Narayanappa Gayathri

2.3k total citations
136 papers, 1.5k citations indexed

About

Narayanappa Gayathri is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Narayanappa Gayathri has authored 136 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Molecular Biology, 28 papers in Clinical Biochemistry and 20 papers in Rheumatology. Recurrent topics in Narayanappa Gayathri's work include Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (28 papers) and Muscle Physiology and Disorders (27 papers). Narayanappa Gayathri is often cited by papers focused on Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (28 papers) and Muscle Physiology and Disorders (27 papers). Narayanappa Gayathri collaborates with scholars based in India, Australia and United States. Narayanappa Gayathri's co-authors include Atchayaram Nalini, M. M. Srinivas Bharath, Sanjib Sinha, Arun B. Taly, Parayil Sankaran Bindu, T.C. Yasha, S. Thilagar, R. Karthik, D. Kumar and Madhu Nagappa and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Narayanappa Gayathri

129 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Narayanappa Gayathri India 21 872 274 212 211 202 136 1.5k
Gavin Falkous United Kingdom 20 1.1k 1.2× 269 1.0× 218 1.0× 304 1.4× 280 1.4× 43 1.5k
Naïg Guéguen France 34 1.7k 2.0× 456 1.7× 368 1.7× 395 1.9× 91 0.5× 70 2.6k
Martín A. Baraibar France 24 951 1.1× 476 1.7× 204 1.0× 118 0.6× 133 0.7× 33 1.6k
Till Voigtländer Austria 19 1.0k 1.2× 397 1.4× 129 0.6× 287 1.4× 146 0.7× 47 1.7k
S. Priya Narayanan United States 23 1.1k 1.2× 368 1.3× 241 1.1× 108 0.5× 79 0.4× 47 2.4k
Kazunori Sato Japan 17 546 0.6× 278 1.0× 301 1.4× 101 0.5× 108 0.5× 76 1.5k
Danielle Château France 24 2.0k 2.3× 303 1.1× 368 1.7× 168 0.8× 177 0.9× 44 2.7k
Hongwei Xu China 22 556 0.6× 279 1.0× 83 0.4× 146 0.7× 139 0.7× 76 1.6k
Lorenzo Fumagalli Italy 22 684 0.8× 306 1.1× 199 0.9× 42 0.2× 143 0.7× 76 1.7k
Mauro Patrone Italy 26 948 1.1× 199 0.7× 136 0.6× 612 2.9× 77 0.4× 79 2.1k

Countries citing papers authored by Narayanappa Gayathri

Since Specialization
Citations

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

Fields of papers citing papers by Narayanappa Gayathri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Narayanappa Gayathri

This figure shows the co-authorship network connecting the top 25 collaborators of Narayanappa Gayathri. A scholar is included among the top collaborators of Narayanappa Gayathri 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 Narayanappa Gayathri. Narayanappa Gayathri 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.
Prasad, Pramada, Jayashree Aiyar, Saurabh Joshi, et al.. (2023). An ultrastructural and genomic study on the SARS-CoV-2 variant B.1.210 circulating during the first wave of COVID-19 pandemic in India. Indian Journal of Medical Microbiology. 41. 45–52. 1 indexed citations
2.
Dey, Gourav, Gajanan Sathe, Nupur Pruthi, et al.. (2023). Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events. Journal of Neurochemistry. 167(2). 218–247. 4 indexed citations
3.
Preethish‐Kumar, Veeramani, Kiran Polavarapu, Kapaettu Satyamoorthy, et al.. (2021). A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein. Journal of Molecular Neuroscience. 71(12). 2468–2473. 8 indexed citations
4.
Kumar, Krishna, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2020). Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations. European Journal of Neurology. 28(3). 992–1003. 9 indexed citations
5.
Kumar, Manish, Sruthi Unni, Narayanappa Gayathri, et al.. (2019). Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle. Journal of Proteomics. 211. 103556–103556. 10 indexed citations
6.
Vengalil, Seena, Veeramani Preethish‐Kumar, Kiran Polavarapu, et al.. (2017). MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India. BMC Medical Genetics. 18(1). 67–67. 18 indexed citations
7.
Vandana, V.P., Periyasamy Govindaraj, Arun B. Taly, et al.. (2016). Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome. Clinical Neurology and Neurosurgery. 148. 17–21. 13 indexed citations
8.
Singh, Nivedita, Vishwanath Kumble Bhat, Parayil Sankaran Bindu, et al.. (2016). Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex. PLoS ONE. 11(5). e0155605–e0155605. 27 indexed citations
9.
Bindu, Parayil Sankaran, Arun B. Taly, Narayanappa Gayathri, et al.. (2015). Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India. Mitochondrion. 25. 6–16. 22 indexed citations
10.
Chandra, Sadanandavalli Retnaswami, et al.. (2015). Schwartz-Jampel syndrome. Journal of Pediatric Neurosciences. 10(2). 169–169. 9 indexed citations
11.
Bindu, Parayil Sankaran, Arun B. Taly, Atchayaram Nalini, et al.. (2014). Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency. Journal of Clinical Neuromuscular Disease. 16(2). 69–73. 2 indexed citations
12.
Nalini, Atchayaram, Madhu Nagappa, & Narayanappa Gayathri. (2013). Major histocompatibility complex and inflammatory cell subtype expression in inflammatory myopathies and muscular dystrophies. Neurology India. 61(6). 614–614. 12 indexed citations
13.
Khan, Nahid, Parayil Sankaran Bindu, Arun B. Taly, et al.. (2013). Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations. Brain and Development. 36(9). 807–812. 21 indexed citations
14.
Gayathri, Narayanappa, et al.. (2012). Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association. Annals of Indian Academy of Neurology. 15(4). 332–332. 2 indexed citations
15.
Bindu, Parayil Sankaran, Arun B. Taly, Rita Christopher, et al.. (2012). Electro-clinical features and magnetic resonance imaging correlates in Menkes disease. Brain and Development. 35(5). 398–405. 13 indexed citations
16.
Gayathri, Narayanappa, et al.. (2010). Familial amyloidotic polyneuropathy with muscle, vitreous, leptomeningeal, and cardiac involvement: Phenotypic, pathological, and MRI description. SHILAP Revista de lepidopterología. 1 indexed citations
17.
Nalini, Atchayaram, et al.. (2010). Distal myopathy with rimmed vacuoles: Report on clinical characteristics in 23 cases. Neurology India. 58(2). 235–235. 15 indexed citations
18.
Pandit, Lekha, et al.. (2008). Autosomal recessive tubular aggregate myopathy in an Indian family. European Journal of Paediatric Neurology. 13(4). 373–375. 1 indexed citations
19.
Nair, K P Sivaraman, et al.. (2001). DISABILITIES IN CHILDREN WITH DUCHENNE MUSCULAR DYSTROPHY: A PROFILE. Journal of Rehabilitation Medicine. 33(4). 147–149. 26 indexed citations
20.
Gayathri, Narayanappa, et al.. (1999). Metabolic Disorders Presenting as Vacuolar Myopathy. SHILAP Revista de lepidopterología. 2 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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