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2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.Moutsianas, L., Agarwala V., Fuchsberger C., Flannick J., Rivas MA, Gaulton KJ, Albers PK, GoT2D Consortium, McVean G., Boehnke M., Altshuler D., and McCarthy MI PLoS genetics, 2015/04/01, Volume 11, Issue 4, p.e1005165, (2015) Read More / View Supplemental Materials
Abstract
2014
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.Damotte, V., Guillot-Noel L., Patsopoulos NA, Madireddy L., El Behi M., International Multiple Sclerosis Genetics Consortium, Ban M., Baranzini S., Barcellos L., Beecham G., Beecham A., Bernardinelli L., Booth D., Bos S., Buck D., Bush W., Comabella M., Compston A., Cotsapas C., Cournu-Rebeix I., et al. Genes and immunity, 2014/01/16, (2014) Read More / View Supplemental Materials
Abstract
2010
Integrating common and rare genetic variation in diverse human populations.International HapMap 3, Consortium, Altshuler DM, Gibbs RA, Peltonen L., Altshuler DM, Gibbs RA, Peltonen L., Dermitzakis E., Schaffner SF, Yu F., Peltonen L., Dermitzakis E., Bonnen PE, Altshuler DM, Gibbs RA, de Bakker PI, Deloukas P., Gabriel SB, Gwilliam R., Hunt S., et al. Nature, 2010/09/02, Volume 467, Issue 7311, p.52-8, (2010) Read More / View Supplemental Materials
Abstract
  • Showing 1-3 of 3 Results