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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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Potential of ayurgenomics approach in complex trait research: leads from a pilot study on rheumatoid arthritis

PloS one, 2012-09, Vol.7 (9), p.e45752-e45752

2012

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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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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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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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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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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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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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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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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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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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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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Purine biosynthetic pathway genes and methotrexate response in rheumatoid arthritis patients among north Indians

Pharmacogenetics and genomics, 2009-10, Vol.19 (10), p.823-828

2009

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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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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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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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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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Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinsonʼs disease among North Indians

Pharmacogenetics and genomics, 2010-07, Vol.20 (7), p.435-441

2010

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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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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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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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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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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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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

Potential of ayurgenomics approach in complex trait research: leads from a pilot study on rheumatoid arthritis

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

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

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

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

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

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

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

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

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

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

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

Purine biosynthetic pathway genes and methotrexate response in rheumatoid arthritis patients among north Indians

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

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

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

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

Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinsonʼs disease among North Indians

Complex phenotypes in an Indian family with homozygous SCA2 mutations

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

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

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

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

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