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Academic Achievements

Wang Yu-Meng；Zheng Yu-Fang；Yang Si-Yu；Yang Zhang-Min；Zhang Lin-Na；He Yan-Qin；Gong Xiao-Hong；Liu Dong；Finnell Richard H.；Qiu Zi-Long；Du Ya-Song；Wang Hong-Yan,Wang Yu-Meng；Qiu Zi-Long；Du Ya-Song；Wang Hong-Yan；Zheng Yu-Fang；Yang Si-Yu；Yang Zhang-Min；Zhang Lin-Na；He Yan-Qin；Gong Xiao-Hong；Liu Dong；Finnell Richard H., MicroRNA-197 controls ADAM10 expression to mediate MeCP2's role in the differentiation of neuronal progenitors -CELL DEATH AND DIFFERENTIATION -2019-01-01 -26
Qin Qi-Yun；Zeng Wei-Jia；Peng Chu-Yue；Zheng Yu-Fang；Wang Hong-Yan, Deficiency of Antisense lncRNA Gm48853 Resulted in Embryonic Lethality and Impaired Placental Development in Mice -Reproductive and Developmental Medicine -2019-01-01 -3
Zhang Henan；Guo Yi；Gu Hui；Wei Xiaowei；Ma Wei；Liu Dan；Yu Kun；Luo Wenting；Ma Ling；Liu Yusi；Xue Jia；Huang Jieting；Wang Yanfu；Jia Shanshan；Dong Naixuan；Wang Hongyan；Yuan Zhengwei,Zhang Henan；Liu Yusi；Xue Jia；Huang Jieting；Wang Yanfu；Jia Shanshan；Dong Naixuan；Wang Hongyan；Yuan Zhengwei；Guo Yi；Gu Hui；Wei Xiaowei；Ma Wei；Liu Dan；Yu Kun；Luo Wenting；Ma Ling, TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis -Clinical Epigenetics -2019-01-01 -11
Xie Yifang；Ma Anyun；Wang Boshi；Peng Rui；Jing Yingchun；Wang Deqian；Finnell Richard H.；Qiao Bin；Wang Yongming；Wang Hongyan；Zheng Yufang,Xie Yifang；Wang Hongyan；Zheng Yufang；Ma Anyun；Wang Boshi；Peng Rui；Jing Yingchun；Wang Deqian；Finnell Richard H.；Qiao Bin；Wang Yongming, Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling -CLINICAL SCIENCE -2019-01-01 -133
Dong Shuangshuang；Wang Chunyan；Li Xueping；Shen Qian；Fu Xiaoyi；Wu Mingyan；Song Chengcheng；Yang Nan；Wu Yanhua；Wang Hongyan；Jin Li；Xu Hong；Zhang Feng,Dong Shuangshuang；Wang Hongyan；Jin Li；Xu Hong；Zhang Feng；Wang Chunyan；Li Xueping；Shen Qian；Fu Xiaoyi；Wu Mingyan；Song Chengcheng；Yang Nan；Wu Yanhua, Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract -MOLECULAR GENETICS AND GENOMICS -2019-01-01 -294
Shi Zhiwen；Chen Shuxia；Han Xiao；Peng Rui；Luo Jin；Yang Luming；Zheng Yufang；Wang Hongyan, The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects -Molecular Cytogenetics -2019-01-01 -12
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella -JOURNAL OF MEDICAL GENETICS -2019-01-01 -56
Li Q.；Li Y.；Yang S.；Huang S.；Yan M.；Ding Y.；Tang W.；Lou X.；Yin Q.；Sun Z.；Lu L.；Shi H.；Wang H.；Chen Y.；Li J.,Li Q.；Sun Z.；Lu L.；Shi H.；Wang H.；Chen Y.；Li J.；Li Y.；Yang S.；Huang S.；Yan M.；Ding Y.；Tang W.；Lou X.；Yin Q., Author Correction: CRISPR–Cas9-mediated base-editing screening in mice identifies DND1 amino acids that are critical for primordial germ cell development (Nature Cell Biology, (2018), 20, 11, (1315-1325), 10.1038/s41556-018-0202-4) -NATURE CELL BIOLOGY -2019-01-01 -21
Wang Daqi；Zhang Chengdong；Wang Bei；Li Bin；Wang Qiang；Liu Dong；Wang Hongyan；Zhou Yan；Shi Leming；Lan Feng；Wang Yongming,Wang Daqi；Lan Feng；Wang Yongming；Zhang Chengdong；Wang Bei；Li Bin；Wang Qiang；Liu Dong；Wang Hongyan；Zhou Yan；Shi Leming, Optimized CRISPR guide RNA design for two high-fidelity Cas9 variants by deep learning -Nature Communications -2019-01-01 -10
Ye Z.；Huang Y.；Zheng C.；Wang Y.；Lu J.；Wang H.；Wu B.；Wang X.；Zhang R.；Wang J.,Ye Z.；Wang J.；Huang Y.；Zheng C.；Wang Y.；Lu J.；Wang H.；Wu B.；Wang X.；Zhang R., Clinical and genetic spectrum of children with congenital diarrhea and enteropathy in China -GENETICS IN MEDICINE -2019-01-01 -21

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