
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
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| Development and human disease – a synthesis of evolutionary, medical, anthropological, and economic perspectives. | Lancet, 373:1-8. |
2009
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| Genetic mechanisms underlying the pathogenesis of tropical calcific pancreatitis | World J Gastroenterol, January 21; 15(3): 264-269 |
2009
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| 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
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| 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
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| Genetic landscape of the people of India: a canvas for disease gene exploration | J Genet., 87(1): 3-20 |
2008
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| High Prevalence of Infantile Encephalitic Beriberi with Overlapping Features of Leigh’s Disease | Journal of Tropical Pediatrics, 6 |
2008
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| Trypsinogen Copy Number Mutations in Patients with Idiopathic Chronic Pancreatitis | Clinical Gastroenterology and Hepatology., 6: 82-88 |
2008
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| Evaluation of Genetic Markers linked to Hemophilia A Locus: An Indian Experience | Haematologica., 92: 1725-26 |
2007
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| 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
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| 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
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| Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population | Diabetologia., 50: 63-67 |
2007
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| 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
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| Triglyceride altering polymorphisms of the ApoAV gene have very different allele frequencies in India compared to Europeans | BMC Medical Genetics., 7: 76-81 |
2006
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| A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients | BMC Medical Genetics., 7: 73-78 |
2006
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| Juvenile Fibrocalculous Pancreatopathy-A Patient Report | Journal of Pediatric Endocrinology & Metabolism., 19: 947-950 |
2006
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| Association of Cathepsin B Polymorphisms with Tropical Calcific Pancreatitis | Gut., 55: 1270-1275 |
2006
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| 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
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| 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
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| Genotype-phenotype correlation of 5q13 region genes in Spinal Muscular Atrophy patients from India | Experimental and Molecular Medicine., 37: 134-141 |
2005
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| The Indian Genome Variation Consortium. The Indian Genome Variation database (IGVdb): a project overview | Human Genetics., 1: 1-11 |
2005
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| Mutations in Anionic Trypsinogen Gene are not associated with Tropical calcific Pancreatitis | Gut., 54: 705-707 |
2005
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| Absence of PRSS1 Mutations and Association of SPINK1 Trypsin Inhibitor Mutations in Hereditary and Non-Hereditary Chronic Pancreatitis | Gut., 53: 72-727 |
2004
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| Molecular Pathology of Haemophilia-B: Identification of Five Novel Mutations including a LINE1 Insertion in Indian Patients | Haemophilia., 10: 259-263 |
2004
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| Dystrophy Gene Deletions in South Indian Duchenne Muscular Dystrophy Patients | Ind J Med Sciences., 57: 1-6 |
2003
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| Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India | Human Biology., 74: 683-693 |
2002
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| 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
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| Pancreatic Cancer in Hereditary Pancreatitis: Consensus Guidelines for Prevention, Screening and Treatment | Pancreatology., 1: 416-422 |
2001
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| Consensus Statement on Genetic Testing for Hereditary Pancreatitis: Guidelines for Indications, Counselling, Consent and Privacy Issues | Pancreatology., 1: 405-415 |
2001
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| Sickle Cell Gene Haplotypes in Relli and Thurpu Kapu Populations of Andhra Pradesh | Human Biology., 72: 535-540 |
2000
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