Veeramani Preethish-Kumar

12PUBLICATIONS
51CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsCancer diagnosisMedical infection agents (incl. prions)
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Publications (12)

|Jul 20, 2026
Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene.

|Oct 23, 2021
Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis.

Akshata Huddar, Kiran Polavarapu, Veeramani Preethish-Kumar

|Jun 29, 2021
Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review.

Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa

|Nov 21, 2020
Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies.

Zhongbo Chen, Reza Maroofian, A Nazlı Başak

|Oct 30, 2020
Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Shamita Sanga, Arnab Ghosh, Krishna Kumar

|Jul 04, 2020
In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI.

V Preethish-Kumar, A Shah, M Kumar

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Frequent Collaborators

5 joint publications

Atchayaram Nalini

3 joint publications

Mainak Bardhan

3 joint publications

Kiran Polavarapu

3 joint publications

Seena Vengalil