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Veeramani Preethish-Kumar

11PUBLICATIONS

28CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesNeurogeneticsCancer diagnosisMedical infection agents (incl. prions)

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Publications (11)

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|Oct 23, 2021

Expanding the Phenotypic Spectrum of <i>ECEL1</i>-Associated Distal Arthrogryposis.

Akshata Huddar, Kiran Polavarapu, Veeramani Preethish-Kumar

|Jun 29, 2021

Nemaline Rod/Cap Myopathy Due to Novel Homozygous <i>MYPN</i> 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

|Aug 03, 2019

Family Caregivers' Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India.

Manjusha G Warrier, Priya Treesa Thomas, Arun Sadasivan

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Frequent Collaborators

4 joint publications

Atchayaram Nalini

3 joint publications

Mainak Bardhan

2 joint publications

Leena Shingavi

2 joint publications

Kiran Polavarapu

2 joint publications

Seena Vengalil

2 joint publications

Saraswati Nashi

1 joint publications

A Shah

1 joint publications

M Kumar

1 joint publications

M Afsar

1 joint publications

J Rajeswaran

Frequent Collaborators

4 joint publications

Atchayaram Nalini

3 joint publications

Mainak Bardhan

2 joint publications

Leena Shingavi

2 joint publications

Kiran Polavarapu

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