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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.

Mannan, Ashraf U and Singh, Jaya and Lakshmikeshava, Ravikiran and Thota, Nishita and Singh, Suhasini and Sowmya, TS and Mishra, Avshesh and Sinha, Aditi and Deshwal, Shivani and Soni, Megha R and Chandrasekar, Anbukayalvizhi and Ramesh, Bhargavi and Ramamurthy, Bharat and Padhi, Shila and Manek, Payal and Ramalingam, Ravi and Kapoor, Suman and Ghosh, Mithua and Sankaran, Satish and Ghosh, Arunabha and Veeramachaneni, Vamsi and Ramamoorthy, Preveen and Hariharan, Ramesh and Subramanian, Kalyanasundaram (2016) Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India. In: JOURNAL OF HUMAN GENETICS, 61 (6). pp. 515-522.

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.