已發(fā)表的SCI和EI收錄論文：
1.Chen C-Y, Xu C-M, Du Z-F, Chen X-L, Ren G-L, Zhang XN*. A c.1363C>T (p.R455X) nonsense mutation of RB1 gene in a southern Chinese retinoblastoma pedigree. Genetic Testing and Molecular Biomarkers 2010;（印刷中)（*通訊作者)（SCI。2008年IF= 1.120。)
2.Chen X-L, Xu C-M, Cai S-R, Chen C-Y, Zhang XN*. Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred. Prenatal Diagnosis 2009;29(9):911-913（*通訊作者)（SCI。2008年IF= 1.596。)
3.Xu C-M, Chen X-L, Chen C-Y, Zhang XN*. Missense mutation of keratin 9 (c.487C>T (p.R163W) in southern Chinese patients with epidermolytic palmoplantar keratoderma. European Journal of Dermatology 2009;19(3):265-266（*通訊作者)（SCI。2008年IF= 1.968。)
4.Liang Y-H, Chen X-L, Yu Z-S, Chen C-Y, Bi S, Mao L-G, Zhou B-L, Zhang X-N*. Deletion analysis of SMN1 and NAIP genes in southern Chinese children with spinal muscular atrophy. Journal of Zhejiang University Science B,2009; 10(1):29-34（*通訊作者)（SCI。2008年IF= 1.679。)
quanxiangyun.cn5.Zhang X-N*, Qi M. Mitochondrion and its related disorders: Making a comeback. Journal of Zhejiang University Science B,2008; 9(2):90-92（*通訊作者)（SCI。2008年IF= 1.679。)
6.Zhang X-N, Zhou M-N, Qiu Y-Q, Ding S-P, Qi M, Li J-C. Genetic analysis of RET, EDNRB and EDN3 genes and three SNPs in MCS+9.7 in Chinese patients with isolated Hirschsprung disease. Biochemical Genetics,2007;45(7/8): 523-527（SCI。2008年IF=0.750)
quanxiangyun.cn7.Yu R, Zhang X-N*, Huang X-X, Ding S-P, Li J-C. Association analysis of COMT polymorphisms and schizophrenia in a Chinese Han population: A case-control study. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics,2007;144B(4):570-573（*通訊作者)（SCI。2008年IF=3.932)
8.Yu R, Lai Z, Zhou W, Ti D-D, Zhang X-N*. Recurrent FBN1 mutation (R62C) in a Chinese family with isolated ectopia lentis. American Journal of Ophthalmology，2006;141(6): 1136-1138（*通訊作者)（SCI。2008年IF=3.102)
9.Guo J-M, Xiao B-X, Kang G-Z, Liu D-H, Chen H, Zhang S, Zhang X-N. Suppression of telomerase activity and arrest at G1 phase in human cervical cancer HeLa cells by all-trans retinoic acid. International Journal of Gynecological Cancer, 2006;16(1):341-346（SCI。2008年IF=1.932)
10.Lai Z, Zhang X-N*, Zhou W, Yu R, Le Y-P. Evaluation of the ELOVL4 gene in a Chinese family with autosomal dominant STGD3-like macular dystrophy. Journal of Cellular and Molecular Medicine,2005; 9(4):961-965（*通訊作者)（SCI。2008年IF=5.114)
11.Zhang X-N, He X-H, Lai Z, Mao W, He X-L, Li J-C. An insertion-deletion mutation in keratin 9 in three Chinese families with epidermolytic palmoplantar keratoderma. British Journal of Dermatology,2005; 152(4):804-806（SCI。2008年IF=3.489)
12.He X-H, Zhang X-N*, Mao W, Chen H-P, Xu L-R, Chen H, He X-L, Le Y-P. A novel mutation of keratin 9 in a large Chinese family with epidermolysis palmoplantar keratoderma. British Journal of Dermatology,2004;150(4):647-651（*通訊作者)（SCI。2008年IF=3.489)
13.Zhang X-N*, Jiang S-D, He X-H, Zhang L-N. 102T/C SNP in the 5-hydroxytryptamine receptor 2A (HTR2A) gene and schizophrenia in two southern Han Chinese populations: Lack of association. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics,2004; 126B(1):16-18（*通訊作者)（SCI。2008年IF=3.932)
14.張咸寧*,阮列敏,樂燕萍,張野.注意缺陷多動障礙與
兒茶酚-O-甲基轉移酶基因Vall58 Met多態(tài)性的關聯分析.
中華醫(yī)學遺傳學雜志,2003；20(4):322-324（*通訊作者)（EI)
15.Dai FY, Yu L, He H, Zhao Y, Yang J, Zhang X-N, Zhao S-Y. Cloning and mapping of a novel human serum/glucocorticoid regulated kinase-like gene, SGKL, to chromosome 8q12.3-q13.1. Genomics,1999; 62(1):95-97（SCI。2008年IF=3.075)
16.Li X, Fan Y-X, Ji B-X, Zhang X-N, Zhu D-L, Geng Z-C. The association of different Human leucocyte antigen-DQ with myasthenia gravis. Chinese Medical Journal,1998; 111(9):802（SCI。2008年IF= 0.858)
主要教學、科研等獎勵和榮譽：
1.2009年度浙江大學醫(yī)學部先進工作者。
2.2009年度浙江大學醫(yī)學部“獎教金”。
3.2007年度浙江大學醫(yī)學院先進工作者。
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