Bedia A. Barkoh

3.3k total citations
45 papers, 2.4k citations indexed

About

Bedia A. Barkoh is a scholar working on Cancer Research, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Bedia A. Barkoh has authored 45 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cancer Research, 21 papers in Molecular Biology and 14 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Bedia A. Barkoh's work include Cancer Genomics and Diagnostics (21 papers), Acute Myeloid Leukemia Research (12 papers) and Lung Cancer Treatments and Mutations (10 papers). Bedia A. Barkoh is often cited by papers focused on Cancer Genomics and Diagnostics (21 papers), Acute Myeloid Leukemia Research (12 papers) and Lung Cancer Treatments and Mutations (10 papers). Bedia A. Barkoh collaborates with scholars based in United States, Venezuela and Netherlands. Bedia A. Barkoh's co-authors include Rajyalakshmi Luthra, L. Jeffrey Medeiros, Keyur P. Patel, Rajesh R. Singh, Russell R. Broaddus, Mark J. Routbort, Kenneth Aldape, Rashmi Kanagal‐Shamanna, Neelima G. Reddy and Sinchita Roy‐Chowdhuri and has published in prestigious journals such as Blood, PLoS ONE and Cancer.

In The Last Decade

Bedia A. Barkoh

45 papers receiving 2.4k citations

Peers

Bedia A. Barkoh
Ming‐Tseh Lin United States
Gavin Ha United States
Alison M. Schram United States
K. Hacène France
Peter Ulz Austria
Mark Sausen United States
Stephen Lade Australia
Ming‐Tseh Lin United States
Bedia A. Barkoh
Citations per year, relative to Bedia A. Barkoh Bedia A. Barkoh (= 1×) peers Ming‐Tseh Lin

Countries citing papers authored by Bedia A. Barkoh

Since Specialization
Citations

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

Fields of papers citing papers by Bedia A. Barkoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bedia A. Barkoh. 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 Bedia A. Barkoh. The network helps show where Bedia A. Barkoh may publish in the future.

Co-authorship network of co-authors of Bedia A. Barkoh

This figure shows the co-authorship network connecting the top 25 collaborators of Bedia A. Barkoh. A scholar is included among the top collaborators of Bedia A. Barkoh 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 Bedia A. Barkoh. Bedia A. Barkoh 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.
Grosu, Horiana B., Sharjeel Sabir, F. Anthony San Lucas, et al.. (2021). Adequacy of small biopsy and cytology specimens for comprehensive genomic profiling of patients with non-small-cell lung cancer to determine eligibility for immune checkpoint inhibitor and targeted therapy. Journal of Clinical Pathology. 75(9). 612–619. 20 indexed citations
2.
Hannigan, B. M., Meenakshi Mehrotra, Vincent K. Lam, et al.. (2019). Liquid biopsy assay for lung carcinoma using centrifuged supernatants from fine-needle aspiration specimens. Annals of Oncology. 30(6). 963–969. 36 indexed citations
3.
Roy‐Chowdhuri, Sinchita, Meenakshi Mehrotra, Rashmi Kanagal‐Shamanna, et al.. (2018). Salvaging the supernatant: next generation cytopathology for solid tumor mutation profiling. Modern Pathology. 31(7). 1036–1045. 55 indexed citations
4.
Mehrotra, Meenakshi, Rajesh R. Singh, Wei Chen, et al.. (2017). Study of Preanalytic and Analytic Variables for Clinical Next-Generation Sequencing of Circulating Cell-Free Nucleic Acid. Journal of Molecular Diagnostics. 19(4). 514–524. 21 indexed citations
5.
Ballester, Leomar Y., Sanam Loghavi, Rashmi Kanagal‐Shamanna, et al.. (2016). Clinical Validation of a CXCR4 Mutation Screening Assay for Waldenstrom Macroglobulinemia. Clinical Lymphoma Myeloma & Leukemia. 16(7). 395–403.e1. 14 indexed citations
6.
Goswami, Rashmi S., Rajyalakshmi Luthra, Rajesh R. Singh, et al.. (2016). Identification of Factors Affecting the Success of Next-Generation Sequencing Testing in Solid Tumors. American Journal of Clinical Pathology. 145(2). 222–237. 90 indexed citations
7.
Mehrotra, Meenakshi, Rajyalakshmi Luthra, Rajesh R. Singh, et al.. (2015). Clinical Validation of a Multipurpose Assay for Detection and Genotyping ofCALRMutations in Myeloproliferative Neoplasms. American Journal of Clinical Pathology. 144(5). 746–755. 9 indexed citations
8.
Mehrotra, Meenakshi, L. Jeffrey Medeiros, Rajyalakshmi Luthra, et al.. (2014). Identification of putative pathogenic microRNA and its downstream targets in anaplastic lymphoma kinase–negative anaplastic large cell lymphoma. Human Pathology. 45(10). 1995–2005. 11 indexed citations
9.
Singh, Rajesh R., Keyur P. Patel, Mark J. Routbort, et al.. (2014). Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours. British Journal of Cancer. 111(10). 2014–2023. 65 indexed citations
10.
Kanagal‐Shamanna, Rashmi, Bryce P. Portier, Rajesh R. Singh, et al.. (2013). Next-generation sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: promises and challenges for routine clinical diagnostics. Modern Pathology. 27(2). 314–327. 158 indexed citations
11.
Djordjevic, Bojana, Bedia A. Barkoh, Rajyalakshmi Luthra, & Russell R. Broaddus. (2013). Relationship between PTEN, DNA mismatch repair, and tumor histotype in endometrial carcinoma: retained positive expression of PTEN preferentially identifies sporadic non-endometrioid carcinomas. Modern Pathology. 26(10). 1401–1412. 39 indexed citations
12.
Singh, Rajesh R., Keyur P. Patel, Mark J. Routbort, et al.. (2013). Clinical Validation of a Next-Generation Sequencing Screen for Mutational Hotspots in 46 Cancer-Related Genes. Journal of Molecular Diagnostics. 15(5). 607–622. 239 indexed citations
13.
Jour, George, Matthew Johnson, Jason Reidy, et al.. (2013). Primary cutaneous carcinosarcoma: insights into its clonal origin and mutational pattern expression analysis through next-generation sequencing. Human Pathology. 44(12). 2853–2860. 23 indexed citations
14.
Greaves, Wesley O., Shalini Verma, Keyur P. Patel, et al.. (2012). Frequency and Spectrum of BRAF Mutations in a Retrospective, Single-Institution Study of 1112 Cases of Melanoma. Journal of Molecular Diagnostics. 15(2). 220–226. 173 indexed citations
15.
Bartley, Angela N., Hui Yao, Bedia A. Barkoh, et al.. (2011). Complex Patterns of Altered MicroRNA Expression during the Adenoma-Adenocarcinoma Sequence for Microsatellite-Stable Colorectal Cancer. Clinical Cancer Research. 17(23). 7283–7293. 57 indexed citations
16.
Kanagal‐Shamanna, Rashmi, Carlos E. Bueso‐Ramos, Bedia A. Barkoh, et al.. (2011). Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild‐type TP53. Cancer. 118(11). 2879–2888. 49 indexed citations
17.
Patel, Keyur P., Bedia A. Barkoh, Chen Zhao, et al.. (2011). Diagnostic Testing for IDH1 and IDH2 Variants in Acute Myeloid Leukemia. Journal of Molecular Diagnostics. 13(6). 678–686. 41 indexed citations
18.
Lennon, Patrick A., Srđan Verstovšek, Bedia A. Barkoh, et al.. (2010). Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations. Cancer Genetics and Cytogenetics. 197(1). 1–7. 14 indexed citations
19.
Yin, C. Cameron, Jörge E. Cortes, Bedia A. Barkoh, et al.. (2006). t(3;21)(q26;q22) in myeloid leukemia. Cancer. 106(8). 1730–1738. 45 indexed citations
20.
Goy, André, Yvonne Remache, Jun Gu, et al.. (2004). Establishment and Characterization of a New Mantle Cell Lymphoma Cell Line M-1. Leukemia & lymphoma. 45(6). 1255–1260. 21 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026