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

Yazar: Ladouceur, Martin, Zheng, Hou-Feng, Greenwood, Celia M T, Richards, J Brent
Baskı/Yayın Bilgisi 2013

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

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

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

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

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

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

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

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

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

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

Genetic interactions affecting human gene expression identified by variance association mapping

Yazar: 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
Baskı/Yayın Bilgisi 2014

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

Yazar: 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
Yayımlandı Sci Rep (2016)

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

Yazar: 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
Yayımlandı Sci Rep (2016)

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

Yazar: 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.
Yayımlandı BMC Genomics (2016)

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

Yazar: 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
Yayımlandı Lipids Health Dis (2019)

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

Yazar: 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
Yayımlandı Nat Commun (2015)

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

Yazar: 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.
Yayımlandı 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...

Yazar: 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.
Baskı/Yayın Bilgisi 2013

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

Yazar: 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
Yayımlandı Eur J Hum Genet (2016)

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

Yazar: 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
Baskı/Yayın Bilgisi 2013

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

Yazar: 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
Yayımlandı BMJ Open (2021)

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

Yazar: 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
Baskı/Yayın Bilgisi 2014

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

Yazar: 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
Yayımlandı 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

Yazar: 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
Baskı/Yayın Bilgisi 2012