饶佳

医疗专长：常见儿童肾脏疾病，包括儿童肾病综合征，泌尿道感染，先天性肾脏及尿路畸形简要工作经历：毕业于复旦大学上海医学院临床医学专业，在复旦大学儿科医院取得博士学位。长期从事儿童肾脏病临床工作，致力于探索小儿肾病的致病机制，并不断优化诊疗策略。在儿童遗传性肾脏疾病新致病基因的发现与功能研究工作中取得了突破性进展，研究成果先后在NatureGenetics,JCI等期刊获得发表。进修学习情况：悉尼儿童医院进行儿童肾移植专科培训哈佛医学院波士顿儿童医院完成博士后工作科研成果及论著：1.   *RaoJ,*AshrafS,TanW,vanderVenAT,GeeHY,BraunDA,FehérK,GeorgeSP, EsmaeilniakooshkghaziA,ChoiWI,Jobst-SchwanT,SchneiderR,SchmidtJM,WidmeierE,WarejkoJK,HermleT,SchapiroD,LovricS,ShrilS,DagaA,NayirA,ShenoyM,TseY,BaldM,HelmchenU,MirS,BerdeliA,KariJA,ElDesokyS,SolimanNA,BaggaA,ManeS,JairajpuriMA,LiftonRP,KhuranaS,MartinsJC,HildebrandtF.AdvillinactsupstreamofphospholipaseCϵ1insteroid-resistant nephroticsyndrome.JClinInvest.2017;127(12):4257-4256(共同第一作者，IF12.784)2.   *BraunDA,*RaoJ,*MolletG,SchapiroD,DaugeronMC,TanW,GribouvalO,Boyer O,RevyP,Jobst-SchwanT,SchmidtJM,LawsonJA,SchanzeD,AshrafS,UllmannJFP,HoogstratenCA,BoddaertN,CollinetB,MartinG,LigerD,LovricS,FurlanoM,GuerreraIC,Sanchez-FerrasO,HuJF,BoschatAC,SanquerS,MentenB,VergultS,DeRockerN,AirikM,HermleT,ShrilS,WidmeierE,GeeHY,ChoiWI,SadowskiCE,PabstWL,WarejkoJK,DagaA,BastaT,MatejasV,ScharmannK,KienastSD,BehnamB,BeesonB,BegtrupA,BruceM,Ch'ngGS,LinSP,ChangJH,ChenCH,Cho MT,GaffneyPM,GipsonPE,HsuCH,KariJA,KeYY,Kiraly-BorriC,LaiWM,LemyreE,LittlejohnRO,MasriA,MoghtaderiM,NakamuraK,OzaltinF,PraetM,PrasadC,PrytulaA,RoederER,RumpP,SchnurRE,ShiiharaT,SinhaMD,SolimanNA,SoulamiK,SweetserDA,TsaiWH,TsaiJD,TopalogluR,VesterU,ViskochilDH,VatanavicharnN,WaxlerJL,WierengaKJ,WolfMTF,WongSN,LeidelSA,TruglioG,DedonPC,PoduriA,ManeS,LiftonRP,BouchardM,KannuP,ChitayatD,MagenD, CallewaertB,vanTilbeurghH,ZenkerM,AntignacC,HildebrandtF.MutationsinKEOPS-complexgenescausenephroticsyndromewithprimarymicrocephaly.NatGenet.2017;49(10):1529-1538.（共同第一作者，IF27.959）3.   *RaoJ,*LiuX,MaoJ,etal.Geneticspectrumofrenaldiseasefor1001Chinesechildrenbasedonamulticenterregistrationsystem..ClinGenet.2019;96(5):402-4104.   SunS,XuL,BiY,WangJ,ZhangZ,TangX,CaoQ,ZhaiY,ChenJ,FangX,LiuJ,FangY,XiangT,QianY,WuB,WangH,ZhouW,ShenJ,DongK,LiuX,ZhengB,ZhangA,WangX,WuY,MaD,ShenQ,RaoJ#,XuH#.EarlydiagnosisofWT1nephropathyandfollowupinaChinesemulticentercohort.EurJMedGenet.2020Sep4;63(11):104047.5.   SongX,FangX,TangX,CaoQ,ZhaiY,ChenJ,LiuJ,ZhangZ,XiangT,QianY,WuB,WangH,ZhouW,LiuC,ShenQ,XuH,RaoJ#.COQ8Bnephropathy:Earlydetectionandoptimaltreatment.MolGenetGenomicMed.2020Jun16:e1360.6.   方晓燕沈剑沈茜毕允力汤小山刘佳璐张致庆翟亦晖陈径李国民吴冰冰钱琰琰徐虹饶佳。WT1基因检测时机对Wilms肿瘤合并慢性肾脏疾病预后影响的回顾性队列研究。中国循证儿科杂志,2019年第4期；266-270页   （通讯作者）7.   WeiL,FangY,CaoG,ZhangS,TianM,ShenQ,XuH,LiuC#,RaoJ#.GeneticandpathologicalfindingsinaboywithpsoriasisandC3glomerulonephritis:Acasereportandliteraturereview.MolGenetGenomicMed.2020Jul28:e1430学术任职：中华医学会儿科分会肾脏病学组青年学组副组长，上海市医学会肾脏病分会青年委员，上海市医学会遗传学会青年委员，Frontiers　Medicine杂志审稿人，中华肾脏病杂志审稿人所获荣誉：2018年国家自然科学基金委优秀青年基金2018年上海市青年优秀学术带头人计划