Publications

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Mitochondrion 32:42-49.

Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation.

J Invest Dermatol. 137:670-677.

Reconstructing the population history of the largest tribe of India: the Dravidian speaking Gond.

Eur J Hum Genet. 25:493-498.

Ancient DNA Reveals Late Pleistocene Existence of Ostriches in Indian Sub-Continent.

PLoS One. 12:e0164823.

Origin and spread of human mitochondrial DNA haplogroup U7.

Sci Rep; 7:46044.

3`-UTR SNP rs2229611 in G6PC1 affects mRNA stability, expression and Glycogen Storage Disease type-Ia risk.

Clin Chim Acta. 471:46-54.

Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Neurol Genet. 2017 3(3):e149.

Geographical distribution of complement receptor type 1 variants and their associated disease risk.

PLoS One. 2017 12(5):e0175973.

&sdquo;Like sugar in milk&sdquo: reconstructing the genetic history of the Parsi population.

Genome Biol. 18:110.

MPV17 hepatocerebral mitochondrial DNA depletion syndrome presenting as acute flaccid paralysis - A case report. Mitochondrion.

Jun 30. doi: 10.1016/j.mito.2017.06.006. [Epub ahead of print].