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

door Ladouceur, Martin, Zheng, Hou-Feng, Greenwood, Celia M T, Richards, J Brent
Gepubliceerd in 2013

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

door Sun, Jianping, Oualkacha, Karim, Forgetta, Vincenzo, Zheng, Hou-Feng, Brent Richards, J, Ciampi, Antonio, Greenwood, Celia MT
Gepubliceerd in Eur J Hum Genet (2016)

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

door Zheng, Hou-Feng, Rong, Jing-Jing, Liu, Ming, Han, Fang, Zhang, Xing-Wei, Richards, J. Brent, Wang, Li
Gepubliceerd in PLoS One (2015)

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

door Niu, Yao-Fang, Ye, Chengyin, He, Ji, Han, Fang, Guo, Long-Biao, Zheng, Hou-Feng, Chen, Guo-Bo
Gepubliceerd in G3 (Bethesda) (2017)

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

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

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

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

Genetic interactions affecting human gene expression identified by variance association mapping

door 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
Gepubliceerd in 2014

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

door 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
Gepubliceerd in Sci Rep (2016)

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

door 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
Gepubliceerd in Sci Rep (2016)

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

door 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.
Gepubliceerd in BMC Genomics (2016)

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

door 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
Gepubliceerd in Lipids Health Dis (2019)

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

door 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
Gepubliceerd in Nat Commun (2015)

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

door 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.
Gepubliceerd in 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...

door 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.
Gepubliceerd in 2013

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

door 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
Gepubliceerd in Eur J Hum Genet (2016)

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

door 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
Gepubliceerd in 2013

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

door 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
Gepubliceerd in BMJ Open (2021)

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

door 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
Gepubliceerd in 2014

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

door 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
Gepubliceerd in 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

door 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
Gepubliceerd in 2012