夏欣一，教授、主任医师，博士生导师
1978年12月出生，江苏东台人，2008年南京大学医学院外科学专业博士毕业、博士后。现任东部战区总医院（原南京军区南京总医院，南京大学医学院附属金陵医院）主任医师、教授，博士生导师、博士后联系导师，主要从事生殖遗传和分子诊断专业。入选国家人社部“香江****计划”、江苏省 “333工程”培养对象、江苏省科教兴（强）卫工程医学重点人才（2011年和2016年）、原南京军区“334”高层次科技人才、享受军队优秀专业技术人才岗位津贴。任国家重点临床专科--全军检验医学研究所所长助理、检验科（临床中心实验科）副主任、《中华男科学杂志》编辑部主任，学术任职包括中国中西医结合学会男科专业委员会青年委员、中国医师协会中国Y染色体微缺失质控联盟委员会副会长、中国医师协会男科医师分会性功能障碍专家委员会委员、中国中西医结合学会检验医学专业委员会肿瘤专家委员会委员、世界中医药学会联合会男科专业委员会常委、中国医疗保健国际交流促进会泌尿生殖分会委员兼江苏学组常委、江苏省医学会男科分会青年委员、江苏省医学会检验分会青年委员、世界中医药学会联合会男科专委会常委、江苏省妇幼健康研究会生育调控专业委员会副主委、全军检验医学专委会青年委员、南京医学会男科分会委员、《中华男科学杂志》编委、《临床检验杂志》编委、《东南国防医药》青年编委等。主持国家自然科学基金、江苏省自然科学基金、江苏省重点研发计划项目（临床前沿技术）、中央军委军事医学创新工程等项目。以第一作者/通讯作者发表SCI论文30余篇，副主编《实用流式细胞术彩色图谱》、《实用男科学》等专著5部，主要执笔中华医学会《男性生殖遗传学检查专家共识》等规范共识4部。获中国妇幼健康科技成果一等奖、军队科技进步二等奖、军队医疗成果二等奖、江苏省科技进步三等奖、江苏省医学新技术引进一等奖等成果。我院为南京大学附属医院，本学科是国家重点临床专科、江苏省和军队重点学科，具有良好的科研条件，欢迎有志青年加入本实验室，攻读硕、博士学位或从事博士后研究工作。
联系方式：南京中山东路305号东部战区总医院（210002）；电话：；E-mail: xxybio@126.com
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近3年部分论文：（*, corresponding author）
Wu J, Dai W, Wu L, Li W, Xia X*, Wang J*. Decoding genetic and epigenetic information embedded in cell free DNA with adapted SALP-seq. Int J Cancer. 2019, 145(9):2395-2406.
Liu S, Zhu P, Ni M, Zhang M, Jiang W, Yu M, Zhang J, Wu Q, Li W, Xue C, Xia X*. A novel mutation of MIP in a Chinese family with congenital nuclear cataract identified by whole-exome sequencing. Ophthalmic Genet. 2018, 39(1): 139-140.
Zhang B, Xia Q, Wang Q, Xia X*, Wang J*. Detecting and typing target DNA with a novel CRISPR-typing PCR (ctPCR) technique. Anal Biochem. 2018, (561-562), 37-46.
Zhang B, Wang Q, Xu X, Xia Q, Long F, Li W, Shui Y, Xia X*, Wang J*. Detection of target DNA with a novel Cas9/sgRNAs-associated reverse PCR (CARP) technique. Anal Bioanal Chem, 2018, 410(12), 2889-2900.
Jiang W, Shi L, Liu H, Cao J, Zhu P, Zhang J, Yu M, Guo Y, Cui Y, Xia X*.Systematic review and meta-analysis of the genetic association between protamine polymorphism and male infertility. Andrologia. 2018,50(5), e12990.
Zhu P, Li W, Ni M, Zhang C, Liu S, Wu Q, Jiang W, Zhang J, Zhang M, Li X, Cui Y, Xue C, Xia X*. The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells. Biochem Biophys Res Commun. 2017, 483(1):463-467.
Wu Q, Zhang J, Zhu P, Jiang W, Liu S, Ni M, Zhang M, Li W, Zhou Q, Cui Y, Xia X*. The susceptibility of FSHB -211G?>?T and FSHR G-29A, 919A?>?G, 2039A?>?G polymorphisms to men infertility: an association study and meta-analysis. BMC Med Genet. 2017, 18(1):81.
Ni M, Ding H, Liu S, Zhu P, Wu Q, Li W, Zhang J, Jiang W, Xia X*. Application of next-generation sequencing for molecular diagnosis in a large Chinese family with osteogenesis imperfecta type I. Mol Med Rep,2017. 16(5):6846-6849.
Liu SM, Ni MX, Zhang MC, Zhu PR, Wu QY, Jiang WJ, Zhang J, Li WW, Xia XY*. A novel missense mutation of ADAR1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review. J Genet,?96(6): 1021-1026.
Liu S, Zhang M, Ni M, Zhu P, Xia X*. A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: a case report. BMC Pediatr. 2017, 17(1):217.
Jiang W, Xiong L, Yang B, Li W, Zhang J, Zhou Q, Wu Q, Li T, Zhang C, Zhang M, Xia X*. Hyperhomocysteinaemia in rats is associated with erectile dysfunction by impairing endothelial nitric oxide synthase activity. Sci Rep. 2016, 6:26647.
Ye YH, Xie HQ, Shao XB, Wei Y, Liu YH, Zhao WB *, Xia XY *. Amperometric glucose biosensor based on effective self-assembly technology for preparation of poly(allylamine hydrochloride)/Au nanoparticles multilayers. J Nanosci Nanotechno, 2016, 16(3): 2270-2276.
Zhang J, Jiang W, Zhou Q, Ni M, Liu S, Zhu P, Wu Q, Li W, Zhang M, Xia X*. CAG-repeat polymorphisms in the polymerase γ gene and male infertility: a meta-analysis. Andrologia. 2016 , 2016(9): 882-889.
Yang R, Hu Z, Kong Q, Li W, Zhang L, Du X, Huang S, Xia X*, Sang H*. A known mutation in GJB6 in a large Chinese family with hidrotic ectodermal dysplasia. J Eur Acad Dermatol Venereol. 2016, 30(8):1362-1365.