Li-Mei Yu - NARA Discovery

Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic herniaNARA Subscribed

Human Genetics · 2025 · Vol. 144 · Issue 9-10 · Springer

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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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Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association studyNARA Subscribed

Human Genetics · 2014 · Vol. 133 · Issue 5 · Springer

Wei Liu; Hai-Ning Wang; Zhao-Hui Gu; Shao-Ying Yang; Xiao-Ping Ye; Chun-Ming Pan; Shuang-Xia Zhao; Li-Qiong Xue; Hui-Jun Xie; Sha-Sha Yu; Cui-Cui Guo; Wen-Hua Du; Jun Liang; Xiao-Mei Zhang; Guo-Yue Yuan; Chang-Gui Li; Qing Su; Guan-Qi Gao; Huai-Dong Song

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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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A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing lossNARA Subscribed

Human Genetics · 2010 · Vol. 127 · Issue 2 · Springer

Hui-Mei Hong; Jiann-Jou Yang; Ching-Chyuan Su; Juan-Yu Chang; Tung-Cheng Li; Shuan-Yow Li

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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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Genome-wide association scan for stature in Chinese: evidence for ethnic specific lociNARA Subscribed

Human Genetics · 2009 · Vol. 125 · Issue 1 · Springer

Shu-Feng Lei; Tie-Lin Yang; Li-Jun Tan; Xiang-Ding Chen; Yan Guo; Yan-Fang Guo; Liang Zhang; Xiao-Gang Liu; Han Yan; Feng Pan; Zhi-Xin Zhang; Yu-Mei Peng; Qi Zhou; Li-Na He; Xue-Zhen Zhu; Jing Cheng; Yao-Zhong Liu; Christopher J. Papasian; Hong-Wen Deng

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