A Caenorhabditis elegans Tissue Model of Radiation-Induced Reproductive Cell Death von Weidhaas, J. B., Eisenmann, D. M., Holub, J. M., Nallur, S. V.

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MicroRNA profiling of triple negative breast cancer: predicting outcome and targets von Paranjape, TS, Nallur, SV, Keanie, K, Martel, M, Haffty, BG, Tuck, DP, Slack, F, Weidhaas, JB

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A decentralized self-adaptation mechanism for service-based applications in the cloud von Nallur, V., Bahsoon, R.

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Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders von S Niranjana Murthy, Ashitha, V Suresh, Raviraj, Nallur B, Ramachandra

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Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes von Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, Megha, Suresh, Raviraj V, Manjegowda, Dinesh S, Ramachandra, Nallur B

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Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression von Veerappa, Avinash M, Murthy, Megha N, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Suresh, Raviraj V, Nachappa, Somanna Ajjamada, Prashali, Nelchi, Yadav, Sangeetha Nuggehalli, Srikanta, Manjula Arsikere, Manjegowda, Dinesh S, Seshachalam, Keshava B, Ramachandra, Nallur B

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Comparable effects of 0.5 ms and 1.5 ms pulse-widths on cardiovascular response in schizophrenia patients receiving electroconvulsive therapy von Ithal, Dhruva, Mitra, Sayantanava, Nallur, Shreya V., Arumugham, Shyam Sundar, Kumar, Channaveerachari Naveen, Ramesh, Venkatapura J., Thirthalli, Jagadisha, Gangadhar, Bangalore N.

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Occupational Hazards Among the Agricultural Workers in a Rural Area of South India von SV, Bhavana, Cheluvaraj, Pavithra, Bidare Sastry, Nanda Kumar, Nallur Somanna, Shivaraj

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Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach von Suresh, Raviraj V, Lingaiah, Kusuma, Veerappa, Avinash M, Ramachandra, Nallur B

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Signal amplification by rolling circle amplification on DNA microarrays von Nallur, Girish, Luo, Chenghua, Fang, Linhua, Cooley, Stephanie, Dave, Varshal, Lambert, Jeremy, Kukanskis, Kari, Kingsmore, Stephen, Lasken, Roger, Schweitzer, Barry

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A conserved RAS/mitogen-activated protein kinase pathway regulates DNA damage-induced cell death postirradiation in radelegans von WEIDHAAS, Joanne B, EISENMANN, David M, HOLUB, Justin M, NALLUR, Sunitha V

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Insertion-deletions burden in copy number polymorphisms of the Tibetan population von Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, N Megha, Suresh, Raviraj V, Belur, Keshava, Ramachandra, Nallur B, Tejaswini, Patel, Niveditha B, Gowda, P K Supriya

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Association of RFC1 A80G gene polymorphism with advanced maternal age in risk of Down syndrome von Suresh, Raviraj V., Narayannapa, Savitha, Udupa, Ambika S., Lingaiah, Kusuma, Polapalli, Sunil Kumar, Ramachandra, Nallur B.

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The embryonic development of the flatworm Macrostomum sp von Morris, Joshua, Nallur, Ramachandra, Ladurner, Peter, Egger, Bernhard, Rieger, Reinhard, Hartenstein, Volker

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Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes: e0121846 von Veerappa, Avinash M, Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, Megha, Suresh, Raviraj V, Manjegowda, Dinesh S, Ramachandra, Nallur B

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Embryonic development in the primitive bilaterian Neochildia fusca: normal morphogenesis and isolation of POU genes Brn-1 and Brn-3 von Ramachandra, Nallur B, Gates, Ruth D, Ladurner, Peter, Jacobs, David K, Hartenstein, Volker

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Allelic variants of DYX1C1 are not associated with dyslexia in India von Saviour, Pushpa, Kumar, Satish, Kiran, U, Ravuri, Rajasekhara Reddy, Rao, V R, Ramachandra, Nallur Basappa

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POSTER SESSION 2, HRC 2011 von Shetty, A. K., Mehta, P. A., Squirrel, M., Bostock, J., Rinaldi, C. A., Wright, G. A., Lines, I., Tomlinson, D. R., Haywood, G. A., Neiderer, S., Ginks, M., Duckett, S. G., Ma, Y., Chen, Z., Sohal, M., Mehta, P., Kapetanakis, S., Carr-White, G., Kyriacou, A., Pabari, P., Lefroy, D., Davies, D. W., Peters, N., Kanagaratnam, P., Mayet, J., Hughes, A., Francis, D. P., Whinnett, Z. I., Khoo, C. W., Krishnamoorthy, S., Dwivedi, G., Lip, G. Y. H., Lim, H. S., Nallur Shivu, G., Brooks, V., Johns, M. J., Bleasdale, R. A., Yung, L. T. M., Wilson, S., Slade, A. K. B., Johnston, R. T., Chernyshev, A. A., Kovalev, I. A., Zavadovsky, K. V., Popov, S. V., Garg, P., Khan, I., Douglas, H.

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Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization von VEERAPPA, AVINASH M., SURESH, RAVIRAJ V., VISHWESWARAIAH, SANGEETHA, LINGAIAH, KUSUMA, MURTHY, MEGHA, MANJEGOWDA, DINESH S., PADAKANNAYA, PRAKASH, RAMACHANDRA, NALLUR B.

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Allelic variants of DYX1C1 are not associated with dyslexia in India von Saviour, Pushpa, Kumar, Satish, Kiran, U, Ravuri, Rajasekhara Reddy, Rao, VR, Ramachandra, Nallur Basappa

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