Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.
Br J Radiol. 87:20130478
2014
Unravelling the distinct strains of Tharu ancestry.
Eur. J. Hum. Genet. (March 26)
2014
RAF1 mutations in childhood-onset dilated cardiomyopathy.
Nature Genetics (April 28)
2014
A novel androgen receptor gene mutation in a patient with congenital adrenal hyperplasia associated with penoscrotal hypospadias.
Transl Res. (May 6)
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
Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G.
PLoS One. 9(7):e102763
2014
Mitochondria in health and disease.
Mitochondrion 16: 1
2014
Genetics of male infertility: Indian scenario
Mol Cytogenet. 21: 7 (Suppl.)
2014
Reduced prevalence of placental malaria in primiparae with blood group O
Malar J. 13: 289
2014
Ancient human genomes suggest three ancestral populations for present-day Europeans
Nature 513: 409
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
Mitochondrial Myopathy, Cardiomyopathy, and Pontine Signal Changes in an Adult Patient With Isolated Complex II Deficiency.
J. Clin. Neuromuscul. Dis. 16:69-73
2014
Analysis of genetic variants in the IL4 promoter and VNTR loci in Indian patients with Visceral Leishmaniasis.
Hum. Immunol. 75:1177-1181
2014
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
Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis
Clin Endocrinol (Oxf). 2014 Nov;81(5):702-10. doi: 10.1111/cen.12428. Epub 2014 Mar 13.
2014
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