Article

Naushad, S.M. and Sai Shruti, P. and Bharathi, V. and Krishnaprasad, C. and Hussain, T. and Alrokayan, S.A. and Naik, U. and Radha Rama Devi, A. (2016) Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders. Psychiatric Genetics, 26 (6). pp. 281-286. ISSN 0955-8829

Uttarilli, Anusha and Ranganath, P. and Matta, D. and Jain, J.M.N. and Krishnaprasad, C. and Sobhan Babu, A. and Girisha, K.M. and Verma, I.C. and Phadke, S.R. and Mandal, K. and Puri, R.D. and Aggarwal, Shagun and Danda, S. and Sankar, V.H. and Kapoor, S. and Bhat, M. and Gowrishankar, K. and Hasan, A.Q. and Nair, M. and Nampoothiri, S. and Dalal, Ashwin (2016) Identification and Characterization of 20 Novel Pathogenic Variants in 60 unrelated Indian patients with Mucopolysaccharidoses (MPS) type I and type II. Clinical Genetics, 90 (6). pp. 496-508. ISSN 0009-9163

Uttarilli, Anusha and Ranganath, P. and Jain, S.J.M.N. and Krishnaprasad, C. and Sinha, A. and Verma, I.C. and Phadke, S.R. and Puri, R.D. and Danda, S. and Muranjan, M. and Jevalikar, G. and Nagarajaram, H.A. and Dalal, Ashwin (2015) Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI. Indian Journal of Medical Research, 142 (4). pp. 414-425. ISSN 0971-5916

Naushad, S.M. and Krishnaprasad, C. and Radha Rama Devi, A. (2014) Adaptive developmental plasticity in methylene tetrahydrofolate reductase (MTHFR) C677T polymorphism limits its frequency in South Indians. Molecular Biology Reports, 41 (5). pp. 3045-50. ISSN 1573-4978

Love, J.M. and Prosser, D. and Love, D.R. and Krishnaprasad, C. and Dalal, Ashwin and Aggarwal, Shagun (2014) A novel glycine decarboxylase gene mutation in an Indian family with nonketotic hyperglycinemia. Journal of Child Neurology, 29 (1). pp. 122-7. ISSN 1708-8283

Naushad, S.M. and Jain, J.M.N. and Krishnaprasad, C. and Naik, U. and Radha Rama Devi, A. (2013) Autistic children exhibit distinct plasma amino acid profile. Indian Journal of Biochemistry and Biophysics, 50 (5). pp. 474-478. ISSN 0301-1208

Naushad, S.M. and Jain, J.M.N. and Krishnaprasad, C. and Singh, R.P. and Naik, U. and Radha Rama Devi, A. (2009) Aberrations in folate metabolic pathway and altered susceptibility to autism. Psychiatric Genetics, 19 (4). pp. 171-176. ISSN 0955-8829

Govindaiah, V. and Naushad, S.M. and Jain, J.M.N. and Krishnaprasad , C. and Radha Rama Devi , A. (2009) Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians. Clinica Chimica Acta, 405 (1-2). pp. 127-131. ISSN 0009-8981

Govindaiah, V. and Naushad, S.M. and Prabhakara, K. and Krishnaprasad, C. and Radha Rama Devi, A. (2009) Association of parental hyperhomocysteinemia and C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss. Clinical Biochemistry, 42 (4-5). pp. 380-386. ISSN 0009-9120

Naushad, S.M. and Jain, J.M.N. and Krishnaprasad, C. and Radha Rama Devi, A. (2008) Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians. Clinical Chemistry and Laboratory Medicine, 46 (1). pp. 73-79. ISSN 1434-6621

Radha Rama Devi, A. and Naushad, S.M. and Krishnaprasad, C. (2006) Evaluation of total plasma homocysteine in Indian newborns using heel-prick samples. The Indian Journal of Pediatrics, 73 (6). pp. 503-508. ISSN 0019-5456