Afreen Khan

Genomics of rare genetic diseases—experiences from India

V. R. Rajendran, K. M. Cherian, Sruthi S. Nair, 2019, Human Genomics.

Next Generation Sequencing and Cytogenetic Based Evaluation of Indian Pierre Robin Sequence Families Reveals CNV Regions of Modest Effect and a Novel LOXL3 Mutation

O. Kharbanda, M. Kabra, M. Faruq, 2021, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Integrated whole exome sequencing and functional approach delineate genetic heterogeneity in cerebellar ataxias

R. Kumari, M. Faruq, M. Mukerji, 2021 .

N Gene Target Failure (NGTF) for detection of Omicron: a way out for the "stealth" too?

S. Nair, Sudeep Gupta, V. Murthy, 2022, medRxiv.

Genomics of rare genetic diseases—experiences from India

V. R. Rajendran, K. M. Cherian, Sruthi S. Nair, 2019, Human Genomics.

Oral

Rajkumar, S. Prakash, B. Meena, 2016, Journal of Medical Physics.

Genomics of rare genetic diseases—experiences from India

V. R. Rajendran, K. M. Cherian, Sruthi S. Nair, 2019, Human Genomics.

Oral N-acetylcysteine as an adjunct to standard medical therapy improved heart function in cases with stable class II and III systolic heart failure

Rajkumar, S. Prakash, B. Meena, 2021, Irish Journal of Medical Science (1971 -).