Sneha Arya

Phenotype–genotype spectrum of AAA syndrome from Western India and systematic review of literature

Hiren Patt, Katrin Koehler, Sailesh Lodha et al. · Endocrine Connections · 2017 · 38 citations · Full text

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Madhur Maheshwari, Sneha Arya, Anurag Lila et al. · Journal of the Endocrine Society · 2022 · 17 citations · Full text

Expanding genetic spectrum and discriminatory role of steroid profiling by LC‐MS/MS in 11β‐hydroxylase deficiency

Manjiri Karlekar, Vijaya Sarathi, Anurag Lila et al. · Clinical Endocrinology · 2020 · 16 citations

Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity

Shantanu Kale, Jugal V. Gada, Swati Jadhav et al. · Pituitary · 2020 · 14 citations

Developmental Biology, Pituitary Gland, Growth Hormone +11

Implications of MGMT methylation status in pituitary adenoma

Sneha Arya, M.A. Majaid, S Shwetha et al. · Pathology - Research and Practice · 2014 · 13 citations

Pituitary Gland, Dna Methylation, Pathology +4