Veeramani Preethish‐Kumar

1.2k total citations
72 papers, 652 citations indexed

About

Veeramani Preethish‐Kumar is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Veeramani Preethish‐Kumar has authored 72 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 20 papers in Neurology and 16 papers in Genetics. Recurrent topics in Veeramani Preethish‐Kumar's work include Muscle Physiology and Disorders (24 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Cardiomyopathy and Myosin Studies (13 papers). Veeramani Preethish‐Kumar is often cited by papers focused on Muscle Physiology and Disorders (24 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Cardiomyopathy and Myosin Studies (13 papers). Veeramani Preethish‐Kumar collaborates with scholars based in India, Canada and United Kingdom. Veeramani Preethish‐Kumar's co-authors include Atchayaram Nalini, Kiran Polavarapu, Seena Vengalil, Saraswati Nashi, Priya Treesa Thomas, Ravinder‐Jeet Singh, Narayanappa Gayathri, Chandrajit Prasad, Jitender Saini and Meera Purushottam and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Cell Biology and Neurology.

In The Last Decade

Veeramani Preethish‐Kumar

68 papers receiving 639 citations

Peers

Veeramani Preethish‐Kumar

NEURO

GENET

SURGE

CMN

Kiran Polavarapu India

Seena Vengalil India

Carlos de Sousa United Kingdom

Alberto Palladino Italy

Saraswati Nashi India

Julie C. Fitzgerald United States

Pierre‐Yves Jeannet Switzerland

Claudio Bruno Italy

Sonya Wang United States

D Fontan France

Kiran Polavarapu India

Veeramani Preethish‐Kumar

292 ×0.9

178 ×0.9

NEURO

91 ×0.8

GENET

102 ×0.9

SURGE

111 ×1.1

CMN

Citations per year, relative to Veeramani Preethish‐Kumar Veeramani Preethish‐Kumar (= 1×) peers Kiran Polavarapu

Countries citing papers authored by Veeramani Preethish‐Kumar

Since Specialization

Citations

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

Fields of papers citing papers by Veeramani Preethish‐Kumar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veeramani Preethish‐Kumar. 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 Veeramani Preethish‐Kumar. The network helps show where Veeramani Preethish‐Kumar may publish in the future.

Co-authorship network of co-authors of Veeramani Preethish‐Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Veeramani Preethish‐Kumar. A scholar is included among the top collaborators of Veeramani Preethish‐Kumar 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 Veeramani Preethish‐Kumar. Veeramani Preethish‐Kumar 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:

20 of 20 papers shown

Adoor, Meghana, Veeramani Preethish‐Kumar, Kiran Polavarapu, et al.. (2025). Cardiac dysregulation in Duchenne muscular dystrophy: An ECG analysis. Journal of Electrocardiology. 91. 154015–154015.

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

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

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

Vengalil, Seena, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2022). Mutation Spectrum of Primary Lipid Storage Myopathies. Annals of Indian Academy of Neurology. 25(1). 106–113. 7 indexed citations

Bardhan, Mainak, Kiran Polavarapu, Veeramani Preethish‐Kumar, et al.. (2022). Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C. Neurogenetics. 23(3). 187–202. 7 indexed citations

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

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

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

10.

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

11.

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

12.

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

13.

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

14.

Preethish‐Kumar, Veeramani, et al.. (2021). Customized and Cost-Effective 3D Printed Mold for Cranioplasty. Neurology India. 69(3). 611–617. 10 indexed citations

15.

Preethish‐Kumar, Veeramani, Kiran K. Mangalaparthi, Sruthi Unni, et al.. (2021). A Dominant C150Y Mutation in FHL1 Induces Structural Alterations in LIM2 Domain Causing Protein Aggregation In Human and Drosophila Indirect Flight Muscles. Journal of Molecular Neuroscience. 71(11). 2324–2335. 2 indexed citations

16.

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

17.

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

18.

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

19.

Polavarapu, Kiran, Veeramani Preethish‐Kumar, Seena Vengalil, et al.. (2016). Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern. Neuromuscular Disorders. 26(11). 768–774. 38 indexed citations

20.

Preethish‐Kumar, Veeramani, Atchayaram Nalini, Ravinder‐Jeet Singh, et al.. (2015). Distal bimelic amyotrophy (DBMA): Phenotypically distinct but identical on cervical spine MR imaging with brachial monomelic amyotrophy/Hirayama disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(5-6). 338–344. 10 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