现任上海交通大学医学院附属新华医院院长，国家教委重点学科儿科学学科带头人，担任第六届亚太小儿心血管学会主席，兼任中华医师协会等多个学术组织重要职位。
1. Liu C, Cao R, Xu Y, Li T, Li F, Chen S, Xu R, Sun K.Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects. Genome Med. 2018 May 30;10(1):40.
2. Pu T, Liu Y, Xu R, Li F, Chen S, Sun K.Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients. Mol Genet Genomics. 2018 Feb;293(1):217-223.
3. Du Q, Salem Y, Liu HH, Zhou X, Chen S, Chen N, Yang X, Liang J, Sun K.A home-based exercise program for children with congenital heart disease following interventional cardiac catheterization: study protocol for a randomized controlled trial .Trials. 2017 Jan 23;18(1):38.
4. Zhang E, Hong N, Chen S, Fu Q, Li F, Yu Y, Sun K.Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects. Gene. 2018 Jan 30;641:341-348.
5. Yao LP, Zhang L, Li HM, Ding M, Yu LW, Yang X, Li XM, Sun K.Assessment of coronary artery by prospective ECG-triggered 256 multi-slice CT on children with congenital heart disease .Int J Cardiovasc Imaging. 2017 Dec;33(12):2021-2028.
6. Liu Y, Li B, Xu Y, Sun K.Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population .Pediatr Cardiol. 2017 Mar;38(3):506-512.
7. Li WJ, Guo QQ, Gharibeh L, Xu R, Chen S, Sun K.Inhibition of Cardiomyogenesis in Embryocarcinoma Cells induced by longterm High level of Glucose. Cell Physiol Biochem. 2016;38(5):2041-52.
8. Zhao L, Wu Y, Chen S, Ren Y, Chen P, Niu J, Li C, Sun K.Screening using fourdismensional ultrasound with spatiotemporal image correlation: a multicenter study .PLoS One. 2016 Jun 17;11(6):e0157477.
9. Zhang X, Wang J, Wang B, Chen S, Fu Q, Sun K.A novel missense mutation of GATA4 in a Chinese family with congenital heart disease.PLoS One. 2016 Jul 8;11(7):e0158904.
10. Wang Q, Wu YR, Zhang LN, Zhang YJ, Xie LJ, Chen S, Sun K.Evaluating the risk factors of reintervention of neonates with PA/IVS and CPS/IVS after PBPV as initial intervention method .J Cardiol. 2016 Sep;68(3):190-5.
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11. Guo Q, Shen J, Liu Y, Pu T, Sun K, Chen S. Exome Sequencing Identifies a c.148-1G>C mutation of TBX5 in a Holt-Oram family with unusual genotype-phenotype correlations. Cell Physiol Biochem. 2015; 37(3): 1066-1074. (2.88)
12. Pu T, Guo Q, Cao R, Xu R, Sun K, Chen S. Using exome sequencing to identify the cause of myocardial hypertrophy in a Chinese family. Mol Med Rep. 2015; 12(3): 3662-3666.
13. Cao R, Long F, Wang L, Xu Y, Guo Y, Li F, Chen S, Sun K, Xu R. Duplication and Deletion of CFC1 Associated with Heterotaxy Syndrome. DNA Cell Biol. 2015; 34(2): 101-106.
14.Cao R, Pu T, Fang S, Long F, Xie J, Xu Y, Chen S, Sun K, Xu R. Patients Carrying 9p31.1-q32 deletion share common features with Cornelia de Lange Syndrome. Cell Physiol Biochem. 2015; 35(1): 270-280.
15.Guo QQ, Xu YJ, Wang XK, Guo Y, Xu R, Sun K, Chen S. Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy. DNA Cell Biol. 2014; 33(10): 699-704. (1.99)
16. Long F, Wang XK, Fang SH, Xu YJ, Sun K, Chen S, Xu R. A potential relationship among beta-defensins Haplotype, SOX7 duplication and Cardiac defects. PLoS One 2013; 8(8): e72515.
17. Yan Y, Huang J, Ding F, Mei J, Zhu J, Liu H, Sun K. Aquaporin 1 plays an important role in myocardial edema caused by cardiopulmonary bypass surgery in goat. Int J Mol Med. 2013; 31(3): 637-643.
