任下列學術期刊的特邀審稿人：Human Molecular Genetics，Neuroscience Letters， Journal of Clinical Psychiatry，American Journal of Medical Genetics， Biological Psychiatry & Schizophrenia Research.
著作論文
自2005年以來，代表性論文包括發表在NEJM，Circulation，Cell research，PNAS，Human Mutation，Cancer，Human Molecular Genetics,Molecular Psychiatry 及 American Journal of Medical Genetics 等期刊中的文章。
Yun-Ping Lei, Ting Zhang, Hong Li, Bai-Lin Wu, Li Jin,Hong-Yan Wang*(2010). VANGL2 Mutations Identified in Human Cranial Neural-Tube Defects.New EnglandJournal of Medicine362 (23):2232-2235.(IF=54)
Wang D, Wang F, Shi KH, Tao H, Li Y, Zhao R, Lu H, Duan WY, Qiao, B, Zhao SM*,Wang HY*,Zhao JY* (2017). The Circulating Folate Decrease Induced by a Fidgetin Intronic Variant Is Associated with Reduced Congenital Heart Disease Susceptibility.Circulation.(IF=19.31)
Zhou, Xiangyu, and Hongyan Wang*(2017). ACOX2 deficiency in primary malignant cardiac tumors.Proceedings of the National Academy of Sciences.(IF=9.66)
Zhao JY#, Qiao B#, Duan WY#, Gong XH, Jiang SS, Ye ZZ, Wang J, Gu ZY, Shen HB, Shi KH, Sun SN, Huang GY*, Jin L*,Wang HY*(2013). Genetic variants reducing MTR gene expression increase risk of congenital heart disease in a Chinese population.European Heart Journal(DOI: 10.1093 /eurheartj/eht221)(IF 14.1)
Zhao JY, Yang XY#, Shi KH#, Sun SN, Hou J, Ye ZZ, Wang J, Duan WY, Qiao Bin, Chen YJ, Shen HB, Huang GY, Jin L,Wang HY*(2013). A Functional Variant in the Cystathionine b-Synthase Gene Promoter Significantly Reduces Congenital Heart Disease Susceptibility in Han Chinese Population.Cell Research( 23:242-253)(IF 10.53 )
Zhao JY, Yang XY, Gong XH，Gu ZY, Duan WY, Wang J, Ye ZZ, Shen HB, Shi KH, Hou J, Huang GY, Jin L, Qiao B*, andWang HY*(2012). A functional variant in MTRR intron-1 significantly increases risk of congenital heart disease in Han Chinese population.Circulation125:482-490,（IF=19.31）
Yang, XY, Zhou, XY, Wang, QQ,Wang, H Y*,Mutations in the COPII vesicle component gene SEC24B are associated with humanneural tube defects.Hum Mutation, 2013. 34(8): p. 1094-101.(IF=5.6)
Shi, Y, Ding, Y, Lei, YP,Wang, H Y*,Identification of novel rare mutations of DACT1 in human neural tube defects.Hum Mutation, 2012. 33(10): p. 1450-5.(IF=5.6)
Wang，HY, Sammel MD, Tromp G, Gotsch F, Halder I, Shriver MD, Romero R, Strauss JF et al (2008). A 12 bp deletion in the 5’-flanking region of the SERPINH1 gene affects promoter activity and protects against preterm premature rupture of membranes in African Americans.Human Mutation29(2):332.(IF=5.6)
Wang，HY,Ogawa M, Wood JR, Bartolomei MS, Sammel MD, Kusanovic JP, Walsh SW, Romero R, Strauss JFet al (2008). Genetic and epigenetic mechanisms combine to control MMP1 expression and its association with preterm premature rupture of membranes.Human Molecular Genetics17(8):1087-1096.(IF=7.54)
Wang HY, Parry S, Macones G, Sammel MD, Kuivaniemi H, Tromp G, Halder I, Shriver MD, Romero R, Strauss JF (2006). A Functional SNP in the Promoter of the SERPINH1 Gene Encoding Hsp47 Increases Risk of Preterm Premature Rupture of Membranes and Preterm Birth in African-Americans.Proceedings of the National Academy of Sciences of United States of America(IF=9.8)
Wang HY,Parry S, Macones G, Sammel MD, Ferrand PE, Kuivaniemi H, Tromp G, Halder I, Shriver MD, Romero R, Strauss JF (2004). Functionally significant SNP MMP8 promoter haplotypes and preterm premature rupture of membranes (PPROM).Human Molecular Genetics 13(21):2659-2669.(IF=7.54)
Wang, H.Y., et al., Apolipoprotein E is a genetic risk factor for fetal iodine deficiency disorder in China. Mol Psychiatry, 2000. 5(4): p. 363-8.（IF=13.7）
Wang, H., et al., Congenital absence of permanent teeth in a six-generation Chinese kindred. Am J Med Genet, 2000. 90(3): p. 193-8.（IF=3.65)。
