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Journal of Pediatric Genetics|November 6, 2024
CDKN1C -Related Beckwith-Wiedemann Syndrome: First Patient from IndiaVeronica Arora, Aashita Takkar, Sudhisha Dubey, et al.Indian Journal of Pediatrics|July 13, 2026
Artificial Intelligence in Clinical Genetics: Current Applications and ChallengesRohit Sadanand, Neerja GuptaJournal of Biomedical Science|March 11, 2009
A novel 9-bp insertion detected in steroid 21-hydroxylase gene (CYP21A2): prediction of its structural and functional implications by computational methodsSudhisha Dubey, Susan Idicula-Thomas, Mohammad Anwaruddin, et al.Pediatric Dermatology|June 20, 2006
Cutis laxa type II and wrinkly skin syndrome: distinct phenotypesNeerja Gupta, Shubha R PhadkeIndian Pediatrics|August 14, 2012
Mutation analysis of Indian patients with urea cycle defectsNeerja Gupta, Madhulika Kabra, J HäberleActa Reumatologica Portuguesa|August 10, 2018
My Phenotype speaks: please do not harm me with biopsy needleIsha Saini, Narendra Bagri, Neerja GuptaIndian Journal of Cancer|April 8, 2024
Concordance of breast cancer services in an urban tertiary care institute in India to EUSOMA guidelines: An audit of Indian breast cancer practicesGeeta Kadayaprath, Sandhya Gupta, Neerja GuptaCase Reports in Genetics|August 29, 2013
Prenatal diagnosis of fetal peters' plus syndrome: a case reportNeerja Gupta, Anita Kaul, Madhulika KabraIndian Journal of Pediatrics|March 4, 2016
Genetic Studies in AutismShruthi Sudarshan, Neerja Gupta, Madhulika KabraIndian Journal of Pediatrics|September 12, 2021
Combined Methylmalonic Aciduria and Homocystinuria Presenting as Pulmonary HypertensionAmbika Gupta, Madhulika Kabra, Neerja GuptaPageof 20