1.国家自然科学基金项目（81170002），原发性自发性气胸的分子和临床遗传学研究，第一完成人，2012-2015 年，60 万。2. 省临床医学科技专项基金，在原发性自发性气胸病人中筛查和鉴定BHD综合征的诊断策略，第一完成人，2014-2016年，75万。3，国家高技术研究发展计划（863计划）子课题（2014AA022204），药食同源生物资源挖掘关键技术与产品研发, 2014-2016年，50万

. Haiyan Min, Chengchu Zhu，Wei Zou，Yibing Ding，Dehua Ma， Baofu Chen， Minhua Ye, Yanqing Pan, Lei Cao, Yueming Wan,Yong Wang， Hongwei Wang, Long Yi*（易龙），Qian Gao. Plasma let-7d and miR-424 as biomarkers to distinguish BHDS in PSP patients. Chest 2014(submitted).

2. Shen L, Gu H, Wang D, Yang C, Xu Z, Jing H, Jiang Y, Ding Y, Hou H, Ge Z, Chen S, Mo X, Yi L*（易龙）.Influence of chromosome 22q11.2 microdeletion on postoperative calcium level after cardiac-correction surgery. Pediatr Cardiol. 2011;32(7):904-9.

3． Yang C, Shen L, Xu Z, Wu X, Mo X, Zhang J, Wang D, Wang Y, Peng Y, Cao L, Jiang Y, Gu H, Chen S, Bian X, Liu J, Qiao D, Yi L*（易龙）. A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations. Electrophoresis. 2009, 30:465-71.

4. Ren HZ, Zhu CC, Yang C, Chen SL, Xie J, Hou YY, Xu ZF, Wan DJ, Mu DK, Ma DH, Wang Y, Ye MH, Ye ZR, Chen BF, Wang CG, Lin J, Qiao D, Yi L*（易龙）. Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax. Clin Genet. 2008, 74:178-183

5. Xie J, Yi L*（易龙）, Xu ZF, Mo XM, Hu YL, Wang DJ, Ren HZ, Han B, Wang Y, Yang C, Zhao YL, Shi DQ, Jiang YZ, Shen L, Qiao D, Chen SL, Yu BJ. VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies. Eur J Hum Genet. 2007，15:1246-1251.