Thomas Hollander

2.1k total citations
48 papers, 883 citations indexed

About

Thomas Hollander is a scholar working on Oncology, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Thomas Hollander has authored 48 papers receiving a total of 883 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Oncology, 25 papers in Surgery and 25 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Thomas Hollander's work include Pancreatic and Hepatic Oncology Research (17 papers), Gastric Cancer Management and Outcomes (16 papers) and Colorectal Cancer Screening and Detection (12 papers). Thomas Hollander is often cited by papers focused on Pancreatic and Hepatic Oncology Research (17 papers), Gastric Cancer Management and Outcomes (16 papers) and Colorectal Cancer Screening and Detection (12 papers). Thomas Hollander collaborates with scholars based in United States. Thomas Hollander's co-authors include Dayna S. Early, Christine E. Hovis, Reena V. Chokshi, Jean S. Wang, Daniel Mullady, Steven A. Edmundowicz, Vladimir Kushnir, Faris Murad, Riad R. Azar and Matt Hall and has published in prestigious journals such as Gastroenterology, Cancer Research and Scientific Reports.

In The Last Decade

Thomas Hollander

45 papers receiving 860 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Hollander United States 14 640 619 468 136 57 48 883
Dai Hirasawa Japan 18 246 0.4× 828 1.3× 833 1.8× 264 1.9× 57 1.0× 59 1.1k
William Tam Australia 12 498 0.8× 630 1.0× 465 1.0× 186 1.4× 17 0.3× 32 873
Toshiki Sugawara Japan 17 307 0.5× 501 0.8× 559 1.2× 116 0.9× 56 1.0× 34 695
Claudio Tombazzi United States 13 419 0.7× 539 0.9× 602 1.3× 58 0.4× 60 1.1× 38 773
R. Hawes United States 10 323 0.5× 412 0.7× 468 1.0× 137 1.0× 73 1.3× 31 677
Milton T. Smith United States 18 628 1.0× 407 0.7× 919 2.0× 33 0.2× 80 1.4× 34 1.1k
R. H. Diament United Kingdom 12 392 0.6× 343 0.6× 271 0.6× 24 0.2× 33 0.6× 17 533
N. D’Imperio Italy 15 406 0.6× 423 0.7× 692 1.5× 206 1.5× 125 2.2× 53 893
Antonino Granata Italy 16 228 0.4× 481 0.8× 560 1.2× 175 1.3× 39 0.7× 81 710
Sarto C. Paquin Canada 10 380 0.6× 238 0.4× 462 1.0× 52 0.4× 208 3.6× 34 671

Countries citing papers authored by Thomas Hollander

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Hollander

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Hollander

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Hollander. A scholar is included among the top collaborators of Thomas Hollander 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 Hollander. Thomas Hollander 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.
Dbouk, Mohamad, Thomas Hollander, Ahmad Najdat Bazarbashi, et al.. (2025). EUS-guided fine-needle biopsy sampling of solid pancreatic masses with and without rapid onsite evaluation for commercial next-generation genomic profiling. Gastrointestinal Endoscopy. 102(6). 855–862.e1.
2.
Altayar, Osama, Tala Mahmoud, Dayna S. Early, et al.. (2024). Clinical predictors of significant findings on EUS for the evaluation of incidental common bile duct dilation. Gastrointestinal Endoscopy. 100(4). 670–678.e1. 1 indexed citations
3.
Li, Shuying, Chao Zhou, Thomas Hollander, et al.. (2024). In vivo evaluation of complex polyps with endoscopic optical coherence tomography and deep learning during routine colonoscopy: a feasibility study. Scientific Reports. 14(1). 27930–27930. 3 indexed citations
4.
Mittal, Chetan, V. Raman Muthusamy, Violette C. Simon, et al.. (2022). Threshold evaluation for optimal number of endoscopic treatment sessions to achieve complete eradication of Barrett’s metaplasia. Endoscopy. 54(10). 927–933. 1 indexed citations
5.
Hasak, Stephen, Michael Weaver, Arvind Rengarajan, et al.. (2021). Validation of choledocholithiasis predictors from the “2019 ASGE Guideline for the role of endoscopy in the evaluation and management of choledocholithiasis.”. Surgical Endoscopy. 36(6). 4199–4206. 9 indexed citations
6.
Cosgrove, Natalie, Anup S. Shetty, Richard G. McLean, et al.. (2021). Radiologic Predictors of Increased Number of Necrosectomies During Endoscopic Management of Walled-off Pancreatic Necrosis. Journal of Clinical Gastroenterology. 56(5). 457–463. 3 indexed citations
7.
Das, Koushik K., Stephen Hasak, Sherif Elhanafi, et al.. (2020). Performance and Predictors of Migration of Partially and Fully Covered Esophageal Self-Expanding Metal Stents for Malignant Dysphagia. Clinical Gastroenterology and Hepatology. 19(12). 2656–2663.e2. 13 indexed citations
8.
Wani, Sachin, Samuel Han, Vladimir Kushnir, et al.. (2020). Recurrence Is Rare Following Complete Eradication of Intestinal Metaplasia in Patients With Barrett’s Esophagus and Peaks at 18 Months. Clinical Gastroenterology and Hepatology. 18(11). 2609–2617.e2. 28 indexed citations
9.
Thaker, Adarsh M., Sachin Wani, Violette C. Simon, et al.. (2019). Anatomic location of Barrett’s esophagus recurrence after endoscopic eradication therapy: development of a simplified surveillance biopsy strategy. Gastrointestinal Endoscopy. 90(3). 395–403. 20 indexed citations
10.
Murphy, Ian, Vladimir Kushnir, Koushik K. Das, et al.. (2018). Mo1330 USE OF FNB WITHOUT ROSE FOR SOLID PANCREATIC MASSES DECREASES PROCEDURE TIME WHILE ACHIEVING SIMILAR DIAGNOSTIC YIELD VERSUS FNA WITH ROSE. Gastrointestinal Endoscopy. 87(6). AB448–AB448. 1 indexed citations
11.
Smith, Zachary L., Gabriel Lang, Dayna S. Early, et al.. (2018). The importance of early recognition in management of ERCP-related perforations. Surgical Endoscopy. 32(12). 4841–4849. 14 indexed citations
12.
Lang, Gabriel, Daniel Mullady, Dayna S. Early, et al.. (2018). Utility of Endoscopic Ultrasound in Evaluating Local Recurrence After Surgery for Pancreatic Cancer. Clinical Gastroenterology and Hepatology. 16(11). 1834–1835. 1 indexed citations
13.
Smith, Zachary L., Daniel Mullady, Gabriel Lang, et al.. (2018). A randomized controlled trial evaluating general endotracheal anesthesia versus monitored anesthesia care and the incidence of sedation-related adverse events during ERCP in high-risk patients. Gastrointestinal Endoscopy. 89(4). 855–862. 58 indexed citations
14.
Fritz, Cassandra, et al.. (2018). Prolonged Cecal Insertion Time Is Not Associated with Decreased Adenoma Detection When a Longer Withdrawal Time Is Achieved. Digestive Diseases and Sciences. 63(11). 3120–3125. 9 indexed citations
15.
Kushnir, Vladimir, Young S. Oh, Thomas Hollander, et al.. (2015). Impact of Retroflexion Vs. Second Forward View Examination of the Right Colon on Adenoma Detection: A Comparison Study. The American Journal of Gastroenterology. 110(3). 415–422. 87 indexed citations
16.
Sayuk, Gregory S., Thomas Hollander, Steven A. Edmundowicz, et al.. (2014). Resect and Discard Approach to Colon Polyps: Real-World Applicability Among Academic and Community Gastroenterologists. Digestive Diseases and Sciences. 60(2). 502–508. 29 indexed citations
17.
Kushnir, Vladimir, Thomas Hollander, Christine E. Hovis, et al.. (2013). Long-Term Outcomes After Single-Balloon Enteroscopy in Patients with Obscure Gastrointestinal Bleeding. Digestive Diseases and Sciences. 58(9). 2572–2579. 23 indexed citations
18.
Wani, Sachin, Dayna S. Early, Christine E. Hovis, et al.. (2012). Take-home Message. Gastrointestinal Endoscopy. 2(76). 328–335. 39 indexed citations
19.
Wani, Sachin, Gregory A. Coté, Rajesh N. Keswani, et al.. (2012). Learning curves for EUS by using cumulative sum analysis: implications for American Society for Gastrointestinal Endoscopy recommendations for training. Gastrointestinal Endoscopy. 77(4). 558–565. 101 indexed citations
20.
Wani, Sachin, Dayna S. Early, Christine E. Hovis, et al.. (2012). Diagnostic yield of malignancy during EUS-guided FNA of solid lesions with and without a stylet: a prospective, single blind, randomized, controlled trial. Gastrointestinal Endoscopy. 76(2). 328–335. 68 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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