Publications

Novel NR5A1 Pathogenic Variants Cause Phenotypic Heterogeneity in 46,XY Disorders of Sex Development

Sex Dev. Feb 1. [Epub ahead of print].

Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach

PLoS One. 2020 Jan 29;15(1):e0228269. doi: 10.1371/journal.pone.0228269. eCollection 2020.

Maternal vitamin B(12) deficiency in rats alters DNA methylation in metabolically important genes in their offspring

Mol Cell Biochem. 2020 May;468(1-2):83-96. doi: 10.1007/s11010-020-03713-x. Epub 2020 Mar 18.

Novel p.P298L SURF1 mutation in thiamine deficient Leigh syndrome patients compromises cytochrome c oxidase activity

Mitochondrion. 2020 Jul;53:91-98. doi: 10.1016/j.mito.2020.04.009. Epub 2020 May 4.

Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India

Sci Rep. 2020 Jun 11;10(1):9450. doi: 10.1038/s41598-020-65317-1.

Periconceptional environment predicts leukocyte telomere length in a cross-sectional study of 7-9 year old rural Gambian children

Sci Rep. 2020 Jun 15;10(1):9675. doi: 10.1038/s41598-020-66729-9.

Genetic Architecture of Parkinson\'s Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson\'s Disease Research

Front Neurol. 2020 Jun 18;11:524. doi: 10.3389/fneur.2020.00524. eCollection 2020.

Effect of maternal preconceptional and pregnancy micronutrient interventions on children\'s DNA methylation: Findings from the EMPHASIS study

Am J Clin Nutr. 2020 Oct 1;112(4):1099-1113. doi: 10.1093/ajcn/nqaa193.

Mitochondrial chaperone, TRAP1 as a potential pharmacological target to combat cancer metabolism

Mitochondrion. 2019 Oct 25. pii: S1567-7249(19)30019-4. doi: 10.1016/j.mito.2019.09.011.

Compromising the constitutive p16(INK4a) expression sensitizes human neuroblastoma cells to Hsp90 inhibition and promotes premature senescence.

J Cell Biochem. 2019 Nov 6. doi:10.1002/jcb.29493.