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

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

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

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

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

Complex phenotypes in an Indian family with homozygous SCA2 mutations

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

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

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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