Arabandi Ramesh

1.6k total citations
30 papers, 775 citations indexed

About

Arabandi Ramesh is a scholar working on Molecular Biology, Sensory Systems and Plant Science. According to data from OpenAlex, Arabandi Ramesh has authored 30 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Sensory Systems and 6 papers in Plant Science. Recurrent topics in Arabandi Ramesh's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), RNA regulation and disease (5 papers) and Connexins and lens biology (4 papers). Arabandi Ramesh is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), RNA regulation and disease (5 papers) and Connexins and lens biology (4 papers). Arabandi Ramesh collaborates with scholars based in India, United States and Belgium. Arabandi Ramesh's co-authors include C. R. Srikumari Srisailapathy, Richard J. Smith, Sathiyavedu Thyagarajan Santhiya, P Arumugam, Kumpati Premkumar, P. Ramamurthy, Ross I. S. Zbar, Guy Van Camp, Saima Riazuddin and Thomas B. Friedman and has published in prestigious journals such as Nature Communications, PLoS ONE and Genome Research.

In The Last Decade

Arabandi Ramesh

29 papers receiving 749 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arabandi Ramesh India 16 457 396 164 91 74 30 775
Sara Letizia Maria Eramo Italy 14 456 1.0× 275 0.7× 168 1.0× 131 1.4× 52 0.7× 16 786
Shuan‐Yow Li Taiwan 18 316 0.7× 544 1.4× 94 0.6× 75 0.8× 175 2.4× 51 955
Thomas F.J. Wagner Germany 8 607 1.3× 368 0.9× 45 0.3× 40 0.4× 91 1.2× 8 933
Liping Nie China 20 346 0.8× 1.0k 2.6× 87 0.5× 76 0.8× 95 1.3× 45 1.4k
Daniela Buckiová Czechia 12 141 0.3× 116 0.3× 64 0.4× 56 0.6× 42 0.6× 17 437
Jesse Peterson United States 14 333 0.7× 239 0.6× 67 0.4× 18 0.2× 38 0.5× 19 1.1k
Yue Qiu China 16 100 0.2× 323 0.8× 75 0.5× 40 0.4× 164 2.2× 40 661
Rui Lin China 15 95 0.2× 326 0.8× 141 0.9× 9 0.1× 170 2.3× 30 736
Désirée Griesemer Germany 15 298 0.7× 301 0.8× 45 0.3× 56 0.6× 24 0.3× 15 694
Tatjana I. Kichko Germany 15 505 1.1× 315 0.8× 41 0.3× 10 0.1× 74 1.0× 18 1.0k

Countries citing papers authored by Arabandi Ramesh

Since Specialization
Citations

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

Fields of papers citing papers by Arabandi Ramesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arabandi Ramesh

This figure shows the co-authorship network connecting the top 25 collaborators of Arabandi Ramesh. A scholar is included among the top collaborators of Arabandi Ramesh 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 Arabandi Ramesh. Arabandi Ramesh 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.
Ramesh, Arabandi, et al.. (2014). High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications. Journal of Genetics. 93(1). 207–213. 5 indexed citations
3.
Ramesh, Arabandi, et al.. (2014). Is Screening for Mitochondrial A1555G Mutation among Assortative Mating Hearing Impaired Families Important? : A Prefatory Quest. 3(1). 1–7. 3 indexed citations
4.
Srisailapathy, C. R. Srikumari, Vikas Malhotra, Meenakshi Sharma, et al.. (2014). Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE. PLoS ONE. 9(1). e84773–e84773. 48 indexed citations
5.
Padmaja, Mekala, et al.. (2012). PARK2 gene mutations in early onset Parkinson's disease patients of South India. Neuroscience Letters. 523(2). 145–147. 12 indexed citations
6.
Lelli, Andrea, Margit Schraders, Kausik K. Ray, et al.. (2011). Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. Nature Communications. 2(1). 201–201. 78 indexed citations
7.
Manickaraj, Ashok Kumar, et al.. (2010). Associations for Lipoprotein Lipase and Peroxisome Proliferator-activated Receptor-γ Gene and Coronary Artery Disease in an Indian Population. Archives of Medical Research. 41(1). 19–25.e1. 17 indexed citations
8.
Manickaraj, Ashok Kumar, et al.. (2009). Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians. Molecular Biology Reports. 37(1). 521–527. 20 indexed citations
9.
10.
Arumugam, P, et al.. (2009). Superoxide radical scavenging and antibacterial activities of different fractions of ethanol extract of Mentha spicata (L.). Medicinal Chemistry Research. 19(7). 664–673. 15 indexed citations
11.
Mani, Ram S., C. R. Srikumari Srisailapathy, Vikas Malhotra, et al.. (2008). Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss. European Journal of Human Genetics. 17(4). 502–509. 63 indexed citations
12.
Khan, Shahid Y., Zubair M. Ahmed, Shin‐ichiro Kitajiri, et al.. (2007). Mutations of theRDXgene cause nonsyndromic hearing loss at theDFNB24locus. Human Mutation. 28(5). 417–423. 60 indexed citations
13.
Arumugam, P, P. Ramamurthy, Sathiyavedu Thyagarajan Santhiya, & Arabandi Ramesh. (2006). Antioxidant activity measured in different solvent fractions obtained from Mentha spicata Linn.: an analysis by ABTS*+ decolorization assay.. PubMed. 15(1). 119–24. 57 indexed citations
14.
Guo, Yingshi, Valentina Pilipenko, Lynne Hsueh Yee Lim, et al.. (2004). Refining the DFNB17 interval in consanguineous Indian families. Molecular Biology Reports. 31(2). 97–105. 2 indexed citations
15.
Premkumar, Kumpati, et al.. (2004). Interactive effects of saffron with garlic and curcumin against cyclophosphamide induced genotoxicity in mice.. PubMed. 13(3). 292–4. 26 indexed citations
16.
Naz, Sadaf, Chantal Giguère, David C. Kohrman, et al.. (2002). Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus. The American Journal of Human Genetics. 71(3). 632–636. 100 indexed citations
17.
Stephan, Dietrich, Tama Hasson, Kunihiro Fukushima, et al.. (2001). MYO1F as a Candidate Gene for Nonsyndromic Deafness, DFNB15. Archives of Otolaryngology - Head and Neck Surgery. 127(8). 921–921. 23 indexed citations
18.
Greinwald, John H., Daryl A. Scott, Jacquie Marietta, et al.. (1997). Construction of P1-Derived Artificial Chromosome and Yeast Artificial Chromosome Contigs Encompassing the DFNB7 andDFNB11 Region of Chromosome 9q13–21. Genome Research. 7(9). 879–886. 7 indexed citations
19.
Fukushima, Kunihiro, Arabandi Ramesh, C. R. Srikumari Srisailapathy, et al.. (1995). Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Human Molecular Genetics. 4(9). 1643–1648. 41 indexed citations
20.
Jain, Pawan Kumar, Kunihiro Fukushima, Dilip Deshmukh, et al.. (1995). A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus. Human Molecular Genetics. 4(12). 2391–2394. 51 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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