Ramesh C. Juyal

Aruna Asaf Ali Road
New Delhi, DL, India

Last Updated: 09/26/2026

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Found 16 publications

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

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

Journal: Journal of Ayurveda and integrative medicine

Published: July 19, 2021

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

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

Journal: Parkinsonism & related disorders

Published: September 29, 2020

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

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

Journal: Parkinsonism & related disorders

Published: December 09, 2015

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

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

Journal: Journal of medical genetics

Published: November 03, 2015

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

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

Journal: Journal of medical genetics

Published: August 15, 2015

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

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

Journal: Nature genetics

Published: October 30, 2014

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

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

Journal: Gut

Published: May 20, 2014

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

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

Journal: Pharmacogenetics and genomics

Published: March 04, 2014

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

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

Journal: The Journal of nutritional biochemistry

Published: May 04, 2013

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

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

Journal: Neurobiology of aging

Published: April 12, 2013

A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians.

A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians.

Journal: Arthritis and rheumatism

Published: March 13, 2013

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

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

Journal: Journal of gastroenterology and hepatology

Published: February 13, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026