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List of works by Meera Purushottam

An exploratory association study of the influence of dysbindin and neuregulin polymorphisms on brain morphometry in patients with schizophrenia and healthy subjects from South India.

scientific article published on 21 April 2014

ApoE4 and late onset depression in Indian population.

scientific article

Apolipoprotein E polymorphism and dementia: a hospital-based study from southern India.

scientific article published in January 2010

Association of N-Methyl-D-Aspartate receptor 2B Subunit (GRIN2B) polymorphism with earlier age at onset of withdrawal symptoms in Indian alcohol dependent subjects

scientific article published on 15 January 2016

Association of serotonin transporter gene polymorphisms with obsessive-compulsive disorder (OCD) in a south Indian population

scientific article

Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment.

scientific article published in March 2009

BDNF gene and obsessive compulsive disorder risk, symptom dimensions and treatment response

scientific article published on 18 October 2017

Cellular models to study schizophrenia: A systematic review.

scientific article published on 17 October 2016

Common psychiatric diseases and human genetic variation.

scientific article published in January 2002

Deletion analysis of spinal muscular atrophy in southern Indian population.

scientific article published in July 2008

Dementia and diabetes mellitus: association with apolipoprotein e4 polymorphism from a hospital in southern India.

scientific article

Derivation of iPSC lines from two patients with familial Alzheimer's disease from India

scientific article published on 19 December 2018

Determinants of Onset of Huntington's Disease with Behavioral Symptoms: Insight from 92 Patients.

scientific article published on 11 December 2015

Differential expression levels of collagen 1A2, tissue inhibitor of metalloproteinase 4, and cathepsin B in intracranial aneurysms

scientific article published in July 2016

Discovery biology of neuropsychiatric syndromes (DBNS): a center for integrating clinical medicine and basic science.

scientific article published on 18 April 2018

Does GRIN2B gene influence obsessive-compulsive disorder risk, symptom dimensions and treatment response?

scientific article published on 21 December 2017

Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort

scientific article published on January 2017

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

scientific article published in November 2009

Effect of CLU and PICALM polymorphisms on AD risk: A study from south India.

scientific article published on 29 December 2016

Effect of polymorphisms of three genes mediating monoamine signalling on brain morphometry in schizophrenia and healthy subjects

scientific article published on April 2015

Electrophysiological evaluation of spinocerebellar ataxias 1, 2 and 3 ⬇️

scientific article published on August 31, 2011

Erratum: Figure Correction.

scientific article

Estrogen pathway related genes and their association with risk of postpartum psychosis: A case control study

scientific article published on 19 January 2017

GSK-3b 50 T/C polymorphism in bipolar disorder and its relationship with clinical phenotypes and treatment response

scientific article published on 17 August 2018

Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population ⬇️

scientific article published on June 7, 2012

Gene Expression in Intracranial Aneurysms-Comparison Analysis of Aneurysmal Walls and Extracranial Arteries with Real-Time Polymerase Chain Reaction and Immunohistochemistry

scientific article published on 13 June 2019

Generation and characterization of individual-specific induced pluripotent cells from patient-derived lymphoblastoid cell lines.

scientific article

Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing

scientific article published on 28 June 2019

Genetic analysis of a family from India with Machado-Joseph disease

scientific article published on 01 March 2019

Genetic studies indicate a potential target 5-HTR(3B) for drug therapy in schizophrenia patients

scientific article published on 17 October 2012

Genetic testing for clinically suspected spinocerebellar ataxias: report from a tertiary referral centre in India

scientific article published on 01 March 2018

Higher interleukin-33 levels in aggressive periodontitis cases

scientific article published on 01 September 2019

Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance

scientific article published on 22 October 2019

Influence of early adversity on cortisol reactivity, SLC6A4 methylation and externalizing behavior in children of alcoholics

scientific article published on 10 May 2019

Insulin resistance in patients with Alzheimer's dementia: A controlled study from India

scientific article published on 28 October 2018

Lower levels of serum copper in patients with Alzheimer's dementia: A controlled study from India

scientific article published on 2 December 2017

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

scientific article

Manganese- and 1-methyl-4-phenylpyridinium-induced neurotoxicity display differences in morphological, electrophysiological and genome-wide alterations: implications for idiopathic Parkinson's disease

scientific article published on 12 August 2017

Mutation burden profile in familial Alzheimer's disease cases from India.

scientific article published on 12 December 2017

Non-ataxic manifestations of Spinocerebellar ataxia-2, their determinants and predictors

scientific article published on 01 September 2018

Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.

scientific article published on 26 November 2007

Phylogenetic analysis and selection pressures of 5-HT receptors in human and non-human primates: receptor of an ancient neurotransmitter.

scientific article

Protective Effect of Antioxidants on Neuronal Dysfunction and Plasticity in Huntington's Disease

scientific article published on 12 January 2017

Reduced telomere length in subjects with dementia and diabetes mellitus type 2 is independent of apolipoprotein E4 genotype.

scientific article published on 30 June 2014

Serotonergic candidate genes and puerperal psychosis: an association study.

scientific article published in October 2007

Shortened telomere in unremitted schizophrenia

scientific article published on 12 January 2015

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