Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project - Feifan Xiao; Bingbing Wu; Chenbin Dong; Guoqiang Cheng; Yun Cao; Laishuan Wang; Xinran Dong; Yulan Lu; Lin Yang; Liping Chen; Long Li; Xinnian Pan; et al. (Human Genetics, 2023)

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium - Qing Li; Robert Wojciechowski; Claire L. Simpson; Pirro G. Hysi; Virginie J. M. Verhoeven; Mohammad Kamran Ikram; René Höhn; Veronique Vitart; Alex W. Hewitt; Konrad Oexle; Kari-Matti Mäkelä; Stuart MacGregor; et al. (Human Genetics, 2015)

Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients - Lei Yu; Ji-Cheng Lv; Xu-jie Zhou; Li Zhu; Ping Hou; Hong Zhang (Human Genetics, 2011)

Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14 - Hui Li; Jia-Xin Wang; Cheng-Ye Wang; Ping Yu; Qiang Zhou; Yong-Gang Chen; Lu-Hang Zhao; Ya-Ping Zhang (Human Genetics, 2008)