U. Mittal

发表

SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies

N. Pandey, A. Srivastava, M. Mukerji, 2004, Journal of Human Genetics.

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

Ashutosh Kumar Singh, Amitabh Sharma, J. Kumar, 2008, Journal of Genetics.

Complex phenotypes in an Indian family with homozygous SCA2 mutations

Mona Ragothaman, U. Muthane, M. Mukerji, 2004, Annals of neurology.

Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family

A. Srivastava, M. Mukerji, Satish Jain, 2005, Journal of Human Genetics.

The Indian Genome Variation database (IGVdb): a project overview

Debasis Dash, Ashutosh Kumar Singh, Arijit Mukhopadhyay, 2005, Human Genetics.

Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies.

Sanjeev Jain, A. Srivastava, M. Mukerji, 2005, Archives of neurology.

Consortium IGVThe Indian Genome Variation database (IGVdb): a project overview. Hum Genet 118:1-11

B. C. Mishra, Gajendra P.S. Raghava, Amitabh Sharma, 2005 .

Evidence of a Common Founder for SCA12 in the Indian Population

R. Margolis, S. Bahl, A. Srivastava, 2005, Annals of human genetics.

Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms

A. Srivastava, M. Mukerji, P. Pal, 2005, Human Genetics.

SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.

M. Mukerji, P. Pal, B. S. Yashavantha, 2007, The Indian journal of medical research.

Psychological Correlates of Breast Cancer: An Exploratory Study

U. Mittal, Sushila Pareek, Asha Hingar, 2009 .