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Ganapathy, Aparna and Mishra, Avshesh and Soni, Megha Rani and Kumar, Priyanka and Sadagopan, Mukunth and Kanthi, Anil Vittal and Patric, Irene Rosetta Pia and George, Sobha and Sridharan, Aparajit and Thyagarajan, T C and Aswathy, S L and Vidya, H K and Chinnappa, Swathi M and Nayanala, Swetha and Prakash, Manasa B and Raghavendrachar, Vijayashree G and Parulekar, Minothi and Gowda, Vykuntaraju K and Nampoothiri, Sheela and Menon, Ramshekhar N and Pachat, Divya and Udani, Vrajesh and Naik, Neeta and Kamate, Mahesh and Devi, A Radha Rama and Kunju, P A Mohammed and Nair, Mohandas and Hegde, Anaita Udwadia and Kumar, M. Pradeep and Sundaram, Soumya and Tilak, Preetha and Puri, Ratna D and Shah, Krati and Sheth, Jayesh and Hasan, Qurratulain and Sheth, Frenny and Agrawal, Pooja and Katragadda, Shanmukh and Veeramachaneni, Vamsi and Chandru, Vijay and Hariharanu, Ramesh and Manna, Ashraf U (2019) Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients. In: JOURNAL OF NEUROLOGY, 266 (8). pp. 1919-1926.

Singh, Jaya and Thota, Nishita and Singh, Suhasini and Padhi, Shila and Mohan, Puja and Deshwal, Shivani and Sur, Soumit and Ghosh, Mithua and Agarwal, Amit and Sarin, Ramesh and Ahmed, Rosina and Almel, Sachin and Chakraborti, Basumita and Raina, Vinod and DadiReddy, Praveen K and Smruti, B K and Rajappa, Senthil and Dodagoudar, Chandragouda and Aggarwal, Shyam and Singhal, Manish and Joshi, Ashish and Kumar, Rajeev and Kumar, Ajai and Mishra, Deepak K and Arora, Neeraj and Karaba, Aarati and Sankaran, Satish and Katragadda, Shanmukh and Ghosh, Arunabha and Veeramachaneni, Vamsi and Hariharan, Ramesh and Mannan, Ashraf U (2018) Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations. In: BREAST CANCER RESEARCH AND TREATMENT, 170 (1). pp. 189-196.

Singh, Jaya and Mishra, Avshesh and Pandian, Arunachalam Jayamuruga and Mallipatna, Ashwin C and Khetan, Vikas and Sripriya, S and Kapoor, Suman and Agarwal, Smita and Sankaran, Satish and Katragadda, Shanmukh and Veeramachaneni, Vamsi and Hariharan, Ramesh and Subramanian, Kalyanasundaram and Mannan, Ashraf U (2016) Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort. In: MOLECULAR VISION, 22 . pp. 1036-1047.