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Genetic variants in novel pathways influence blood pressure and cardiovascular disease riskNew insights from monogenic diabetes for "common" type 2 diabetesHigh resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding regionChronic maternal vitamin B12 restriction induced changes in body composition & glucose metabolism in the Wistar rat offspring are partly correctable by rehabilitationDirectional dominance on stature and cognition in diverse human populationsThe genetic architecture of type 2 diabetesBirth size, risk factors across life and cognition in late life: protocol of prospective longitudinal follow-up of the MYNAH (MYsore studies of Natal effects on Ageing and Health) cohortTCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatitis but may interact with SPINK1 and CTSB mutations in predicting diabetes.Association of common genetic variants with lipid traits in the Indian population.Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians.Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signaling and other protein groups of regulatory functions.Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis.Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals.Association between common polymorphism near the MC4R gene and obesity risk: a systematic review and meta-analysis.Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs.Study of 11 BMI-associated loci identified in GWAS for associations with central obesity in the Chinese childrenGenetic and phenotypic heterogeneity in tropical calcific pancreatitisRelationship of APOA5, PPARγ and HL gene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood.Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans.Assessing the pathological relevance of SPINK1 promoter variants.Association of cathepsin B gene polymorphisms with tropical calcific pancreatitisEvaluation of seven common lipid associated loci in a large Indian sib pair study.Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia.FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians.Identification of urinary proteins potentially associated with diabetic kidney disease.Towards a new developmental synthesis: adaptive developmental plasticity and human disease.Variants in CPA1 are strongly associated with early onset chronic pancreatitis.No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations.Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene.Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy.GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians.Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype.Juvenile fibrocalculous pancreatopathy--a patient report.Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model.Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis.Cardiac beriberi: often a missed diagnosis.High prevalence of infantile encephalitic beriberi with overlapping features of Leigh's disease.Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians.
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P50
description
researcher ORCID ID = 0000-0002-3095-9453
@en
wetenschapper
@nl
name
Giriraj R Chandak
@ast
Giriraj R Chandak
@en
Giriraj R Chandak
@es
Giriraj R Chandak
@nl
type
label
Giriraj R Chandak
@ast
Giriraj R Chandak
@en
Giriraj R Chandak
@es
Giriraj R Chandak
@nl
altLabel
Giriraj Ratan Chandak
@en
prefLabel
Giriraj R Chandak
@ast
Giriraj R Chandak
@en
Giriraj R Chandak
@es
Giriraj R Chandak
@nl
P106
P1153
6602765139
P31
P496
0000-0002-3095-9453