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Amitabh Joshi Anuranjan Anand Balasubramanian Sundaram Bivas Saha C. P. Rajendran 
C.N.R Rao C.N.R Rao Chandrabhas Narayana Diwakar S. Venkatesan Eswaramoorthy M
G.U. Kulkarni Ganesh Subramanian Govindaraju T H Ila Hemalatha Balaram 
James P. Clement Chelliah Jayanta Haldar K. B. Sinha K.S. Narayan Kanishka Biswas 
Kaustuv Sanyal Kavita Jain Krishnan V.Kundu Tapas K.M. R. S. Rao 
Maneesha Inamdar Meheboob Alam Meher K. Prakash Namita Surolia Narasimha Roddam 
Premkumar Senguttuvan Rajesh Ganapathy Ranjan Datta Ranjani Viswanatha Ravi Manjithaya 
S. N. Bhat Santosh Ansumali Santosh Ansumali Sarit S. Agasti Sebastian C Peter 
Sheeba Vasu Shivaprasad S. M.Shobhana Narasimhan Sreenivas K. R.Sridhar Rajaram 
Srikanth Sastry Subi Jacob George Subir K. Das Sundaresan A.Swapan Pati 
Tapas Kumar Maji Udaykumar Ranga Umesh V. Waghmare Valdiya K. S.Vidhyadhiraja N. S.
Vidya T. N. C. 

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  1. Q. Saleem, S. Roy, U. Murgood, R. Saxena, I. C. Verma, A. Anand, U. Muthane, S. Jain and S. K. Brahmachari, Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population, Acta Neurol. Scand. 108, 281 - 286 (2003).

  2. J. Vijai, A. Kapoor, H. M .Ravishankar, P. J. Cherian, A. S. Girija, B. Rajendran, G. Rangan, S. Jayalakshmi, S. Mohandas, K. Radhakrishnan and A. Anand, Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population, Human Genetics 113, 461 - 463 (2003).

  3. A. Kapoor, J. Vijai, H. M. Ravishankar, P. Satishchandra, K. Radhakrishnan and A. Anand, Absence of Ala322Asp, a GABRA1 mutation in Juvenile Myoclonic Epilepsy families from South India, Journal of Genetics 82, 17 - 21 (2003).

  4. M. RamShankar, S. Girirajan, O. Dagan, H. M. Ravi Shankar, R. Jalvi, R. Rangasayee, K. B. Avraham and A. Anand, Contribution of connexin 26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India, Journal of Medical Genetics 40, (2003).

  5. J. Vijai, P. J. Cherian, P. N. Sylaja, A. Anand and K. Radhakrishnan, Clinical characteristics of a South Indian cohort of juvenile myoclonic epilepsy probands, Seizure 12, 490 - 496 (2003).

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