Vigneshwar Senthivel

890 total citations
14 papers, 110 citations indexed

About

Vigneshwar Senthivel is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Vigneshwar Senthivel has authored 14 papers receiving a total of 110 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Infectious Diseases. Recurrent topics in Vigneshwar Senthivel's work include Genomics and Rare Diseases (5 papers), SARS-CoV-2 and COVID-19 Research (2 papers) and BRCA gene mutations in cancer (2 papers). Vigneshwar Senthivel is often cited by papers focused on Genomics and Rare Diseases (5 papers), SARS-CoV-2 and COVID-19 Research (2 papers) and BRCA gene mutations in cancer (2 papers). Vigneshwar Senthivel collaborates with scholars based in India and United States. Vigneshwar Senthivel's co-authors include Sridhar Sivasubbu, Vinod Scaria, Mohamed Imran, Abhinav Jain, Rahul C. Bhoyar, Bani Jolly, Shamsudheen Karuthedath Vellarikkal, Disha Sharma, Rijith Jayarajan and Mercy Rophina and has published in prestigious journals such as Journal of Medical Virology, Cancer Causes & Control and Mitochondrion.

In The Last Decade

Vigneshwar Senthivel

13 papers receiving 107 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vigneshwar Senthivel India	6	39	37	25	22	14	14	110
Suhua Zhou China	4	76 1.9×	27 0.7×	12 0.5×	20 0.9×	11 0.8×	5	125
Misha R. Agarwal United States	5	67 1.7×	62 1.7×	7 0.3×	42 1.9×	19 1.4×	6	319
Irene Dapía Spain	7	48 1.2×	36 1.0×	19 0.8×	45 2.0×	15 1.1×	9	126
Ritika Kapoor Singapore	7	24 0.6×	7 0.2×	11 0.4×	27 1.2×	9 0.6×	16	131
Marius Cotic United Kingdom	5	40 1.0×	10 0.3×	21 0.8×	8 0.4×	18 1.3×	10	108
Mobin Wan China	8	42 1.1×	13 0.4×	38 1.5×	16 0.7×	13 0.9×	15	362
Yuka Maruyama Japan	5	56 1.4×	58 1.6×	6 0.2×	25 1.1×	24 1.7×	10	157
Touch Ativitavas Thailand	6	34 0.9×	41 1.1×	5 0.2×	50 2.3×	62 4.4×	13	125
Stefan Lueth Germany	4	17 0.4×	16 0.4×	17 0.7×	11 0.5×	14 1.0×	7	187
Marcela Galoppo Argentina	8	20 0.5×	29 0.8×	13 0.5×	8 0.4×	7 0.5×	9	188

Countries citing papers authored by Vigneshwar Senthivel

Since Specialization

Citations

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

Fields of papers citing papers by Vigneshwar Senthivel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vigneshwar Senthivel

This figure shows the co-authorship network connecting the top 25 collaborators of Vigneshwar Senthivel. A scholar is included among the top collaborators of Vigneshwar Senthivel 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 Vigneshwar Senthivel. Vigneshwar Senthivel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Bhoyar, Rahul C., Mohamed Imran, Vigneshwar Senthivel, et al.. (2025). Understanding the genetic epidemiology of hereditary breast cancer in India using whole genome data from 1029 healthy individuals. Cancer Causes & Control. 36(7). 673–682. 1 indexed citations

Imran, Mohamed, Arvinden VR, Bhaskar Jyoti Saikia, et al.. (2024). Understanding the variant landscape, and genetic epidemiology of Multiple Endocrine Neoplasia in India. Endocrine. 86(3). 1178–1187.

Senthivel, Vigneshwar, Bani Jolly, Arvinden VR, et al.. (2024). Whole genome sequencing of families diagnosed with cardiac channelopathies reveals structural variants missed by whole exome sequencing. Journal of Human Genetics. 69(9). 455–465. 1 indexed citations

Sivadas, Ambily, Bani Jolly, Rahul C. Bhoyar, et al.. (2024). Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population. BMJ Open Diabetes Research & Care. 12(2). e003769–e003769. 12 indexed citations

Imran, Mohamed, Rahul C. Bhoyar, Abhinav Jain, et al.. (2023). Genetic epidemiology of monogenic dyslipidemia and statin-associated adverse drug phenotypes in Indian population from whole-genomes of 1029 self-declared healthy individuals. Human Gene. 39. 201252–201252. 2 indexed citations

Divakar, Mohit Kumar, Abhinav Jain, Rahul C. Bhoyar, et al.. (2023). Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants. Journal of Human Genetics. 68(6). 409–417. 2 indexed citations

Rophina, Mercy, Rahul C. Bhoyar, Mohamed Imran, et al.. (2022). Genetic landscape of human neutrophil antigen variants in India from population‐scale genomes. HLA. 101(3). 262–269. 1 indexed citations

Senthivel, Vigneshwar, Rahul C. Bhoyar, Abhinav Jain, et al.. (2022). 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants. Human Genomics. 16(1). 30–30. 3 indexed citations

Bhoyar, Rahul C., Ambily Sivadas, Abhinav Jain, et al.. (2022). Pharmacogenomic landscape of Indian population using whole genomes. Clinical and Translational Science. 15(4). 866–877. 17 indexed citations

10.

Bhoyar, Rahul C., Vigneshwar Senthivel, Bani Jolly, et al.. (2021). An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms. STAR Protocols. 2(3). 100755–100755. 9 indexed citations

11.

Singh, Urvashi B., Mercy Rophina, Rama Chaudhry, et al.. (2021). Variants of concern responsible for SARS‐CoV‐2 vaccine breakthrough infections from India. Journal of Medical Virology. 94(4). 1696–1700. 17 indexed citations

12.

Sharma, Disha, Shamsudheen Karuthedath Vellarikkal, Rijith Jayarajan, et al.. (2018). Organellar transcriptome sequencing reveals mitochondrial localization of nuclear encoded transcripts. Mitochondrion. 46. 59–68. 5 indexed citations

13.

Vellarikkal, Shamsudheen Karuthedath, Ankit Verma, Rijith Jayarajan, et al.. (2018). SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes. Database. 2018. 1–10. 18 indexed citations

14.

Vellarikkal, Shamsudheen Karuthedath, K Pavithran, Ankit Verma, et al.. (2017). Pharmacogenetic Landscape of DPYD Variants in South Asian Populations by Integration of Genome-Scale Data. Pharmacogenomics. 19(3). 227–241. 22 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