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Madhu Singh

Researcher at Indian Institute of Toxicology Research

Publications -  9
Citations -  745

Madhu Singh is an academic researcher from Indian Institute of Toxicology Research. The author has contributed to research in topics: Genotype & Haplotype. The author has an hindex of 8, co-authored 9 publications receiving 697 citations. Previous affiliations of Madhu Singh include Institute of Genomics and Integrative Biology & Council of Scientific and Industrial Research.

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Genetic landscape of the people of India: A canvas for disease gene exploration

Samir K. Brahmachari, +150 more
- 01 Apr 2008 - 
TL;DR: High levels of genetic divergence are observed between groups of populations that cluster largely on the basis of ethnicity and language in diverse populations of India.
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The Indian Genome Variation database (IGVdb): a project overview

Samir K. Brahmachari, +98 more
- 01 Nov 2005 - 
TL;DR: The Indian Genome Variation (IGV) consortium as discussed by the authors is the first large-scale comprehensive study of the structure of the Indian population with wide-reaching implications, which aims to provide data on validated SNPs and repeats, both novel and reported, along with gene duplications, in over a thousand genes, in 15,000 individuals drawn from Indian subpopulations.
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Association of genetic polymorphisms in glutathione S-transferases and susceptibility to head and neck cancer.

TL;DR: Evidence that GST polymorphism modifies the susceptibility to head and neck squamous cell carcinoma is provided and importance of gene-environment interaction in modulating the risk is demonstrated in modifying the risk to HNSCC is demonstrated.
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Polymorphism in environment responsive genes and association with Parkinson disease.

TL;DR: The data suggest that polymorphism in the genes involved in detoxification and dopamine regulation may modulate the susceptibility to PD and could be important risk factors in the pathogenesis of PD.
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Interaction of cytochrome P4501A1 genotypes with other risk factors and susceptibility to lung cancer.

TL;DR: The lung cancer risk was increased several two-to fourfold in the patients carrying the genotype combinations of CYP1A1*2A and GSTM1 suggesting the role of gene-gene interaction in lung cancer.