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✓Human Genetics10
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Rui-Rui Zhang results 10 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Rui-Rui Zhang ×Clear All Filters
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Identification of novel loci regulating circulating melatonin and its causal relationship with hypertensionNARA Subscribed
Human Genetics · 2026 · Vol. 145 · Issue 1 · Springer
Lin Yan; Yang Qiu; Zhiwen Mo; Mingli Li; Xueran Huang; Yongfen Gao; Boteng Yan; Qiantu Hu; Haiying Zhang; Zengnan Mo; Rui Lin
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Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain developmentNARA Subscribed
Human Genetics · 2025 · Vol. 144 · Issue 5 · Springer
Bo Chen; Chenyang Zhang; Huanwen Rui; Dan Shen; Zhuxi Huang; Weijun Feng
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Leveraging molecular quantitative trait loci to comprehend complex diseases/traits from the omics perspectiveNARA Subscribed
Human Genetics · 2023 · Vol. 142 · Issue 11 · Springer
Zijun Zhu; Xinyu Chen; Sainan Zhang; Rui Yu; Changlu Qi; Liang Cheng; Xue Zhang
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Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesisNARA Subscribed
Human Genetics · 2017 · Vol. 136 · Issue 11-12 · Springer
Tang Hai; Weiwei Guo; Jing Yao; Chunwei Cao; Ailing Luo; Meng Qi; Xianlong Wang; Xiao Wang; Jiaojiao Huang; Ying Zhang; Hongyong Zhang; Dayu Wang; Haitao Shang; Qianlong Hong; Rui Zhang; Qitao Jia; Qiantao Zheng; Guosong Qin; Yongshun Li; Tao Zhang; Weiwu Jin; Zheng-Yi Chen; Hongmei Wang; Qi Zhou; Anming Meng; Hong Wei; Shiming Yang; Jianguo Zhao
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Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trialNARA Subscribed
Human Genetics · 2016 · Vol. 135 · Issue 3 · Springer
Nicola G. Ghazi; Emad B. Abboud; Sawsan R. Nowilaty; Hisham Alkuraya; Abdulrahman Alhommadi; Huimin Cai; Rui Hou; Wen-Tao Deng; Sanford L. Boye; Abdulrahman Almaghamsi; Fahad Al Saikhan; Hassan Al-Dhibi; David Birch; Christopher Chung; Dilek Colak; Matthew M. LaVail; Douglas Vollrath; Kirsten Erger; Wenqiu Wang; Thomas Conlon; Kang Zhang; William Hauswirth; Fowzan S. Alkuraya
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Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinementsNARA Subscribed
Human Genetics · 2014 · Vol. 133 · Issue 3 · Springer
Feng Wang; Hui Wang; Han-Fang Tuan; Duy H. Nguyen; Vincent Sun; Vafa Keser; Sara J. Bowne; Lori S. Sullivan; Hongrong Luo; Ling Zhao; Xia Wang; Jacques E. Zaneveld; Jason S. Salvo; Sorath Siddiqui; Louise Mao; Dianna K. Wheaton; David G. Birch; Kari E. Branham; John R. Heckenlively; Cindy Wen; Ken Flagg; Henry Ferreyra; Jacqueline Pei; Ayesha Khan; Huanan Ren; Keqing Wang; Irma Lopez; Raheel Qamar; Juan C. Zenteno; Raul Ayala-Ramirez; Beatriz Buentello-Volante; Qing Fu; David A. Simpson; Yumei Li; Ruifang Sui; Giuliana Silvestri; Stephen P. Daiger; Robert K. Koenekoop; Kang Zhang; Rui Chen
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A miR-570 binding site polymorphism in the B7-H1 gene is associated with the risk of gastric adenocarcinomaNARA Subscribed
Human Genetics · 2013 · Vol. 132 · Issue 6 · Springer
Weipeng Wang; Fang Li; Yong Mao; Huan Zhou; Jing Sun; Rui Li; Cuiping Liu; Weichang Chen; Dong Hua; Xueguang Zhang
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Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populationsNARA Subscribed
Human Genetics · 2012 · Vol. 131 · Issue 7 · Springer
Jing He; Li-Xin Qiu; Meng-Yun Wang; Rui-Xi Hua; Ruo-Xin Zhang; Hong-Ping Yu; Ya-Nong Wang; Meng-Hong Sun; Xiao-Yan Zhou; Ya-Jun Yang; Jiu-Cun Wang; Li Jin; Qing-Yi Wei; Jin Li
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Ascertainment adjustment in genetic studies of ordinal traitsNARA Subscribed
Human Genetics · 2006 · Vol. 119 · Issue 4 · Springer
Rui Feng; Heping Zhang
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A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophyNARA Subscribed
Human Genetics · 2005 · Vol. 117 · Issue 5 · Springer
Laura Lucarini; Betti Giusti; Rui-Zhu Zhang; Te-Cheng Pan; Cecilia Jimenez-Mallebrera; Eugenio Mercuri; Francesco Muntoni; Guglielmina Pepe; Mon-Li Chu
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