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Nature Genetics|March 8, 2011
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone lossMichael A Simpson, Melita D Irving, Esra Asilmaz, et al.American Journal of Human Genetics|May 14, 2011
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomaliesLaura Southgate, Rajiv D Machado, Katie M Snape, et al.Cancer Research|October 3, 2007
FBXW7/hCDC4 is a general tumor suppressor in human cancerShahab Akhoondi, Dahui Sun, Natalie von der Lehr, et al.Science Signaling|August 21, 2014
The ErbB4 CYT2 variant protects EGFR from ligand-induced degradation to enhance cancer cell motilityTai Kiuchi, Elena Ortiz-Zapater, James Monypenny, et al.International Journal of Cancer|July 17, 2010
Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancerMaria Notaridou, Lydia Quaye, Dimitra Dafou, et al.Pageof 6