CCMB

CSIR - Centre for Cellular & Molecular Biology

The Innovation Engine of India

G R Chandak

G R Chandak

G R Chandak

J C Bose Fellow
Genomic Research on Complex Diseases
+91-040-27192748
chandakgrc[at]ccmb[dot]res[dot]in

Research Interests

Our group is interested in understanding the genetic basis of complex disorders such as type 2 diabetes mellitus and chronic pancreatitis and its interaction with various environmental factors (epigenetic basis). The major focus is on identifying various genetic and nutritional factors (and interaction between them), which influence The Thin Fat Indian Phenotype, and various intermediate traits that predict higher risk of developing diabetes and metabolic syndrome. These determinants could be both maternal and fetal in origin and we believe that the variable clinical phenotype of these complex disorders in Indians has different genetic basis that is regulated differently and is programmed in-utero (Developmental Origins of Adult Common Diseases,). The larger goal is to have comprehensive knowledge of gene-gene and gene-nutrient interaction that will enable to alleviate and/or modulate the clinical course and complications of these disorders by modification of life style and diet, especially micronutrients.

Selected Publications

C S Yajnik, G R Chandak, C Joglekar, P Katre, D S Bhat, S N Singh, C S Janipalli, H Refsum, G Krishnaveni, S Veena, C Osmond, CHD Fall. Maternal homocysteine in pregnancy and offspring birthweight: Epidemiological associations and Mendelian randomizationanalysis. Int J Epidemiology 22 July 2014. Epub ahead of print. PMID: 25052622.
[Accompanied by Editorial Commentary, Sarah J Lewis (2014). “One-carbon metabolism has major implications for fetal growth and development beyond neural tube defects” Int. J. of Epidemiol., 1-2 doi: 10.1093/ije/dyu175].

Heiko Witt, Sebastian Beer, Jonas Rosendahl, Jian-Min Chen, GirirajRatanChandak, et al. Loss-of-function mutations in CPA1 are strongly associated with early-onset chronic pancreatitis. Nature Genetics 2013 Oct;45(10):1216-20. doi: 10.1038/ng.2730. Epub 2013 Aug 18.

Ganesh Chauhan, Charles J Spurgeon, 12 more authors and G R Chandak (2010). Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC3018, HHEX, CDKN2A, IGF2BP2 AND CDKAL1 on the risk of type 2 diabetes in 5148 Indians. Diabetes ;59(8):2068-74.

P D Gluckman, P Bateson, A S Beedle, Z A Bhutta, M A Hanson, C Law, K V Anokhin, P Bougneres, G R Chandak, P Dasupta, G D Smith, P T Ellison, T Forrester, S F Gilbert, E Jablonka, H Kaplan, A M Prentice, S J Simpson, R Uauy & M J West-Eberhard (2009).”Development and human disease – a synthesis of evolutionary, medical, anthropological, and economic perspectives”. Lancet 373(9675):1654-1657.

G R Chandak, C S Janipalli, S Bhaskar, S R Kulkarni, P Mohankrishna, A T Hattersley, T M Frayling, C S Yajnik (2007). Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population. Diabetologia50(1):63-67.

[This paper is accompanied by an Editorial Commentary, Zeggini E and McCarthy MI “TCF7L2: the biggest story in diabetes genetics since HLA ?” Diabetologia 50: 1-4.]
DEEP Project Network

Education & Experience

P.G:

Biochemistry ; Banaras Hindu University ; 1993

Ph.D:

Genetic basis of tropical calcific pancreatitis ; Osmania University ; 2009

Post.Doc:

Disease Genomics ; CSIR-CCMB ; 1994-96

Experience:
  • 2016 onwards Scientist F Centre for Cellular and Molecular Biology, Hyderabad, India
  • 2015-2016 Director(On lien) Centre for DNA Fingerprinting & Diagnostics, Hyderabad, India
  • 2011-2015 Scientist F Centre for Cellular and Molecular Biology, Hyderabad, India
  • 2006-2011 Scientist EII Centre for Cellular and Molecular Biology, Hyderabad, India
  • 2003-2006 Scientist EI (Merit) Centre for Cellular and Molecular Biology, Hyderabad, India
  • 1999-2003 Scientist C Centre for Cellular and Molecular Biology, Hyderabad, India
  • 1996-1999 Scientist III Centre for DNA Fingerprinting & Diagnostics, Hyderabad, India

Team Members

team-members-pic
G R Chandak
G R Chandak

J C Bose Fellow

J C Bose Fellow

P Ashok
P Ashok

Lab Attendant(2)

Lab Attendant(2)

Seema Bhaskar
Seema Bhaskar

Project Manager

Project Manager

Suraj Singh Nongmaithem
Suraj Singh Nongmaithem

Project Scientist-II

Project Scientist-II

Sumit Paliwal
Sumit Paliwal

Project Scientist-II

Project Scientist-II

Sara Sajjadi
Sara Sajjadi

Senior Research Fellow

Senior Research Fellow

Swati Bayyana
Swati Bayyana

Senior Research Fellow

Senior Research Fellow

Alagu Sankareswaran
Alagu Sankareswaran

Senior Project Associate

Senior Project Associate

Sohail Rafik Mansuri
Sohail Rafik Mansuri

Senior Research Fellow(CSIR)

Senior Research Fellow(CSIR)

Manisha Arumalla
Manisha Arumalla

Project Associate - II

Project Associate - II

P S K D B Punya Sri
P S K D B Punya Sri

Project Assistant

Project Assistant

Archana D
Archana D

Project Associate-I

Project Associate-I

Jukanti Akshitha
Jukanti Akshitha

Project Associate-I

Project Associate-I

Dimple Lavanuru
Dimple Lavanuru

Project Associate-I

Project Associate-I

Pranavi Garimella
Pranavi Garimella

Project Assistant

Project Assistant

Patents

Invention

Countries of Filing

Application Number

Publication Number

Status

Grant Number


A kit for detection of mutations causing genetic disorders using unprocessed blood or dried blood spot
India
201911038617
Filed
Under process
A kit for detection of mutations causing genetic disorders using unprocessed blood or dried blood spot
PCT
PCT/IN2020/050189
Filed
Under process

Publications

Title

Journal

Year

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries
Lancet Diabetes and Endocrinology
2026
Burden of MASLD and liver fibrosis: evidence from Phenome India cohort
Lancet Reg Health Southeast Asia
2026
Plasma proteome signatures in sickle cell anaemia and effect of hydroxyurea treatment
medRxiv (Preprint)
2026
Performance of a Type 1 Diabetes Genetic Risk Score in a Multicentric Study from India and its Implications in Clinical Practice
medRxiv (Preprint)
2026
Development of a Clinical Severity Score for Indian Sickle Cell Anaemia Patients
eJHaem
2026
Unveiling the burden of MASLD and liver fibrosis in India: Novel insights from the phenome India study into fibrosis without MASLD
medRxiv
2025
Sickle cell allele distribution in southern India: a population-based study in a rural–tribal context
BMJ Public health
2025
Anaemia and iron deficiency in India: a venous blood-based survey of adolescents, adults, and the elderly in eight states.
Eur J Clin Nutr.
2025
Investigating misclassification of type 1 diabetes in a population-based cohort of British Pakistanis and Bangladeshis using polygenic risk scores.
Sci Rep
2025
HLA haplotype diversity, islet autoantibody status and discriminative ability of type 1 diabetes genetic risk score in Indians.
Diabet Med
2025
Cardiometabolic Risk factors among adults in rural, urban, and urban slum population in eight states of India.
Indian Heart J.
2025
Polygenic prediction of body mass index and obesity through the life course and across ancestries
Nat Med
2025
Maternal age is related to offspring DNA methylation: a meta-analysis of results from the PACE consortium
Aging Cell (Accpted)
2024
Anaemia and iron deficiency in India: a venous blood-based survey of adolescents, adults, and the elderly in eight states
European Journal of Clinical Nutrition (Accepted)
2024
Investigating misclassification of type 1 diabetes in a population- based cohort of British Pakistanis and Bangladeshis using polygenic risk scores
Scientific Reports (Accepted)
2024
Maternal peri-conceptional vitamin B12 deficiency in Wistar rats leads to sex-specific programming for cardiometabolic disease risk in the next generationÂ
The Journal of Nutrition (Accepted)
2023
Genetic architecture of adiposity measures among Asians: Findings from GWAS
Annals of Human Genetics
2023
DNA methylation at the suppressor of cytokine signaling 3 (SOCS3) gene influences height in childhood
Nature Communications (Accepted)
2023
Differential expression of genes influencing mitotic processes in cord blood mononuclear cells after a pre-conceptional micronutrient-based randomised controlled trial: Pune Rural Intervention in Young Adolescents (PRIYA).
J Dev Orig Health Dis. 2023, doi: 10.1017/S204017442200068X
2023
Hypoxia Inducible factors (HIF1α and HIF3α) are differentially methylated in preeclampsia placentae and are associated with birth outcomes
Molecular and Cellular Biochemistry (Accepted)
2023
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome Biology
2022
A saturated map of common genetic vatiants associate with human height from 5.4 million individuals of diverse ancestries.
Nature. 2022 Oct;610(7933):704-712
2022
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome Biology (Accepted)
2022
The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitis
Pancreatology
2022
DNA methylation at the suppressor of cytokine signaling 3 (SOCS3) gene influences height in childhood
bioRxiv
2022
Differential expression of genes influence mitotic processes in cord blood mononuclear cells after a pre-conceptional micronutrient-based randomized controlled trial: Pune Rural Intervention in Young Adolescents (PRIYA)
medRxiv
2022
Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo
Nucleic Acids Res
2022
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
Am J Hum Genet
2022
Evaluation of pharmacological efficacy and safety of Hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India
Pediatric Hematology and Oncology
2022
Association of placental fatty acid desaturase 2 (FADS2) methylation with maternal fatty acid levels in women with preeclampsia
Prostaglandins, Leukotrienes and Essential Fatty Acids(Accepted)
2022
Sexual dimorphism in the relationship between brain complexity, volume and general intelligence (g): a cross-cohort study
Scientific Reports
2022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Nat Genet. 2022 May;54(5):560-572. doi: 10.1038/s41588-022-01058-3. Epub 2022 May 12.
2022
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Commun Biol. 2022 May 5;5(1):441. doi: 10.1038/s42003-022-03404-x.
2022
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Commun Biol. 2022 Apr 7;5(1):329. doi: 10.1038/s42003-022-03248-5.
2022
Environmentally sensitive hotspots in the methylome of the early human embryo
Elife. 2022 Feb 21;11:e72031. doi: 10.7554/eLife.72031.
2022
Babies of South Asian and European Ancestry Show Similar Associations With Genetic Risk Score for Birth Weight Despite the Smaller Size of South Asian Newborns
Diabetes. 2022 Apr 1;71(4):821-836. doi: 10.2337/db21-0479.
2022
DNA methylation signatures associated with cardiometabolic risk factors in children from India and The Gambia: results from the EMPHASIS study
Clin Epigenetics. 2022 Jan 9;14(1):6. doi: 10.1186/s13148-021-01213-3.
2022
Placental growth factor?and Fms related tyrosine kinase-1?are hypomethylated in preeclampsia placentae
Epigenomics. 2021 Feb;13(4):257-269. doi: 10.2217/epi-2020-0318. Epub 2021 Jan 20.
2021
Protocol for a cluster randomised trial evaluating a multifaceted intervention starting preconceptionally-Early Interventions to Support Trajectories for Healthy Life in India (EINSTEIN): a Healthy Life Trajectories Initiative (HeLTI) Study
BMJ Open. 2021 Feb 16;11(2):e045862. doi: 10.1136/bmjopen-2020-045862.
2021
Rapid and accurate nucleobase detection using FnCas9 and its application in COVID-19 diagnosis
Biosens Bioelectron. 2021 Jul 1;183:113207. doi: 10.1016/j.bios.2021.113207. Epub 2021 Apr 5.
2021
Insights from a Pan India Sero-Epidemiological survey (Phenome-India Cohort) for SARS-CoV2
Elife. 2021 Apr 20;10:e66537. doi: 10.7554/eLife.66537.
2021
Size at birth, lifecourse factors, and cognitive function in late life: findings from the MYsore study of Natal effects on Ageing and Health (MYNAH) cohort in South India
Int Psychogeriatr. 2021 Oct 20:1-14. doi: 10.1017/S1041610221001186. Online ahead of print.
2021
The power of genetic diversity in genome-wide association studies of lipids
Nature. 2021 Dec;600(7890):675-679. doi: 10.1038/s41586-021-04064-3. Epub 2021 Dec 9.
2021
Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach
PLoS One. 2020 Jan 29;15(1):e0228269. doi: 10.1371/journal.pone.0228269. eCollection 2020.
2020
Maternal vitamin B(12) deficiency in rats alters DNA methylation in metabolically important genes in their offspring
Mol Cell Biochem. 2020 May;468(1-2):83-96. doi: 10.1007/s11010-020-03713-x. Epub 2020 Mar 18.
2020
Novel p.P298L SURF1 mutation in thiamine deficient Leigh syndrome patients compromises cytochrome c oxidase activity
Mitochondrion. 2020 Jul;53:91-98. doi: 10.1016/j.mito.2020.04.009. Epub 2020 May 4.
2020
Type 1 diabetes genetic risk score is discriminative of diabetes in non-Europeans: evidence from a study in India
Sci Rep. 2020 Jun 11;10(1):9450. doi: 10.1038/s41598-020-65317-1.
2020
Periconceptional environment predicts leukocyte telomere length in a cross-sectional study of 7-9 year old rural Gambian children
Sci Rep. 2020 Jun 15;10(1):9675. doi: 10.1038/s41598-020-66729-9.
2020
Genetic Architecture of Parkinson\'s Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson\'s Disease Research
Front Neurol. 2020 Jun 18;11:524. doi: 10.3389/fneur.2020.00524. eCollection 2020.
2020
Effect of maternal preconceptional and pregnancy micronutrient interventions on children\'s DNA methylation: Findings from the EMPHASIS study
Am J Clin Nutr. 2020 Oct 1;112(4):1099-1113. doi: 10.1093/ajcn/nqaa193.
2020
Protease-Sensitive Pancreatic Lipase Variants Are Associated With Early Onset Chronic Pancreatitis
Am J Gastroenterol. 2019 Jun;114(6):974-983. doi: 10.14309/ajg.0000000000000051.
2019
The REVAMP study: research exploring various aspects and mechanisms in preeclampsia: study protocol
BMC Pregnancy Childbirth. 2019 Aug 23;19(1):308. doi: 10.1186/s12884-019-2450-0.
2019
Associations of autozygosity with a broad range of human phenotypes
Nat Commun. 2019 Oct 31;10(1):4957. doi: 10.1038/s41467-019-12283-6.
2019
Vitamin B(12) supplementation influences methylation of genes associated with Type 2 diabetes and its intermediate traits
Epigenomics. 2018 Jan;10(1):71-90. doi: 10.2217/epi-2017-0102. Epub 2017 Nov 14.
2018
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Sci Data. 2018 Jan 23;5:180002. doi: 10.1038/sdata.2018.2.
2018
Identification and characterization of cis-regulatory elements \'insulator and repressor\' in PPARD gene
Epigenomics. 2018 May;10(5):613-627. doi: 10.2217/epi-2017-0139. Epub 2018 Mar 27.
2018
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
Int J Epidemiol. 2018 Dec 1;47(6):1910-1937. doi: 10.1093/ije/dyy153.
2018
Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians
Blood Cells Mol Dis. 2018 Nov;73:14-21. doi: 10.1016/j.bcmd.2018.08.003. Epub 2018 Aug 27.
2018
GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians
Hum Mol Genet. 2017 Jul 1;26(13):2551-2564. doi: 10.1093/hmg/ddx071.
2017
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
Diabetes. 2017 Jul;66(7):2019-2032. doi: 10.2337/db16-1329. Epub 2017 Mar 24.
2017
GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians
Hum Mol Genet. 2017 Jul 1;26(13):2589. doi: 10.1093/hmg/ddx156.
2017
Identification of a functional enhancer variant within the chronic pancreatitis-associated SPINK1 c.101A>G (p.Asn34Ser)-containing haplotype
Hum Mutat. 2017 Aug;38(8):1014-1024. doi: 10.1002/humu.23269. Epub 2017 Jun 15.
2017
Hypermethylated CpG sites in the MTR gene promoter in preterm placenta
Epigenomics. 2017 Jul;9(7):985-996. doi: 10.2217/epi-2016-0173. Epub 2017 Jun 15.
2017
Inclusion of Population-specific Reference Panel from India to the 1000 Genomes Phase 3 Panel Improves Imputation Accuracy
Sci Rep. 2017 Jul 27;7(1):6733. doi: 10.1038/s41598-017-06905-6.
2017
Protocol for the EMPHASIS study; epigenetic mechanisms linking maternal pre-conceptional nutrition and children\'s health in India and Sub-Saharan Africa
BMC Nutr. 2017 Oct 30;3:81. doi: 10.1186/s40795-017-0200-0.
2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
Sci Data. 2017 Dec 19;4:170179. doi: 10.1038/sdata.2017.179.
2017
Association Analysis of PRSS1-PRSS2 and CLDN2-MORC4 Variants in Nonalcoholic Chronic Pancreatitis Using Tropical Calcific Pancreatitis as Model
Pancreas. 2016 Sep;45(8):1153-7. doi: 10.1097/MPA.0000000000000608.
2016
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Nat Commun. 2016 Jan 21;7:10023. doi: 10.1038/ncomms10023.
2016
Lack of replication of association of THSD7A with obesity
Int J Obes (Lond). 2016 Apr;40(4):725-6. doi: 10.1038/ijo.2016.15. Epub 2016 Feb 23.
2016
No Association Between CEL-HYB Hybrid Allele and Chronic Pancreatitis in Asian Populations
Gastroenterology. 2016 Jun;150(7):1558-1560.e5. doi: 10.1053/j.gastro.2016.02.071. Epub 2016 Mar 3.
2016
The genetic architecture of type 2 diabetes
Nature. 2016 Aug 4;536(7614):41-47. doi: 10.1038/nature18642. Epub 2016 Jul 11.
2016
Identification of urinary proteins potentially associated with diabetic kidney disease
Indian J Nephrol. 2016 Nov-Dec;26(6):434-445. doi: 10.4103/0971-4065.176144.
2016
New genetic loci link adipose and insulin biology to body fat distribution
Nature. 2015 Feb 12;518(7538):187-196. doi: 10.1038/nature14132.
2015
Genetic studies of body mass index yield new insights for obesity biology
Nature. 2015 Feb 12;518(7538):197-206. doi: 10.1038/nature14177.
2015
Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups
J Proteomics. 2015 Sep 8;127(Pt A):178-84. doi: 10.1016/j.jprot.2015.04.035. Epub 2015 May 14.
2015
Directional dominance on stature and cognition in?diverse human populations
Nature. 2015 Jul 23;523(7561):459-462. doi: 10.1038/nature14618. Epub 2015 Jul 1.
2015
New insights from monogenic diabetes for \"common\" type 2 diabetes
Front Genet. 2015 Aug 7;6:251. doi: 10.3389/fgene.2015.00251. eCollection 2015.
2015
Intrauterine Programming of Diabetes and Adiposity
Curr Obes Rep. 2015 Dec;4(4):418-28. doi: 10.1007/s13679-015-0175-6.
2015
Association of common variants in/near six genes (ATP2B1, CSK, MTHFR, CYP17A1, STK39 and FGF5) with blood pressure/hypertension risk in Chinese children
J Hum Hypertens. 2014 Jan;28(1):32-6. doi: 10.1038/jhh.2013.50. Epub 2013 Jun 13.
2014
Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis
Clin Endocrinol (Oxf). 2014 Nov;81(5):702-10. doi: 10.1111/cen.12428. Epub 2014 Mar 13.
2014
FTO gene variant and risk of hypertension: a meta-analysis of 57,464 hypertensive cases and 41,256 controls
Metabolism. 2014 May;63(5):633-9. doi: 10.1016/j.metabol.2014.02.008. Epub 2014 Feb 17.
2014
Altered methylation and expression patterns of genes regulating placental angiogenesis in preterm pregnancy
Reprod Sci. 2014 Dec;21(12):1508-17. doi: 10.1177/1933719114532838. Epub 2014 May 6.
2014
Association of common genetic variants with lipid traits in the Indian population
PLoS One. 2014 Jul 3;9(7):e101688. doi: 10.1371/journal.pone.0101688. eCollection 2014.
2014
Maternal homocysteine in pregnancy and offspring birthweight: epidemiological associations and Mendelian randomization analysis
Int J Epidemiol. 2014 Oct;43(5):1487-97. doi: 10.1093/ije/dyu132. Epub 2014 Jul 22.
2014
Chronic maternal vitamin B12 restriction induced changes in body composition & glucose metabolism in the Wistar rat offspring are partly correctable by rehabilitation
PLoS One. 2014 Nov 14;9(11):e112991. doi: 10.1371/journal.pone.0112991. eCollection 2014.
2014
Genetic and phenotypic heterogeneity in tropical calcific pancreatitis
World J Gastroenterol. 2014 Dec 14;20(46):17314-23. doi: 10.3748/wjg.v20.i46.17314.
2014
Comprehensive screening of chymotrypsin C (CTRC) gene in tropical calcific pancreatitis identifies novel variants
Gut. 2013 Nov;62(11):1602-6. doi: 10.1136/gutjnl-2012-302448. Epub 2012 May 12.
2013
Maternal dietary folate and/or vitamin B12 restrictions alter body composition (adiposity) and lipid metabolism in Wistar rat offspring
J Nutr Biochem. 2013 Jan;24(1):25-31. doi: 10.1016/j.jnutbio.2012.01.004. Epub 2012 Jun 14.
2013
Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk
Gut. 2013 Nov;62(11):1616-24. doi: 10.1136/gutjnl-2012-303090. Epub 2012 Sep 1.
2013
Migration and DNA methylation: a comparison of methylation patterns in type 2 diabetes susceptibility genes between indians and europeans
J Diabetes Res Clin Metab. 2013;2:6. doi: 10.7243/2050-0866-2-6. Epub 2013 Feb 6.
2013
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs
PLoS One. 2013;8(1):e53944. doi: 10.1371/journal.pone.0053944. Epub 2013 Jan 17.
2013
Study of 11 BMI-associated loci identified in GWAS for associations with central obesity in the Chinese children
PLoS One. 2013;8(2):e56472. doi: 10.1371/journal.pone.0056472. Epub 2013 Feb 12.
2013
STK39 polymorphism is associated with essential hypertension: a systematic review and meta-analysis
PLoS One. 2013;8(3):e59584. doi: 10.1371/journal.pone.0059584. Epub 2013 Mar 18.
2013
Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children
Am J Hypertens. 2013 Aug;26(8):990-6. doi: 10.1093/ajh/hpt046. Epub 2013 Apr 16.
2013
Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia
Clin Epigenetics. 2013 Apr 26;5(1):6. doi: 10.1186/1868-7083-5-6.
2013
PPAR signaling pathway is a key modulator of liver proteome in pups born to vitamin B(12) deficient rats
J Proteomics. 2013 Oct 8;91:297-308. doi: 10.1016/j.jprot.2013.07.027. Epub 2013 Aug 6.
2013
Variants in CPA1 are strongly associated with early onset chronic pancreatitis
Nat Genet. 2013 Oct;45(10):1216-20. doi: 10.1038/ng.2730. Epub 2013 Aug 18.
2013
Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians
Diabet Med. 2012 Jan;29(1):121-7. doi: 10.1111/j.1464-5491.2011.03438.x.
2012
Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs
Diabetologia. 2012 Feb;55(2):349-57. doi: 10.1007/s00125-011-2355-6. Epub 2011 Nov 4.
2012
Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians
Diabetologia. 2012 Apr;55(4):981-95. doi: 10.1007/s00125-011-2370-7. Epub 2011 Nov 23.
2012
LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signaling and other protein groups of regulatory functions
Mol Cell Proteomics. 2012 Jun;11(6):M111.013565. doi: 10.1074/mcp.M111.013565. Epub 2012 Jan 4.
2012
Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population
J Hum Genet. 2012 Mar;57(3):184-90. doi: 10.1038/jhg.2011.150. Epub 2012 Jan 26.
2012
High resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding region
PLoS One. 2012;7(2):e31621. doi: 10.1371/journal.pone.0031621. Epub 2012 Feb 15.
2012
Presence of strong association of the major histocompatibility complex (MHC) class I allele HLA-A*26:01 with idiopathic hypoparathyroidism
J Clin Endocrinol Metab. 2012 Sep;97(9):E1820-4. doi: 10.1210/jc.2012-1328. Epub 2012 Jun 20.
2012
Common polymorphism near the MC4R gene is associated with type 2 diabetes: data from a meta-analysis of 123,373 individuals
Diabetologia. 2012 Oct;55(10):2660-2666. doi: 10.1007/s00125-012-2655-5. Epub 2012 Aug 7.
2012
Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy
Mol Vis. 2012;18:2022-32. Epub 2012 Jul 20.
2012
H63D mutation in HFE gene is common in Indians and is associated with the European haplotype
J Genet. 2012 Aug;91(2):229-32. doi: 10.1007/s12041-012-0163-5.
2012
Proteins with altered levels in plasma from glioblastoma patients as revealed by iTRAQ-based quantitative proteomic analysis
PLoS One. 2012;7(9):e46153. doi: 10.1371/journal.pone.0046153. Epub 2012 Sep 28.
2012
Association between common polymorphism near the MC4R gene and obesity risk: a systematic review and meta-analysis
PLoS One. 2012;7(9):e45731. doi: 10.1371/journal.pone.0045731. Epub 2012 Sep 25.
2012
Evaluation of seven common lipid associated loci in a large Indian sib pair study
Lipids Health Dis. 2012 Nov 14;11:155. doi: 10.1186/1476-511X-11-155.
2012
What\'s there in a name: tropical calcific pancreatitis and idiopathic chronic pancreatitis in India
Gut. 2011 Oct;60(10):1440-1; author reply 1441-2. doi: 10.1136/gut.2010.228452. Epub 2010 Oct 27.
2012
Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians
J Gastroenterol Hepatol. 2011 Apr;26(4):694-9. doi: 10.1111/j.1440-1746.2010.06533.x.
2011
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Hum Mol Genet. 2011 Jun 1;20(11):2273-84. doi: 10.1093/hmg/ddr092. Epub 2011 Mar 4.
2011
Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes
Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):507-12. doi: 10.1089/gtmb.2010.0207. Epub 2011 Mar 25.
2011
Relationship of APOA5, PPAR? and HL gene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood
Lipids Health Dis. 2011 May 8;10:68. doi: 10.1186/1476-511X-10-68.
2011
Glioblastoma cell secretome: analysis of three glioblastoma cell lines reveal 148 non-redundant proteins
J Proteomics. 2011 Sep 6;74(10):1918-25. doi: 10.1016/j.jprot.2011.05.002. Epub 2011 May 11.
2011
Assessing the pathological relevance of SPINK1 promoter variants
Eur J Hum Genet. 2011 Oct;19(10):1066-73. doi: 10.1038/ejhg.2011.79. Epub 2011 May 25.
2011
A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India
Haemophilia. 2011 Sep;17(5):e928-35. doi: 10.1111/j.1365-2516.2011.02584.x. Epub 2011 Jun 22.
2011
Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India
Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):848-56. doi: 10.1002/bdra.20841. Epub 2011 Jul 18.
2011
Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier
J Obes. 2011;2011:307542. doi: 10.1155/2011/307542. Epub 2011 May 17.
2011
Obscure pathogenesis of primary iron overload in Indians warrants more focused research
Indian J Gastroenterol. 2011 Jul;30(4):154-5. doi: 10.1007/s12664-011-0119-3. Epub 2011 Aug 17.
2011
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Nature. 2011 Sep 11;478(7367):103-9. doi: 10.1038/nature10405.
2011
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Nat Genet. 2011 Oct 16;43(11):1131-8. doi: 10.1038/ng.970.
2011
Cardiac beriberi: often a missed diagnosis
J Trop Pediatr. 2010 Aug;56(4):284-5. doi: 10.1093/tropej/fmp108. Epub 2009 Nov 24.
2010
Low prevalence of GJB2 mutations in non-syndromic hearing loss in Western India
Indian J Otolaryngol Head Neck Surg. 2010 Jan;62(1):60-3. doi: 10.1007/s12070-010-0009-5. Epub 2010 Jun 4.
2010
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
Diabetes. 2010 Aug;59(8):2068-74. doi: 10.2337/db09-1386. Epub 2010 Apr 27.
2010
EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda
Proc Natl Acad Sci U S A. 2010 Nov 2;107(44):18961-6. doi: 10.1073/pnas.1006108107. Epub 2010 Oct 18.
2010
FTO gene variants are strongly associated with type 2 diabetes in South Asian Indians
Diabetologia. 2009 Feb;52(2):247-52. doi: 10.1007/s00125-008-1186-6. Epub 2008 Nov 13.
2009
Genetic mechanisms underlying the pathogenesis of tropical calcific pancreatitis
World J Gastroenterol. 2009 Jan 21;15(3):264-9. doi: 10.3748/wjg.15.264.
2009
Towards a new developmental synthesis: adaptive developmental plasticity and human disease
Lancet. 2009 May 9;373(9675):1654-7. doi: 10.1016/S0140-6736(09)60234-8.
2009
The G191R variant in the PRSS2 gene does not play a role in protection against tropical calcific pancreatitis
Gut. 2009 Jun;58(6):881-2. doi: 10.1136/gut.2008.170753.
2009
Trypsinogen copy number mutations in patients with idiopathic chronic pancreatitis
Clin Gastroenterol Hepatol. 2008 Jan;6(1):82-8. doi: 10.1016/j.cgh.2007.10.004. Epub 2007 Dec 11.
2008
High prevalence of infantile encephalitic beriberi with overlapping features of Leigh\'s disease
J Trop Pediatr. 2008 Oct;54(5):328-32. doi: 10.1093/tropej/fmn031. Epub 2008 May 8.
2008
Genetic landscape of the people of India: a canvas for disease gene exploration
J Genet. 2008 Apr;87(1):3-20. doi: 10.1007/s12041-008-0002-x.
2008
TCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatitis but may interact with SPINK1 and CTSB mutations in predicting diabetes
BMC Med Genet. 2008 Aug 16;9:80. doi: 10.1186/1471-2350-9-80.
2008
Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population
Diabetologia. 2007 Jan;50(1):63-7. doi: 10.1007/s00125-006-0502-2. Epub 2006 Nov 9.
2008
Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India
World J Gastroenterol. 2007 Jun 7;13(21):2956-9. doi: 10.3748/wjg.v13.i21.2956.
2007
Comprehensive screening for reg1alpha gene rules out association with tropical calcific pancreatitis
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2007
Evaluation of genetic markers linked to hemophilia A locus: an Indian experience
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2007
Association of cathepsin B gene polymorphisms with tropical calcific pancreatitis
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2006
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
Lipids Health Dis. 2006 May 2;5:11. doi: 10.1186/1476-511X-5-11.
2006
Juvenile fibrocalculous pancreatopathy--a patient report
J Pediatr Endocrinol Metab. 2006 Jul;19(7):947-50. doi: 10.1515/jpem.2006.19.7.947.
2006
A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients
BMC Med Genet. 2006 Sep 30;7:73. doi: 10.1186/1471-2350-7-73.
2006
Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans
BMC Med Genet. 2006 Oct 10;7:76. doi: 10.1186/1471-2350-7-76.
2006
Lack of significant association of an insertion/deletion polymorphism in the angiotensin converting enzyme (ACE) gene with tropical calcific pancreatitis
BMC Gastroenterol. 2006 Dec 12;6:42. doi: 10.1186/1471-230X-6-42.
2006
Remarkable variation in the informativeness of RFLP markers linked to hemophilia B locus in Indian population groups: implication in the strategy for carrier detection
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2006
Mutations in anionic trypsinogen gene are not associated with tropical calcific pancreatitis
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2005
Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy patients from India
Exp Mol Med. 2005 Jun 30;37(3):147-54. doi: 10.1038/emm.2005.20.
2005
Absence of PRSS1 mutations and association of SPINK1 trypsin inhibitor mutations in hereditary and non-hereditary chronic pancreatitis
Gut. 2004 May;53(5):723-8. doi: 10.1136/gut.2003.026526.
2004
Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients
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2004
Dystrophin gene deletions in South Indian Duchenne muscular dystrophy patients
Indian J Med Sci. 2003 Jan;57(1):1-6.
2003
Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis
J Med Genet. 2002 May;39(5):347-51. doi: 10.1136/jmg.39.5.347.
2002
Apolipoprotein E and presenilin-1 allelic variation and Alzheimer\'s disease in India
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2002
Sickle cell gene haplotypes in Relli and Thurpu Kapu populations of Andhra Pradesh
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2000
Fetus-in-fetu: a case report with molecular analysis
J Pediatr Surg. 1999 Apr;34(4):641-4. doi: 10.1016/s0022-3468(99)90095-7.
1999
Some atypical and rare sickle cell gene haplotypes in populations of Andhra Pradesh, India
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1999

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