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Journal of Genetics|April 2, 2025
Gonadal mosaicism and paradoxical phenotype in <i>NEXMIF</i> encephalopathy: a case report of two siblingsNaik Adarsha, Haseena SaitInternational Journal of General Medicine|May 31, 2022
Integrated Management Strategies for Epidermolysis Bullosa: Current InsightsHaseena Sait, Somya Srivastava, Deepti SaxenaAmerican Journal of Medical Genetics. Part A|April 24, 2025
Clinical and Radiological Characterization of TEFM-Associated Neurological DisorderNaik Adarsha, Haseena Sait, Deepak RavichandranJournal of Genetics|July 31, 2024
COQ7 splice site variant causing a spastic paraparesis phenotype in siblingsHaseena Sait, Manmohan Pandey, Shubha R PhadkeThe Indian Journal of Medical Research|September 20, 2022
Haemophilia management programme: Transformation during COVID-19Haseena Sait, Shruti M Sajjan, Shubha R PhadkeJournal of Reproduction & Infertility|January 6, 2022
Kallmann Syndrome and X-linked Ichthyosis Caused by Translocation Between Chromosomes X and Y: A Case ReportHaseena Sait, Priyanka Srivastava, Preeti Dabadghao, et al.American Journal of Medical Genetics. Part A|February 23, 2022
Autosomal recessive spinocerebellar ataxia-20 due to a novel SNX14 variant in an Indian girlHaseena Sait, Amita Moirangthem, Vinita Agrawal, et al.Indian Journal of Pediatrics|February 19, 2022
Congenital Hyperinsulinemia of Infancy: Role of Molecular Testing in Management and Genetic CounselingHaseena Sait, Lokesh Sharma, Preeti Dabadghao, et al.Journal of Clinical and Experimental Hepatology|November 19, 2025
Nuances in <i>ATP7B</i> Genetic Testing and Interpretation in IndiaAmresh K Mishra, Moinak Sen Sarma, Amita Moirangthem, et al.Journal of Clinical and Experimental Hepatology|June 30, 2026
Corrigendum to "Nuances in ATP7B Genetic Testing and Interpretation in India" [J Clin Exp Hepatol 16 (1) (2026) 103205]Amresh K Mishra, Moinak Sen Sarma, Amita Moirangthem, et al.Pageof 3