Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hou-Feng Zheng"'
Autor:
Hou-Feng Zheng, Xing-Wei Zhang, Pian-Pian Zhao, Liang-Cai Wu, Xiao-Bo Wang, Lu Zheng, Jiangwei Xia, Wei-Yang Bai, Qiong Yin, Ming-Yu Han, Xiao-Wei Zhu, Li-Ya Hu
Publikováno v:
Archives of Dermatological Research. 310:711-728
Previous studies have reported that genes relating to JAK-STAT pathway (IFIH1, TYK2 and IL-10) conferred the susceptibility to SLE. In this study, we performed a meta-analysis (including 43 studies) to evaluate the association between IFIH1 (9288 pat
Autor:
Zhi Cheng, Bo Zhang, Li-Ya Hu, Hou-Feng Zheng, Xiao-Bo Wang, Qiong Yin, Pian-Pian Zhao, Ming-Yu Han, Xiao-Wei Zhu
Publikováno v:
Archives of dermatological research. 309(6)
Previous studies have explored the relationship of PTPN22 and TLR9 polymorphisms with systemic lupus erythematosus (SLE). In consideration of the population stratification, conflicting results and updating data, we conducted a comprehensive meta-anal
Autor:
Lu Zheng, Hua Zhang, Hou-Feng Zheng, Ying Pan, Fang-Fang Shen, Li-Dong Wang, Qi-Si Xue, Fu-You Zhou
Publikováno v:
Molecular Biology Reports. 40:6035-6042
Cytochrome P4501A1 (CYP1A1) enzyme is a member of the CYP superfamily of enzymes. CYP1A1 A2455G and T3801C are two most commonly studied polymorphisms loci. Previous studies have reported that CYP1A1 polymorphisms increase esophageal cancer (EC) risk
Autor:
Nicholas J. Timpson, Klaudia Walter, Josine L. Min, Ioanna Tachmazidou, Giovanni Malerba, So Youn Shin, Lu Chen, Marta Futema, Lorraine Southam, Valentina Iotchkova, Jie Huang, Yasin Memari, Shane McCarthy, Petr Danecek, Dawn Muddyman, Massimo Mangino, Cristina Menni, John R. B. Perry, Susan M. Ring, Amadou Gaye, George Dedoussis, Aliki Eleni Farmaki, Paul Burton, Philippa J. Talmud, Giovanni Gambaro, Tim D. Spector, George Davey Smith, Richard Durbin, J. Brent Richards, Steve E. Humphries, Eleftheria Zeggini, Nicole Soranzo, Saeed Al Turki, Carl Anderson, Richard Anney, Dinu Antony, Maria Soler Artigas, Muhammad Ayub, Senduran Balasubramaniam, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Krishna Chatterjee, Antonio Ciampi, Sebhattin Cirak, Peter Clapham, Gail Clement, Guy Coates, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Aaron Day Williams, Ian N. M. Day, Thomas Down, Yuanping Du, Ian Dunham, Sarah Edkins, Peter Ellis, David Evans, Sadaf Faroogi, Ghazaleh Fatemifar, David R. Fitzpatrick, Paul Flicek, James Flyod, A. Reghan Foley, Christopher S. Franklin, Louise Gallagher, Tom Gaunt, Matthias Geihs, Daniel Geschwind, Celia Greenwood, Heather Griffin, Detelina Grozeva, Xueqin Guo, Xiaosen Guo, Hugh Gurling, Deborah Hart, Audrey Hendricks, Peter Holmans, Bryan Howie, Liren Huang, Tim Hubbard, Matthew E. Hurles, Pirro Hysi, David K. Jackson, Yalda Jamshidi, Tian Jing, Chris Joyce, Jane Kaye, Thomas Keane, Julia Keogh, John Kemp, Karen Kennedy, Anja Kolb Kokocinski, Genevieve Lachance, Cordelia Langford, Daniel Lawson, Irene Lee, Monkol Lek, Jieqin Liang, Hong Lin, Rui Li, Yingrui Li, Ryan Liu, Jouko Lönnqvist, Margarida Lopes, Valentina Lotchkova, Daniel MacArthur, Jonathan Marchini, John Maslen, Mangino Massimo, Iain Mathieson, Gaëlle Marenne, Peter McGuffin, Andrew McIntosh, Andrew G. McKechanie, Andrew McQuillin, Sarah Metrustry, Josine Min, Hannah Mitchison, Alireza Moayyeri, James Morris, Francesco Muntoni, Kate Northstone, Michael O'Donnovan, Alexandros Onoufriadis, Stephen O'Rahilly, Karim Oualkacha, Michael J. Owen, Aarno Palotie, Kalliope Panoutsopoulou, Victoria Parker, Jeremy R. Parr, Lavinia Paternoster, Tiina Paunio, Felicity Payne, John Perry, Olli Pietilainen, Vincent Plagnol, Lydia Quaye, Michael A. Quail, Lucy Raymond, Karola Rehnström, Brent Richards, Susan Ring, Graham R. S. Ritchie, Nicola Roberts, David B. Savage, Peter Scambler, Stephen Schiffels, Miriam Schmidts, Nadia Schoenmakers, Robert K. Semple, Eva Serra, Sally I. Sharp, Hasheem Shihab, David Skuse, Kerrin Small, Olivera Spasic Boskovic, Tim Spector, David St Clair, Jim Stalker, Elizabeth Stevens, Beate St Pourcian, Jianping Sun, Gabriela Surdulescu, Jaana Suvisaari, Ionna Tachmazidou, Nicholas Timpson, Martin D. Tobin, Ana Valdes, Margriet Van Kogelenberg, Parthiban Vijayarangakannan, Peter M. Visscher, Louise V. Wain, James T. R. Walters, Guangbiao Wang, Jun Wang, Yu Wang, Kirsten Ward, Elanor Wheeler, Tamieka Whyte, Hywel Williams, Kathleen A. Williamson, Crispian Wilson, Scott G. Wilson, Kim Wong, ChangJiang Xu, Jian Yang, Fend Zhang, Pingbo Zhang, Hou Feng Zheng, COCCA, MASSIMILIANO
Publikováno v:
Nature Communications
Timpson, N J, Walter, K, Min, J L, Tachmazidou, I, Malerba, G, Shin, S-Y, Chen, L, Futema, M, Southam, L, Iotchkova, V, Cocca, M, Huang, J, Memari, Y, McCarthy, S, Danecek, P, Muddyman, D, Mangino, M, Menni, C, Perry, J R B, Ring, S M, Gaye, A, Dedoussis, G, Farmaki, A-E, Burton, P, Talmud, P J, Gambaro, G, Spector, T D, Smith, G D, Durbin, R, Richards, J B, Humphries, S E, Zeggini, E, Soranzo, N 2014, ' A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans ', Nature Communications, vol. 5, 4871 . https://doi.org/10.1038/ncomms5871
Timpson, N J, Walter, K, Min, J L, Tachmazidou, I, Malerba, G, Shin, S-Y, Chen, L, Futema, M, Southam, L, Iotchkova, V, Cocca, M, Huang, J, Memari, Y, McCarthy, S, Danecek, P, Muddyman, D, Mangino, M, Menni, C, Perry, J R B, Ring, S M, Gaye, A, Dedoussis, G, Farmaki, A-E, Burton, P, Talmud, P J, Gambaro, G, Spector, T D, Smith, G D, Durbin, R, Richards, J B, Humphries, S E, Zeggini, E, Soranzo, N 2014, ' A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans ', Nature Communications, vol. 5, 4871 . https://doi.org/10.1038/ncomms5871
The analysis of rich catalogues of genetic variation from population-based sequencing provides an opportunity to screen for functional effects. Here we report a rare variant in APOC3 (rs138326449-A, minor allele frequency ~0.25% (UK)) associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::239f3f327a3d8bed252dfd05c2a94d0b
Autor:
Jing-Jing Rong, Yi-Hua Wei, Xing-Wei Zhang, Li Wang, Wen-Ying Zhong, Hou-Feng Zheng, Xiao-Wei Zhu, Yong Wang, Xiao-Bo Wang, Pian-Pian Zhao
Publikováno v:
Scientific Reports
We performed a meta analysis to assess the relationship of FCGRs polymorphisms with the risk of SLE. Thirty-five articles (including up to 5741 cases and 6530 controls) were recruited for meta-analysis. The strongest association was observed between
Publikováno v:
Nature Reviews Genetics. 13:576-588
Osteoporosis is among the most common and costly diseases and is increasing in prevalence owing to the ageing of our global population. Clinically defined largely through bone mineral density, osteoporosis and osteoporotic fractures have reasonably h
Autor:
Yun Qing Ren, Wen Sheng Lu, Sen Yang, Yong Cui, Xianyong Yin, Hou-Feng Zheng, Xian Bo Zuo, Chi Zhang, Xuejun Zhang, Yang Li, Kun Ju Zhu, Feng Yu Zhang, Wen Ju Wang, Liangdan Sun, Hui Cheng
Publikováno v:
Journal of Dermatological Science. 61:124-128
Background Psoriasis has long been considered as a complex disease, and gene–gene or gene–environment interactions may jointly influence the etiology for psoriasis. Objective We evaluated the associations of single nucleotide polymorphisms (SNPs)
Autor:
Hou-Feng Zheng, Qiang Xu, Li-Qiong Cai, Sheng-Xin Xu, Sen Yang, Sheng-Quan Zhang, Kun-Ju Zhu, Xuejun Zhang, Zheng Zhang, Xianbo Zuo, Jan-Wen Han, Hui Cheng, Cheng Quan, Liangdan Sun
Publikováno v:
Archives of Dermatological Research. 302:619-624
Systemic lupus erythematosus (SLE) is an autoimmune disease influenced by genetic and environmental factors. Recently, single nucleotide polymorphisms (SNPs) in the region of B lymphoid tyrosine kinase (BLK) have been shown to be associated with SLE
Autor:
Hui Qi Low, Sheng-Quan Zhang, Fusheng Zhou, Hou-Feng Zheng, Wei-fang Zhu, Kun-Ju Zhu, Guoping Zhao, Pei-Lian Zhang, Xiao Yan Zhang, Feng-Yu Zhang, Yujun Sheng, Wei Huang, Zaixing Wang, Xuejun Zhang, Li Ma, Bo Li, Jianlin Huang, Qing Guo, Ying Wang, Da Lin, Hongfu Xie, Zhiming Cai, Jian-Qiang Yang, Hui Li, Fan-Qin Zeng, Zhi Hu, Sen Yang, Songke Shen, Cheng Quan, Yi-Lin Cheng, Chi Zhang, Jianwen Han, Anping Zhang, Yong Cui, Feng-Li Xiao, Jian Li, Xiangpei Li, Wen-Ming Zhou, Xiaoxia Zuo, Qing-Wen Wang, Zheng Zhang, Yi Li, Fei Hao, Wen-Hui Du, Pei-Guang Wang, Hong Fang, Jianjun Liu, Liangdan Sun, Min Shen, Yang Li, Yunqing Ren, Zhi-Fang Zhai, Da-Yan Hu, Yunfeng Pan, Dan-Qi Deng, Wen-Sheng Lu, Jianhua Xu, Zhi-Zhong Ye, Min Gao, Jinhua Xu, Qian-Jin Lu, Fei Gao, Xianbo Zuo, Shengxiu Liu, Chun-Jun Yang, Dong-Qing Ye, Yongmei Lv
Publikováno v:
Nature Genetics. 41:1234-1237
We performed a genome-wide association study (GWAS) of systemic lupus erythematosus (SLE) in a Chinese Han population by genotyping 1,047 cases and 1,205 controls using Illumina Human610-Quad BeadChips and replicating 78 SNPs in two additional cohort
Autor:
Tuuli Lappalainen, Hou-Feng Zheng, Andrew A. Brown, Daniel Glass, Alfonso Buil, Emmanouil T. Dermitzakis, Kerrin S. Small, Tim D. Spector, J. Brent Richards, Ana Viñuela, Richard Durbin, Matthew N. Davies
Understanding the genetic architecture of gene expression is an intermediate step to understand the genetic architecture of complex diseases. RNA-seq technologies have improved the quantification of gene expression and allow to measure allelic specif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa7ac6b3033ca430ad04b4602ef542e2