Shruti R. Pande

Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling

K. Girisha, A. Shukla, S. Nampoothiri, 2021, European Journal of Human Genetics.

Untapped opportunities for rare disease gene discovery in India

S. Phadke, K. Girisha, A. Dalal, 2020, American journal of medical genetics. Part A.