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The Journal of Clinical Investigation|July 12, 2016
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalisSilvia Martin-Almedina, Ines Martinez-Corral, Rita Holdhus, et al.American Journal of Human Genetics|January 31, 2012
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathyPia Ostergaard, Michael A Simpson, Antonella Mendola, et al.Human Molecular Genetics|November 11, 2011
Gene-gene interactions in breast cancer susceptibilityClare Turnbull, Sheila Seal, Anthony Renwick, et al.Nature Genetics|August 9, 2011
Germline mutations in RAD51D confer susceptibility to ovarian cancerChey Loveday, Clare Turnbull, Emma Ramsay, et al.Nature|December 18, 2012
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancerElise Ruark, Katie Snape, Peter Humburg, et al.Pageof 4