Publications

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.

FTO gene variant and risk of hypertension: a meta-analysis of 57,464 hypertensive cases and 41,256 controls

Metabolism. 2014 May;63(5):633-9. doi: 10.1016/j.metabol.2014.02.008. Epub 2014 Feb 17.

Altered methylation and expression patterns of genes regulating placental angiogenesis in preterm pregnancy

Reprod Sci. 2014 Dec;21(12):1508-17. doi: 10.1177/1933719114532838. Epub 2014 May 6.

Association of common genetic variants with lipid traits in the Indian population

PLoS One. 2014 Jul 3;9(7):e101688. doi: 10.1371/journal.pone.0101688. eCollection 2014.

Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis

Int J Epidemiol. 2014 Oct;43(5):1487-97. doi: 10.1093/ije/dyu132. Epub 2014 Jul 22.

Chronic maternal vitamin B12 restriction induced changes in body composition & glucose metabolism in the Wistar rat offspring are partly correctable by rehabilitation

PLoS One. 2014 Nov 14;9(11):e112991. doi: 10.1371/journal.pone.0112991. eCollection 2014.

Genetic and phenotypic heterogeneity in tropical calcific pancreatitis

World J Gastroenterol. 2014 Dec 14;20(46):17314-23. doi: 10.3748/wjg.v20.i46.17314.

IRF-1-binding site in the first intron mediates interferon-?-induced optineurin promoter activation.

Biochem Biophys Res Commun. 437, 179-184.

M98K-OPTN induces transferrin receptor degradation and RAB12-mediated autophagic death in retinal ganglion cells.

Autophagy 9:4, 510-527.

A cataract-causing connexin-50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain.

FEBS Open Bio. 3, 22-29.