Lista de obras - Giriraj R Chandak - Dominio Público Uruguay

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

artículo científico publicado en 2017

A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India.

artículo científico publicado en 2011

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

artículo científico

Altered methylation and expression patterns of genes regulating placental angiogenesis in preterm pregnancy.

artículo científico publicado en 2014

Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians

Assessing the pathological relevance of SPINK1 promoter variants

artículo científico publicado en 2011

Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model

artículo científico publicado en 2016

Association between common polymorphism near the MC4R gene and obesity risk: a systematic review and meta-analysis.

artículo científico publicado en 2012

Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes.

artículo científico publicado en 2011

Association of cathepsin B gene polymorphisms with tropical calcific pancreatitis

artículo científico publicado en 2006

Association of common genetic variants with lipid traits in the Indian population

artículo científico publicado en 2014

Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.

artículo científico publicado en 2011

Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs

artículo científico publicado en 2013

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis

artículo científico publicado en 2014

Birth 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) cohort

artículo científico publicado en 2017

Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism

artículo científico publicado en 2018

Cardiac beriberi: often a missed diagnosis.

artículo científico publicado en 2009

Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach

scientific article published on 29 January 2020

Chronic maternal vitamin B12 restriction induced changes in body composition & glucose metabolism in the Wistar rat offspring are partly correctable by rehabilitation

artículo científico publicado en 2014

Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals.

artículo científico publicado en 2012

Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians.

artículo científico publicado en 2011

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population.

artículo científico publicado en 2006

Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population

Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk ⬇️

artículo científico publicado el 1 de septiembre de 2012

Comprehensive screening of chymotrypsin C (CTRC) gene in tropical calcific pancreatitis identifies novel variants ⬇️

artículo científico publicado el 12 de mayo de 2012

Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia.

artículo científico publicado en 2013

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Evaluation of genetic markers linked to hemophilia A locus: an Indian experience

artículo científico publicado en 2007

Evaluation of seven common lipid associated loci in a large Indian sib pair study

artículo científico publicado en 2012

FTO gene variant and risk of hypertension: A meta-analysis of 57,464 hypertensive cases and 41,256 controls

article

FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians.

artículo científico publicado en 2008

Fetus-in-fetu: a case report with molecular analysis

scientific article published on 01 April 1999

GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

artículo científico publicado en 2017

GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

artículo científico publicado en 2017

Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy ⬇️

artículo científico publicado el 20 de julio de 2012

Genetic and phenotypic heterogeneity in tropical calcific pancreatitis

artículo científico publicado en 2014

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

H63D mutation in HFE gene is common in Indians and is associated with the European haplotype

scientific article published on 01 August 2012

High prevalence of infantile encephalitic beriberi with overlapping features of Leigh's disease.

artículo científico publicado en 2008

High resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding region

artículo científico publicado en 2012

Hypermethylated CpG sites in the MTR gene promoter in preterm placenta.

artículo científico publicado en 2017

Identification and characterization of cis-regulatory elements 'insulator and repressor' in PPARD gene.

artículo científico publicado en 2018

Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype

artículo científico publicado en 2017

Identification of urinary proteins potentially associated with diabetic kidney disease.

artículo científico publicado en 2016

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. ⬇️

artículo científico publicado en 2010

Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy.

artículo científico publicado en 2017

Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children.

artículo científico publicado en 2013

Juvenile fibrocalculous pancreatopathy--a patient report.

artículo científico publicado en 2006

LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signaling and other protein groups of regulatory functions.

artículo científico publicado en 2012

Lack of replication of association of THSD7A with obesity

scientific article published on 23 February 2016

Maternal dietary folate and/or vitamin B12 restrictions alter body composition (adiposity) and lipid metabolism in Wistar rat offspring

artículo científico publicado en 2012

Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis.

artículo científico publicado en 2014

Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups.

artículo científico publicado en 2015

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

artículo científico publicado en 2011

Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.

artículo científico publicado en 2004

New insights from monogenic diabetes for "common" type 2 diabetes

artículo científico publicado en 2015

No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations

artículo científico publicado en 2016

Obscure pathogenesis of primary iron overload in Indians warrants more focused research

artículo científico publicado en 2011

PPAR signaling pathway is a key modulator of liver proteome in pups born to vitamin B(12) deficient rats.

artículo científico publicado en 2013

Relationship of APOA5, PPARγ and HL gene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood.

artículo científico publicado en 2011

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Study of 11 BMI-associated loci identified in GWAS for associations with central obesity in the Chinese children

artículo científico publicado en 2013

TCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatitis but may interact with SPINK1 and CTSB mutations in predicting diabetes.

artículo científico publicado en 2008

The G191R variant in the PRSS2 gene does not play a role in protection against tropical calcific pancreatitis.

artículo científico publicado en 2009

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The power of genetic diversity in genome-wide association studies of lipids

Towards a new developmental synthesis: adaptive developmental plasticity and human disease

artículo científico publicado en 2009

Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans

artículo científico publicado en 2006

Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India

artículo científico publicado en 2020

Variants in CPA1 are strongly associated with early onset chronic pancreatitis

artículo científico publicado en 2013

Vitamin B12 supplementation influences methylation of genes associated with Type 2 diabetes and its intermediate traits.

artículo científico publicado en 2017

What's there in a name: tropical calcific pancreatitis and idiopathic chronic pancreatitis in India

scientific article published on 27 October 2010

Lista de obras de Giriraj R Chandak

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India.

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

Altered methylation and expression patterns of genes regulating placental angiogenesis in preterm pregnancy.

Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians

Assessing the pathological relevance of SPINK1 promoter variants

Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model

Association between common polymorphism near the MC4R gene and obesity risk: a systematic review and meta-analysis.

Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes.

Association of cathepsin B gene polymorphisms with tropical calcific pancreatitis

Association of common genetic variants with lipid traits in the Indian population

Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.

Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs

Associations of autozygosity with a broad range of human phenotypes

Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis

Birth 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) cohort

Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism

Cardiac beriberi: often a missed diagnosis.

Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach

Chronic maternal vitamin B12 restriction induced changes in body composition & glucose metabolism in the Wistar rat offspring are partly correctable by rehabilitation

Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals.

Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians.

Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population.

Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population

Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk ⬇️

Comprehensive screening of chymotrypsin C (CTRC) gene in tropical calcific pancreatitis identifies novel variants ⬇️

Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia.

Directional dominance on stature and cognition in diverse human populations

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Evaluation of genetic markers linked to hemophilia A locus: an Indian experience

Evaluation of seven common lipid associated loci in a large Indian sib pair study

FTO gene variant and risk of hypertension: A meta-analysis of 57,464 hypertensive cases and 41,256 controls

FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians.

Fetus-in-fetu: a case report with molecular analysis

GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians

Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy ⬇️

Genetic and phenotypic heterogeneity in tropical calcific pancreatitis

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

H63D mutation in HFE gene is common in Indians and is associated with the European haplotype

High prevalence of infantile encephalitic beriberi with overlapping features of Leigh's disease.

High resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding region

Hypermethylated CpG sites in the MTR gene promoter in preterm placenta.

Identification and characterization of cis-regulatory elements 'insulator and repressor' in PPARD gene.

Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype

Identification of urinary proteins potentially associated with diabetic kidney disease.

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. ⬇️

Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy.

Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children.

Juvenile fibrocalculous pancreatopathy--a patient report.

LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signaling and other protein groups of regulatory functions.

Lack of replication of association of THSD7A with obesity

Maternal dietary folate and/or vitamin B12 restrictions alter body composition (adiposity) and lipid metabolism in Wistar rat offspring

Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis.

Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups.

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.

New insights from monogenic diabetes for "common" type 2 diabetes

No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations

Obscure pathogenesis of primary iron overload in Indians warrants more focused research

PPAR signaling pathway is a key modulator of liver proteome in pups born to vitamin B(12) deficient rats.

Relationship of APOA5, PPARγ and HL gene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Study of 11 BMI-associated loci identified in GWAS for associations with central obesity in the Chinese children

TCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatitis but may interact with SPINK1 and CTSB mutations in predicting diabetes.

The G191R variant in the PRSS2 gene does not play a role in protection against tropical calcific pancreatitis.

The genetic architecture of type 2 diabetes

The power of genetic diversity in genome-wide association studies of lipids

Towards a new developmental synthesis: adaptive developmental plasticity and human disease

Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans

Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India

Variants in CPA1 are strongly associated with early onset chronic pancreatitis

Vitamin B12 supplementation influences methylation of genes associated with Type 2 diabetes and its intermediate traits.

What's there in a name: tropical calcific pancreatitis and idiopathic chronic pancreatitis in India