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Springer Nature15
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✓Human Genetics15
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Li-Cheng Wang results 15 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Cheng Wang ×Clear All Filters
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Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes ProjectNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 12 · Springer
Feifan Xiao; Bingbing Wu; Chenbin Dong; Guoqiang Cheng; Yun Cao; Laishuan Wang; Xinran Dong; Yulan Lu; Lin Yang; Liping Chen; Long Li; Xinnian Pan; Qiufen Wei; Deyi Zhuang; Dongmei Chen; Zhaoqing Yin; Qi Ni; Rencao Liu; Suzhen Xu; Gang Li; Ping Zhang; Yanyan Qian; Xu Li; Xiaomin Peng; Yao Wang; Huijun Wang; Wenhao Zhou
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Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 6 · Springer
Ruibin Huang; Fang Fu; Hang Zhou; Lu Zhang; Tingying Lei; Ken Cheng; Shujuan Yan; Fei Guo; You Wang; Chunling Ma; Ru Li; Qiuxia Yu; Qiong Deng; Lushan Li; Xin Yang; Jin Han; Dongzhi Li; Can Liao
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Whole exome sequencing improves genetic diagnosis of fetal clubfootNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 3 · Springer
Ruibin Huang; Hang Zhou; Chunling Ma; Fang Fu; Ken Cheng; You Wang; Ru Li; Tingying Lei; Qiuxia Yu; Dan Wang; Shujuan Yan; Xin Yang; Dongzhi Li; Can Liao
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Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humansNARA Subscribed
Human Genetics · 2022 · Vol. 141 · Issue 11 · Springer
Huan Wu; Xin Zhang; Rong Hua; Yuqian Li; Li Cheng; Kuokuo Li; Yiyuan Liu; Yang Gao; Qunshan Shen; Guanxiong Wang; Mingrong Lv; Yuping Xu; Xiaojin He; Yunxia Cao; Mingxi Liu
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DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing lossNARA Subscribed
Human Genetics · 2022 · Vol. 141 · Issue 3-4 · Springer
Fengxiao Bu; Mingjun Zhong; Qinyi Chen; Yumei Wang; Xia Zhao; Qian Zhang; Xiarong Li; Kevin T. Booth; Hela Azaiez; Yu Lu; Jing Cheng; Richard J. H. Smith; Huijun Yuan
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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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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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Mutations in IL36RN are associated with geographic tongueNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 2 · Springer
Jianying Liang; Peichen Huang; Huaguo Li; Jia Zhang; Cheng Ni; Yirong Wang; Jinwen Shen; Chunxiao Li; Lu Kang; Jie Chen; Hui Zhang; Zhen Wang; Zhen Zhang; Ming Li; Zhirong Yao
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Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 2 · Springer
Luis G. Carvajal-Carmona; Tracy A. O’Mara; Jodie N. Painter; Felicity A. Lose; Joe Dennis; Kyriaki Michailidou; Jonathan P. Tyrer; Shahana Ahmed; Kaltin Ferguson; Catherine S. Healey; Karen Pooley; Jonathan Beesley; Timothy Cheng; Angela Jones; Kimberley Howarth; Lynn Martin; Maggie Gorman; Shirley Hodgson; Nicholas Wentzensen; Peter A. Fasching; Alexander Hein; Matthias W. Beckmann; Stefan P. Renner; Thilo Dörk; Peter Hillemanns; Matthias Dürst; Ingo Runnebaum; Diether Lambrechts; Lieve Coenegrachts; Stefanie Schrauwen; Frederic Amant; Boris Winterhoff; Sean C. Dowdy; Ellen L. Goode; Attila Teoman; Helga B. Salvesen; Jone Trovik; Tormund S. Njolstad; Henrica M. J. Werner; Rodney J. Scott; Katie Ashton; Tony Proietto; Geoffrey Otton; Ofra Wersäll; Miriam Mints; Emma Tham; Per Hall; Kamila Czene; Jianjun Liu; Jingmei Li; John L. Hopper; Melissa C. Southey; Arif B. Ekici; Matthias Ruebner; Nichola Johnson; Julian Peto; Barbara Burwinkel; Frederik Marme; Hermann Brenner; Aida K. Dieffenbach; Alfons Meindl; Hiltrud Brauch; Annika Lindblom; Jeroen Depreeuw; Matthieu Moisse; Jenny Chang-Claude; Anja Rudolph; Fergus J. Couch; Janet E. Olson; Graham G. Giles; Fiona Bruinsma; Julie M. Cunningham; Brooke L. Fridley; Anne-Lise Børresen-Dale; Vessela N. Kristensen; Angela Cox; Anthony J. Swerdlow; Nicholas Orr; Manjeet K. Bolla; Qin Wang; Rachel Palmieri Weber; Zhihua Chen; Mitul Shah; Paul D. P. Pharoah; Alison M. Dunning; Ian Tomlinson; Douglas F. Easton; Amanda B. Spurdle; Deborah J. Thompson
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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 2 · Springer
Qing Li; Robert Wojciechowski; Claire L. Simpson; Pirro G. Hysi; Virginie J. M. Verhoeven; Mohammad Kamran Ikram; René Höhn; Veronique Vitart; Alex W. Hewitt; Konrad Oexle; Kari-Matti Mäkelä; Stuart MacGregor; Mario Pirastu; Qiao Fan; Ching-Yu Cheng; Beaté St Pourcain; George McMahon; John P. Kemp; Kate Northstone; Jugnoo S. Rahi; Phillippa M. Cumberland; Nicholas G. Martin; Paul G. Sanfilippo; Yi Lu; Ya Xing Wang; Caroline Hayward; Ozren Polašek; Harry Campbell; Goran Bencic; Alan F. Wright; Juho Wedenoja; Tanja Zeller; Arne Schillert; Alireza Mirshahi; Karl Lackner; Shea Ping Yip; Maurice K. H. Yap; Janina S. Ried; Christian Gieger; Federico Murgia; James F. Wilson; Brian Fleck; Seyhan Yazar; Johannes R. Vingerling; Albert Hofman; André Uitterlinden; Fernando Rivadeneira; Najaf Amin; Lennart Karssen; Ben A. Oostra; Xin Zhou; Yik-Ying Teo; E. Shyong Tai; Eranga Vithana; Veluchamy Barathi; Yingfeng Zheng; Rosalynn Grace Siantar; Kumari Neelam; Youchan Shin; Janice Lam; Ekaterina Yonova-Doing; Cristina Venturini; S. Mohsen Hosseini; Hoi-Suen Wong; Terho Lehtimäki; Mika Kähönen; Olli Raitakari; Nicholas J. Timpson; David M. Evans; Chiea-Chuen Khor; Tin Aung; Terri L. Young; Paul Mitchell; Barbara Klein; Cornelia M. van Duijn; Thomas Meitinger; Jost B. Jonas; Paul N. Baird; David A. Mackey; Tien Yin Wong; Seang-Mei Saw; Olavi Pärssinen; Dwight Stambolian; Christopher J. Hammond; Caroline C. W. Klaver; Cathy Williams; Andrew D. Paterson; Joan E. Bailey-Wilson; Jeremy A. Guggenheim
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Polymorphisms of the Interleukin 6 gene contribute to cervical cancer susceptibility in Eastern Chinese womenNARA Subscribed
Human Genetics · 2013 · Vol. 132 · Issue 3 · Springer
Ting-Yan Shi; Mei-Ling Zhu; Jing He; Meng-Yun Wang; Qiao-Xin Li; Xiao-Yan Zhou; Meng-Hong Sun; Zhi-Ming Shao; Ke-Da Yu; Xi Cheng; Xiaohua Wu; Qingyi Wei
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Two novel mutations of the IRX4 gene in patients with congenital heart diseaseNARA Subscribed
Human Genetics · 2011 · Vol. 130 · Issue 5 · Springer
Zhi Cheng; Jing Wang; Dongmei Su; Hong Pan; Guoying Huang; Xiaotian Li; Zhongzhi Li; Adong Shen; Xiaodong Xie; Binbin Wang; Xu Ma
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Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationNARA Subscribed
Human Genetics · 2011 · Vol. 129 · Issue 3 · Springer
Cong Li; Fan Wang; Yanzong Yang; Fenfen Fu; Chengqi Xu; Lisong Shi; Sisi Li; Yunlong Xia; Gang Wu; Xiang Cheng; Hui Liu; Chuchu Wang; Pengyun Wang; Jianjun Hao; Yuhe Ke; Yuanyuan Zhao; Mugen Liu; Rongfeng Zhang; Lianjun Gao; Bo Yu; Qiutang Zeng; Yuhua Liao; Bo Yang; Xin Tu; Qing K. Wang
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Protein C -1641A/-1654C haplotype is associated with organ dysfunction and the fatal outcome of severe sepsis in Chinese Han populationNARA Subscribed
Human Genetics · 2008 · Vol. 123 · Issue 3 · Springer
Qi Xing Chen; Shui Jing Wu; Hai Hong Wang; Chen Lv; Bao Li Cheng; Guo Hao Xie; Xiang Ming Fang
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Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14NARA Subscribed
Human Genetics · 2008 · Vol. 122 · Issue 6 · Springer
Hui Li; Jia-Xin Wang; Cheng-Ye Wang; Ping Yu; Qiang Zhou; Yong-Gang Chen; Lu-Hang Zhao; Ya-Ping Zhang
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