Research Group Publications

Research Group | Year Index | Home

Amitabh Joshi Anuranjan Anand Balasubramanian Sundaram C. P. Rajendran C.N.R Rao 
C.N.R Rao Chandrabhas Narayana Diwakar S. Venkatesan Eswaramoorthy MG.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 
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. 

20172016201520142013201220112010
20092008200720062005200420032002
20012000199919981997199619951994
PreviousAll

  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).

Research Units

           

Dean Offices &

Administrative Units

           

Academic Programmes

           

Information for Visitors

           

JNC Quick Links


Tenders

Search Person


Jncasr News   

Announcements