Research output per year
Research output per year
Search results
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2016
Reply to 'Lack of replication of association of THSD7A with obesity'
Nizamuddin, S., Govindaraj, P., Saxena, S., Kashyap, M., Mishra, A., Singh, S., Rotti, H., Raval, R., Nayak, J., Bhat, B. K., Prasanna, B. V., Dhumal, V. R., Bhale, S., Joshi, K. S., Dedge, A. P., Bharadwaj, R., Gangadharan, G. G., Nair, S., Gopinath, P. M., Patwardhan, B., & 4 others, 01-04-2016, In: International Journal of Obesity. 40, 4, p. 727-728 2 p.Research output: Contribution to journal › Letter › peer-review
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Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum
Chakrabarty, S., Vijayakumar, N., Radhakrishnan, K. & Satyamoorthy, K., 01-10-2016, In: Journal of Neurology. 263, 10, p. 2130-2132 3 p.Research output: Contribution to journal › Letter › peer-review
5 Citations (Scopus) -
2015
Association of GRIN1, ABCB1, and DRD4 genes and response to antipsychotic drug treatment in schizophrenia
Pai, P., Arathil, P., Kotambail, A., Nair, R., Gupta, M., Moily, N. S., Kukreti, R., Jain, S., Rai, P. S., Gopinath, P. M., Sharma, P. S. & Satyamoorthy, K., 13-05-2015, In: Psychiatric Genetics. 25, 3, p. 135-136 2 p.Research output: Contribution to journal › Letter › peer-review
5 Citations (Scopus) -
GADL1 gene polymorphisms and lithium response in bipolar i disorder: Lack of association from an Indian population
Kotambail, A., Mathur, A., Bhat, S. M., Rai, P. S., Sharma, P. S. & Satyamoorthy, K., 03-02-2015, In: Psychiatric Genetics. 25, 1, p. 39-40 2 p.Research output: Contribution to journal › Letter › peer-review
19 Citations (Scopus) -
2013
Cytogenetic study in recurrent pregnancy loss: An experience from tertiary care centre
Rajasekhar, M., Sreelakshm, K., Gopinath, P. M. & Satyamoorthy, K., 2013, In: Genetic Counseling. 24, 3, p. 347-349 3 p.Research output: Contribution to journal › Letter › peer-review
1 Citation (Scopus) -
2012
Mucolipidosis type II α/β with a homozygous missense mutation in the GNPTAB gene
Coutinho, M. F., Santos, L. D. S., Girisha, K. M., Satyamoorthy, K., Lacerda, L., Prata, M. J. & Alves, S., 05-2012, In: American Journal of Medical Genetics, Part A. 158 A, 5, p. 1225-1228 4 p.Research output: Contribution to journal › Letter › peer-review
10 Citations (Scopus) -
2010
Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis
Girisha, K. M., Vahab, S. A., Dalal, A. B., Gopinath, P. M. & Satyamoorthy, K., 06-2010, In: Annals of Hematology. 89, 6, p. 625-626 2 p.Research output: Contribution to journal › Letter › peer-review
2 Citations (Scopus)