Publications

A Novel Arginine to Tryptophan (R144W) Mutation in Troponin T (cTnT) Gene in an Indian Multigenerational Family with Dilated Cardiomyopathy (FDCM)

PLoS One. 9(7):e101451

Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G.

PLoS One. 9(7):e102763

Mitochondria in health and disease.

Mitochondrion 16: 1

Genetics of male infertility: Indian scenario

Mol Cytogenet. 21: 7 (Suppl.)

Reduced prevalence of placental malaria in primiparae with blood group O

Malar J. 13: 289

Ancient human genomes suggest three ancestral populations for present-day Europeans

Nature 513: 409

Determinants of prakriti, the human constitution types of Indian traditional medicine and its correlation with contemporary science.

J. Ayurveda Integr. Med. 5:167-75

Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency.

J. Clin. Neuromuscul. Dis. 16:69-73

Analysis of genetic variants in the IL4 promoter and VNTR loci in Indian patients with Visceral Leishmaniasis.

Hum. Immunol. 75:1177-1181

Association of common variants in/near six genes (ATP2B1, CSK, MTHFR, CYP17A1, STK39 and FGF5) with blood pressure/hypertension risk in Chinese children

J Hum Hypertens. 2014 Jan;28(1):32-6. doi: 10.1038/jhh.2013.50. Epub 2013 Jun 13.