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List of works by Mainak Sengupta

A meta-analysis and in silico analysis of polymorphic variants conferring breast cancer risk in the Indian subcontinent

scientific article published on 01 August 2020

A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient.

scientific article published on 15 June 2010

Association of 12 polymorphic variants conferring genetic risk to lung cancer in Indian population: An extensive meta-analysis

scientific article

Association of Interleukin-1 beta and tumor necrosis factor-alpha genetic polymorphisms with gastric cancer in India

scientific article published on 09 August 2018

Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene.

scientific article published on 26 April 2010

Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water.

scientific article

Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients

scientific article published on 23 July 2019

Genetic defects in Indian Wilson disease patients and genotype-phenotype correlation

scientific article published on 25 September 2013

Indian genetic disease database

scientific article

Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease.

scientific article

Mapping the TYR gene reveals novel and previously reported variants in Eastern Indian patients highlighting preponderance of the same changes in multiple unrelated ethnicities

scientific article published on 02 March 2020

Meta-analysis and prioritization of human skin pigmentation-associated GWAS-SNPs using ENCODE data-based web-tools

scientific article published on 13 February 2019

Molecular and Functional Studies of Tyrosinase Variants Among Indian Oculocutaneous Albinism Type 1 Patients

scientific article published on 23 September 2010

OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene.

scientific article published in September 2006

Potential Role of Brain-Derived Neurotrophic Factor and Dopamine Receptor D2 Gene Variants as Modifiers for the Susceptibility and Clinical Course of Wilson's Disease

scientific article published on 10 July 2018

Structure-function correlation analysis of connexin50 missense mutations causing congenital cataract: electrostatic potential alteration could determine intracellular trafficking fate of mutants.

scientific article published on 6 May 2014

The aging eye.

scientific article

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