• Publications
  • Influence
Homozygous loss‐of‐function mutation of the LEPREL1 gene causes severe non‐syndromic high myopia with early‐onset cataract
High myopia is a severe visual impairment which can increase the risk of retinal degeneration, subretinal hemorrhage, choroidal neovascularization, cataract and retinal detachment. We recruited anExpand
Mandibulofacial dysostosis, microtia, and limb anomalies in a newborn: a new form of acrofacial dysostosis syndrome?
Zhang Y, Dai Y, Liu Y, Ren J. Mandibulofacial dysostosis, microtia, and limb anomalies in a newborn: a new form of acrofacial dysostosis syndrome?
Superconductivity and Mossbauer effect of FexCu1-xBa2YCu2O7+y superconductors synthesized by high pressure
The superconductivity in FexCu1-xBa2YCu2O7+y superconductors (0.00 <= x <= 0.70) is improved by high-pressure (HP) synthesis. The HP samples have higher oxygen content than the ambient pressure (AM)Expand
Ovarian stimulation and endometrial gene expression
The 2nd International Symposium on Reproductive Endocrinology and Genetics, Jinan, China, 19-21 June 2009.
Association of serum uric acid levels with suicide risk in female patients with major depressive disorder: a comparative cross-sectional study
Background Individuals with major depressive disorder (MDD) have a high suicide risk. Some evidence suggests that uric acid (UA) may be involved in the pathophysiology of MDD. The purpose of thisExpand