Leveraging prior information to detect causal variants via multi-variant regression. by Nanye Long, Samuel P Dickson, Jessica M Maia, Hee Shin Kim, Qianqian Zhu, Andrew S Allen

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Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strain. by Pablo M Casillas-Espinosa, Kim L Powell, Mingfu Zhu, C Ryan Campbell, Jessica M Maia, Zhong Ren, Nigel C Jones, Terence J O'Brien, Slavé Petrovski

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A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population. by Ian R White, Sarah E Kleinstein, Christophe Praet, Chris Chamberlain, Duncan McHale, Jessica M Maia, Pingxing Xie, David B Goldstein, Thomas J Urban, Patrick R Shea

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A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population by Ian R. White, Sarah E. Kleinstein, Christophe Praet, Chris Chamberlain, Duncan McHale, Jessica M. Maia, Pingxing Xie, David B. Goldstein, Thomas J. Urban, Patrick R. Shea

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The characterization of twenty sequenced human genomes. by Kimberly Pelak, Kevin V Shianna, Dongliang Ge, Jessica M Maia, Mingfu Zhu, Jason P Smith, Elizabeth T Cirulli, Jacques Fellay, Samuel P Dickson, Curtis E Gumbs, Erin L Heinzen, Anna C Need, Elizabeth K Ruzzo, Abanish Singh, C Ryan Campbell, Linda K Hong, Katharina A Lornsen, Alexander M McKenzie, Nara L M Sobreira, Julie E Hoover-Fong, Joshua D Milner, Ruth Ottman, Barton F Haynes, James J Goedert, David B Goldstein

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