Govardhan Bale
Hyderabad, TG, India
Last Updated: 09/26/2026
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Found 11 publications
Wilson Disease in India: Common but Genetically Enigmatic.
Journal: Journal of clinical and experimental hepatology
Published: December 09, 2025
Genetics of Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) in the Indian Ethnicity: An Update.
Journal: Journal of clinical and experimental hepatology
Published: November 05, 2025
Clinical and Genetic Profile of Pediatric and Adult Wilson's Disease in India.
Journal: Gastro hep advances
Published: March 31, 2025
A Pilot Study Based on the Correlation Between Whole Exome and Transcriptome Reveals Potent Variants in the Indian Population of Cervical Cancer.
Journal: Indian journal of microbiology
Published: January 09, 2024
Comparing rare variants versus common in the pathogenesis of nonalcoholic fatty liver disease: a whole exome sequencing approach.
Journal: Journal of gastroenterology and hepatology
Published: August 28, 2023
NUDT15 C415T variant compared with TPMT genotyping in predicting azathioprine-induced leucopenia: prospective analysis of 1014 inflammatory bowel disease patients in India.
Journal: Alimentary pharmacology & therapeutics
Published: May 04, 2020
Whole-Exome Sequencing Identifies a Variant in Phosphatidylethanolamine N-Methyltransferase Gene to be Associated With Lean-Nonalcoholic Fatty Liver Disease.
Journal: Journal of clinical and experimental hepatology
Published: September 27, 2018
Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population.
Journal: Journal of clinical and experimental hepatology
Published: October 18, 2017
PRSS1 (R122H) mutation in an Indian family with low penetrance is associated with pancreatitis phenotype.
Journal: Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology
Published: July 17, 2017
Regional differences in genetic susceptibility to non-alcoholic liver disease in two distinct Indian ethnicities.
Journal: World journal of hepatology
Published: April 27, 2017
Hereditary Persistence of Alpha-Fetoprotein Is Associated with the -119G>A Polymorphism in AFP Gene.
Hereditary Persistence of Alpha-Fetoprotein Is Associated with the -119G>A Polymorphism in AFP Gene.
Journal: ACG case reports journal
Published: September 20, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026