UB Paderborn / Katalog / Suche / in CDI

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

Nature genetics, 2015-09, Vol.47 (9), p.979-986

2015

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An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians

PloS one, 2011-01, Vol.6 (1), p.e16565-e16565

2011

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

BMC medical genetics, 2010-03, Vol.11 (1), p.52-52, Article 52

2010

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

BMC medical genetics, 2007-04, Vol.8 (1), p.20-20, Article 20

2007

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De novo deletion in MECP2 in a monozygotic twin pair: a case report

BMC medical genetics, 2011-08, Vol.12 (1), p.113-113, Article 113

2011

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

BMC medical genetics, 2006-05, Vol.7 (1), p.42-42, Article 42

2006

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Genetic underpinnings of tardive dyskinesia: passing the baton to pharmacogenetics

Pharmacogenomics, 2008-09, Vol.9 (9), p.1285-1306

2008

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Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism

Journal of medical genetics, 2016-07, Vol.53 (7), p.450-456

2016

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

Journal of psychopharmacology (Oxford), 2020-03, Vol.34 (3), p.358-369

2020

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SA120FAMILY BASED RARE VARIANT STUDY SUPPORTS THE CUMULATIVE CONTRIBUTION OF NEURODEVELOPMENTAL PATHWAY GENES IN SCHIZOPHRENIA ETIOLOGY

European neuropsychopharmacology, 2019, Vol.29, p.S1254-S1255

2019

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Rare And Ultra-Rare Variants In Familial Schizophrenia - An Update From India

European neuropsychopharmacology, 2019, Vol.29, p.S744-S745

2019

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Targeted Deep Resequencing Identifies MID2 Mutation for X-Linked Intellectual Disability with Varied Disease Severity in a Large Kindred from India

Human mutation, 2014-01, Vol.35 (1), p.41-44

2014

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Factors Associated with Transient Neonatal Hyperthyrotropinemia

Indian journal of pediatrics, 2020-06, Vol.87 (6), p.482-483

2020

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Replication Study Of Gwas And Other Strongly Associated Markers From Chromosome 6 In North Indian Population

European neuropsychopharmacology, 2017, Vol.27, p.S457

2017

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T40 - Replication Study Of Gwas And Other Strongly Associated Markers From Chromosome 6 In North Indian Population

European neuropsychopharmacology, 2017, Vol.27, p.S457-S457

2017

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Findings From Continuing Gene Hunt In Families With Schizophrenia

European neuropsychopharmacology, 2017, Vol.27, p.S490-S490

2017

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LBOS 02-05 INHIBITORS OF DOPAMINE-β-HYDROXYLASE OBTAINED BY STRUCTURE BASED METHODS EXHIBITED ANTI-HYPERTENSIVE EFFECT IN L-NAME INDUCED HYPERTENSIVE RATS

Journal of hypertension, 2016-09, Vol.34 Suppl 1 - ISH 2016 Abstract Book (Supplement 1), p.e550-e550

2016

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A preliminary study of association of genetic variants with early response to olanzapine in schizophrenia

Indian journal of psychiatry, 2018-01, Vol.60 (1), p.10-16

2018

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Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study

Indian journal of human genetics, 2006-01, Vol.12 (1), p.17-22

Chowdhury MadhumitaRoy, Kabra Madhulika, Sharma Deepti, Singh Deepika, Dabral Anjali, Thelma BK, Kalra Veena

2006

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HLA sequencing identifies novel associations and suggests clinical relevance of DPB104:01 in ANCA-associated Granulomatosis with polyangiitis

Gene, 2024-02, Vol.896, p.148024-148024, Article 148024

2024

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Association of polymorphisms of CYP2C9, CYP2C19, and ABCB1, and activity of P-glycoprotein with response to anti-epileptic drugs

Journal of postgraduate medicine, 2014-07, Vol.60 (3), p.265-269

2014

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Evaluation of cytochrome P4502E1 polymorphisms in healthy adult Western Indians and patients with antituberculous drug-induced hepatotoxicity

Indian journal of pharmacology, 2016-01, Vol.48 (1), p.42-46

2016

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Genetic susceptibility to tardive dyskinesia in chronic schizophrenia subjects: III. Lack of association of CYP3A4 and CYP2D6 gene polymorphisms

Schizophrenia research, 2005-06, Vol.75 (1), p.21-26

2005

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Clinical and genetic correlates of severity in schizophrenia in India: An ordinal logistic regression approach

Psychiatry research, 2011-09, Vol.189 (2), p.321-323

2011

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Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians

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

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

De novo deletion in MECP2 in a monozygotic twin pair: a case report

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

Genetic underpinnings of tardive dyskinesia: passing the baton to pharmacogenetics

Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism

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

SA120FAMILY BASED RARE VARIANT STUDY SUPPORTS THE CUMULATIVE CONTRIBUTION OF NEURODEVELOPMENTAL PATHWAY GENES IN SCHIZOPHRENIA ETIOLOGY

Rare And Ultra-Rare Variants In Familial Schizophrenia - An Update From India

Targeted Deep Resequencing Identifies MID2 Mutation for X-Linked Intellectual Disability with Varied Disease Severity in a Large Kindred from India

Factors Associated with Transient Neonatal Hyperthyrotropinemia

Replication Study Of Gwas And Other Strongly Associated Markers From Chromosome 6 In North Indian Population

T40 - Replication Study Of Gwas And Other Strongly Associated Markers From Chromosome 6 In North Indian Population

Findings From Continuing Gene Hunt In Families With Schizophrenia

LBOS 02-05 INHIBITORS OF DOPAMINE-β-HYDROXYLASE OBTAINED BY STRUCTURE BASED METHODS EXHIBITED ANTI-HYPERTENSIVE EFFECT IN L-NAME INDUCED HYPERTENSIVE RATS

A preliminary study of association of genetic variants with early response to olanzapine in schizophrenia

Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study

HLA sequencing identifies novel associations and suggests clinical relevance of DPB104:01 in ANCA-associated Granulomatosis with polyangiitis

Association of polymorphisms of CYP2C9, CYP2C19, and ABCB1, and activity of P-glycoprotein with response to anti-epileptic drugs

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

Evaluation of cytochrome P4502E1 polymorphisms in healthy adult Western Indians and patients with antituberculous drug-induced hepatotoxicity

Genetic susceptibility to tardive dyskinesia in chronic schizophrenia subjects: III. Lack of association of CYP3A4 and CYP2D6 gene polymorphisms

Clinical and genetic correlates of severity in schizophrenia in India: An ordinal logistic regression approach

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