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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.Kushagra Bansal 
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. R. Ratnapriya, J. Vijai, J. Kadandale, R. Iyer, K. Radhakrishnan and A. Anand, A locus for juvenile myoclonic epilepsy maps to 2q33-q36, Human Genetics (2010). In Press.

  2. R. Ratnapriya, P. Satishchandra, S. Dilip, G. Gadre and A. Anand, Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28, Human Genetics 126, 677 - 683 (2009).

  3. R. Ratnapiya, P. Satishchandra, S. Dilip Kumar, G. Gadre, R. Reddy and A. Anand, A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3, Human Genetics 125, 541 - 549 (2009).

  4. Arunima Chatterjee, R. Jalvi, Nishtha Pandey, R. Rangasayee and A. Anand, A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3, Human Genetics 124, 669 - 675 (2009).

  5. M. RamShankar, Aparna G, R. Jalvi, CR Srikumari Srisailapathy, V. Malhotra, S Chadha, A Agarwal, A Ramesh, R. Rangasayee and A. Anand, Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss, European Journal of Human Genetics 1 - 8 (2008).

  6. A. Kapoor, P. Satishchandra, R. Ratnapriya, Ramesh Reddy, Jayaram Kadandale, Susarla K Shankar and A. Anand, An idiopathic epilepsy syndrome linked to 3q13.3-q21 and missense mutations in the extracellular calcium sensing receptor gene, Annals of Neurology 64, 158 - 167 (2008).

  7. G. L. Cavalleri, N. M. Walley, N. Soranzo, J. Mulley, C. P. Doherty, A. Kapoor, C. Depondt, J. M. Lynch, I. E. Scheffer, A. Heils, A. Gehrmann, P. Kinirons, S. Gandhi, P. Satishchandra, N. W. Wood, A. Anand, T. Sander, S. F. Berkovic, N. Delanty, D. B. Goldstein and S. M. Sisodiya, A multicenter study of BRD2 as a risk factor for Juvenile Myoclonic Epilepsy, Epilepsia 48, 706 - 712 (2007).

  8. G. S. Shekhwat, M. Ramshankar, R. Jalvi, R. Rangasayee and A. Anand, Implications of disclosing auditory genetic mutation to a family: A case study, International Journal of Audiology 46, 384 - 387 (2007).

  9. A. Kapoor, R. Ratnapriya, G Kuruttukulam and A. Anand, A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12-q14, Human Genetics 121, 655 - 662 (2007).

  10. H. M. Ravishankar, A Kishore and A. Anand, Mutational screening of the Parkin gene among South Indians with early onset Parkinson's disease, Journal of Neurology, Neurosurgery and Psychiatry 76, 1588 - 1590 (2005).

  11. J. Vijai, A. Kapoor, H. M. Ravishankar, P. J. Cherian, G Kuruttukulam, B. Rajendran, R Sridharan, G. Rangan, A. S. Girija, S. Jayalakshmi, S. Mohandas, K. S. Mani and A. Anand, Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy, Journal of Medical Genetics 42, 439 - 442 (2005).

  12. 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).

  13. 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).

  14. 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).

  15. 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).

  16. 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).

  17. O. Mukherjee, Q Saleem, A. Anand, S. K. Brahmachari and S. Jain, Common psychiatric diseases and human genetic variation, Community Genetics 5, 171 - 177 (2002).

  18. A. Anand, A Villella, LC Ryner, T. Carlos, SF Goodwin, HJ Song, DA Gailey, A Morles, JC Hall, BS Baker and BJ Taylor, Molecular dissection of the sex-specific and vital functions of the Drosophila melanogaster sex determination gene fruitless, Genetics 158, 1569 - 1595 (2001).

  19. K. J. Sheikh, D. Naveen, T. Sherrin, A. Murthy, K. Thennarasu, A. Anand, V. Benegal and S. Jain, Polymorphisms at the DRD2 locus in early onset alcoholism in the Indian population, Addication Biology 6, 331 - 335 (2001).

  20. Q. Saleem, A. Anand, S. K. Brahmachari, S. Jain and U. Muthane, A clinical study of patients with genetically confirmed Huntington's disease from India, J. Neurological Sciences 15, 73 - 78 (2001).

  21. Q Saleem, A. Anand, S. Jain and S. K. Brahmachari, The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans, Human Genetics 109, 136 - 142 (2001).

  22. Q. Saleem, V. S. Sreevidya, J. Sudhir, J. V. Savithri, Y. Gowda, C. B. Rao, V. Benegal, P. P. Majumder, A. Anand, S. K. Brahmachari and S. Jain, Association analysis of CAG repeat at the KCNN3 locus in Indian patients with Bipolar Disorder and Schizophrenia, American Journal of Medical Genetics: Neuropsychiatric Genetics 96, 744 - 748 (2000).

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