Samarth Kulshreshtha

NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study

R. Saxena, S. Nair, Kanika Singh, 2020, BMC medical genetics.

COASY related pontocerebellar hypoplasia type 12: A common Indian mutation with expansion of the phenotypic spectrum

Suzena Masih, A. Moirangthem, S. Phadke, 2022, American journal of medical genetics. Part A.

NGS based expanded pilot carrier screening study in North Indian population reveals unexpected results.

Kanika Singh, S. Bijarnia-Mahay, S. Kohli, 2020 .

Robinow Syndrome and Brachydactyly: An Interplay of High-Throughput Sequencing and Deep Phenotyping in a Kindred

R. Saxena, D. Gupta, I. Verma, 2020, Molecular Syndromology.

HoneyBadgerMPC and AsynchroMix: Practical Asynchronous MPC and its Application to Anonymous Communication

Aniket Kate, Thomas Yurek, Rahul Govind, 2019, IACR Cryptol. ePrint Arch..

A Further Case of Larsen's Syndrome: Clinical and Genotypic Challenges in Diagnosis

I. Verma, S. Pal, Veronica Arora, 2020, Journal of Pediatric Genetics.