about
Evaluation of European coeliac disease risk variants in a north Indian populationA genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North IndiansDense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseChronic renal insufficiency among Asian Indians with type 2 diabetes: I. Role of RAAS gene polymorphisms.Association of TGFbeta1, TNFalpha, CCR2 and CCR5 gene polymorphisms in type-2 diabetes and renal insufficiency among Asian IndiansGenetics of schizophrenia from a clinicial perspective.Low hygiene and exposure to infections may be associated with increased risk for ulcerative colitis in a North Indian population.Differing correlates for suicide attempts among patients with schizophrenia or schizoaffective disorder in India and USA.Evaluation of familial influences on the course and severity of schizophrenia among US and Indian cases.Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition.Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north IndiansLimited evidence for parent-of-origin effects in inflammatory bowel disease associated lociFragile X CGG repeat variation in Tamil Nadu, South India: a comparison of radioactive and methylation-specific polymerase chain reaction in CGG repeat sizing.Evaluation of cytochrome P4502E1 polymorphisms in healthy adult Western Indians and patients with antituberculous drug-induced hepatotoxicity.Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort.Functional characterization of rare variants in human dopamine receptor D4 gene by genotype-phenotype correlations.Attempts to replicate genetic associations with schizophrenia in a cohort from north India.Possible role of rare variants in Trace amine associated receptor 1 in schizophrenia.Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India.A cross-ethnic survey of CFB and SLC44A4, Indian ulcerative colitis GWAS hits, underscores their potential role in disease susceptibility.Normative genetic profiles of RAAS pathway gene polymorphisms in North Indian and South Indian populations.Identification of critical variants within SLC44A4, an ulcerative colitis susceptibility gene identified in a GWAS in north Indians.Dopaminergic pathway gene polymorphisms and genetic susceptibility to schizophrenia among north Indians.Population and genomic lessons from genetic analysis of two Indian populations.Association of polymorphisms of CYP2C9, CYP2C19, and ABCB1, and activity of P-glycoprotein with response to anti-epileptic drugs.Polymorphism of the p53 codon 72 Arg/Pro and the risk of HPV type 16/18-associated cervical and oral cancer in India.Correlates of response to Olanzapine in a North Indian Schizophrenia sample.Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism.II. Serotonin receptor gene polymorphisms and their association with tardive dyskinesia among schizophrenia patients from North India.Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation.FMR1 haplotype analysis among Indian communities.Characterization of SNPs in the dopamine-β-hydroxylase gene providing new insights into its structure-function relationship.Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome Patients.Genetic susceptibility to Parkinson's disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.Functional characterisation of ADP ribosylation factor-like protein 15 in rheumatoid arthritis synovial fibroblasts.Distinct de novo deletions in a brother-sister pair with RTT: a case report.Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.Parkin mutations in familial and sporadic Parkinson's disease among Indians.
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P50
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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B.K Thelma
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P108
P106
P31
P496
0000-0002-2154-5443