

Fritcher, Emily G. Barr, Shannon M. Brankley, Benjamin R. Kipp, et al.. (2008). A comparison of conventional cytology, DNA ploidy analysis, and fluorescence in situ hybridization for the detection of dysplasia and adenocarcinoma in patients with Barrett's esophagus. Human Pathology. 39(8). 1128–1135. 45 indexed citations

18.

Kipp, Benjamin R., Harmony L. Tyner, Michael B. Campion, et al.. (2008). Chromosomal Alterations Detected by Fluorescence In Situ Hybridization in Urothelial Carcinoma and Rarer Histologic Variants of Bladder Cancer. American Journal of Clinical Pathology. 130(4). 552–559. 25 indexed citations

19.

Соколова, И. А., Alicia Algeciras‐Schimnich, Benjamin R. Kipp, et al.. (2007). Chromosomal Biomarkers for Detection of Human Papillomavirus Associated Genomic Instability in Epithelial Cells of Cervical Cytology Specimens. Journal of Molecular Diagnostics. 9(5). 604–611. 38 indexed citations

20.

Hill, James R., et al.. (1976). A Horse with One Kidney, Partially Obstructed Ureter, and Contralateral Urogenital Anomalies. Journal of the American Veterinary Medical Association. 169(2). 217–219. 5 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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