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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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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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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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Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS

Journal of ayurveda and integrative medicine, 2022-07, Vol.13 (3), p.100578-100578, Article 100578

2022

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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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Role of immunodeficient animal models in the development of fructose induced NAFLD

The Journal of nutritional biochemistry, 2014-02, Vol.25 (2), p.219-226

2014

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VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

Neurobiology of aging, 2013-10, Vol.34 (10), p.2442.e1-2442.e3

2013

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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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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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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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Sex and strain-related differences in the peripheral blood cell values of mutant mouse strains

Comparative clinical pathology, 2012-12, Vol.21 (6), p.1577-1585

2012

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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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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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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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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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Mosaicism for del(17) (p11.2p11.2) underlying the Smith-Magenis syndrome

American journal of medical genetics, 1996-12, Vol.66 (2), p.193-196

1996

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Smith-Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization

American journal of medical genetics, 1995-09, Vol.58 (3), p.286-291

1995

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

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

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

Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS

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

Role of immunodeficient animal models in the development of fructose induced NAFLD

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

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

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

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

Sex and strain-related differences in the peripheral blood cell values of mutant mouse strains

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

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

Haploinsufficiency of cytosolic serine hydroxymethyltransferase in the Smith-Magenis syndrome

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

Mosaicism for del(17) (p11.2p11.2) underlying the Smith-Magenis syndrome

Smith-Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization

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

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