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Springer Nature7
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✓Human Genetics7
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Li-Ping Chen results 7 · Newest (Page 1/1, per page 25)
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Journal: Human Genetics ×Author: Li-Ping Chen ×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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Discovery of structural deletions in breast cancer predisposition genes using whole genome sequencing data from > 2000 women of African-ancestryNARA Subscribed
Human Genetics · 2021 · Vol. 140 · Issue 10 · Springer
Zhishan Chen; Xingyi Guo; Jirong Long; Jie Ping; Bingshan Li; Mary Kay Fadden; Thomas U. Ahearn; Daniel O. Stram; Xiao-Ou Shu; Guochong Jia; Jonine Figueroa; Robertson Adjei; Lucy Afriyie; Anthony Adjei; Florence Dedey; Verna Vanderpuye; Victoria Okyne; Naomi Ohene Oti; Evelyn Tay; Adu‐Aryee; Angela Kenu; Obed Ekpedzor; Marion Alcpaloo; Isaac Boakye; Bernard Arhin; Emmanuel Assimah; Samuel Ka‐chungu; Joseph Oppong; Ernest Osei‐Bonsu; Margaret Frempong; Emma Brew Abaidoo; Bridget Nortey Mensah; Samuel Amanama; Prince Agyapong; Debora Boateng; Ansong Thomas Agyei; Richard Opoku; Kofi Owusu Gyimah; Louise Brinton; Michelle Brotzman; Shelley Niwa; Usha Singh; Ann Truelove; Richard Biritwum; Julie R. Palmer; Maureen Sanderson; Christopher A. Haiman; William J. Blot; Montserrat Garcia-Closas; Qiuyin Cai; Wei Zheng
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Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regionsNARA Subscribed
Human Genetics · 2015 · Vol. 134 · Issue 6 · Springer
Ye Wang; Peiqiang Su; Bin Hu; Wenjuan Zhu; Qibin Li; Ping Yuan; Jiangchao Li; Xinyuan Guan; Fucheng Li; Xiangyi Jing; Ru Li; Yongling Zhang; Claude Férec; David N. Cooper; Jun Wang; Dongsheng Huang; Jian-Min Chen; Yiming Wang
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Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association studyNARA Subscribed
Human Genetics · 2013 · Vol. 132 · Issue 2 · Springer
Yan-Fang Guo; Li-Shu Zhang; Yong-Jun Liu; Hong-Gang Hu; Jian Li; Qing Tian; Ping Yu; Feng Zhang; Tie-Lin Yang; Yan Guo; Xiang-Lei Peng; Meng Dai; Wei Chen; Hong-Wen Deng
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A miRNA-492 binding-site polymorphism in BSG (basigin) confers risk to psoriasis in Central South Chinese populationNARA Subscribed
Human Genetics · 2011 · Vol. 130 · Issue 6 · Springer
Li-Sha Wu; Fang-Fang Li; Liang-Dan Sun; Dai Li; Juan Su; Ye-Hong Kuang; Gang Chen; Xiao-Ping Chen; Xiang Chen
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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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Molecular characterization of germline mutations in the BRCA1 and BRCA2 genes from breast cancer families in TaiwanNARA Subscribed
Human Genetics · 1999 · Vol. 104 · Issue 3 · Springer
Steven Shoei-Lung Li; H.-M. Tseng; Tsui-Ping Yang; Chia-Han Liu; Shiuh-Jen Teng; Hung-Wen Huang; L.-M. Chen; Hsiao-Wei Kao; Jimmy H. Chen; Jau-Neng Tseng; Angela Chen; Ming-Feng Hou; Tsung-Jen Huang; Hong-Tai Chang; King-Tong Mok; Juei-Hsiung Tsai
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