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.

2014

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

Hum. Immunol. 75:1177-1181

2014

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

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

2014

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

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

2014

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

Nature 513: 409

2014

Reduced prevalence of placental malaria in primiparae with blood group O

Malar J. 13: 289

2014

Genetics of male infertility: Indian scenario

Mol Cytogenet. 21: 7 (Suppl.)

2014

Mitochondria in health and disease.

Mitochondrion 16: 1

2014

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

PLoS One. 9(7):e102763

2014

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

2014

A novel androgen receptor gene mutation in a patient with congenital adrenal hyperplasia associated with penoscrotal hypospadias.

Transl Res. (May 6)

2014

RAF1 mutations in childhood-onset dilated cardiomyopathy.

Nature Genetics (April 28)

2014

Unravelling the distinct strains of Tharu ancestry.

Eur. J. Hum. Genet. (March 26)

2014

Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.

Br J Radiol. 87:20130478

2014

Novel mutations in ATPase 8, ND1 and ND5 genes associated with peripheral neuropathy of diabetes.

Diabetes Res Clin Pract. (Jan 5)

2014