1. Genetic diversity of NDUFV1-dependent mitochondrial complex I deficiency. (November 2018) Authors: Srivastava, Anshika; Srivastava, Kinshuk; Hebbar, Malavika; Galada, Chelna; Kadavigrere, Rajagopal; Su, Fengyun; Cao, Xuhong; Chinnaiyan, Arul; Girisha, Katta; Shukla, Anju; Bielas, Stephanie Journal: European journal of human genetics Issue: Volume 26:Number 11(2018) Page Start: 1582 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Pseudoachondroplasia: Phenotype and genotype in 11 Indian patients. Issue 3 (9th November 2021) Authors: Jacob, Prince; Bhavani, Gandham Sri Lakshmi; Shah, Hitesh; Galada, Chelna; Nampoothiri, Sheela; Kamath, Nutan; Phadke, Shubha R.; Muranjan, Mamta; Datar, Chaitanya A.; Shukla, Anju; Girisha, Katta M. Journal: American journal of medical genetics Issue: Volume 188:Issue 3(2022) Page Start: 751 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature. (20th February 2018) Authors: Galada, Chelna; Hebbar, Malavika; Lewis, Leslie; Soans, Santosh; Kadavigere, Rajagopal; Srivastava, Anshika; Bielas, Stephanie; Girisha, Katta M.; Shukla, Anju Journal: Congenital anomalies Issue: Volume 58:Number 5(2018) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗