Publications

1. M D Bashyam, A K Chaudhary, E C Reddy, V Reddy, V Acharya, H A Nagarajaram, A R R Devi, L Bashyam, A B Dalal, N Gupta, M Kabra, M Agarwal, S R Phadke, R Tainwala, R Kumar, S V Hariharan (2011). An Ectodysplasin A receptor (EDAR) founder mutation results in a high frequency of the autosomal recessive form of Hypohidrotic Ectodermal Dysplasia in India. Br J Dermatol (In Press).
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2. Vishal Acharya and H.A.Nagarajaram (2011) Hansa: An automated method for discriminating disease and neutral human nsSNPs Hum Mutat (In Press)
   
   
3. Murali Bashyam, Guroji Purushotham, Ajay K Chaudhary, Madhumohan Rao, Vishal Acharya, Tabrez Mohammad, Hampapatalu Nagarajaram, Vuppaladadhiam Hariram, Calambur Narasimhan(2011). A low prevalence of MYH7/MYBPC3 mutations among Familial Hypertrophic Cardiomyopathy patients in India. Mol Cell Biochem. 00:000-000; in press.
   
   
4. VishalAcharya Anil Kumar, H.A. Nagarajaram (2011). Hansa: The web-server forprediction of deleterious mutations (Manuscript under preparation). (hansa.cdfd.org.in:8080).

Posters presented

1. Vishal Acharya, HA Nagarajaram (2010): “Prediction of disease-associated single nucleotide polymorphisms mapping on to human proteins” presented at 4^th ESF Conference on Functional Genomics and Disease, Dresden, Germany.
   
   
2. Vishal Acharya, HA Nagarajaram (2008): Prediction of deleterious Human Membrane Transporter Polymorphisms presented at HUGO's 13^th Human Genome Meeting “Genomics and the Future of Medicine”, Hyderabad, India .
   
   
3. Vishal Acharya, HA Nagarajaram (2007): In silico analysis of candidate nsSNPs from public NCBI SNP database in Human Membrane Transport Proteins” presented at Indo-Australian Conference on Human Variations and Pharmacogenomics, Manipal, India.

Oral talk presented

1. Invited and presented the oral talk "Hansa:An automated method fordiscriminating disease and neutral human nsSNPs"atIndo-French Bioinformatics Meetings on 23^rd - 25^th March, 2011,Hyderabad, India.
   
   
2. Invited for oral talk at HUGO's 13th Human Genome Meeting “Genomics and the Future of Medicine”, Hyderabad, India.