Arundhati Sharma

A novel VSX1 mutation identified in an individual with keratoconus in India.

Preeti Paliwal, Radhika Tandon, Jeevan S. Titiyal et al. · PubMed · 2009 · 46 citations · Full text

Congenital hereditary endothelial dystrophy - mutation analysis of SLC4A11 and genotype-phenotype correlation in a North Indian patient cohort.

Preeti Paliwal, Arundhati Sharma, Radhika Tandon et al. · PubMed · 2010 · 41 citations · Full text

Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus.

Preeti Paliwal, Radhika Tandon, Divya Dube et al. · PubMed · 2011 · 32 citations · Full text

Identification of novel SRY mutations and SF1 (NR5A1) changes in patients with pure gonadal dysgenesis and 46,XY karyotype

Preeti Paliwal, Anshul Sharma, Shweta Birla et al. · Molecular Human Reproduction · 2011 · 32 citations · Full text

Genetics, Disease Gene Identification, Reproductive Biology +16

TGFBI mutation screening and genotype-phenotype correlation in north Indian patients with corneal dystrophies.

Preeti Paliwal, Arundhati Sharma, Radhika Tandon et al. · PubMed · 2010 · 32 citations