De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India by Pande, Shruti, Majethia, Purvi, Nair, Karthik, Rao, Lakshmi Priya, Mascarenhas, Selinda, Kaur, Namanpreet, do Rosario, Michelle C., Neethukrishna, Kausthubham, Chaurasia, Ankur, Hunakunti, Bhagesh, Jadhav, Nalesh, Xavier, Sruthy, Kumar, Jeevan, Bhat, Vivekananda, Bhavani, Gandham SriLakshmi, Narayanan, Dhanya Lakshmi, Yatheesha, B. L., Patil, Siddaramappa J., Nampoothiri, Sheela, Kamath, Nutan, Aroor, Shrikiran, Bhat Y, Ramesh, Lewis, Leslie E., Sharma, Suvasini, Bajaj, Shruti, Sankhyan, Naveen, Siddiqui, Shahyan, Nayak, Shalini S., Bielas, Stephanie, Girisha, Katta Mohan, Shukla, Anju

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Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities by Kaur, Parneet, Rosario, Michelle C, Hebbar, Malavika, Sharma, Suvasini, Kausthubham, Neethukrishna, Nair, Karthik, A, Shrikiran, Bhat Y, Ramesh, Lewis, Leslie Edward S, Nampoothiri, Sheela, Patil, Siddaramappa J, Suresh, Narayanaswami, Bijarnia Mahay, Sunita, Dua Puri, Ratna, Pai, Shivanand, Kaur, Anupriya, KC, Rakshith, Kamath, Nutan, Bajaj, Shruti, Kumble, Ali, Shetty, Rajesh, Shenoy, Rathika, Kamate, Mahesh, Shah, Hitesh, Muranjan, Mamta N, BL, Yatheesha, Avabratha, K Shreedhara, Subramaniam, Girish, Kadavigere, Rajagopal, Bielas, Stephanie, Girisha, Katta Mohan, Shukla, Anju

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Second report of SHMT2 related neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities by Majethia, Purvi, Bhat, Vivekananda, Yatheesha, B.L., Siddiqui, Shahyan, Shukla, Anju

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Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population by Kaur, Namanpreet, Rosario, Michelle C., Majethia, Purvi, Mascarenhas, Selinda, Rao, Lakshmi Priya, Nair, Karthik Vijay, Hunakunti, Bhagesh, Prasannakumar, Adarsh Pooradan, Naik, Rohit, Narayanan, Dhanya Lakshmi, Nayak, Shalini S., Bhat, Vivekananda, Sharma, Suvasini, Ramesh Bhat, Y., Yatheesha, B. L., Kulkarni, Rajesh, Patil, Siddaramappa J., Nampoothiri, Sheela, Siddiqui, Shahyan, Girisha, Katta Mohan, Bielas, Stephanie, Shukla, Anju

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Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications by Majethia, Purvi, Kaur, Namanpreet, Mascarenhas, Selinda, Rao, Lakshmi Priya, Pande, Shruti, Narayanan, Dhanya Lakshmi, Bhat, Vivekananda, Nayak, Shalini S., Nair, Karthik Vijay, Prasannakumar, Adarsh Pooradan, Chaurasia, Ankur, Hunakunti, Bhagesh, Jadhav, Nalesh, Farooqui, Sheeba, Yeole, Mayuri, Kothiwale, Vishaka, Naik, Rohit, Bhat, Veena, Aroor, Shrikiran, Lewis, Leslie, Purkayastha, Jayashree, Bhat, Y. Ramesh, Praveen, B. K., Yatheesha, B. L., Patil, Siddaramappa J., Nampoothiri, Sheela, Kamath, Nutan, Siddiqui, Shahyan, Bielas, Stephanie, Girisha, Katta Mohan, Sharma, Suvasini, Shukla, Anju

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Reactive Hemophagocytic syndrome by Rajam, L., Prasad, Vinitha, Yatheesha, B.L.

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