Scientific Research Groups

Amit Chattopadhyay Chandak G R Ghanshyam Swarup Gopal Pande Imran Siddiqi Jyotsna Dhawan
Kasbekar D P Kshitish Majumdar Lalji Singh Madhusudhana Rao N Malay K Ray Mohan Rao Ch
Nagaraj R Purnima Bhargava Rakesh Kumar Mishra Ramesh K Aggarwal Ramesh V Sonti Rajan Sankaranarayanan
Satish Kumar Shashidhara L S Shivaji S Sirdeshmukh R Somdatta Sinha Thangaraj K
Utpal Bhadra Veena K Parnaik Yogendra Sharma . . .

 

 

 

Anant B Patel Guruprasad K Jagannadham M V Lakshmi Rao K Murthy B S N Prabir Kumar De
Rachel A J Radha V Ramakrishna Murti T Shailendra K Saxena Shashi Singh Shrish Tiwari
Sreedhar A S Tushar Vaidya . . . .




G R Chandak Group Publication

Title Journal Year Article
The G191R variant in PRSS2 gene does not play a role in protection against tropical calcific pancreatitis. Gut.,  58:6
2009
Development and human disease – a synthesis of evolutionary, medical, anthropological, and economic perspectives. Lancet,  373:1-8.
2009
Genetic mechanisms underlying the pathogenesis of tropical calcific pancreatitis World J Gastroenterol,  January 21; 15(3): 264-269
2009
FTO Gene Variants are Associated with Type 2 Diabetes but not with Obesity in South Asian Indians Diabetologia,  DOI: 10.1007/s00125-008-1186-6
2008
TCF7L2 gene polymorphisms do not predict susceptibility to diabetes in tropical calcific pancreatis but may interact with SPINK1 and CTSB mutations in predicting diabetes BMC Med. Genet., 16:9(1): 80
2008
Genetic landscape of the people of India: a canvas for disease gene exploration J Genet., 87(1): 3-20
2008
High Prevalence of Infantile Encephalitic Beriberi with Overlapping Features of Leigh’s Disease Journal of Tropical Pediatrics, 
2008
Trypsinogen Copy Number Mutations in Patients with Idiopathic Chronic Pancreatitis Clinical Gastroenterology and Hepatology., 6: 82-88
2008
Evaluation of Genetic Markers linked to Hemophilia A Locus: An Indian Experience Haematologica., 92: 1725-26
2007
Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India World Journal of Gastroenterology., 13(21): 2956-2959
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
2007
Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population Diabetologia., 50: 63-67
2007
Lack of significant association of an insertion/deletion polymorphism in the angiotensin converting enzyme (ACE) gene with tropical calcific pancreatitis BMC Gastroenterol., 6: 42-48
2006
Triglyceride altering polymorphisms of the ApoAV gene have very different allele frequencies in India compared to Europeans BMC Medical Genetics., 7: 76-81
2006
A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients BMC Medical Genetics., 7: 73-78
2006
Juvenile Fibrocalculous Pancreatopathy-A Patient Report Journal of Pediatric Endocrinology & Metabolism., 19: 947-950
2006
Association of Cathepsin B Polymorphisms with Tropical Calcific Pancreatitis Gut., 55: 1270-1275
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: 11-16
2006
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.., 26: 677-680
2005
Genotype-phenotype correlation of 5q13 region genes in Spinal Muscular Atrophy patients from India Experimental and Molecular Medicine., 37: 134-141
2005
The Indian Genome Variation Consortium. The Indian Genome Variation database (IGVdb): a project overview Human Genetics., 1: 1-11
2005
Mutations in Anionic Trypsinogen Gene are not associated with Tropical calcific Pancreatitis Gut., 54: 705-707
2005
Absence of PRSS1 Mutations and Association of SPINK1 Trypsin Inhibitor Mutations in Hereditary and Non-Hereditary Chronic Pancreatitis Gut., 53: 72-727
2004
Molecular Pathology of Haemophilia-B: Identification of Five Novel Mutations including a LINE1 Insertion in Indian Patients Haemophilia., 10: 259-263
2004
Dystrophy Gene Deletions in South Indian Duchenne Muscular Dystrophy Patients Ind J Med Sciences., 57: 1-6
2003
Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India Human Biology., 74: 683-693
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
2002
Pancreatic Cancer in Hereditary Pancreatitis: Consensus Guidelines for Prevention, Screening and Treatment Pancreatology., 1: 416-422
2001
Consensus Statement on Genetic Testing for Hereditary Pancreatitis: Guidelines for Indications, Counselling, Consent and Privacy Issues Pancreatology., 1: 405-415
2001
Sickle Cell Gene Haplotypes in Relli and Thurpu Kapu Populations of Andhra Pradesh Human Biology., 72: 535-540
2000