Use of Polygenic Scores to Select Embryos von Kumar, Akash, Im, Kate, Rabinowitz, Matthew, Treff, Nathan R, Tellier, Laurent C.A.M, Hsu, Stephen D.H

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POLYGENIC RISK SCORES, PGT-P, AND IVF: SIBLING AND NON-EUROPEAN ANCESTRY VALIDATIONS von Lello, Louis, Tellier, Laurent C.A.M.

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Second-generation PLINK: rising to the challenge of larger and richer datasets von Chang, Christopher C, Chow, Carson C, Tellier, Laurent CAM, Vattikuti, Shashaank, Purcell, Shaun M, Lee, James J

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Genomic Prediction of 16 Complex Disease Risks Including Heart Attack, Diabetes, Breast and Prostate Cancer von Lello, Louis, Raben, Timothy G., Yong, Soke Yuen, Tellier, Laurent C. A. M., Hsu, Stephen D. H.

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Preimplantation Genetic Testing for Polygenic Disease Risk von Treff, Nathan, Marin, Diego, Lello, Louis, Hsu, Stephen, Tellier, Laurent Cam

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Utility and First Clinical Application of Screening Embryos for Polygenic Disease Risk Reduction von Treff, Nathan R, Eccles, Jennifer, Lello, Lou, Bechor, Elan, Hsu, Jeffrey, Plunkett, Kathryn, Zimmerman, Raymond, Rana, Bhavini, Samoilenko, Artem, Hsu, Steven, Tellier, Laurent C A M

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Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs von Treff, Nathan R, Eccles, Jennifer, Marin, Diego, Messick, Edward, Lello, Louis, Gerber, Jessalyn, Xu, Jia, Tellier, Laurent C A M

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An integrated tool to study MHC region: accurate SNV detection and HLA genes typing in human MHC region using targeted high-throughput sequencing von Cao, Hongzhi, Wu, Jinghua, Wang, Yu, Jiang, Hui, Zhang, Tao, Liu, Xiao, Xu, Yinyin, Liang, Dequan, Gao, Peng, Sun, Yepeng, Gifford, Benjamin, D'Ascenzo, Mark, Liu, Xiaomin, Tellier, Laurent C A M, Yang, Fang, Tong, Xin, Chen, Dan, Zheng, Jing, Li, Weiyang, Richmond, Todd, Xu, Xun, Wang, Jun, Li, Yingrui

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Embryo Screening for Polygenic Disease Risk: Recent Advances and Ethical Considerations von Tellier, Laurent C A M, Eccles, Jennifer, Treff, Nathan R, Lello, Louis, Fishel, Simon, Hsu, Stephen

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De novo assembly of a haplotype-resolved human genome von Cao, Hongzhi, Wu, Honglong, Luo, Ruibang, Huang, Shujia, Sun, Yuhui, Tong, Xin, Xie, Yinlong, Liu, Binghang, Yang, Hailong, Zheng, Hancheng, Li, Jian, Li, Bo, Wang, Yu, Yang, Fang, Sun, Peng, Liu, Siyang, Gao, Peng, Huang, Haodong, Sun, Jing, Chen, Dan, He, Guangzhu, Huang, Weihua, Huang, Zheng, Li, Yue, Tellier, Laurent C A M, Liu, Xiao, Feng, Qiang, Xu, Xun, Zhang, Xiuqing, Bolund, Lars, Krogh, Anders, Kristiansen, Karsten, Drmanac, Radoje, Drmanac, Snezana, Nielsen, Rasmus, Li, Songgang, Wang, Jian, Yang, Huanming, Li, Yingrui, Wong, Gane Ka-Shu, Wang, Jun

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A Short-Read Multiplex Sequencing Method for Reliable, Cost-Effective and High-Throughput Genotyping in Large-Scale Studies von Cao, Hongzhi, Wang, Yu, Zhang, Wei, Chai, Xianghua, Zhang, Xiandong, Chen, Shiping, Yang, Fan, Zhang, Caifen, Guo, Yulai, Liu, Ying, Tang, Zhoubiao, Chen, Caifen, Xue, Yaxin, Zhen, Hefu, Xu, Yinyin, Rao, Bin, Liu, Tao, Zhao, Meiru, Zhang, Wenwei, Li, Yingrui, Zhang, Xiuqing, Tellier, Laurent C. A. M., Krogh, Anders, Kristiansen, Karsten, Wang, Jun, Li, Jian

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