Role of miRNA binding site SNPs in candidate genes in a North Indian schizophrenia cohort

Por John, Jibin, Deshpande, Smita N, Nimgaonkar, Vishwajit L, Thelma, BK
Publicado em 2014

Association of dopaminergic pathway gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes

Por Gupta Arvind, Ammini AC, Kumar KM Prasanna, Prasad Pushplata, Gupta Rajeev, Thelma BK
Publicado em 2008-03-01

Association of dopaminergic pathway gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes

Por Prasad, Pushplata, Kumar, KM Prasanna, Ammini, AC, Gupta, Arvind, Gupta, Rajeev, Thelma, BK
Publicado em 2008

Genetic susceptibility to Tardive Dyskinesia in chronic schizophrenia subjects: Role of oxidative stress pathway genes

Por Tiwari, Arun K, Deshpande, Smita N, Lerer, Bernard, Nimgaonkar, Vishwajit L, Thelma, BK
Publicado em 2007

Fragile X CGG Repeat Variation in Tamil Nadu, South India: A Comparison of Radioactive and Methylation-Specific Polymerase Chain Reaction in CGG Repeat Sizing

Por Indhumathi, Nagarathinam, Singh, Deepika, Chong, Samuel S., Thelma, B.K., Arabandi, Ramesh, Srisailpathy, C.R. Srikumari
Publicado em 2012

Differing correlates for suicide attempts among patients with schizophrenia or schizoaffective disorder in India and USA

Por Bhatia, Triptish, Thomas, Pramod, Semwal, Prachi, Thelma, B.K., Nimgaonkar, V.L., Deshpande, Smita N.
Publicado no Schizophr Res (2006)

Association of TGFβ1, TNFα, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian Indians

Por Prasad, Pushplata, Tiwari, Arun K, Kumar, KM Prasanna, Ammini, AC, Gupta, Arvind, Gupta, Rajeev, Thelma, BK
Publicado em 2007

Association analysis of ADPRT1, AKR1B1, RAGE, GFPT2 and PAI-1 gene polymorphisms with chronic renal insufficiency among Asian Indians with type-2 diabetes

Por Prasad, Pushplata, Tiwari, Arun K, Kumar, KM Prasanna, Ammini, AC, Gupta, Arvind, Gupta, Rajeev, Thelma, BK
Publicado em 2010

Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition

Por John, Jibin, Bhatia, Triptish, Kukshal, Prachi, Chandna, Puneet, Nimgaonkar, Vishwajit L., Deshpande, Smita N., Thelma, B.K.
Publicado no Schizophr Res (2016)

Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia

Por John, Jibin, Kukshal, Prachi, Bhatia, Triptish, Chowdari, K.V., Nimgaonkar, V.L., Deshpande, S.N., Thelma, B.K.
Publicado no Schizophr Res (2017)

Association studies of cytosolic phospholipase A2 polymorphisms and schizophrenia among two independent family-based samples

Por Chowdari, Kodavali V., Brandstaetter, Bernard, Semwal, Prachi, Bhatia, Triptish, Deshpande, Smita, Reddy, Ravi, Wood, Joel, Weinberg, Clarice R., Thelma, B.K., Nimgaonkar, Vishwajit L.
Publicado no Psychiatr Genet (2001)

Clinical and genetic correlates of severity in schizophrenia in India: An Ordinal Logistic Regression Approach

Por Thomas, Pramod, Chandra, Abha, Bhatia, Triptish, Mishra, N.N., Sharma, Vikash Ranjan, Gauba, Deepak, Wood, Joel, Chowdari, Kodavali, Semwal, Prachi, Thelma, BK, Nimgaonkar, Vishwajit L, Deshpande, Smita N
Publicado em 2011

Chronic renal insufficiency among Asian Indians with type 2 diabetes: I. Role of RAAS gene polymorphisms

Por Prasad, Pushplata, Tiwari, Arun K, Kumar, KM Prasanna, Ammini, AC, Gupta, Arvind, Gupta, Rajeev, Sharma, AK, Rao, AR, Nagendra, R, Chandra, T Satish, Tiwari, SC, Rastogi, Priyanka, Gupta, B Lal, Thelma, BK
Publicado em 2006

Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples

Por Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O’Donovan, Michael C., Owen, Michael J., Richard, Christian, Semwal, Prachi, Sobell, Janet L., Clair, David St, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel M., Wood, Joel, Zhang, Feng, Devlin, Bernie, Nimgaonkar, Vishwajit L.
Publicado em 2006

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

Por Trynka, Gosia, Hunt, Karen A, Bockett, Nicholas A, Romanos, Jihane, Mistry, Vanisha, Szperl, Agata, Bakker, Sjoerd F, Bardella, Maria Teresa, Bhaw-Rosun, Leena, Castillejo, Gemma, de la Concha, Emilio G., de Almeida, Rodrigo Coutinho, Dias, Kerith-Rae M, van Diemen, Cleo C., Dubois, Patrick CA, Duerr, Richard H., Edkins, Sarah, Franke, Lude, Fransen, Karin, Gutierrez, Javier, Heap, Graham AR, Hrdlickova, Barbara, Hunt, Sarah, Izurieta, Leticia Plaza, Izzo, Valentina, Joosten, Leo AB, Langford, Cordelia, Mazzilli, Maria Cristina, Mein, Charles A, Midah, Vandana, Mitrovic, Mitja, Mora, Barbara, Morelli, Marinita, Nutland, Sarah, Núñez, Concepción, Onengut-Gumuscu, Suna, Pearce, Kerra, Platteel, Mathieu, Polanco, Isabel, Potter, Simon, Ribes-Koninckx, Carmen, Ricaño-Ponce, Isis, Rich, Stephen S., Rybak, Anna, Santiago, José Luis, Senapati, Sabyasachi, Sood, Ajit, Szajewska, Hania, Troncone, Riccardo, Varadé, Jezabel, Wallace, Chris, Wolters, Victorien M, Zhernakova, Alexandra, Thelma, B.K., Cukrowska, Bozena, Urcelay, Elena, Bilbao, Jose Ramon, Mearin, M Luisa, Barisani, Donatella, Barrett, Jeffrey C, Plagnol, Vincent, Deloukas, Panos, Wijmenga, Cisca, van Heel, David A
Publicado em 2011