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Antigen peptide transporter 1 is involved in the development of fructose-induced hepatic steatosis in mice

Journal of gastroenterology and hepatology, 2013-08, Vol.28 (8), p.1403-1409

2013

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APOE Polymorphism in a Rural Older Population-Based Sample in India

Human biology, 2001-02, Vol.73 (1), p.135-144

2001

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APOE polymorphisms in a rural older population-based sample in India

Human biology, 2001-02, Vol.73 (1), p.135

2001

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Apolipoprotein E polymorphism and Alzheimer disease: The Indo-US Cross-National Dementia Study

Archives of neurology (Chicago), 2000-06, Vol.57 (6), p.824

2000

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Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient

American journal of medical genetics, 1995-11, Vol.59 (3), p.406-407

1995

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Association of Cullin1 haplotype variants with rheumatoid arthritis and response to methotrexate

Pharmacogenetics and genomics, 2011-09, Vol.21 (9), p.590-593

2011

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Association of N-acetyl transferase 2 gene polymorphism and slow acetylator phenotype with young onset and late onset Parkinsonʼs disease among Indians

Pharmacogenetics and genomics, 2005-10, Vol.15 (10), p.731-735

2005

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Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians

PloS one, 2012-02, Vol.7 (2), p.e31584-e31584

2012

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Complex phenotypes in an Indian family with homozygous SCA2 mutations

Annals of neurology, 2004-01, Vol.55 (1), p.130-133

2004

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Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease

Parkinsonism & related disorders, 2021-03, Vol.84, p.61-67

2021

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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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Early Onset Parkinson's disease due to DJ1 mutations: An Indian study

Parkinsonism & related disorders, 2016-11, Vol.32, p.20-24

2016

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Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes

Journal of medical genetics, 2016-08, Vol.53 (8), p.559-566

2016

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The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis syndrome patients

Human molecular genetics, 1995-04, Vol.4 (4), p.589-597

1995

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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

Neurogenetics, 2008-02, Vol.9 (1), p.73-73

2008

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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

Neurogenetics, 2006-11, Vol.7 (4), p.223-229

2006

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Genetically modified mouse models for the study of nonalcoholic fatty liver disease

World journal of gastroenterology : WJG, 2012-03, Vol.18 (11), p.1141-1153

2012

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Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation

Pharmacogenetics and genomics, 2014-04, Vol.24 (4), p.211-219

2014

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Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis

Gut, 2015-04, Vol.64 (4), p.571-579

2015

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A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians

Arthritis & rheumatology (Hoboken, N.J.), 2013-12, Vol.65 (12), p.3026-3035

2013

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Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome

American journal of human genetics, 1995-12, Vol.57 (6), p.1342-1350

1995

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Interaction of genes from influx-metabolism-efflux pathway and their influence on methotrexate efficacy in rheumatoid arthritis patients among Indians

Pharmacogenetics and genomics, 2008-12, Vol.18 (12), p.1041-1049

2008

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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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Leads from xenobiotic metabolism genes for Parkinson’s disease among north Indians

Pharmacogenetics and genomics, 2011-12, Vol.21 (12), p.790-797

2011

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Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients

American journal of human genetics, 1996-05, Vol.58 (5), p.998-1007

1996

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Antigen peptide transporter 1 is involved in the development of fructose-induced hepatic steatosis in mice

APOE Polymorphism in a Rural Older Population-Based Sample in India

APOE polymorphisms in a rural older population-based sample in India

Apolipoprotein E polymorphism and Alzheimer disease: The Indo-US Cross-National Dementia Study

Apparent mosaicism for del(17)(p11.2) ruled out by fluorescence in situ hybridization in a Smith-Magenis syndrome patient

Association of Cullin1 haplotype variants with rheumatoid arthritis and response to methotrexate

Association of N-acetyl transferase 2 gene polymorphism and slow acetylator phenotype with young onset and late onset Parkinsonʼs disease among Indians

Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians

Complex phenotypes in an Indian family with homozygous SCA2 mutations

Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease

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

Early Onset Parkinson's disease due to DJ1 mutations: An Indian study

Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes

The gene for a human microfibril-associated glycoprotein is commonly deleted in Smith-Magenis 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

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

Genetically modified mouse models for the study of nonalcoholic fatty liver disease

Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation

Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis

A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome

Interaction of genes from influx-metabolism-efflux pathway and their influence on methotrexate efficacy in rheumatoid arthritis patients among Indians

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

Leads from xenobiotic metabolism genes for Parkinson’s disease among north Indians

Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients

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