Qin Y#, et al…,Gong XH* and Wang HY*. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Mol Psychiatry 2022 Jul;27(7):2985-98.
Li C#, et al…,Zhao JY* and Wang HY*. Master microRNA-222 regulates cardiac microRNA maturation and triggers Tetralogy of Fallot. Signal Transduct Target Ther. 2022;7(1):165.
Wang YL#, et al…,Wang CJ* and Wang HY*. KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses. Sci Adv. 2022;8(31):eabm5578.
Chen ZZ#, et al…,Zhang T*, Finnell R*, Wang HY*. Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell Res 2018; 28(10):1039-41
Zhou X#, Wang HY*. ACOX2 deficiency in primary malignant cardiac tumors.Proc Natl Acad Sci U S A.2017; 114(18):E3590-E3591
Wang D#, et al…,Zhao SM*, Wang HY*, Zhao JY*. Lower Circulating Folate Induced by a Fidgetin Intronic Variant is Associated with Reduced Congenital Heart Disease Susceptibility.Circulation. 2017;135(18):1733-1748
Zhao JY#, et al…, Huang GY*, Jin L*, Wang HY*. Genetic variants reducing MTR gene expression increase risk of congenital heart disease in a Chinese population. Eur Heart J. 2014;35(11):733-42
Zhao JY#, et al…, Wang HY*. A Functional Variant in the Cystathionine b-Synthase Gene Promoter Significantly Reduces Congenital Heart Disease Susceptibility in Han Chinese Population. Cell Res, 2013;23:242-253
Qin Y#, et al…,Gong XH* and Wang HY*. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Mol Psychiatry 2022 Jul;27(7):2985-98.
Li C#, et al…,Zhao JY* and Wang HY*. Master microRNA-222 regulates cardiac microRNA maturation and triggers Tetralogy of Fallot. Signal Transduct Target Ther. 2022;7(1):165.
Wang YL#, et al…,Wang CJ* and Wang HY*. KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses. Sci Adv. 2022;8(31):eabm5578.
Chen ZZ#, et al…,Zhang T*, Finnell R*, Wang HY*. Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell Res 2018; 28(10):1039-41
Zhou X#, Wang HY*. ACOX2 deficiency in primary malignant cardiac tumors.Proc Natl Acad Sci U S A.2017; 114(18):E3590-E3591
Wang D#, et al…,Zhao SM*, Wang HY*, Zhao JY*. Lower Circulating Folate Induced by a Fidgetin Intronic Variant is Associated with Reduced Congenital Heart Disease Susceptibility.Circulation. 2017;135(18):1733-1748
Zhao JY#, et al…, Huang GY*, Jin L*, Wang HY*. Genetic variants reducing MTR gene expression increase risk of congenital heart disease in a Chinese population. Eur Heart J. 2014;35(11):733-42
Zhao JY#, et al…, Wang HY*. A Functional Variant in the Cystathionine b-Synthase Gene Promoter Significantly Reduces Congenital Heart Disease Susceptibility in Han Chinese Population. Cell Res, 2013;23:242-253
新发突变致出生缺陷的发生机理,全国妇幼健康自然科学一等奖,第一完成人,2016
中国人群重大出生缺陷的遗传分析,教育部自然科学一等奖,第一完成人,2015
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