Prabodh Kumar

Distribution of head and neck lesions diagnosed on histopathology in Western U.P.: A retrospective study

S. Agarwal, R. Agrawal, Prachi Gupta, 2018 .

Primary Cardiac Involvement in the Rare Transthyretin Ile73Val Mutation: A Case Series.

K. Nayak, Prabodh Kumar, Prakashini K, 2020, Circulation. Genomic and precision medicine.

A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation.

K. Nayak, Prabodh Kumar, Rajasekhar Moka, 2022, Indian journal of clinical biochemistry : IJCB.

Treacher -Collins syndrome

Prabodh Kumar, L. Sarella, K. Kumari, 2014 .

A novel FLNC variation associated with restrictive cardiomyopathy with an unusually long clinical course — A case report

Prabodh Kumar, T. Devasia, M. Prabhu, 2023, Gene Reports.