Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals

著者: Ladouceur, Martin, Zheng, Hou-Feng, Greenwood, Celia M T, Richards, J Brent
出版事項 2013

A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects

著者: Sun, Jianping, Oualkacha, Karim, Forgetta, Vincenzo, Zheng, Hou-Feng, Brent Richards, J, Ciampi, Antonio, Greenwood, Celia MT
出版年 Eur J Hum Genet (2016)

Performance of Genotype Imputation for Low Frequency and Rare Variants from the 1000 Genomes

著者: Zheng, Hou-Feng, Rong, Jing-Jing, Liu, Ming, Han, Fang, Zhang, Xing-Wei, Richards, J. Brent, Wang, Li
出版年 PLoS One (2015)

Reproduction and In-Depth Evaluation of Genome-Wide Association Studies and Genome-Wide Meta-analyses Using Summary Statistics

著者: Niu, Yao-Fang, Ye, Chengyin, He, Ji, Han, Fang, Guo, Long-Biao, Zheng, Hou-Feng, Chen, Guo-Bo
出版年 G3 (Bethesda) (2017)

Exome-wide rare variant analyses of two bone mineral density phenotypes: the challenges of analyzing rare genetic variation

著者: Sun, Jianping, Oualkacha, Karim, Forgetta, Vincenzo, Zheng, Hou-Feng, Richards, J. Brent, Evans, Daniel S., Orwoll, Eric, Greenwood, Celia M. T.
出版年 Sci Rep (2018)

Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study

著者: Trajanoska, Katerina, Morris, John A, Oei, Ling, Zheng, Hou-Feng, Evans, David M, Kiel, Douglas P, Ohlsson, Claes, Richards, J Brent, Rivadeneira, Fernando
出版年 BMJ (2018)

Genetic interactions affecting human gene expression identified by variance association mapping

著者: Brown, Andrew Anand, Buil, Alfonso, Viñuela, Ana, Lappalainen, Tuuli, Zheng, Hou-Feng, Richards, J Brent, Small, Kerrin S, Spector, Timothy D, Dermitzakis, Emmanouil T, Durbin, Richard
出版事項 2014

A combined reference panel from the 1000 Genomes and UK10K projects improved rare variant imputation in European and Chinese samples

著者: Chou, Wen-Chi, Zheng, Hou-Feng, Cheng, Chia-Ho, Yan, Han, Wang, Li, Han, Fang, Richards, J. Brent, Karasik, David, Kiel, Douglas P., Hsu, Yi-Hsiang
出版年 Sci Rep (2016)

Comprehensive Assessment of the Association between FCGRs polymorphisms and the risk of systemic lupus erythematosus: Evidence from a Meta-Analysis

著者: Zhu, Xiao-Wei, Wang, Yong, Wei, Yi-Hua, Zhao, Pian-Pian, Wang, Xiao-Bo, Rong, Jing-Jing, Zhong, Wen-Ying, Zhang, Xing-Wei, Wang, Li, Zheng, Hou-Feng
出版年 Sci Rep (2016)

Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density

著者: Mullin, Benjamin H., Walsh, John P., Zheng, Hou-Feng, Brown, Suzanne J., Surdulescu, Gabriela L., Curtis, Charles, Breen, Gerome, Dudbridge, Frank, Richards, J. Brent, Spector, Tim D., Wilson, Scott G.
出版年 BMC Genomics (2016)

Effect of CD14 polymorphisms on the risk of cardiovascular disease: evidence from a meta-analysis

著者: Xu, Jin-Jian, Liu, Ke-Qi, Ying, Zhi-Min, Zhu, Xiao-Wei, Xu, Xue-Jin, Zhao, Pian-Pian, Bai, Wei-Yang, Qiu, Mo-Chang, Zhang, Xing-Wei, Zheng, Hou-Feng
出版年 Lipids Health Dis (2019)

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

著者: Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole
出版年 Nat Commun (2015)

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

著者: Mullin, Benjamin H., Zhao, Jing Hua, Brown, Suzanne J., Perry, John R.B., Luan, Jian'an, Zheng, Hou-Feng, Langenberg, Claudia, Dudbridge, Frank, Scott, Robert, Wareham, Nick J., Spector, Tim D., Richards, J. Brent, Walsh, John P., Wilson, Scott G.
出版年 Hum Mol Genet (2017)

Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based...

著者: Wood, Andrew R., Perry, John R. B., Tanaka, Toshiko, Hernandez, Dena G., Zheng, Hou-Feng, Melzer, David, Gibbs, J. Raphael, Nalls, Michael A., Weedon, Michael N., Spector, Tim D., Richards, J. Brent, Bandinelli, Stefania, Ferrucci, Luigi, Singleton, Andrew B., Frayling, Timothy M.
出版事項 2013

Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

著者: Ruth, Katherine S, Campbell, Purdey J, Chew, Shelby, Lim, Ee Mun, Hadlow, Narelle, Stuckey, Bronwyn GA, Brown, Suzanne J, Feenstra, Bjarke, Joseph, John, Surdulescu, Gabriela L, Zheng, Hou Feng, Richards, J Brent, Murray, Anna, Spector, Tim D, Wilson, Scott G, Perry, John RB
出版年 Eur J Hum Genet (2016)

Meta-Analysis of Genome-Wide Studies Identifies MEF2C SNPs Associated with Bone Mineral Density at Forearm

著者: Zheng, Hou-Feng, Duncan, Emma, Yerges-Armstrong, Laura M., Eriksson, Joel, Bergström, Ulrica, Leo, Paul J., Leslie, William D., Goltzman, David, Blangero, John, Hanley, David A., Carless, Melanie A., Streeten, Elizabeth A., Lorentzon, Mattias, Brown, Matthew A., Spector, Tim D., Pettersson-Kymmer, Ulrika, Ohlsson, Claes, Mitchell, Braxton D., Richards, J. Brent
出版事項 2013

Cohort profile: the Westlake BioBank for Chinese (WBBC) pilot project

著者: Zhu, Xiao-Wei, Liu, Ke-Qi, Wang, Ping-Yu, Liu, Jun-Quan, Chen, Jin-Yang, Xu, Xue-Jin, Xu, Jin-Jian, Qiu, Mo-Chang, Sun, Yi, Liu, Chun, Bai, Wei-Yang, Zhao, Pian-Pian, Xia, Jiangwei, Gai, Si-Rui, Guan, Peng-Lin, Qian, Yu, Cong, Pei-Kuan, Xie, Shu-Yang, Zheng, Hou-Feng
出版年 BMJ Open (2021)

Expression of Phosphofructokinase in Skeletal Muscle Is Influenced by Genetic Variation and Associated With Insulin Sensitivity

著者: Keildson, Sarah, Fadista, Joao, Ladenvall, Claes, Hedman, Åsa K., Elgzyri, Targ, Small, Kerrin S., Grundberg, Elin, Nica, Alexandra C., Glass, Daniel, Richards, J. Brent, Barrett, Amy, Nisbet, James, Zheng, Hou-Feng, Rönn, Tina, Ström, Kristoffer, Eriksson, Karl-Fredrik, Prokopenko, Inga, Spector, Timothy D., Dermitzakis, Emmanouil T., Deloukas, Panos, McCarthy, Mark I., Rung, Johan, Groop, Leif, Franks, Paul W., Lindgren, Cecilia M., Hansson, Ola
出版事項 2014

A regulatory mutant on TRIM26 conferring the risk of nasopharyngeal carcinoma by inducing low immune response

著者: Lyu, Xiao‐Ming, Zhu, Xiao‐Wei, Zhao, Manli, Zuo, Xian‐Bo, Huang, Zhong‐Xi, Liu, Xiao, Jiang, Tao, Yang, Xue‐Xi, Li, Xin, Long, Xiao‐Bing, Wang, Jian‐Guo, Li, Jin‐Bang, Han, Ming‐Yu, Wang, Shuang, Liu, Teng‐Fei, Zhang, Bo, Sun, Tao, Cheng, Zhi, Qiu, Mo‐Chang, Dong, Lei, Zheng, Lu, Zhang, Long‐Cheng, Wang, Jia‐Hong, Wei, Gan‐Guan, Yao, Kaitai, Wang, Qian, Zheng, Hou‐Feng, Li, Xin
出版年 Cancer Med (2018)

Meta-Analysis of Genome-Wide Scans for Total Body BMD in Children and Adults Reveals Allelic Heterogeneity and Age-Specific Effects at the WNT16 Locus

著者: Medina-Gomez, Carolina, Kemp, John P., Estrada, Karol, Eriksson, Joel, Liu, Jeff, Reppe, Sjur, Evans, David M., Heppe, Denise H. M., Vandenput, Liesbeth, Herrera, Lizbeth, Ring, Susan M., Kruithof, Claudia J., Timpson, Nicholas J., Zillikens, M. Carola, Olstad, Ole K., Zheng, Hou-Feng, Richards, J. Brent, St. Pourcain, Beate, Hofman, Albert, Jaddoe, Vincent W. V., Smith, George Davey, Lorentzon, Mattias, Gautvik, Kaare M., Uitterlinden, André G., Brommage, Robert, Ohlsson, Claes, Tobias, Jonathan H., Rivadeneira, Fernando
出版事項 2012