FACULTY


Nishtha Pandey, PhD
Visiting Scientist

Publications:

Functional analysis of a novel connexin30 mutation in a large family with hearing loss, pesplanus, ichthyosis, cutaneous nodules, and keratoderma.Annals of Human Genetics, 80: 11-19 (2016). Pandey N, Xavier DF, Chatterjee A, Mani RS, Hiremagalore R, Tharakan A, Rajashekhar B, Anand A

Mutations in OTOF, CLDN14 and SLC26A4 are a major cause of hearing impairment in Dhadhaki village, Jammu and Kashmir, India. Indian Journal of Medical Research. 146(4): 489-497 (2017). Pandey N, Sharma M, Rashid T, Jalvi R, Andrabi R, Rangasayee R, Anand A