Seena Vengalil

1.4k total citations
103 papers, 620 citations indexed

About

Seena Vengalil is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Seena Vengalil has authored 103 papers receiving a total of 620 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 33 papers in Neurology and 20 papers in Surgery. Recurrent topics in Seena Vengalil's work include Muscle Physiology and Disorders (26 papers), Amyotrophic Lateral Sclerosis Research (16 papers) and Neurogenetic and Muscular Disorders Research (16 papers). Seena Vengalil is often cited by papers focused on Muscle Physiology and Disorders (26 papers), Amyotrophic Lateral Sclerosis Research (16 papers) and Neurogenetic and Muscular Disorders Research (16 papers). Seena Vengalil collaborates with scholars based in India, Canada and United Kingdom. Seena Vengalil's co-authors include Atchayaram Nalini, Kiran Polavarapu, Veeramani Preethish‐Kumar, Saraswati Nashi, Priya Treesa Thomas, Narayanappa Gayathri, Ravi Yadav, Chandrajit Prasad, Anita Mahadevan and Jitender Saini and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Seena Vengalil

88 papers receiving 609 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seena Vengalil India 15 250 184 96 89 87 103 620
Kiran Polavarapu India 15 292 1.2× 178 1.0× 102 1.1× 111 1.2× 91 1.0× 85 617
Veeramani Preethish‐Kumar India 17 317 1.3× 190 1.0× 112 1.2× 100 1.1× 113 1.3× 72 652
Meral Özmen Türkiye 17 148 0.6× 120 0.7× 91 0.9× 85 1.0× 40 0.5× 67 830
Saraswati Nashi India 12 138 0.6× 151 0.8× 64 0.7× 54 0.6× 51 0.6× 85 416
Melinda Nolan Australia 14 142 0.6× 88 0.5× 30 0.3× 139 1.6× 124 1.4× 21 953
Ahsan N. Moosa United States 17 85 0.3× 181 1.0× 56 0.6× 199 2.2× 44 0.5× 53 863
Colin Quinn United States 17 116 0.5× 343 1.9× 72 0.8× 105 1.2× 144 1.7× 58 682
Jayashri Srinivasan United States 14 130 0.5× 335 1.8× 172 1.8× 230 2.6× 98 1.1× 42 916
Daniele Imperiale Italy 17 366 1.5× 233 1.3× 49 0.5× 265 3.0× 25 0.3× 62 1.2k
Alfred Peter Born Denmark 15 158 0.6× 201 1.1× 37 0.4× 36 0.4× 54 0.6× 52 644

Countries citing papers authored by Seena Vengalil

Since Specialization
Citations

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

Fields of papers citing papers by Seena Vengalil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seena Vengalil

This figure shows the co-authorship network connecting the top 25 collaborators of Seena Vengalil. A scholar is included among the top collaborators of Seena Vengalil 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 Seena Vengalil. Seena Vengalil 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.
Christopher, Rita, Gautham Arunachal, Kiran Polavarapu, et al.. (2025). Acute myeloneuropathy due to Glutaric aciduria-1: Expanding the phenotypic spectrum. PubMed. 12(2). 100036–100036.
2.
Philip, Mariamma, et al.. (2025). Cardiac MRI for early detection of subclinical cardiac dysfunction in dysferlinopathy. Neuromuscular Disorders. 54. 106205–106205.
3.
4.
Padmanabha, Hansashree, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2024). Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India. Journal of Neuromuscular Diseases. 11(5). 935–957. 1 indexed citations
5.
Polavarapu, Kiran, Veeramani Preethish‐Kumar, Seena Vengalil, et al.. (2024). Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent ADSSL1 Missense Variant. Neurology Genetics. 10(1). e200122–e200122. 5 indexed citations
6.
7.
Vengalil, Seena, Saraswati Nashi, Mainak Bardhan, et al.. (2023). MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO). Journal of Neuromuscular Diseases. 10(4). 727–730. 1 indexed citations
8.
Thomas, Priya Treesa, Shoba Arun, Seena Vengalil, et al.. (2022). An individualised psychosocial intervention program for persons with MND/ALS and their families in low resource settings. Chronic Illness. 19(2). 458–471. 1 indexed citations
9.
Holla, Vikram V., Seena Vengalil, Nitish Kamble, et al.. (2022). Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse‐Sakati syndrome.. Journal of Neuroendocrinology. 34(10). e13185–e13185. 2 indexed citations
10.
Vengalil, Seena, et al.. (2022). The Spectrum of Neuro-COVID. Annals of Indian Academy of Neurology. 25(2). 194–202. 1 indexed citations
11.
Bardhan, Mainak, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2021). Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome. Journal of Human Genetics. 66(8). 813–823. 8 indexed citations
12.
Saini, Jitender, Seena Vengalil, Saraswati Nashi, et al.. (2021). Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis. Journal of Clinical Ultrasound. 50(2). 286–291. 4 indexed citations
13.
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
14.
Polavarapu, Kiran, Seena Vengalil, Veeramani Preethish‐Kumar, et al.. (2021). Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes – A recognizable clinical phenotype. European Journal of Paediatric Neurology. 31. 54–60. 7 indexed citations
15.
Polavarapu, Kiran, Mainak Bardhan, Seena Vengalil, et al.. (2021). Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review. Journal of Clinical Neurology. 17(3). 409–409. 1 indexed citations
16.
Polavarapu, Kiran, Veeramani Preethish‐Kumar, Mainak Bardhan, et al.. (2021). Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis. Children. 8(10). 909–909. 4 indexed citations
17.
Saini, Jitender, Seena Vengalil, Saraswati Nashi, et al.. (2021). Diaphragmatic ultrasound: Prospects as a tool to assess respiratory muscle involvement in amyotrophic lateral sclerosis. Journal of Clinical Ultrasound. 50(1). 131–135. 4 indexed citations
18.
Netravathi, M, Vikram V. Holla, Atchayaram Nalini, et al.. (2020). Myelin oligodendrocyte glycoprotein-antibody-associated disorder: a new inflammatory CNS demyelinating disorder. Journal of Neurology. 268(4). 1419–1433. 32 indexed citations
19.
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
20.
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

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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