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Springer Nature9
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✓Human Genetics9
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Li-Fei Liu results 9 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Fei Liu ×Clear All Filters
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Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic herniaNARA Subscribed
Human Genetics · 2025 · Vol. 144 · Issue 9-10 · Springer
Ruibin Huang; Fang Fu; Shanshan Mei; Liyuan Liu; Wei Zhong; Jin Han; Qiuxia Yu; Hang Zhou; Chunling Ma; Li Zhen; Min Pan; Qiong Deng; Jianqin Lu; Xinyi Zhao; Na Zhang; Fei Guo; Huanyi Chen; Xinyue Tan; Fucheng Li; Dongzhi Li; Ru Li; Can Liao
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TMEM151A variants associated with paroxysmal kinesigenic dyskinesiaNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 8 · Springer
Hua lin Huang; Qing xia Zhang; Fei Huang; Xiao yan Long; Zhi Song; Bo Xiao; Guo liang Li; Cai yu Ma; Ding Liu
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Retraction Note to: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypesNARA Subscribed
Human Genetics · 2022 · Vol. 141 · Issue 1 · Springer
Michael Nothnagel; Guangyao Fan; Fei Guo; Yongfeng He; Yiping Hou; Shengping Hu; Jiang Huang; Xianhua Jiang; Wook Kim; Kicheol Kim; Chengtao Li; Hui Li; Liming Li; Shilin Li; Zhao Li; Weibo Liang; Chao Liu; Di Lu; Haibo Luo; Shengjie Nie; Meisen Shi; Hongyu Sun; Jianpin Tang; Lei Wang; Chuan-Chao Wang; Dan Wang; Shao-Qing Wen; Hongyan Wu; Weiwei Wu; Jiaxin Xing; Jiangwei Yan; Shi Yan; Hongbing Yao; Yi Ye; Libing Yun; Zhaoshu Zeng; Lagabaiyila Zha; Suhua Zhang; Xiufen Zheng; Sascha Willuweit; Lutz Roewer
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Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCDNARA Subscribed
Human Genetics · 2020 · Vol. 139 · Issue 2 · Springer
Chaofeng Tu; Hongchuan Nie; Lanlan Meng; Weili Wang; Haiyu Li; Shimin Yuan; Dehua Cheng; Wenbin He; Gang Liu; Juan Du; Fei Gong; Guangxiu Lu; Ge Lin; Qianjun Zhang; Yue-Qiu Tan
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Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophyNARA Subscribed
Human Genetics · 2018 · Vol. 137 · Issue 10 · Springer
Shanshan Han; Xiliang Liu; Shanglun Xie; Meng Gao; Fei Liu; Shanshan Yu; Peng Sun; Changquan Wang; Stephen Archacki; Zhaojing Lu; Xuebin Hu; Yayun Qin; Zhen Qu; Yuwen Huang; Yuexia Lv; Jiayi Tu; Jingzhen Li; Tinsae Assefa Yimer; Tao Jiang; Zhaohui Tang; Daji Luo; Fangyi Chen; Mugen Liu
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A genetic variant in the placenta-derived MHC class I chain-related gene A increases the risk of preterm birth in a Chinese populationNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 10 · Springer
Junjiao Song; Jing Li; Han Liu; Yuexin Gan; Yang Sun; Min Yu; Yongjun Zhang; Fei Luo; Ying Tian; Weiye Wang; Jun Zhang; Julian Little; Haidong Cheng; Dan Chen
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RETRACTED ARTICLE: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypesNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 5 · Springer
Michael Nothnagel; Guangyao Fan; Fei Guo; Yongfeng He; Yiping Hou; Shengping Hu; Jiang Huang; Xianhua Jiang; Wook Kim; Kicheol Kim; Chengtao Li; Hui Li; Liming Li; Shilin Li; Zhao Li; Weibo Liang; Chao Liu; Di Lu; Haibo Luo; Shengjie Nie; Meisen Shi; Hongyu Sun; Jianpin Tang; Lei Wang; Chuan-Chao Wang; Dan Wang; Shao-Qing Wen; Hongyan Wu; Weiwei Wu; Jiaxin Xing; Jiangwei Yan; Shi Yan; Hongbing Yao; Yi Ye; Libing Yun; Zhaoshu Zeng; Lagabaiyila Zha; Suhua Zhang; Xiufen Zheng; Sascha Willuweit; Lutz Roewer
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Genome-wide association study identifies HMGN3 locus for spine bone size variation in ChineseNARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer
Shu-Feng Lei; Hui Shen; Tie-Lin Yang; Yan Guo; Shan-Shan Dong; Xiang-Hong Xu; Fei-Yan Deng; Qing Tian; Yong-Jun Liu; Yao-Zhong Liu; Jian Li; Hong-Wen Deng
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Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31NARA Subscribed
Human Genetics · 2009 · Vol. 125 · Issue 1 · Springer
Xue-Zhong Liu; Yongyi Yuan; Denise Yan; Emilie Hong Ding; Xiao Mei Ouyang; Yu Fei; Wenxue Tang; Huijun Yuan; Qing Chang; Li Lin Du; Xin Zhang; Guojian Wang; Shoeb Ahmad; Dong Yang Kang; Xi Lin; Pu Dai
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