Narayanappa Gayathri

2.3k citations

136 papers · 1.5k indexed · h-index 21

Molecular Biology top 10%
Physiology top 10%
Cellular and Molecular Neuroscience top 10%
Clinical Biochemistry top 2%
Neurology top 5%

Co-authors: Atchayaram Nalini M. M. Srinivas Bharath Sanjib Sinha Arun B. Taly Parayil Sankaran Bindu T.C. Yasha S. Thilagar D. Kumar
Topics: Mitochondrial Function and Pathology (37 papers)Metabolism and Genetic Disorders (28 papers)Muscle Physiology and Disorders (27 papers)
Cited by: Clinical Biochemistry Neurology Molecular Biology
Journals: Journal of Biological ChemistrySHILAP Revista de lepidopterologíaPLoS ONE
Partner nations: India Australia United States

In The Last Decade

Narayanappa Gayathri

129 papers receiving 1.5k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	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 2023 ·Indian Journal of Medical Microbiology ·(unknown),(unknown),Pramada Prasad,(unknown),Jayashree Aiyar,Saurabh Joshi,Narayanappa Gayathri,Anita Desai,(unknown),Manjunatha M. Venkataswamy	1
2	Neuroanatomical zones of human traumatic brain injury reveal significant differences in protein profile and protein oxidation: Implications for secondary injury events 2023 ·Journal of Neurochemistry ·(unknown),(unknown),Gourav Dey,(unknown),Gajanan Sathe,Nupur Pruthi,Dhaval Shukla,Narayanappa Gayathri,(unknown),Balasundaram Padmanabhan,Vivek Chandramohan,Anita Mahadevan,M. M. Srinivas Bharath	4
3	A Novel L1 Linker Mutation in DES Resulted in Total Absence of Protein 2021 ·Journal of Molecular Neuroscience ·(unknown),Veeramani Preethish‐Kumar,Kiran Polavarapu,(unknown),(unknown),Kapaettu Satyamoorthy,Seena Vengalil,Saraswati Nashi,(unknown),Aditi Joshi,Atchayaram Nalini,Narayanappa Gayathri	8
4	A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight Muscles 2021 ·Journal of Molecular Neuroscience ·(unknown),Veeramani Preethish‐Kumar,Kiran K. Mangalaparthi,Sruthi Unni,Balasundaram Padmanabhan,(unknown),Upendra Nongthomba,Atchayaram Nalini,Narayanappa Gayathri	2
5	Whole‐exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations 2020 ·European Journal of Neurology ·(unknown),(unknown),Krishna Kumar,Kiran Polavarapu,Veeramani Preethish‐Kumar,Seena Vengalil,Saraswati Nashi,Mainak Bardhan,Gautham Arunachal,(unknown),Narayanappa Gayathri,Nidhan K. Biswas,(unknown),Atchayaram Nalini,Sudipto Roy,Moulinath Acharya	9
6	Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle 2019 ·Journal of Proteomics ·(unknown),Manish Kumar,(unknown),Sruthi Unni,Narayanappa Gayathri,Thottethodi Subrahmanya Keshava Prasad,Atchayaram Nalini,Kiran Polavarapu,Seena Vengalil,Veeramani Preethish‐Kumar,Balasundaram Padmanabhan,M. M. Srinivas Bharath	10
7	MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India 2017 ·BMC Medical Genetics ·(unknown),Seena Vengalil,Veeramani Preethish‐Kumar,Kiran Polavarapu,Atchayaram Nalini,Narayanappa Gayathri,Meera Purushottam	18
8	Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome 2016 ·Clinical Neurology and Neurosurgery ·V.P. Vandana,(unknown),(unknown),Periyasamy Govindaraj,Arun B. Taly,Narayanappa Gayathri,(unknown),(unknown),H.R. Arvinda,(unknown),Sanjib Sinha,Kumarasamy Thangaraj	13
9	Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India 2016 ·Mitochondrion ·(unknown),Parayil Sankaran Bindu,(unknown),Periyasamy Govindaraj,Narayanappa Gayathri,(unknown),(unknown),(unknown),Sanjib Sinha,Nahid Khan,(unknown),Paramasivam Arumugam,Kumarasamy Thangaraj,Arun B. Taly	16
10	Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex 2016 ·PLoS ONE ·(unknown),(unknown),Nivedita Singh,(unknown),Vishwanath Kumble Bhat,(unknown),Parayil Sankaran Bindu,Arun B. Taly,Sanjib Sinha,Madhu Nagappa,Rose Dawn Bharath,Anita Mahadevan,Narayanappa Gayathri,Yasha T. Chickabasaviah,Arun Kumar	27
11	Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India 2015 ·Mitochondrion ·Parayil Sankaran Bindu,(unknown),Arun B. Taly,(unknown),(unknown),(unknown),(unknown),Narayanappa Gayathri,Srinivas Bharath,(unknown),Sanjib Sinha,Nahid Khan,Periyasamy Govindaraj,(unknown),Paramasivam Arumugam,Kumarasamy Thangaraj	22
12	Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency 2014 ·Journal of Clinical Neuromuscular Disease ·(unknown),Parayil Sankaran Bindu,Arun B. Taly,Atchayaram Nalini,(unknown),(unknown),Nahid Khan,Kumarasamy Thangaraj,Narayanappa Gayathri	2
13	Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G 2014 ·PLoS ONE ·Amirtharaj Francis,(unknown),(unknown),Kiran Polavarapu,(unknown),(unknown),M. M. Srinivas Bharath,Narayanappa Gayathri,Atchayaram Nalini,Kumarasamy Thangaraj	23
14	Major histocompatibility complex and inflammatory cell subtype expression in inflammatory myopathies and muscular dystrophies 2013 ·Neurology India ·Atchayaram Nalini,Madhu Nagappa,Narayanappa Gayathri	12
15	Bethlem myopathy: An autosomal dominant myopathy with flexion contractures, keloids, and follicular hyperkeratosis 2013 ·Annals of Indian Academy of Neurology ·Aralikatte Onkarappa Saroja,(unknown),Atchayaram Nalini,Narayanappa Gayathri	11
16	Lipid storage myopathy with clinical markers of Marfan syndrome: A rare association 2012 ·Annals of Indian Academy of Neurology ·(unknown),Narayanappa Gayathri,Rita Christopher	2
17	Familial amyloidotic polyneuropathy with muscle, vitreous, leptomeningeal, and cardiac involvement: Phenotypic, pathological, and MRI description 2010 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),(unknown),(unknown),Narayanappa Gayathri,(unknown),Joy Vijayan	1
18	Distal myopathy with rimmed vacuoles: Report on clinical characteristics in 23 cases 2010 ·Neurology India ·Atchayaram Nalini,Narayanappa Gayathri,(unknown)	15
19	Autosomal recessive tubular aggregate myopathy in an Indian family 2008 ·European Journal of Paediatric Neurology ·Lekha Pandit,Narayanappa Gayathri,(unknown),(unknown)	1
20	Metabolic Disorders Presenting as Vacuolar Myopathy 1999 ·SHILAP Revista de lepidopterología ·Narayanappa Gayathri,(unknown),Subhamoy Das,(unknown),(unknown),Vani Santosh,T.C. Yasha,S. K. Shankar	2

About Narayanappa Gayathri

Narayanappa Gayathri is a scholar working on Clinical Biochemistry, Rheumatology and Genetics, having authored 136 papers that have together received 1.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (28 papers) and Muscle Physiology and Disorders (27 papers). The work is most often cited by research in Clinical Biochemistry (211 citations), Neurology (202 citations) and Molecular Biology (872 citations). Narayanappa Gayathri has collaborated with scholars based in India, Australia and United States. Frequent co-authors include Atchayaram Nalini, M. M. Srinivas Bharath, Sanjib Sinha, Arun B. Taly, Parayil Sankaran Bindu, T.C. Yasha, S. Thilagar, D. Kumar, R. Karthik and Kumarasamy Thangaraj. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

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