P. Kukshal

发表

Association study of Neuregulin-1 gene polymorphisms in a north Indian schizophrenia sample

R. Gur, R. Gur, B. Thelma, 2013, Schizophrenia Research.

The study of expression levels of DNA methylation regulators in patients affected with congenital heart defects (CHDs)

P. Kukshal, Radha O Joshi, S. Chellappan, 2022, Birth defects research.

Association of regulatory variants of dopamine β-hydroxylase with cognition and tardive dyskinesia in schizophrenia subjects

B. Thelma, A. Mukhopadhyay, S. Deshpande, 2020, Journal of psychopharmacology.

Rare variant based evidence for oligogenic contribution of neurodevelopmental pathway genes to schizophrenia

B. Thelma, V. Nimgaonkar, S. Deshpande, 2019, Schizophrenia Research.

Genetic variations in evolutionary accelerated regions disrupt cognition in schizophrenia

B. Thelma, S. Deshpande, T. Bhatia, 2021, Psychiatry Research.

Genetics of schizophrenia from a clinicial perspective

B. Thelma, V. Nimgaonkar, S. Deshpande, 2012, International review of psychiatry.

Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition

B. Thelma, V. Nimgaonkar, S. Deshpande, 2016, Schizophrenia Research.

Attempts to replicate genetic associations with schizophrenia in a cohort from north India

B. Thelma, V. Nimgaonkar, S. Deshpande, 2017, npj Schizophrenia.

Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort.

B. Thelma, V. Nimgaonkar, L. McClain, 2013, Journal of psychiatric research.

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance

B. Thelma, S. Deshpande, T. Bhatia, 2019, Schizophrenia Research.

Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based study

B. Thelma, V. Nimgaonkar, Aditya Sharma, 2019, Schizophrenia Research.

Oligogenic rare variant contributions in schizophrenia and their convergence with genes harbouring de novo mutations in schizophrenia, autism and intellectual disability: Evidence from multiplex families

B. Thelma, V. Nimgaonkar, R. Harripaul, 2019, bioRxiv.

Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16–20 October 2015

Christopher B. Cole, Robert M. Maier, R. Yuen, 2016, Psychiatric genetics.

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis

B. Thelma, V. Nimgaonkar, Aditya Sharma, 2018, Schizophrenia bulletin.

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

B. Thelma, V. Nimgaonkar, K. Chowdari, 2017, Schizophrenia Research.

Exploring the Role of Maternal Nutritional Epigenetics in Congenital Heart Disease

P. Kukshal, Radha O Joshi, S. Chellappan, 2020, Current developments in nutrition.

The effect of rs1076560 (DRD2) and rs4680 (COMT) on tardive dyskinesia and cognition in schizophrenia subjects

B. Thelma, S. Deshpande, T. Bhatia, 2020, Psychiatric genetics.