Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordiaPin‐Xian Xu, Richard L. Maas, Joe C. Adams et al.|Nature Genetics|1999Cited by 718
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexesRainer Ruf, Friedhelm Hildebrandt, Pin‐Xian Xu et al.|Proceedings of the National Academy of Sciences|2004Cited by 420
Mouse <i>Eya</i> homologues of the <i>Drosophila eyes absent</i> gene require <i>Pax6</i> for expression in lens and nasal placodePin‐Xian Xu, Richard L. Maas, Ian Woo et al.|Development|1997Cited by 331
<i>Eya1</i>is required for the morphogenesis of mammalian thymus, parathyroid and thyroidPin‐Xian Xu, Xin Xu, Weiming Zheng et al.|Development|2002Cited by 282
Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal SyndromeBethan E. Hoskins, Friedhelm Hildebrandt, Carl H. Cramer et al.|The American Journal of Human Genetics|2007Cited by 203