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2014
Whole -exome sequencing identifies rare, functional CFH variants in families with macular degeneration.Yu, Y., Triebwasser MP, Wong EK, Schramm EC, Thomas B., Reynolds R., Mardis E., Atkinson JP, Daly M., Raychaudhuri S., Kavanagh D., and Seddon JM Human molecular genetics, 2014/05/20, (2014) Read More / View Supplemental Materials
Abstract
2013
Mutations in eIF4ENIF1 Are Associated With Primary Ovarian Insufficiency.Kasippillai, T., Macarthur DG, Kirby A., Thomas B., Lambalk CB, Daly M. J., and Welt CK The Journal of clinical endocrinology and metabolism, 2013/07/31, (2013) Read More / View Supplemental Materials
Abstract
2012
INRICH: Interval-based Enrichment Analysis for Genome Wide Association Studies.Lee, PH, O'Dushlaine C., Thomas B., and Purcell SM Bioinformatics (Oxford, England), 2012/04/17, (2012) Read More / View Supplemental Materials
Abstract
  • Showing 1-3 of 3 Results