Li-Lin Lin - NARA Discovery

Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese HansNARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer

Ling Lu; Hongguang Sheng; Huaixing Li; Wei Gan; Chen Liu; Jingwen Zhu; Ruth J. F. Loos; Xu Lin

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type IINARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 3 · Springer

Hua Zhang; Hongsheng Chen; Hunjin Luo; Jing An; Lin Sun; Lingyun Mei; Chufeng He; Lu Jiang; Wen Jiang; Kun Xia; Jia-Da Li; Yong Feng

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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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Meta-analysis of new genome-wide association studies of colorectal cancer riskNARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 2 · Springer

Ulrike Peters; Carolyn M. Hutter; Li Hsu; Fredrick R. Schumacher; David V. Conti; Christopher S. Carlson; Christopher K. Edlund; Robert W. Haile; Steven Gallinger; Brent W. Zanke; Mathieu Lemire; Jagadish Rangrej; Raakhee Vijayaraghavan; Andrew T. Chan; Aditi Hazra; David J. Hunter; Jing Ma; Charles S. Fuchs; Edward L. Giovannucci; Peter Kraft; Yan Liu; Lin Chen; Shuo Jiao; Karen W. Makar; Darin Taverna; Stephen B. Gruber; Gad Rennert; Victor Moreno; Cornelia M. Ulrich; Michael O. Woods; Roger C. Green; Patrick S. Parfrey; Ross L. Prentice; Charles Kooperberg; Rebecca D. Jackson; Andrea Z. LaCroix; Bette J. Caan; Richard B. Hayes; Sonja I. Berndt; Stephen J. Chanock; Robert E. Schoen; Jenny Chang-Claude; Michael Hoffmeister; Hermann Brenner; Bernd Frank; Stéphane Bézieau; Sébastien Küry; Martha L. Slattery; John L. Hopper; Mark A. Jenkins; Loic Le Marchand; Noralane M. Lindor; Polly A. Newcomb; Daniela Seminara; Thomas J. Hudson; David J. Duggan; John D. Potter; Graham Casey

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Molecular genetic studies of gene identification for sarcopeniaNARA Subscribed

Human Genetics · 2012 · Vol. 131 · Issue 1 · Springer

Li-Jun Tan; Shan-Lin Liu; Shu-Feng Lei; Christopher J. Papasian; Hong-Wen Deng

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Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patientsNARA Subscribed

Human Genetics · 2011 · Vol. 129 · Issue 5 · Springer

Qiaoli Li; Guizhong Yang; Ying Wang; Xiaoping Zhang; Qing Sang; Huan Wang; Xinzhi Zhao; Qinghe Xing; Lin He; Lei Wang

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Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlationNARA Subscribed

Human Genetics · 2010 · Vol. 128 · Issue 3 · Springer

Jiann-Jou Yang; Wen-Hung Wang; Yen-Chun Lin; Hsu-Huei Weng; Jen-Tsung Yang; Chung-Feng Hwang; Che-Min Wu; Shuan-Yow Li

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The CAG repeat in SCA12 functions as a cis element to up-regulate PPP2R2B expressionNARA Subscribed

Human Genetics · 2010 · Vol. 128 · Issue 2 · Springer

Chih-Hsin Lin; Chiung-Mei Chen; Yi-Ting Hou; Yih-Ru Wu; Hsiu-Mei Hsieh-Li; Ming-Tsan Su; Guey-Jen Lee-Chen

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WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsNARA Subscribed

Human Genetics · 2010 · Vol. 128 · Issue 1 · Springer

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Erratum to: Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing lossNARA Subscribed

Human Genetics · 2010 · Vol. 127 · Issue 5 · Springer

Hui-Mei Hong; Jiann-Jou Yang; Jia-Ching Shieh; Mei-Ling Lin; Shuan-Yow Li

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A meta-analysis of three polymorphisms in the endothelial nitric oxide synthase gene (NOS3) and their effect on the risk of diabetic nephropathyNARA Subscribed

Human Genetics · 2010 · Vol. 127 · Issue 4 · Springer

Zhen Zeng; Lina Li; Zhao Zhang; Yang Li; Zhiyun Wei; Ke Huang; Lin He; Yongyong Shi

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Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male populationNARA Subscribed

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

Binbin Wang; Zhimin Miao; Shiguo Liu; Jing Wang; Shiyi Zhou; Lin Han; Dongmei Meng; Yunlong Wang; Changgui Li; Xu Ma

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Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping resultsNARA Subscribed

Human Genetics · 2009 · Vol. 126 · Issue 6 · Springer

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Non-synonymous GIGYF2 variants in Parkinson’s disease from two Asian populationsNARA Subscribed

Human Genetics · 2009 · Vol. 126 · Issue 3 · Springer

Eng-King Tan; Chin-Hslen Lin; Chun-Hwei Tai; Louis C. Tan; Meng-Ling Chen; R. Li; Hui-Qin Lim; Ratnagopal Pavanni; Yih Yuen; K. M. Prakash; Yi Zhao; Ruey-Meei Wu

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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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A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33NARA Subscribed

Human Genetics · 2008 · Vol. 124 · Issue 4 · Springer

Xiao-Hua Dai; Wen-Wu Chen; Xu Wang; Qi-Hui Zhu; Cong Li; Lin Li; Mu-Gen Liu; Qing-K. Wang; Jing-Yu Liu

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Positive association between OLIG2 and schizophrenia in the Chinese Han populationNARA Subscribed

Human Genetics · 2008 · Vol. 122 · Issue 6 · Springer

Ke Huang; Wei Tang; Ruqi Tang; Zhao Xu; Zhangdong He; Zhiqiang Li; Yifeng Xu; Xingwang Li; Guang He; Guoying Feng; Lin He; YongYong Shi

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Meta-analysis shows association between the tryptophan hydroxylase (TPH) gene and schizophreniaNARA Subscribed

Human Genetics · 2006 · Vol. 120 · Issue 1 · Springer

Dawei Li; Lin He

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Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese populationNARA Subscribed

Human Genetics · 2006 · Vol. 119 · Issue 5 · Springer

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Further clarification of the contribution of the tryptophan hydroxylase (TPH) gene to suicidal behavior using systematic allelic and genotypic meta-analysesNARA Subscribed

Human Genetics · 2006 · Vol. 119 · Issue 3 · Springer

Dawei Li; Lin He

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Phylogenetic relationship of the populations within and around Japan using 105 short tandem repeat polymorphic lociNARA Subscribed

Human Genetics · 2006 · Vol. 118 · Issue 6 · Springer

Shi-Lin Li; Toshimichi Yamamoto; Takashi Yoshimoto; Rieko Uchihi; Masaki Mizutani; Yukihide Kurimoto; Katsushi Tokunaga; Feng Jin; Yoshinao Katsumata; Naruya Saitou

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Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationNARA Subscribed

Human Genetics · 2005 · Vol. 116 · Issue 4 · Springer

Xiao Mei Ouyang; Denise Yan; Li Lin Du; J. Fielding. Hejtmancik; Samuel G. Jacobson; Walter E. Nance; An Ren Li; Simon Angeli; Muriel Kaiser; Valerie Newton; Steve D. M. Brown; Thomas Balkany; Xue Zhong Liu

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Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II)NARA Subscribed

Human Genetics · 2005 · Vol. 116 · Issue 3 · Springer

Jui-Hung Chang; Shuan-Pei Lin; Shu-Chuan Lin; Kai-Li Tseng; Chia-Ling Li; Chih-Kuang Chuang; Guey-Jen Lee-Chen

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Localized aggressive periodontitis is linked to human chromosome 1q25NARA Subscribed

Human Genetics · 2004 · Vol. 114 · Issue 3 · Springer

Yefu Li; Lin Xu; Hatice Hasturk; Alpdogan Kantarci; Steven R. DePalma; Thomas E. Van Dyke

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