2015
Ashutosh Singh Tomar, Divya Sri Priyanka Tallapragada, Suraj Singh Nongmaithem, Smeeta Shrestha, Chittaranjan S. Yajnik, Giriraj Ratan Chandak. Intrauterine Programming of Diabetes and Adiposity. Curr Obes Rep (2015); 4:418–428. doi:10.1007/s13679-015-0175-6
Divya Sri Priyanka Tallapragada, Seema Bhaskar, Giriraj R Chandak. New insights from monogenic diabetes for "common type 2 diabetes. Front Genet 2015; 6:251. doi: 10.3389/fgene.2015.00251
Shadab Ahmad, Trayambak Basak, K Anand Kumar, Gourav Bhardwaj, Lalitha A, Dilip K Yadav, Giriraj Ratan Chandak, Manchala Raghunath, Shantanu Sengupta. Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups. J Proteomics 2015 May 14. pii: S1874-3919(15)00235-3. doi: 10.1016/j.jprot.2015.04.035
Joshi PK, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 2015 Jul 23;523(7561):459-62. doi: 10.1038/nature14618
Locke AE, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015 Feb 12;518(7538):197-206. doi: 10.1038/nature14177.
(As part of the International Consortium, ICBP Consortium).
Shungin D et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 2015 Feb 12;518(7538):187-96. doi: 10.1038/nature14132.
(As part of the International Consortium, ICBP Consortium).
Mahajan A et al. Identification and functional characterisation of G6PC2 coding variants influencing glycemic traits defines effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 2015 Jan 27;11(1):e1004876. doi: 10.1371/journal.pgen.1004876
(As part of the International Consortium, T2D-GENES Consortium).
Divya Sri Priyanka Tallapragada, Seema Bhaskar, Giriraj R Chandak. New insights from monogenic diabetes for "common type 2 diabetes. Front Genet 2015; 6:251. doi: 10.3389/fgene.2015.00251
Shadab Ahmad, Trayambak Basak, K Anand Kumar, Gourav Bhardwaj, Lalitha A, Dilip K Yadav, Giriraj Ratan Chandak, Manchala Raghunath, Shantanu Sengupta. Maternal micronutrient deficiency leads to alteration in the kidney proteome in rat pups. J Proteomics 2015 May 14. pii: S1874-3919(15)00235-3. doi: 10.1016/j.jprot.2015.04.035
Joshi PK, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 2015 Jul 23;523(7561):459-62. doi: 10.1038/nature14618
Locke AE, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015 Feb 12;518(7538):197-206. doi: 10.1038/nature14177.
(As part of the International Consortium, ICBP Consortium).
Shungin D et al. New genetic loci link adipose and insulin biology to body fat distribution. Nature. 2015 Feb 12;518(7538):187-96. doi: 10.1038/nature14132.
(As part of the International Consortium, ICBP Consortium).
Mahajan A et al. Identification and functional characterisation of G6PC2 coding variants influencing glycemic traits defines effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 2015 Jan 27;11(1):e1004876. doi: 10.1371/journal.pgen.1004876
(As part of the International Consortium, T2D-GENES Consortium).
2014
Paliwal S, Bhaskar S, Chandak GR. Genetic and phenotypic heterogeneity in tropical calcific pancreatitis. World J Gastroenterol. 2014 Dec 14;20(46):17314-17323. Review.
Kumar KA, Lalitha A, Reddy U, Chandak GR, Sengupta S, Raghunath M. 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.
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 birth weight: Epidemiological associations and Mendelian randomization analysis. 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].
Walia GK, Gupta V, Aggarwal A, Asghar M, Dudbridge F, Timpson N, Singh NS, Kumar MR, Kinra S, Prabhakaran D, Reddy KS, Chandak GR, Smith GD, Ebrahim S. 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.
Deepali P Sundrani, Umakar S Reddy, Preeti M Chavan-Gautam, Savita S Mehendale, G R Chandak, Sadhana R Joshi. Altered methylation and expression patterns of genes regulating placental angiogenesis in preterm pregnancy. Reproductive Sciences. (Accepted for publication).
He D, Fu M, Miao S, Hotta K, Chandak GR, Xi B. FTO gene variant and risk of hypertension: A meta-analysis of 57,464 hypertensive cases and 41,256 controls. Metabolism. 2014 Feb 17. pii: S0026-0495(14)00047-X. doi: 10.1016/j.metabol.2014.02.008. [Epub ahead of print]
Xi B, Takeuchi F, Meirhaeghe A, Kato N, Chambers JC, Morris AP, Cho YS, Zhang W, Mohlke KL, Kooner JS, Shu XO, Pan H, Tai ES, Pan H, Wu JY, Zhou D, Chandak GR; DIAGRAM Consortium; AGEN-T2D Consortium; SAT2D Consortium. Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis. Clin Endocrinol (Oxf). 2014 Feb 16. doi: 10.1111/cen.12428. [Epub ahead of print].
2013
Heiko Witt, Sebastian Beer, Jonas Rosendahl, Jian-Min Chen, G R Chandak, et al. Loss-of-function mutations 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.
Shadab Ahmad, K Anand Kumar, Trayambak Basak, Gourav Bhardwaj, Dilip Yadav, A Lalitha, G R Chandak, Manchala Raghunath, Shantanu Sengupta. PPAR Signalling Pathway is a Key Modulator of Liver Proteome in Pups Born to B12 Deficient Rats. J Proteomics. 2013 Aug 6;91C:297-308. doi: 10.1016/j.jprot.2013.07.027. [Epub ahead of print]
Xi B, Shen Y, Zhao X, Chandak GR, Cheng H, Hou D, Li Y, Ott J, Zhang Y, Wang X, Mi J. 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. 2013 Jun 13. doi: 10.1038/jhh.2013.50. [Epub ahead of print]
Deepali P Sundrani, Umakar S Reddy, Asmita A Joshi, Savita S, Mehendale, Preeti M Chavan-Gautam, Anandwardhan A Hardikar, GR Chandak and Sadhana R Joshi. Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia. Clinical Epigenetics 2013 Apr 26;5(1):6. doi: 10.1186/1868-7083-5-6
Xi B, Chen M, Chandak GR, Shen Y, Yan L, He J, et al.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
Bo Xi, Xiaoyuan Zhao, G R Chandak, Yue Shen, Hong Cheng, Dongqing Hou, Xingyu Wang, Jie Mi. Influence of Obesity on Association between Genetic Variants Identified by Genome-wide Association Studies and Hypertension Risk in Chinese Children. American Journal of Hypertension. Aug;26(8):990-6. doi: 10.1093/ajh/hpt046. Epub 2013 Mar 16.
Hannah R. Elliott, Gagandeep K. Walia, Aparna Duggirala, Alix Groom, S. Umakar Reddy, G R. Chandak, et al. Migration and DNA methylation: A comparison of methylation patterns in type 2 diabetes susceptibility genes between Indians and Europeans. J Diabetes Research and Clinical Metabolism 01/2013; 2. DOI:10.7243/2050-0866-2-6
Xi B, Cheng H, Shen Y, Chandak GR, Zhao X, Hou D, Wu L, Wang X, Mi J. 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.
Vipin Gupta, D G Vinay, Ulla Sovio, Sajjad Rafiq, M V Kranthi Kumar, C S Janipalli, D M Evans, K Radha Mani, M N Sandeep, A E Taylor, S Kinra, R M Sullivan, L Bowen, N J Timpson, George Davey Smith, Frank Dudbridge, Dorairaj Prabhakaran, Y Ben-Shlomo, K Srinath Reddy, Shah Ebrahim, G R Chandak, and Indian Migration Study Group. 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.
Shadab Ahmad, K Anand Kumar, Trayambak Basak, Gourav Bhardwaj, Dilip Yadav, A Lalitha, G R Chandak, Manchala Raghunath, Shantanu Sengupta. PPAR Signalling Pathway is a Key Modulator of Liver Proteome in Pups Born to B12 Deficient Rats. J Proteomics. 2013 Aug 6;91C:297-308. doi: 10.1016/j.jprot.2013.07.027. [Epub ahead of print]
Xi B, Shen Y, Zhao X, Chandak GR, Cheng H, Hou D, Li Y, Ott J, Zhang Y, Wang X, Mi J. 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. 2013 Jun 13. doi: 10.1038/jhh.2013.50. [Epub ahead of print]
Deepali P Sundrani, Umakar S Reddy, Asmita A Joshi, Savita S, Mehendale, Preeti M Chavan-Gautam, Anandwardhan A Hardikar, GR Chandak and Sadhana R Joshi. Differential placental methylation and expression of VEGF, FLT-1 and KDR genes in human term and preterm preeclampsia. Clinical Epigenetics 2013 Apr 26;5(1):6. doi: 10.1186/1868-7083-5-6
Xi B, Chen M, Chandak GR, Shen Y, Yan L, He J, et al.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
Bo Xi, Xiaoyuan Zhao, G R Chandak, Yue Shen, Hong Cheng, Dongqing Hou, Xingyu Wang, Jie Mi. Influence of Obesity on Association between Genetic Variants Identified by Genome-wide Association Studies and Hypertension Risk in Chinese Children. American Journal of Hypertension. Aug;26(8):990-6. doi: 10.1093/ajh/hpt046. Epub 2013 Mar 16.
Hannah R. Elliott, Gagandeep K. Walia, Aparna Duggirala, Alix Groom, S. Umakar Reddy, G R. Chandak, et al. Migration and DNA methylation: A comparison of methylation patterns in type 2 diabetes susceptibility genes between Indians and Europeans. J Diabetes Research and Clinical Metabolism 01/2013; 2. DOI:10.7243/2050-0866-2-6
Xi B, Cheng H, Shen Y, Chandak GR, Zhao X, Hou D, Wu L, Wang X, Mi J. 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.
Vipin Gupta, D G Vinay, Ulla Sovio, Sajjad Rafiq, M V Kranthi Kumar, C S Janipalli, D M Evans, K Radha Mani, M N Sandeep, A E Taylor, S Kinra, R M Sullivan, L Bowen, N J Timpson, George Davey Smith, Frank Dudbridge, Dorairaj Prabhakaran, Y Ben-Shlomo, K Srinath Reddy, Shah Ebrahim, G R Chandak, and Indian Migration Study Group. 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.
2012
Rafiq S, Venkata KK, Gupta V, Guru VD, Spurgeon CJ, Parameshwaran S, Madana SN, Kinra S, Bowen L, Timpson NJ, Smith GD, Dudbridge F, Prabhakaran D, Ben-Shlomo Y, Reddy KS, Ebrahim S, Chandak GR. Evaluation of seven common lipid associated loci in a large Indian sib pair study. Lipids Health Dis. 2012 Nov 14;11(1):155. [Epub ahead of print]
Xi B, Chandak GR, Shen Y, Wang Q, Zhou D. 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.
Gautam P, Nair SC, Gupta MK, Sharma R, Polisetty RV, Uppin MS, Sundaram C, Puligopu AK, Ankathi P, Purohit AK, Chandak GR, Harsha HC, Sirdeshmukh R. 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.
Beer S, Zhou J, Szabó A, Keiles S, Chandak GR, Witt H, Sahin-Tóth M. Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk. Gut. 2012 Sep 1. [Epub ahead of print]
Dhillon BK, Prakash S, Chandak GR, Chawla YK, Das R. H63D mutation in HFE gene is common in Indians and is associated with the European haplotype. J Genet. 2012 Aug;91(2):229-32.
Kapoor S, Bindu PS, Taly AB, Sinha S, Gayathri N, Rani SV, Chandak GR, Kumar A. 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.
Xi B, Takeuchi F, Chandak GR, Kato N, Pan HW; AGEN-T2D Consortium, Zhou DH, Pan HY, Mi J. (2012).Common polymorphism near the MC4R gene is associated with type 2 diabetes: Data from meta-analysis of 123,373 individuals. Diabetologia. 2012 Oct;55(10):2660-6. doi: 10.1007/s00125-012-2655-5. Epub 2012 Aug 7.
Paliwal S, Bhaskar S, Mani KR, Reddy DN, Rao GV, Singh SP, Thomas V, Chandak GR. (2012). Comprehensive Screening of Chymotrypsin C (CTRC) Gene in Tropical Calcific Pancreatitis Identifies Novel Variants. Gut, May 12, Epub ahead of print.
Tabassum R, Mahajan A, Dwivedi OP, Chauhan G, Spurgeon CJ, Kumar MV, Ghosh S, Madhu SV, Mathur SK, Chandak GR, Tandon N, Bharadwaj D (2012). Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population. J Hum Genet. 57:184-90.
Kumar KA, Lalitha A, Pavithra D, Padmavathi IJ, Ganeshan M, Rao KR, Venu L, Balakrishna N, Shanker NH, Reddy SU, Chandak GR, Sengupta S, Raghunath M. (2012). Maternal Dietary Folate and/or Vitamin B12 Restriction alter body composition (Adiposity) and Lipid Metabolism in Wistar Rat Offspring. J Nutr Biochem. 2012, 24(1):25-31
Sati S, Tanwar VS, Kumar KA, Patowary A, Jain V, Ghosh S, Ahmad S, Singh M, Reddy SU, Chandak GR, Raghunath M, Sivasubbu S, Chakraborty K, Scaria V, Sengupta S (2012). High resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding region and alternative splice site. PLoS One. 2012;7(2):e31621. doi: 10.1371/journal.pone.0031621. Epub 2012 Feb 15.
Polisetty RV, Gautam P, Sharma R, Harsha HC, Nair SC, Gupta MK, Uppin MS, Challa S, Puligopu AK, Ankathi P, Purohit AK, Chandak GR, Pandey A, Sirdeshmukh R. (2012). LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signalling 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.
Xi B, Chandak GR, Shen Y, Wang Q, Zhou D. 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.
Gautam P, Nair SC, Gupta MK, Sharma R, Polisetty RV, Uppin MS, Sundaram C, Puligopu AK, Ankathi P, Purohit AK, Chandak GR, Harsha HC, Sirdeshmukh R. 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.
Beer S, Zhou J, Szabó A, Keiles S, Chandak GR, Witt H, Sahin-Tóth M. Comprehensive functional analysis of chymotrypsin C (CTRC) variants reveals distinct loss-of-function mechanisms associated with pancreatitis risk. Gut. 2012 Sep 1. [Epub ahead of print]
Dhillon BK, Prakash S, Chandak GR, Chawla YK, Das R. H63D mutation in HFE gene is common in Indians and is associated with the European haplotype. J Genet. 2012 Aug;91(2):229-32.
Kapoor S, Bindu PS, Taly AB, Sinha S, Gayathri N, Rani SV, Chandak GR, Kumar A. 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.
Xi B, Takeuchi F, Chandak GR, Kato N, Pan HW; AGEN-T2D Consortium, Zhou DH, Pan HY, Mi J. (2012).Common polymorphism near the MC4R gene is associated with type 2 diabetes: Data from meta-analysis of 123,373 individuals. Diabetologia. 2012 Oct;55(10):2660-6. doi: 10.1007/s00125-012-2655-5. Epub 2012 Aug 7.
Paliwal S, Bhaskar S, Mani KR, Reddy DN, Rao GV, Singh SP, Thomas V, Chandak GR. (2012). Comprehensive Screening of Chymotrypsin C (CTRC) Gene in Tropical Calcific Pancreatitis Identifies Novel Variants. Gut, May 12, Epub ahead of print.
Tabassum R, Mahajan A, Dwivedi OP, Chauhan G, Spurgeon CJ, Kumar MV, Ghosh S, Madhu SV, Mathur SK, Chandak GR, Tandon N, Bharadwaj D (2012). Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population. J Hum Genet. 57:184-90.
Kumar KA, Lalitha A, Pavithra D, Padmavathi IJ, Ganeshan M, Rao KR, Venu L, Balakrishna N, Shanker NH, Reddy SU, Chandak GR, Sengupta S, Raghunath M. (2012). Maternal Dietary Folate and/or Vitamin B12 Restriction alter body composition (Adiposity) and Lipid Metabolism in Wistar Rat Offspring. J Nutr Biochem. 2012, 24(1):25-31
Sati S, Tanwar VS, Kumar KA, Patowary A, Jain V, Ghosh S, Ahmad S, Singh M, Reddy SU, Chandak GR, Raghunath M, Sivasubbu S, Chakraborty K, Scaria V, Sengupta S (2012). High resolution methylome map of rat indicates role of intragenic DNA methylation in identification of coding region and alternative splice site. PLoS One. 2012;7(2):e31621. doi: 10.1371/journal.pone.0031621. Epub 2012 Feb 15.
Polisetty RV, Gautam P, Sharma R, Harsha HC, Nair SC, Gupta MK, Uppin MS, Challa S, Puligopu AK, Ankathi P, Purohit AK, Chandak GR, Pandey A, Sirdeshmukh R. (2012). LC-MS/MS analysis of differentially expressed glioblastoma membrane proteome reveals altered calcium signalling 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.
2011
Das R, Chandak GR. (2011). Obscure pathogenesis of primary iron overload in Indians warrants more focused research. Indian J Gastroenterol. 30(4):154-5.
Gupta V, Vinay DG, Rafiq S, Kranthikumar MV, Janipalli CS, Giambartolomei C, Evans DM, Mani KR, Sandeep MN, Taylor AE, Kinra S, Sullivan RM, Bowen L, Timpson NJ, Smith GD, Dudbridge F, Prabhakaran D, Ben-Shlomo Y, Reddy KS, Ebrahim S, Chandak GR; Indian Migration Study Group. (2012). Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs. Diabetologia. 2011 55(2):349-57.
Chambers JC, Zhang W, Sehmi J, Li X, Wass MN, Van der Harst P, Holm H, Sanna S, Kavousi M, Baumeister SE, Coin LJ, Deng G, Gieger C, et al. 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.
Li H, Kilpeläinen TO, Liu C, Zhu J, Liu Y, Hu C, Yang Z, Zhang W, Bao W, Cha S, Wu Y, Yang T, Sekine A, Choi BY, Yajnik CS, Zhou D, Takeuchi F, Yamamoto K, Chan JC, Mani KR, Been LF, Imamura M, Nakashima E, Lee N, Fujisawa T, Karasawa S, Wen W, Joglekar CV, Lu W, Chang Y, Xiang Y, Gao Y, Liu S, Song Y, Kwak SH, Shin HD, Park KS, Fall CH, Kim JY, Sham PC, Lam KS, Zheng W, Shu X, Deng H, Ikegami H, Krishnaveni GV, Sanghera DK, Chuang L, Liu L, Hu R, Kim Y, Daimon M, Hotta K, Jia W, Kooner JS, Chambers JC, Chandak GR, Ma RC, Maeda S, Dorajoo R, Yokota M, Takayanagi R, Kato N, Lin X, Loos RJ. (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 55(4):981-95.
ICBPGWAS consortium (2011). Genetic variants in novel pathways influence blood pressure and cardiovascular risk. Nature, 478(7367): 103-9.
C. S. Janipalli, M. V. Kranthi Kumar, D. G. Vinay, M. N. Sandeep, S. Bhaskar, S R. Kulkarni, M. Aruna, C V. Joglekar, S. Priyadharshini, Nidhi Maheshwari, C. S. Yajnik, G. R. Chandak (2012). 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. 29(1):121-7
K Godbole, T Gayathri, Smita Ghule, B V N Sasirekha, Amruta Kanitkar-Damle, Nilam Memane, S Suresh, Jayesh Sheth, C S Yajnik, G R Chandak (2011). Maternal One-Carbon Metabolism, MTHFR and TCN2 Genotype and Neural Tube Defects in India. Birth Defects Research Part A: Clinical and Molecular Teratology, 91(9):848-56.
Ravindra Varma Polisetty, Manoj Kumar Gupta, Sudha C. Nair, Kalidoss R, Shivani, Anjali Shiras, G R. Chandak, Ravi Sirdeshmukh (2011).Glioblastoma cell secretome: Proteins secreted by three glioblastoma cell lines reveal 148 non-redundant proteins. J Prot Res 74(10):1918-25.
Atreyee Saha, Subhashree Nayak, G R Chandak, Indian Genome Variation Consortium, Arijit Mukhopadhyay, Kunal Ray (2011). A set of five microsatellite markers linked to F8 gene can detect Hemophilia A carriers across India. Hemophilia. 17(5):e928-35
Arnaud Boulling, Heiko Witt, G R Chandak, Emmanuelle Masson, Sumit Paliwal, Seema Bhaskar, D. Nageshwar Reddy, David N. Cooper, Jian-Min Chen and Claude Férec (2011). Assessing the pathological relevance of SPINK1 promoter variants. Eur J Human Genetics, 19(10):1066-73.
Taylor AE, Sandeep, MN, Janipalli, CS, 15 more authors, Reddy KS, Ebrahim S, Chandak GR for the Indian Migration Study Group (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 Obesity 2011:307542. Epub 2011 May 17.
Ramakrishnan Lakshmy, Harshpal Singh Sachdev, 8 more authors, G R Chandak, Reddy Kolli Srinath, Bhargava Santhosh (2011). Relationship of APOA5, PPARγ andHLgene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood. Lipids Health Dis:10:68-75.
Bhaskar S, Ganesan M, Chandak GR, Mani R, Idris MM, Khaja N, Gulla S, Kumar U, Movva S, Vattam KK, Eppa K, Hasan Q, Pulakurthy UR (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. 15(7-8):507-12
Fox ER, Young JH, Li Y, Dreisbach AW, 20 more authors, Caulfield MJ, Ehret GB, Johnson T; The International Consortium for Blood Pressure Genome-wide Association Studies (ICBP-GWAS); CARDIoGRAM consortium; CKDGen consortium; KidneyGen consortium; EchoGen consortium; CHARGE-HF consortium, Chakravarti A, Zhu X, Levy D (2011). Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Hum Mol Genet;20:2273-84. Epub 2011 Mar 4.
Mahurkar S, Banerjee R, Rani VS, Thakur N, Venkat Rao G, Nageshwar Reddy D, Chandak GR(2011). Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians. J Gastroenterol Hepatol; 26:694-99.
Paliwal S, Bhaskar S, Rao GV, Reddy DN, Chandak GR (2011). What's there in a name: tropical calcific pancreatitis and idiopathic chronic pancreatitis in India. Gut. 10.1136/gut.2010.228452.
Gupta V, Vinay DG, Rafiq S, Kranthikumar MV, Janipalli CS, Giambartolomei C, Evans DM, Mani KR, Sandeep MN, Taylor AE, Kinra S, Sullivan RM, Bowen L, Timpson NJ, Smith GD, Dudbridge F, Prabhakaran D, Ben-Shlomo Y, Reddy KS, Ebrahim S, Chandak GR; Indian Migration Study Group. (2012). Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs. Diabetologia. 2011 55(2):349-57.
Chambers JC, Zhang W, Sehmi J, Li X, Wass MN, Van der Harst P, Holm H, Sanna S, Kavousi M, Baumeister SE, Coin LJ, Deng G, Gieger C, et al. 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.
Li H, Kilpeläinen TO, Liu C, Zhu J, Liu Y, Hu C, Yang Z, Zhang W, Bao W, Cha S, Wu Y, Yang T, Sekine A, Choi BY, Yajnik CS, Zhou D, Takeuchi F, Yamamoto K, Chan JC, Mani KR, Been LF, Imamura M, Nakashima E, Lee N, Fujisawa T, Karasawa S, Wen W, Joglekar CV, Lu W, Chang Y, Xiang Y, Gao Y, Liu S, Song Y, Kwak SH, Shin HD, Park KS, Fall CH, Kim JY, Sham PC, Lam KS, Zheng W, Shu X, Deng H, Ikegami H, Krishnaveni GV, Sanghera DK, Chuang L, Liu L, Hu R, Kim Y, Daimon M, Hotta K, Jia W, Kooner JS, Chambers JC, Chandak GR, Ma RC, Maeda S, Dorajoo R, Yokota M, Takayanagi R, Kato N, Lin X, Loos RJ. (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 55(4):981-95.
ICBPGWAS consortium (2011). Genetic variants in novel pathways influence blood pressure and cardiovascular risk. Nature, 478(7367): 103-9.
C. S. Janipalli, M. V. Kranthi Kumar, D. G. Vinay, M. N. Sandeep, S. Bhaskar, S R. Kulkarni, M. Aruna, C V. Joglekar, S. Priyadharshini, Nidhi Maheshwari, C. S. Yajnik, G. R. Chandak (2012). 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. 29(1):121-7
K Godbole, T Gayathri, Smita Ghule, B V N Sasirekha, Amruta Kanitkar-Damle, Nilam Memane, S Suresh, Jayesh Sheth, C S Yajnik, G R Chandak (2011). Maternal One-Carbon Metabolism, MTHFR and TCN2 Genotype and Neural Tube Defects in India. Birth Defects Research Part A: Clinical and Molecular Teratology, 91(9):848-56.
Ravindra Varma Polisetty, Manoj Kumar Gupta, Sudha C. Nair, Kalidoss R, Shivani, Anjali Shiras, G R. Chandak, Ravi Sirdeshmukh (2011).Glioblastoma cell secretome: Proteins secreted by three glioblastoma cell lines reveal 148 non-redundant proteins. J Prot Res 74(10):1918-25.
Atreyee Saha, Subhashree Nayak, G R Chandak, Indian Genome Variation Consortium, Arijit Mukhopadhyay, Kunal Ray (2011). A set of five microsatellite markers linked to F8 gene can detect Hemophilia A carriers across India. Hemophilia. 17(5):e928-35
Arnaud Boulling, Heiko Witt, G R Chandak, Emmanuelle Masson, Sumit Paliwal, Seema Bhaskar, D. Nageshwar Reddy, David N. Cooper, Jian-Min Chen and Claude Férec (2011). Assessing the pathological relevance of SPINK1 promoter variants. Eur J Human Genetics, 19(10):1066-73.
Taylor AE, Sandeep, MN, Janipalli, CS, 15 more authors, Reddy KS, Ebrahim S, Chandak GR for the Indian Migration Study Group (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 Obesity 2011:307542. Epub 2011 May 17.
Ramakrishnan Lakshmy, Harshpal Singh Sachdev, 8 more authors, G R Chandak, Reddy Kolli Srinath, Bhargava Santhosh (2011). Relationship of APOA5, PPARγ andHLgene variants with serial changes in childhood body mass index and coronary artery disease risk factors in young adulthood. Lipids Health Dis:10:68-75.
Bhaskar S, Ganesan M, Chandak GR, Mani R, Idris MM, Khaja N, Gulla S, Kumar U, Movva S, Vattam KK, Eppa K, Hasan Q, Pulakurthy UR (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. 15(7-8):507-12
Fox ER, Young JH, Li Y, Dreisbach AW, 20 more authors, Caulfield MJ, Ehret GB, Johnson T; The International Consortium for Blood Pressure Genome-wide Association Studies (ICBP-GWAS); CARDIoGRAM consortium; CKDGen consortium; KidneyGen consortium; EchoGen consortium; CHARGE-HF consortium, Chakravarti A, Zhu X, Levy D (2011). Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Hum Mol Genet;20:2273-84. Epub 2011 Mar 4.
Mahurkar S, Banerjee R, Rani VS, Thakur N, Venkat Rao G, Nageshwar Reddy D, Chandak GR(2011). Common variants in NOD2 and IL23R are not associated with inflammatory bowel disease in Indians. J Gastroenterol Hepatol; 26:694-99.
Paliwal S, Bhaskar S, Rao GV, Reddy DN, Chandak GR (2011). What's there in a name: tropical calcific pancreatitis and idiopathic chronic pancreatitis in India. Gut. 10.1136/gut.2010.228452.
2010
Aggarwal S, Negi S, Jha P, Singh PK, 5 more authors; Indian Genome Variation Consortium, Prasher B, Mukerji M (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; 107:18961-66.
Response to: 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(9):e16.
Ganesh Chauhan, Charles J Spurgeon, 12 more authors andG 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.
E Masson, S Paliwal, S Bhaskar, S Prakash, V Scotet, D N Reddy, Cédric Le Maréchal, G R Chandak,J M Chen, C Férec (2010). Genetic Analysis of the Glycoprotein 2 Gene (GP2) in Patients with Chronic Pancreatitis. Pancreas. 39(3):353-58.
Response to: 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(9):e16.
Ganesh Chauhan, Charles J Spurgeon, 12 more authors andG 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.
E Masson, S Paliwal, S Bhaskar, S Prakash, V Scotet, D N Reddy, Cédric Le Maréchal, G R Chandak,J M Chen, C Férec (2010). Genetic Analysis of the Glycoprotein 2 Gene (GP2) in Patients with Chronic Pancreatitis. Pancreas. 39(3):353-58.
2009
Rao SN, Chandak GR (2009). Cardiac Beriberi: Often a Missed Diagnosis. J Trop Pediatr; 56:284-85.
S Mahurkar, S Bhaskar, D N Reddy, G V Rao, S P Singh, V Thomas, G R Chandak (2009). The G191R variant in PRSS2 gene does not play a role in protection against tropical calcific pancreatitis. Gut; 58(6):881-88
[Accompanied by an Editorial Commentary, Weiss FU and Sahin-Toth M (2009). “Variations in trypsinogen expression may influence the protective effect of the p.G191R PRSS2 variant in chronic pancreatitis” Gut 58:748-50].
S Mahurkar, D N Reddy, G V Rao, G R Chandak (2009). Genetic Mechanisms Underlying Pathogenesis of Tropical Calcific Pancreatitis. World J Gastroenterology; 15:264-269.
P D Gluckman, P Bateson, A S Beedle, Z A Bhutta, M A Hanson, C Law, K V Anokhin, P Bougnères, 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.
C S Yajnik, C S Janipalli, S Bhaskar, S R Kulkarni, R M Freathy, S Prakash, K R Mani, M N Weedon,, S D Kale, J Deshpande, G V Krishnaveni, S R Veena, C H D Fall, M I McCarthy, T M Frayling, A T Hattersley, G R Chandak (2009).“FTO Gene Variants are Associated with Type 2 Diabetes but not with Obesity in South Asian Indians”. Diabetologia; 52:247-252.
S Mahurkar, S Bhaskar, D N Reddy, G V Rao, S P Singh, V Thomas, G R Chandak (2009). The G191R variant in PRSS2 gene does not play a role in protection against tropical calcific pancreatitis. Gut; 58(6):881-88
[Accompanied by an Editorial Commentary, Weiss FU and Sahin-Toth M (2009). “Variations in trypsinogen expression may influence the protective effect of the p.G191R PRSS2 variant in chronic pancreatitis” Gut 58:748-50].
S Mahurkar, D N Reddy, G V Rao, G R Chandak (2009). Genetic Mechanisms Underlying Pathogenesis of Tropical Calcific Pancreatitis. World J Gastroenterology; 15:264-269.
P D Gluckman, P Bateson, A S Beedle, Z A Bhutta, M A Hanson, C Law, K V Anokhin, P Bougnères, 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.
C S Yajnik, C S Janipalli, S Bhaskar, S R Kulkarni, R M Freathy, S Prakash, K R Mani, M N Weedon,, S D Kale, J Deshpande, G V Krishnaveni, S R Veena, C H D Fall, M I McCarthy, T M Frayling, A T Hattersley, G R Chandak (2009).“FTO Gene Variants are Associated with Type 2 Diabetes but not with Obesity in South Asian Indians”. Diabetologia; 52:247-252.
2008
S Mahurkar, S Bhaskar, D N Reddy, S Prakash, G V Rao, S P Singh, V Thomas, G R Chandak (2008). TCF7L2 Gene Polymorphisms do not Predict Susceptibility to Diabetes in Tropical Calcific Pancreatitis. BMC Medical Genetics; 9:80-86.
S Narasimha Rao, Shalini Mani, Karuna Madap, M V Kranthi Kumar, Lalji Singh, G R Chandak (2008). High Prevalence of Infantile Encephalitic Beriberi with Overlapping Features of Leigh’s Disease. J Trop Pediatrics; 54: 328-32.
The Indian Genome Variation Database (2008) “Genetic landscape of the people of India: a canvas for disease gene exploration”. J Genetics;87: 3-20.
Emmanuelle Masson, Cédric Le Maréchal, G R Chandak, Jérôme Lamoril, Stephane Bezieau, Swapna Mahurkar, Seema Bhaskar, D Nageshwar Reddy, Jian-Min Chen and Claude Férec (2008). Trypsinogen Copy Number Mutations in Patients with Idiopathic Chronic Pancreatitis. Clinical Gastroenterology and Hepatology 6: 82-88.
S Narasimha Rao, Shalini Mani, Karuna Madap, M V Kranthi Kumar, Lalji Singh, G R Chandak (2008). High Prevalence of Infantile Encephalitic Beriberi with Overlapping Features of Leigh’s Disease. J Trop Pediatrics; 54: 328-32.
The Indian Genome Variation Database (2008) “Genetic landscape of the people of India: a canvas for disease gene exploration”. J Genetics;87: 3-20.
Emmanuelle Masson, Cédric Le Maréchal, G R Chandak, Jérôme Lamoril, Stephane Bezieau, Swapna Mahurkar, Seema Bhaskar, D Nageshwar Reddy, Jian-Min Chen and Claude Férec (2008). Trypsinogen Copy Number Mutations in Patients with Idiopathic Chronic Pancreatitis. Clinical Gastroenterology and Hepatology 6: 82-88.
2007
H V Raghavendra Prasad, Neelima Kharidehal, Shalini Mani, G R Chandak (2007). Leigh’s Syndrome: A Case Report. The Internet Journal of Pediatrics and Neonatology 7(2): 1-14.
Atreyee Saha, Saibal Mukherjee, Mahua Maulik, G RChandak, The Indian Genome Variation Consortium, Kunal Ray (2007). Evaluation of Genetic Markers linked to Hemophilia A Locus: An Indian Experience. Haematologica 92: 1725-26.
S Mahurkar, S Bhaskar, D N Reddy, G V Rao, G R Chandak (2007). Comprehensive screening of reg1a gene rules out association with Tropical calcific pancreatitis. World J Gastroenterology 13:5938-43.
B K Dhillon, R Das, G Garewal, Y K Chawla, R K Dhiman, A Das, A Duseja, G R Chandak (2007). Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India. World J Gastroenterology 13: 2956-59. [Published in the Rapid Publication section).
S Mukherjee, A Saha, P Senthil Kumar, G R Chandak, P P Majumder and K Ray (2007). Remarkable variation in the informativeness of RFLP markers linked to hemophilia B locus in Indian population groups: Implication in the strategy for carrier detection. Disease Markers 22, 327-334.
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. Diabetologia 50(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.]
Atreyee Saha, Saibal Mukherjee, Mahua Maulik, G RChandak, The Indian Genome Variation Consortium, Kunal Ray (2007). Evaluation of Genetic Markers linked to Hemophilia A Locus: An Indian Experience. Haematologica 92: 1725-26.
S Mahurkar, S Bhaskar, D N Reddy, G V Rao, G R Chandak (2007). Comprehensive screening of reg1a gene rules out association with Tropical calcific pancreatitis. World J Gastroenterology 13:5938-43.
B K Dhillon, R Das, G Garewal, Y K Chawla, R K Dhiman, A Das, A Duseja, G R Chandak (2007). Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India. World J Gastroenterology 13: 2956-59. [Published in the Rapid Publication section).
S Mukherjee, A Saha, P Senthil Kumar, G R Chandak, P P Majumder and K Ray (2007). Remarkable variation in the informativeness of RFLP markers linked to hemophilia B locus in Indian population groups: Implication in the strategy for carrier detection. Disease Markers 22, 327-334.
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. Diabetologia 50(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.]
2006
Bhaskar S, Reddy DN, Mahurkar S, Rao GV, Singh L, Chandak GR. (2006). Lack of significant association of an insertion/deletion polymorphism in the angiotensin converting enzyme (ACE) gene with tropical calcific pancreatitis. BMC Gastroenterol 6:42.
G R Chandak, K J Ward, C S Yajnik, A N Pandit, A Bavdekar, C V Joglekar, C H D Fall, P Mohan Krishna, T J Wilkin, B S Metcalf, M N Weedon, T M Frayling,A T Hattersley (2006). “Triglyceride altering polymorphisms of the ApoAV gene have very different allele frequencies in India compared to Europeans”. BMC Medical Genetics 7:76.
N Thakur, D N Reddy, G V Rao, P M Krishna, L Singh, G R Chandak (2006). A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients. BMC Medical Genetics 7:73.
M I Bashir, R A Misgar, A I Wani, V Gupta, S R Masoodi, G R Chandak and A H Zargar (2006). "Juvenile Fibrocalculous Pancreatopathy-A Patient Report". Journal of Pediatric Endocrinology & Metabolism 19(7):947-50.
Swapna Mahurkar, M Mohd Idris, D Nageshwar Reddy, S Bhaskar, G V Rao, V Thomas, Lalji Singh, G R Chandak (2006). Association of Cathepsin B Polymorphisms with Tropical Calcific Pancreatitis. Gut 55: 1270-1275.
[This paper is accompanied by an Editorial Commentary, Lerch MM and Halangk W (2006). “Human Pancreatitis and the role of cathepsin B” Gut 55: 1228-30].
Ward KJ, Ellard S, Yajnik CS, Frayling TM, Hattersley AT, Venigalla PN, Chandak GR (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. 5:11 [Epub ahead of print].
G R Chandak, K J Ward, C S Yajnik, A N Pandit, A Bavdekar, C V Joglekar, C H D Fall, P Mohan Krishna, T J Wilkin, B S Metcalf, M N Weedon, T M Frayling,A T Hattersley (2006). “Triglyceride altering polymorphisms of the ApoAV gene have very different allele frequencies in India compared to Europeans”. BMC Medical Genetics 7:76.
N Thakur, D N Reddy, G V Rao, P M Krishna, L Singh, G R Chandak (2006). A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients. BMC Medical Genetics 7:73.
M I Bashir, R A Misgar, A I Wani, V Gupta, S R Masoodi, G R Chandak and A H Zargar (2006). "Juvenile Fibrocalculous Pancreatopathy-A Patient Report". Journal of Pediatric Endocrinology & Metabolism 19(7):947-50.
Swapna Mahurkar, M Mohd Idris, D Nageshwar Reddy, S Bhaskar, G V Rao, V Thomas, Lalji Singh, G R Chandak (2006). Association of Cathepsin B Polymorphisms with Tropical Calcific Pancreatitis. Gut 55: 1270-1275.
[This paper is accompanied by an Editorial Commentary, Lerch MM and Halangk W (2006). “Human Pancreatitis and the role of cathepsin B” Gut 55: 1228-30].
Ward KJ, Ellard S, Yajnik CS, Frayling TM, Hattersley AT, Venigalla PN, Chandak GR (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. 5:11 [Epub ahead of print].
2005
Parvinder kumar, Mohammed Idris, Vikas Dogra, K Radha Mani, K S Jamwal, W K Balwan, T R Raina, G R Chandak, S Gupta (2005). Analysis of Intron 22 Inversion Mutation of Factor VIII Gene in the Patients with Hemophilia-A in J & K State of India. Journal of Capital University of Medical Sciences, Vol. 26(6), 677-680.
A Kesari, Idris MM, G R Chandak and B Mittal (2005). “Genotype-phenotype correlation of 5q13 region genes in Spinal Muscular Atrophy patients from India”. Experimental and Molecular Medicine; 37(2): 134-141.
The Indian Genome Variation Database (2005) “The Indian Genome Variation database (IGVdb): a project overview”. Human Genetics;1:1-11.
M Mohd Idris, S Bhaskar, D Nageshwar Reddy, K Radha Mani, G V Rao and G R Chandak(2005). “Mutations in Anionic Trypsinogen Gene are not associated with Tropical calcific Pancreatitis”.Gut; 54(5): 705-07.
A Kesari, Idris MM, G R Chandak and B Mittal (2005). “Genotype-phenotype correlation of 5q13 region genes in Spinal Muscular Atrophy patients from India”. Experimental and Molecular Medicine; 37(2): 134-141.
The Indian Genome Variation Database (2005) “The Indian Genome Variation database (IGVdb): a project overview”. Human Genetics;1:1-11.
M Mohd Idris, S Bhaskar, D Nageshwar Reddy, K Radha Mani, G V Rao and G R Chandak(2005). “Mutations in Anionic Trypsinogen Gene are not associated with Tropical calcific Pancreatitis”.Gut; 54(5): 705-07.
Prior to 2005
G R Chandak, M Mohd Idris, D Nageshwar Reddy, K Radha Mani, S Bhaskar, G V Rao and L Singh (2004). “Absence of PRSS1 Mutations and Association of SPINK1 Trypsin Inhibitor Mutations in Hereditary and Non-Hereditary Chronic Pancreatitis”. Gut; 53(5):722-27.
S Mukherjee, A Mukhopadhyay, D Banerjee, G R Chandak and K Ray (2004). “Molecular Pathology of Hemophilia-B: Identification of Five Novel Mutations including a LINE1 Insertion in Indian Patients”. Haemophilia; 10: 259-63.
G N M Rao, T Hussain, N Geetha Devi, Suman Jain, G R Chandak, M P J S Ananda Raj (2003). Dystrophy Gene Deletions in South Indian Duchenne Muscular Dystrophy Patients” Ind J Med Sciences; 57(1): 1-6.
G R Chandak, M Uma Sridevi, C J Vas, D M Panikker and L Singh (2002). "Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India". Human Biology; 74(5): 683-693.
G R Chandak, M Mohd Idris, D Nageshwar Reddy, S Bhaskar, PVJ Sriram and L Singh (2002).“Mutations in Pancreatic Secretory Trypsin Inhibitor (PSTI/SPINK1) rather than Cationic Trypsinogen Gene (PRSS1) are Significantly Associated with Tropical Calcific Pancreatitis”. J Medical Genetics; 39: 347-351.
[Based on this paper, Tropical Calcific Pancreatitis has been recognized as a genetic disease and given a number sign (#) in the Online Mendelian Inheritance in Man (OMIM) and has been assigned a number #608189]
Ulrich CD, Amann ST, Argent BE, Bartsch D, Bell RH, Bhagat L, Bishop MD, Brentnall TA, Bronner MP, Burton FR, G R Chandak, et al (2001). “Pancreatic Cancer in Hereditary Pancreatitis: Consensus Guidelines for Prevention, Screening and Treatment”. Pancreatology;1: 416-422.
Ian Ellis, Markus M Lerch, David C Whitcomb, B E Argent, D Bartsch, R H Bell, M D Bishop, T A Brentall, G R Chandak, et al (2001). “Consensus Statement on Genetic Testing for Hereditary Pancreatitis: Guidelines for Indications, Counselling, Consent and Privacy Issues”.Pancreatology;1: 405-415.
G V Ramana, G R Chandak and L Singh (2000). “Sickle Cell Gene Haplotypes in Relli and Thurpu Kapu Populations of Andhra Pradesh". Human Biology, 72(3): 535-40.
Y Niranjan, G R Chandak, P Veeraraju and L Singh (1999) "Some Atypical and Rare Sickle Gene Haplotypes in Populations of Andhra Pradesh" Human Biology, 71(3): 333-40.
A Narendra Kumar, G R Chandak, N C K Reddy and L Singh (1999) " A Case of Fetus in Fetu with Molecular Analysis", J Pediatric Surgery, vol. 34(4), 1-5.
G R Chandak (1998). "Molecular Diagnosis of Genetic Disorders: The Indian Challenge". Everyman's Science.
S Mukherjee, A Mukhopadhyay, D Banerjee, G R Chandak and K Ray (2004). “Molecular Pathology of Hemophilia-B: Identification of Five Novel Mutations including a LINE1 Insertion in Indian Patients”. Haemophilia; 10: 259-63.
G N M Rao, T Hussain, N Geetha Devi, Suman Jain, G R Chandak, M P J S Ananda Raj (2003). Dystrophy Gene Deletions in South Indian Duchenne Muscular Dystrophy Patients” Ind J Med Sciences; 57(1): 1-6.
G R Chandak, M Uma Sridevi, C J Vas, D M Panikker and L Singh (2002). "Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India". Human Biology; 74(5): 683-693.
G R Chandak, M Mohd Idris, D Nageshwar Reddy, S Bhaskar, PVJ Sriram and L Singh (2002).“Mutations in Pancreatic Secretory Trypsin Inhibitor (PSTI/SPINK1) rather than Cationic Trypsinogen Gene (PRSS1) are Significantly Associated with Tropical Calcific Pancreatitis”. J Medical Genetics; 39: 347-351.
[Based on this paper, Tropical Calcific Pancreatitis has been recognized as a genetic disease and given a number sign (#) in the Online Mendelian Inheritance in Man (OMIM) and has been assigned a number #608189]
Ulrich CD, Amann ST, Argent BE, Bartsch D, Bell RH, Bhagat L, Bishop MD, Brentnall TA, Bronner MP, Burton FR, G R Chandak, et al (2001). “Pancreatic Cancer in Hereditary Pancreatitis: Consensus Guidelines for Prevention, Screening and Treatment”. Pancreatology;1: 416-422.
Ian Ellis, Markus M Lerch, David C Whitcomb, B E Argent, D Bartsch, R H Bell, M D Bishop, T A Brentall, G R Chandak, et al (2001). “Consensus Statement on Genetic Testing for Hereditary Pancreatitis: Guidelines for Indications, Counselling, Consent and Privacy Issues”.Pancreatology;1: 405-415.
G V Ramana, G R Chandak and L Singh (2000). “Sickle Cell Gene Haplotypes in Relli and Thurpu Kapu Populations of Andhra Pradesh". Human Biology, 72(3): 535-40.
Y Niranjan, G R Chandak, P Veeraraju and L Singh (1999) "Some Atypical and Rare Sickle Gene Haplotypes in Populations of Andhra Pradesh" Human Biology, 71(3): 333-40.
A Narendra Kumar, G R Chandak, N C K Reddy and L Singh (1999) " A Case of Fetus in Fetu with Molecular Analysis", J Pediatric Surgery, vol. 34(4), 1-5.
G R Chandak (1998). "Molecular Diagnosis of Genetic Disorders: The Indian Challenge". Everyman's Science.
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