Publications

Genetic affinities of the Jewish populations of India.

Sci Rep. 6:19166

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.

Mitochondrion. 27:1-5

Is MTHFR 677 C>T Polymorphism Clinically Important in Polycystic Ovarian Syndrome (PCOS)? A Case-Control Study, Meta-Analysis and Trial Sequential Analysis.

PLoS One. 11(3):e0151510.

Reply to `Lack of replication of association of THSD7A with obesity`

Int J Obes (Lond). Feb 2. doi: 10.1038

Optimization of purification method and characterization of recombinant human Centrin-1.

Protein Expr. Purif. 124: 48-54.

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.

Sci Rep. 6: 27684.

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Clin Neurol Neurosurg. 148: 17-21

Cryptic Eimeria genotypes are common across the southern but not northern hemisphere.

Int J Parasitol. Jun 28

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.

Nature. 538: 201-206

c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

PLoS One. 11:e0164151.