Apar Pataer

3.6k total citations · 1 hit paper
32 papers, 1.4k citations indexed

About

Apar Pataer is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Apar Pataer has authored 32 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pulmonary and Respiratory Medicine, 14 papers in Molecular Biology and 12 papers in Oncology. Recurrent topics in Apar Pataer's work include Lung Cancer Treatments and Mutations (16 papers), Lung Cancer Diagnosis and Treatment (14 papers) and Cancer Immunotherapy and Biomarkers (7 papers). Apar Pataer is often cited by papers focused on Lung Cancer Treatments and Mutations (16 papers), Lung Cancer Diagnosis and Treatment (14 papers) and Cancer Immunotherapy and Biomarkers (7 papers). Apar Pataer collaborates with scholars based in United States, China and Brazil. Apar Pataer's co-authors include Stephen G. Swisher, Neda Kalhor, William N. William, Ignacio I. Wistuba, Arlene M. Correa, Jack A. Roth, Matthew D. Hellmann, William D. Travis, Mark G. Kris and Valerie W. Rusch and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Apar Pataer

31 papers receiving 1.4k citations

Hit Papers

Pathological response after neoadjuvant chemotherapy in r... 2014 2026 2018 2022 2014 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Apar Pataer United States 18 876 715 293 217 186 32 1.4k
Elena Elimova Canada 21 710 0.8× 529 0.7× 364 1.2× 534 2.5× 185 1.0× 119 1.4k
Jeremy Cetnar United States 14 788 0.9× 905 1.3× 372 1.3× 189 0.9× 62 0.3× 42 1.4k
Jingyu Yu United States 15 439 0.5× 871 1.2× 286 1.0× 102 0.5× 177 1.0× 27 1.3k
Masato Shingyoji Japan 15 847 1.0× 514 0.7× 382 1.3× 99 0.5× 181 1.0× 67 1.3k
Loredana Vecchione Italy 18 444 0.5× 964 1.3× 542 1.8× 213 1.0× 63 0.3× 33 1.5k
Chiara Lazzari Italy 24 738 0.8× 883 1.2× 580 2.0× 71 0.3× 74 0.4× 67 1.5k
Sònia Pernas Spain 20 447 0.5× 1.1k 1.6× 413 1.4× 83 0.4× 312 1.7× 109 1.6k
K.A. Mason United States 11 440 0.5× 687 1.0× 288 1.0× 168 0.8× 123 0.7× 18 1.3k
Angela Listì Italy 19 538 0.6× 701 1.0× 420 1.4× 90 0.4× 40 0.2× 41 1.3k
B. Helfrich United States 13 581 0.7× 726 1.0× 698 2.4× 58 0.3× 193 1.0× 27 1.4k

Countries citing papers authored by Apar Pataer

Since Specialization
Citations

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

Fields of papers citing papers by Apar Pataer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Apar Pataer

This figure shows the co-authorship network connecting the top 25 collaborators of Apar Pataer. A scholar is included among the top collaborators of Apar Pataer 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 Apar Pataer. Apar Pataer 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.
2.
Feldman, Hope, Boris Sepesi, Cheuk Hong Leung, et al.. (2023). Surgical outcomes after chemotherapy plus nivolumab and chemotherapy plus nivolumab and ipilimumab in patients with non–small cell lung cancer. Journal of Thoracic and Cardiovascular Surgery. 167(4). 1444–1453.e4. 8 indexed citations
3.
Pataer, Apar, Annikka Weissferdt, Arlene M. Correa, et al.. (2022). Major Pathologic Response and Prognostic Score Predict Survival in Patients With Lung Cancer Receiving Neoadjuvant Chemotherapy. JTO Clinical and Research Reports. 3(11). 100420–100420. 13 indexed citations
4.
Pataer, Apar, Annikka Weissferdt, Ara A. Vaporciyan, et al.. (2021). Evaluation of Pathologic Response in Lymph Nodes of Patients With Lung Cancer Receiving Neoadjuvant Chemotherapy. Journal of Thoracic Oncology. 16(8). 1289–1297. 32 indexed citations
5.
Weissferdt, Annikka, Apar Pataer, Stephen G. Swisher, et al.. (2021). Controversies and challenges in the pathologic examination of lung resection specimens after neoadjuvant treatment. Lung Cancer. 154. 76–83. 18 indexed citations
6.
Weissferdt, Annikka, Apar Pataer, Ara A. Vaporciyan, et al.. (2020). Agreement on Major Pathological Response in NSCLC Patients Receiving Neoadjuvant Chemotherapy. Clinical Lung Cancer. 21(4). 341–348. 75 indexed citations
7.
Pataer, Apar, Bülent Özpolat, Neil R. Cashman, et al.. (2019). Therapeutic targeting of the PI4K2A/PKR lysosome network is critical for misfolded protein clearance and survival in cancer cells. Oncogene. 39(4). 801–813. 21 indexed citations
8.
Bircan, Ahmet, Nilgün Gürbüz, Apar Pataer, et al.. (2018). Elongation factor-2 kinase (eEF-2K) expression is associated with poor patient survival and promotes proliferation, invasion and tumor growth of lung cancer. Lung Cancer. 124. 31–39. 37 indexed citations
9.
Pu, Xingxiang, Ran Zhang, Li Wang, et al.. (2018). Patient-derived tumor immune microenvironments in patient-derived xenografts of lung cancer. Journal of Translational Medicine. 16(1). 328–328. 11 indexed citations
10.
Weissferdt, Annikka, Boris Sepesi, Apar Pataer, et al.. (2018). Pathologic assessment following neoadjuvant immunotherapy or chemotherapy demonstrates similar patterns in non-small cell lung cancer (NSCLC). Annals of Oncology. 29. viii680–viii680. 4 indexed citations
11.
Cascone, Tina, Kathryn A. Gold, Stephen G. Swisher, et al.. (2017). Induction Cisplatin Docetaxel Followed by Surgery and Erlotinib in Non-Small Cell Lung Cancer. The Annals of Thoracic Surgery. 105(2). 418–424. 20 indexed citations
12.
Gentile, Emanuela, Taro Oba, Jing Lin, et al.. (2017). Cationic liquid crystalline nanoparticles for the delivery of synthetic RNAi-based therapeutics. Oncotarget. 8(29). 48222–48239. 6 indexed citations
13.
Hellmann, Matthew D., Jamie E. Chaft, William N. William, et al.. (2014). Pathological response after neoadjuvant chemotherapy in resectable non-small-cell lung cancers: proposal for the use of major pathological response as a surrogate endpoint. The Lancet Oncology. 15(1). e42–e50. 416 indexed citations breakdown →
14.
William, William N., Apar Pataer, Neda Kalhor, et al.. (2013). Computed Tomography RECIST Assessment of Histopathologic Response and Prediction of Survival in Patients with Resectable Non–Small-Cell Lung Cancer after Neoadjuvant Chemotherapy. Journal of Thoracic Oncology. 8(2). 222–228. 104 indexed citations
15.
Guo, Chengcheng, Ruping Shao, Arlene M. Correa, et al.. (2013). Prognostic Significance of Combinations of RNA-Dependent Protein Kinase and EphA2 Biomarkers for NSCLC. Journal of Thoracic Oncology. 8(3). 301–308. 19 indexed citations
16.
Guo, Chengcheng, Haibo Lu, Wen Gao, et al.. (2013). Insulin-Like Growth Factor Binding Protein-2 Level Is Increased in Blood of Lung Cancer Patients and Associated with Poor Survival. PLoS ONE. 8(9). e74973–e74973. 39 indexed citations
17.
He, Yong, Zhen Zhou, Wayne L. Hofstetter, et al.. (2012). Aberrant Expression of Proteins Involved in Signal Transduction and DNA Repair Pathways in Lung Cancer and Their Association with Clinical Parameters. PLoS ONE. 7(2). e31087–e31087. 33 indexed citations
18.
Pataer, Apar, Neda Kalhor, Arlene M. Correa, et al.. (2012). Histopathologic Response Criteria Predict Survival of Patients with Resected Lung Cancer After Neoadjuvant Chemotherapy. Journal of Thoracic Oncology. 7(5). 825–832. 251 indexed citations
19.
He, Yong, Arlene M. Correa, Maria Gabriela Raso, et al.. (2011). The Role of PKR/eIF2α Signaling Pathway in Prognosis of Non-Small Cell Lung Cancer. PLoS ONE. 6(11). e24855–e24855. 34 indexed citations
20.
Takada, Yuhei, Haruyo Ichikawa, Apar Pataer, Stephen G. Swisher, & Bharat B. Aggarwal. (2006). Genetic deletion of PKR abrogates TNF-induced activation of IκBα kinase, JNK, Akt and cell proliferation but potentiates p44/p42 MAPK and p38 MAPK activation. Oncogene. 26(8). 1201–1212. 86 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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