Yang Bi-Cheng - Key Laboratory of Women's Reproductive Health of Jiangxi Province, P.R. China.

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论文共 59 篇作者统计合作学者相似作者

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A Retrospective Analysis of Robertsonian Translocations from a Single Center in China

Wan Lu,Jihui Zhou,Huihua Rao,Huizhen Yuan,Shuhui Huang,Yanqiu Liu,Bicheng Yang

Reproductive Sciences（2024）

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Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA

Yan Yang,Haiyan Luo,Lijuan Pan, Chuanxin Feng, Zhen Guo,Yongyi Zou,Baitao Zeng,Shuhui Huang,Huizhen Yuan, Ping Wu,Danping Liu, Yi Dan,

Human molecular genetics（2024）

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Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA

Yan Yang,Haiyan Luo,Lijuan Pan, Chuanxin Feng, Zhen Guo,Yongyi Zou,Baitao Zeng,Shuhui Huang,Huizhen Yuan, Ping Wu,Danping Liu, Yi Dan,

Human Molecular Genetics（2024）

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Hereditary deafness carrier screening in 9,993 Chinese individuals

Yanqiu Liu, Lei Wang,Lanlai Yuan, Yaqing Li, Zhengshi Chen,Bicheng Yang, Daqing Wang,Yu Sun

FRONTIERS IN GENETICS (2024): 1327258-1327258

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Association between aberrant amino acid metabolism and nonchromosomal modifications fetal structural anomalies: A cohort study

Huizhen Yuan,Chang Liu,Xinrong Wang,Tingting Huang,Danping Liu,Shuhui Huang,Zeming Wu,Yanqiu Liu,Peiyuan Yin,Bicheng Yang

Front Endocrinol (Lausanne)（2023）

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Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, China

Yongyi Zou, Chuanxin Feng, Jiawei Qin,Xinrong Wang,Tingting Huang,Yan Yang,Kang Xie,Huizhen Yuan,Shuhui Huang,Bicheng Yang,Wan Lu,Yanqiu Liu

Frontiers in Genetics (2023): 1073851-1073851

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Identification of five novel SCN1A variants

Baitao Zeng, Haoyi Zhang,Qing Lu, Qingzi Fu, Yang Yan, Wan Lu,Pengpeng Ma, Chuanxin Feng, Jiawei Qin,Laipeng Luo,Bicheng Yang,Yongyi Zou,

Frontiers in Behavioral Neuroscience (2023): 1272748-1272748

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Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA

Yan Yang, Heng Luo,Lijuan Pan,Feng Chen, Zhen Guo, Ying Zou,Baitao Zeng, San Yuan Huang,Huizhen Yuan, Peng Wu,Danping Liu, Dan Yi,

Research Square (Research Square) (2023)

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Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi province

Baitao Zeng,Qing Lu,Shaohong Chen,Huizhen Guan, Xiaolan Xu,Yongyi Zou,Feng Wang,Shuhui Huang,Yanqiu Liu,Bicheng Yang

Front Genet（2023）

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Developmental Trends in Postnatal Thyroid Hormones and Thyroid Dysfunction in Preterm Infants Born at less than 34 weeks Gestation

Shaohong Chen, Xiaoyan Lu,Bicheng Yang, Jieru Wu,Hui Huang,Yang Zou, Wenyan Tang, Ping Xu, Yu Yang

Fetal and pediatric pathology（2023）

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