Neda Rezaee

3.4k total citations · 1 hit paper
38 papers, 1.9k citations indexed

About

Neda Rezaee is a scholar working on Oncology, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Neda Rezaee has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Oncology, 22 papers in Surgery and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Neda Rezaee's work include Pancreatic and Hepatic Oncology Research (25 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (13 papers) and Pancreatitis Pathology and Treatment (8 papers). Neda Rezaee is often cited by papers focused on Pancreatic and Hepatic Oncology Research (25 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (13 papers) and Pancreatitis Pathology and Treatment (8 papers). Neda Rezaee collaborates with scholars based in United States, Netherlands and China. Neda Rezaee's co-authors include Christopher L. Wolfgang, Matthew J. Weiss, Ralph H. Hruban, Jin He, John L. Cameron, Lei Zheng, Elliot K. Fishman, Wenchuan Wu, Vincent P. Groot and Timothy M. Pawlik and has published in prestigious journals such as Journal of Clinical Oncology, Gastroenterology and PLoS ONE.

In The Last Decade

Neda Rezaee

36 papers receiving 1.9k citations

Hit Papers

Patterns, Timing, and Predictors of Recurrence Following ... 2017 2026 2020 2023 2017 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Patterns, Timing, and Predictors of Recurrence Following Pancreatectomy for Pancreatic Ductal Adenocarcinoma
    2017 477 citations Vincent P. Groot, Neda Rezaee et al. Annals of Surgery profile →

Peers

Neda Rezaee
Takahiro Akahori Japan
Thibault Voron France
Aparna Balachandran United States
Pamela J. Hodul United States
Yohei Mano Japan
Mustafa Suker Netherlands
Yuichiro Nakashima Japan
Yosuke Fukunaga Japan
Ammar A. Javed United States
Naoki Haratake Japan
Takahiro Akahori Japan
Neda Rezaee
Citations per year, relative to Neda Rezaee Neda Rezaee (= 1×) peers Takahiro Akahori

Countries citing papers authored by Neda Rezaee

Since Specialization
Citations

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

Fields of papers citing papers by Neda Rezaee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neda Rezaee

This figure shows the co-authorship network connecting the top 25 collaborators of Neda Rezaee. A scholar is included among the top collaborators of Neda Rezaee 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 Neda Rezaee. Neda Rezaee 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
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Verma, Amanda, Olakanmi Olagoke, Jonathan D. Moreno, et al.. (2022). SARS-CoV-2–Associated Myocarditis: A Case of Direct Myocardial Injury. Circulation Heart Failure. 15(3). e008273–e008273. 8 indexed citations
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Amini, Neda, Joseph R. Habib, Alex B. Blair, et al.. (2020). Invasive and Noninvasive Progression After Resection of Noninvasive Intraductal Papillary Mucinous Neoplasms. Annals of Surgery. 276(2). 370–377. 21 indexed citations
5.
Rezaee, Neda, et al.. (2019). Follicular cholecystitis: clinicopathologic associations. Human Pathology. 88. 1–6. 5 indexed citations
6.
Margonis, Georgios Antonios, Kazunari Sasaki, Sepideh Gholami, et al.. (2018). Genetic And Morphological Evaluation (GAME) score for patients with colorectal liver metastases. British journal of surgery. 105(9). 1210–1220. 111 indexed citations
7.
Noë, Michaël, Neda Rezaee, Kaushal Asrani, et al.. (2018). Immunolabeling of Cleared Human Pancreata Provides Insights into Three-Dimensional Pancreatic Anatomy and Pathology. American Journal Of Pathology. 188(7). 1530–1535. 33 indexed citations
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Barbon, Carlotta, Georgios Antonios Margonis, Nikolaos Andreatos, et al.. (2018). Colorectal Liver Metastases: Does the Future of Precision Medicine Lie in Genetic Testing?. Journal of Gastrointestinal Surgery. 22(7). 1286–1296. 10 indexed citations
10.
Groot, Vincent P., Neda Rezaee, Wenchuan Wu, et al.. (2017). Patterns, Timing, and Predictors of Recurrence Following Pancreatectomy for Pancreatic Ductal Adenocarcinoma. Annals of Surgery. 267(5). 936–945. 477 indexed citations breakdown →
11.
Margonis, Georgios Antonios, Stefan Buettner, Nikolaos Andreatos, et al.. (2017). Preoperative bevacizumab and volumetric recovery after resection of colorectal liver metastases. Journal of Surgical Oncology. 116(8). 1150–1158. 7 indexed citations
12.
Molin, Marco Dal, Amanda L. Blackford, Aaron Brant, et al.. (2017). Duodenal Involvement is an Independent Prognostic Factor for Patients with Surgically Resected Pancreatic Ductal Adenocarcinoma. Annals of Surgical Oncology. 24(8). 2379–2386. 8 indexed citations
13.
Lu, Fengchun, Kevin C. Soares, Jin He, et al.. (2017). Neoadjuvant therapy prior to surgical resection for previously explored pancreatic cancer patients is associated with improved survival. HepatoBiliary Surgery and Nutrition. ６(３). 144–153. 6 indexed citations
14.
Gemenetzis, Georgios, Fabio Bagante, James F. Griffin, et al.. (2016). Neutrophil-to-lymphocyte Ratio is a Predictive Marker for Invasive Malignancy in Intraductal Papillary Mucinous Neoplasms of the Pancreas. Annals of Surgery. 266(2). 339–345. 89 indexed citations
15.
Molin, Marco Dal, Aaron Brant, Amanda L. Blackford, et al.. (2016). Obstructive Sleep Apnea and Pathological Characteristics of Resected Pancreatic Ductal Adenocarcinoma. PLoS ONE. 11(10). e0164195–e0164195. 13 indexed citations
16.
Molin, Marco Dal, Ming Zhang, Roeland F. de Wilde, et al.. (2015). Very Long-term Survival Following Resection for Pancreatic Cancer Is Not Explained by Commonly Mutated Genes: Results of Whole-Exome Sequencing Analysis. Clinical Cancer Research. 21(8). 1944–1950. 74 indexed citations
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Schueneman, Aaron J., Joe Ensor, Burcu Saka, et al.. (2015). Validation of histomolecular classification utilizing histological subtype, MUC1, and CDX2 for prognostication of resected ampullary adenocarcinoma. British Journal of Cancer. 113(1). 64–68. 38 indexed citations
19.
Wu, Wenchuan, Jin He, John L. Cameron, et al.. (2014). The Impact of Postoperative Complications on the Administration of Adjuvant Therapy Following Pancreaticoduodenectomy for Adenocarcinoma. Annals of Surgical Oncology. 21(9). 2873–2881. 159 indexed citations
20.
Molin, Marco Dal, Hanno Matthaei, Jian Wu, et al.. (2013). Clinicopathological Correlates of Activating GNAS Mutations in Intraductal Papillary Mucinous Neoplasm (IPMN) of the Pancreas. Annals of Surgical Oncology. 20(12). 3802–3808. 122 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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