Subrata Kumar Dey

1.7k total citations · 1 hit paper
70 papers, 1.2k citations indexed

About

Subrata Kumar Dey is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Subrata Kumar Dey has authored 70 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Radiology, Nuclear Medicine and Imaging and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Subrata Kumar Dey's work include Effects of Radiation Exposure (8 papers), Radiation Therapy and Dosimetry (7 papers) and DNA Repair Mechanisms (5 papers). Subrata Kumar Dey is often cited by papers focused on Effects of Radiation Exposure (8 papers), Radiation Therapy and Dosimetry (7 papers) and DNA Repair Mechanisms (5 papers). Subrata Kumar Dey collaborates with scholars based in India, China and United States. Subrata Kumar Dey's co-authors include Sujay Ghosh, Chabita Saha, Eleanor Feingold, Santasree Banerjee, Chen Li, Sandip Pal, Heinz‐Bernhard Kraatz, Qing He, Baicheng Xu and Jinxia An and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Langmuir.

In The Last Decade

Subrata Kumar Dey

66 papers receiving 1.2k citations

Hit Papers

Targeted Next Generation Sequencing Revealed a Novel Homo... 2019 2026 2021 2023 2019 100 200 300
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. Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chinese Family
    2019 371 citations Chen Li, Subrata Kumar Dey et al. profile →

Peers

Subrata Kumar Dey
Hitomi Nakamura Japan
Sandra Schulze Germany
Kambiz Gilany Iran
Shujuan Wang China
Rhonda M. Brand United States
Xueqi Wang China
Xiaofei Liu China
Allison Piovesan Italy
Hae‐Won Uh Netherlands
David W. Montgomery United States
Hitomi Nakamura Japan
Subrata Kumar Dey
Citations per year, relative to Subrata Kumar Dey Subrata Kumar Dey (= 1×) peers Hitomi Nakamura

Countries citing papers authored by Subrata Kumar Dey

Since Specialization
Citations

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

Fields of papers citing papers by Subrata Kumar Dey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Subrata Kumar Dey. 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 Subrata Kumar Dey. The network helps show where Subrata Kumar Dey may publish in the future.

Co-authorship network of co-authors of Subrata Kumar Dey

This figure shows the co-authorship network connecting the top 25 collaborators of Subrata Kumar Dey. A scholar is included among the top collaborators of Subrata Kumar Dey 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 Subrata Kumar Dey. Subrata Kumar Dey 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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Zhong, Lijuan, Yin Li, Xiaohong He, et al.. (2023). Identification and functional characterization of a novel truncating splicing variant in COL4A5 gene causing X-linked Alport syndrome with astigmatism. Chinese Medical Journal. 136(21). 2635–2637. 1 indexed citations
3.
Zhang, Rui, Yajing Hao, Ying Xu, et al.. (2022). Whole exome sequencing identified a homozygous novel mutation in SUOX gene causes extremely rare autosomal recessive isolated sulfite oxidase deficiency. Clinica Chimica Acta. 532. 115–122. 6 indexed citations
4.
Nautiyal, Amit, et al.. (2021). Biological Effects Associated with Internal and External Contamination of Diagnostic Nuclear Medicine Sources. Indian Journal of Nuclear Medicine. 36(3). 288–292. 1 indexed citations
5.
Ray, Partha Pratim, et al.. (2019). Potential Effect of Tobacco Consumption through Smoking and Chewing Tobacco on IL1beta Protein Expression in Chronic Periodontitis Patients: In Silico Molecular Docking Study. IEEE/ACM Transactions on Computational Biology and Bioinformatics. 17(4). 1364–1371. 6 indexed citations
6.
Ghosh, Sujay, et al.. (2019). Interleukin gene polymorphisms in chronic periodontitis: A case-control study in the Indian population. Archives of Oral Biology. 101. 156–164. 24 indexed citations
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Ghosh, Priyanka, et al.. (2017). Telomere length analysis in Down syndrome birth. Mechanisms of Ageing and Development. 164. 20–26. 14 indexed citations
9.
Dey, Subrata Kumar, et al.. (2016). Protean presentations of parathyroid adenoma in childhood. Journal of Indian Association of Pediatric Surgeons. 22(1). 40–40. 2 indexed citations
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Pal, Sandip, Subrata Kumar Dey, & Chabita Saha. (2014). Inhibition of Catalase by Tea Catechins in Free and Cellular State: A Biophysical Approach. PLoS ONE. 9(7). e102460–e102460. 45 indexed citations
12.
Ghosh, Debjani, Subrata Kumar Dey, & Chabita Saha. (2014). Mutation Induced Conformational Changes in Genomic DNA from Cancerous K562 Cells Influence Drug-DNA Binding Modes. PLoS ONE. 9(1). e84880–e84880. 21 indexed citations
13.
Ghosh, Sujoy, et al.. (2013). The Autosomal Recessive Inheritance of Hereditary Gingival Fibromatosis. SHILAP Revista de lepidopterología. 2013. 1–4. 15 indexed citations
14.
Dey, Subrata Kumar, et al.. (2013). Altered incidence of meiotic errors and Down syndrome birth under extreme low socioeconomic exposure in the Sundarban area of India. Journal of Community Genetics. 5(2). 119–124. 9 indexed citations
15.
Ghosh, Debjani, Maidul Hossain, Chabita Saha, Subrata Kumar Dey, & Gopinatha Suresh Kumar. (2011). Intercalation and Induction of Strand Breaks by Adriamycin and Daunomycin: A Study with Human Genomic DNA. DNA and Cell Biology. 31(3). 378–387. 16 indexed citations
16.
Ghosh, Priyanka, et al.. (2010). Chromosome 21 non-disjunction and Down syndrome birth in an Indian cohort: analysis of incidence and aetiology from family linkage data. Genetics Research. 92(3). 189–197. 19 indexed citations
17.
Ghosh, Sujay, Eleanor Feingold, & Subrata Kumar Dey. (2009). Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. American Journal of Medical Genetics Part A. 149A(7). 1415–1420. 81 indexed citations
18.
Dey, Subrata Kumar, et al.. (2007). Effect of Kunapajala and Fertilizers on Senna ( Cassia angustifolia Vahl.). Indian Forester. 133(9). 1235–1240. 1 indexed citations
19.
Pathak, Rupak, et al.. (2007). Response to high LET radiation 12 C (LET, 295 keV/μm) in M5 cells, a radio resistant cell strain derived from Chinese hamster V79 cells. International Journal of Radiation Biology. 83(1). 53–63. 10 indexed citations
20.
Roy, Madhumita, et al.. (1993). Characterisation of methotrexate-resistant clones. Mutation Research/Environmental Mutagenesis and Related Subjects. 291(1). 43–51. 9 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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