Molecular genetic aspects of non-syndromic hearing loss in India
Currently, Assistant Professor with a joint appointment in the Departments of Pathology and Urology, and is a member of the Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas
Studies on molecular genetic aspects of idiopathic generalized epilepsies
Currently, Assistant Professor, McGovern Medical School, University of Texas Health Science Center at Houston; 7000 Fannin St, Suite 150, Houston, TX 77030 USA
Studies on molecular genetic aspects of non syndromic hereditary hearing loss
Currently, working at Citadel Precision Medicine LLC, Iselin, New Jersey 08830
Identification of genetic loci for human epilepsies
Currently, Assistant Professor Ophthalmology-Departmental
Baylor College of Medicine
Houston, TX US
On genetic aspects of non-syndromic hearing loss
Currently, Guest lecturer, Centre for Human Genetics, Biotech Park, E-city, Phase-1, Bangalore
Connecting the paralogs: contribution of EFHC1 and EFHC2 in juvenile myoclonic epilepsy
Currently, Postdoctoral Fellow, CHU Sainte-Justine Research Centre, University of Montreal, QC, Canada
Identification of genetic loci and mutations in SLC1A1 for sensory epilepsy triggered by touch and temperature stimuli
Currently, Research Associate @ Weill Cornell Medicine, Ronald G Crystal Lab, Genetic Medicine, WCMC, 1300 York Avenue, New York, NY, 10065
Prospective causal genes for genetic generalized epilepsy
Currently, Scientist II, Clevergene, Bangalore
On genetic aspects of hot water epilepsy, a sensory epilepsy triggered by touch and temperature stimuli
Currently, Senior Project Associate at Institute of Genomics and Integrative Biology, New Delhi
On molecular genetic analysis of juvenile myoclonic epilepsy
© 2021, JNCASR, Jakkur, Bangalore, India