Jian Yang (J Yang)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 94

Top Venues

Nature communications

Nature genetics

NPJ Parkinson's disease

Nature

Westlake University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Westlake University Sep 17 2020

China

Professor :: School of Life Sciences

The University of Queensland Jan 01 2017 - Jun 30 2020

Australia

Professor :: Institute for Molecular Bioscience

Publications

Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loic Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja Maria Nolte, Harold Snieder, null null, Jian Yang, Naomi R Wray, Michael E Goddard, Peter M Visscher, Jian Zeng
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature genetics 56 (5) (2024)
Angli Xue, Zhihong Zhu, Huanwei Wang, Longda Jiang, Peter M Visscher, Jian Zeng, Jian Yang
Unravelling the complex causal effects of substance use behaviours on common diseases. Communications medicine 4 (1) (2024)
Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loic Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja Maria Nolte, Harold Snieder, null null, Jian Yang, Naomi R Wray, Michael E Goddard, Peter M Visscher, Jian Zeng
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature genetics 56 (5) (2024)
Angli Xue, Zhihong Zhu, Huanwei Wang, Longda Jiang, Peter M Visscher, Jian Zeng, Jian Yang
Unravelling the complex causal effects of substance use behaviours on common diseases. Communications medicine 4 (1) (2024)
Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loic Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja Maria Nolte, Harold Snieder, null null, Jian Yang, Naomi R Wray, Michael E Goddard, Peter M Visscher, Jian Zeng
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature genetics 56 (5) (2024)
Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loic Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja Maria Nolte, Harold Snieder, null null, Jian Yang, Naomi R Wray, Michael E Goddard, Peter M Visscher, Jian Zeng
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature genetics (2024)
Alesha B Hatton, Fei-Fei Cheng, Tian Lin, Ren-Juan Shen, Jie Chen, Zhili Zheng, Jia Qu, Fan Lyu, Sarah E Harris, Simon R Cox, Zi-Bing Jin, Nicholas G Martin, Dongsheng Fan, Grant W Montgomery, Jian Yang, Naomi R Wray, Riccardo E Marioni, Peter M Visscher, Allan F McRae
Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature communications 15 (1) (2024)
Alesha B Hatton, Fei-Fei Cheng, Tian Lin, Ren-Juan Shen, Jie Chen, Zhili Zheng, Jia Qu, Fan Lyu, Sarah E Harris, Simon R Cox, Zi-Bing Jin, Nicholas G Martin, Dongsheng Fan, Grant W Montgomery, Jian Yang, Naomi R Wray, Riccardo E Marioni, Peter M Visscher, Allan F McRae
Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature communications 15 (1) (2024)
Alesha B Hatton, Fei-Fei Cheng, Tian Lin, Ren-Juan Shen, Jie Chen, Zhili Zheng, Jia Qu, Fan Lyu, Sarah E Harris, Simon R Cox, Zi-Bing Jin, Nicholas G Martin, Dongsheng Fan, Grant W Montgomery, Jian Yang, Naomi R Wray, Riccardo E Marioni, Peter M Visscher, Allan F McRae
Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature communications 15 (1) (2024)
Zhili Zheng, Shouye Liu, Julia Sidorenko, Ying Wang, Tian Lin, Loic Yengo, Patrick Turley, Alireza Ani, Rujia Wang, Ilja Maria Nolte, Harold Snieder, null null, Jian Yang, Naomi R Wray, Michael E Goddard, Peter M Visscher, Jian Zeng
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature genetics 56 (5) (2024)
Erola Pairo-Castineira, Konrad Rawlik, Andrew D Bretherick, Ting Qi, Yang Wu, Isar Nassiri, Glenn A McConkey, Marie Zechner, Lucija Klarić, Fiona Griffiths, Wilna Oosthuyzen, Athanasios Kousathanas, Anne Richmond, Jonathan Millar, Clark D Russell, Tomas Malinauskas, Ryan S Thwaites, Kirstie Morrice, Sean Keating, David Maslove, Alistair Nichol, Malcolm Gracie Semple, Julian Knight, Manu Shankar-Hari, Charlotte Summers, Charles J Hinds, Peter Horby, Lowell Ling, Daniel Francis McAuley, Hugh E Montgomery, Peter J M Openshaw, Colin Begg, Timothy Walsh, Albert Tenesa, Carlos Flores, José A Riancho, Augusto Rojas-Martinez, Pablo Lapunzina, null null, null null, null null, null null, Jian Yang, Chris Paul Ponting, James F Wilson, Veronique Vitart, Malak Abedalthagafi, Andre D Luchessi, Esteban J Parra, Raquel Cruz, Angel Carracedo, Angie Fawkes, Lee Murphy, Kathryn M Rowan, Alexandre C Pereira, Andrew Law, Benjamin P Fairfax, Sara Clohisey Hendry, John Kenneth Baillie
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19. Nature (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chun-Feng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Liche Zhou, Piu Chan, Hou-Feng Zheng, Jinchen Li, Ji-Feng Guo, Jian Yang, Bei-Sha Tang, null null
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. NPJ Parkinson's disease 9 (1) (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Runshuai Zhang, Jinan Fang, Ting Qi, Shihao Zhu, Luxia Yao, Guicun Fang, Yunsheng Li, Xiao Zang, Weina Xu, Wanyu Hao, Shouye Liu, Dan Yang, Di Chen, Jian Yang, Xianjue Ma, Lianfeng Wu
Maternal aging increases offspring adult body size via transmission of donut-shaped mitochondria. Cell research (2023)
Liyang Song, Xiwei Sun, Ting Qi, Jian Yang
Mixed model-based deconvolution of cell-state abundances (MeDuSA) along a one-dimensional trajectory. Nature computational science 3 (7) (2023)
Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chun-Feng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Liche Zhou, Piu Chan, Hou-Feng Zheng, Jinchen Li, Ji-Feng Guo, Jian Yang, Bei-Sha Tang, null null
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. NPJ Parkinson's disease 9 (1) (2023)
Liyang Song, Xiwei Sun, Ting Qi, Jian Yang
Mixed model-based deconvolution of cell-state abundances (MeDuSA) along a one-dimensional trajectory. Nature computational science 3 (7) (2023)
Liyang Song, Xiwei Sun, Ting Qi, Jian Yang
Mixed model-based deconvolution of cell-state abundances (MeDuSA) along a one-dimensional trajectory. Nature computational science 3 (7) (2023)
Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chun-Feng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Liche Zhou, Piu Chan, Hou-Feng Zheng, Jinchen Li, Ji-Feng Guo, Jian Yang, Bei-Sha Tang, null null
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. NPJ Parkinson's disease 9 (1) (2023)
Carolina Makowski, Hao Wang, Anjali Srinivasan, Anna Qi, Yuqi Qiu, Dennis van der Meer, Oleksandr Frei, Jingjing Zou, Peter M Visscher, Jian Yang, Chi-Hua Chen
Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Proceedings of the National Academy of Sciences of the United States of America 120 (11) (2023)
Erola Pairo-Castineira, Konrad Rawlik, Andrew D Bretherick, Ting Qi, Yang Wu, Isar Nassiri, Glenn A McConkey, Marie Zechner, Lucija Klarić, Fiona Griffiths, Wilna Oosthuyzen, Athanasios Kousathanas, Anne Richmond, Jonathan Millar, Clark D Russell, Tomas Malinauskas, Ryan S Thwaites, Kirstie Morrice, Sean Keating, David Maslove, Alistair Nichol, Malcolm Gracie Semple, Julian Knight, Manu Shankar-Hari, Charlotte Summers, Charles J Hinds, Peter Horby, Lowell Ling, Daniel Francis McAuley, Hugh E Montgomery, Peter J M Openshaw, Colin Begg, Timothy Walsh, Albert Tenesa, Carlos Flores, José A Riancho, Augusto Rojas-Martinez, Pablo Lapunzina, null null, null null, null null, null null, Jian Yang, Chris Paul Ponting, James F Wilson, Veronique Vitart, Malak Abedalthagafi, Andre D Luchessi, Esteban J Parra, Raquel Cruz, Angel Carracedo, Angie Fawkes, Lee Murphy, Kathryn M Rowan, Alexandre C Pereira, Andrew Law, Benjamin P Fairfax, Sara Clohisey Hendry, John Kenneth Baillie
Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19. Nature (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Yeqing Gu, Zimin Song, Qingkui Li, Jinhan Wang, Yanqi Song, Ge Meng, Hongmei Wu, Shunming Zhang, Xuena Wang, Juanjuan Zhang, Xinran Lu, Qiang Liu, Tao Huang, Jian Yang, Kai Jun Niu
Association of thyroid-stimulating hormone with all-cause mortality: A two-sample Mendelian randomization study. The Journal of clinical endocrinology and metabolism (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Yeqing Gu, Zimin Song, Qingkui Li, Jinhan Wang, Yanqi Song, Ge Meng, Hongmei Wu, Shunming Zhang, Xuena Wang, Juanjuan Zhang, Xinran Lu, Qiang Liu, Tao Huang, Jian Yang, Kai Jun Niu
Association of thyroid-stimulating hormone with all-cause mortality: A two-sample Mendelian randomization study. The Journal of clinical endocrinology and metabolism (2023)
Carolina Makowski, Hao Wang, Anjali Srinivasan, Anna Qi, Yuqi Qiu, Dennis van der Meer, Oleksandr Frei, Jingjing Zou, Peter M Visscher, Jian Yang, Chi-Hua Chen
Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Proceedings of the National Academy of Sciences of the United States of America 120 (11) (2023)
Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chun-Feng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Liche Zhou, Piu Chan, Hou-Feng Zheng, Jinchen Li, Ji-Feng Guo, Jian Yang, Bei-Sha Tang, null null
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. NPJ Parkinson's disease 9 (1) (2023)
Liyang Song, Xiwei Sun, Ting Qi, Jian Yang
Mixed model-based deconvolution of cell-state abundances (MeDuSA) along a one-dimensional trajectory. Nature computational science 3 (7) (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Yeqing Gu, Zimin Song, Qingkui Li, Jinhan Wang, Yanqi Song, Ge Meng, Hongmei Wu, Shunming Zhang, Xuena Wang, Juanjuan Zhang, Xinran Lu, Qiang Liu, Tao Huang, Jian Yang, Kai Jun Niu
Association of thyroid-stimulating hormone with all-cause mortality: A two-sample Mendelian randomization study. The Journal of clinical endocrinology and metabolism (2023)
Fengzhe Xu, Evan Yi-Wen Yu, Xue Cai, Liang Yue, Li-Peng Jing, Xinxiu Liang, Yuanqing Fu, Zelei Miao, Min Yang, Menglei Shuai, Wanglong Gou, Congmei Xiao, Zhangzhi Xue, Yuting Xie, Sainan Li, Sha Lu, Meiqi Shi, Xuhong Wang, Wensheng Hu, Claudia Langenberg, Jian Yang, Yu-Ming Chen, Tiannan Guo, Ju-Sheng Zheng
Genome-wide genotype-serum proteome mapping provides insights into the cross-ancestry differences in cardiometabolic disease susceptibility. Nature communications 14 (1) (2023)
Hongxu Pan, Zhenhua Liu, Jinghong Ma, Yuanyuan Li, Yuwen Zhao, Xiaoxia Zhou, Yaqin Xiang, Yige Wang, Xun Zhou, Runcheng He, Yali Xie, Qiao Zhou, Kai Yuan, Qian Xu, Qiying Sun, Junling Wang, Xinxiang Yan, Hainan Zhang, Chunyu Wang, Lifang Lei, Weiguo Liu, Xuejing Wang, Xuebing Ding, Tao Wang, Zheng Xue, Zhentao Zhang, Ling Chen, Qing Wang, Yonghong Liu, Jiayu Tang, Xuewei Zhang, Shifang Peng, Chaodong Wang, Jianqing Ding, Chun-Feng Liu, Lijuan Wang, Haibo Chen, Lu Shen, Hong Jiang, Xinyin Wu, Hongzhuan Tan, Dan Luo, Shuiyuan Xiao, Xiang Chen, Jieqiong Tan, Zhengmao Hu, Chao Chen, Kun Xia, Zhuohua Zhang, Jia Nee Foo, Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton, Liche Zhou, Piu Chan, Hou-Feng Zheng, Jinchen Li, Ji-Feng Guo, Jian Yang, Bei-Sha Tang, null null
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. NPJ Parkinson's disease 9 (1) (2023)
Carolina Makowski, Dennis van der Meer, Weixiu Dong, Hao Wang, Yan Wu, Jingjing Zou, Cin Liu, Sara Brin Rosenthal, Donald J Hagler, Chun-Chieh Fan, William S Kremen, Ole Andreas Andreassen, Terry L Jernigan, Anders M Dale, Kun Zhang, Peter M Visscher, Jian Yang, Chi-Hua Chen
Discovery of genomic loci of the human cerebral cortex using genetically informed brain atlases. Science (New York, N.Y.) 375 (6580) (2022)
Ting Qi, Yang Wu, Hailing Fang, Futao Zhang, Shouye Liu, Jian Zeng, Jian Yang
Genetic control of RNA splicing and its distinct role in complex trait variation. Nature genetics 54 (9) (2022)
Pierrick Wainschtein, Deepti Jain, Zhili Zheng, null null, null null, L Adrienne Cupples, Aladdin H Shadyab, Barbara McKnight, Benjamin M Shoemaker, Braxton D Mitchell, Bruce M Psaty, Charles Kooperberg, Ching-Ti Liu, Christine M Albert, Dan Roden, Daniel I Chasman, Dawood Darbar, Donald M Lloyd-Jones, Donna K Arnett, Elizabeth A Regan, Eric Boerwinkle, Jerome I Rotter, Jeffrey R O'Connell, Lisa R Yanek, Mariza de Andrade, Matthew A Allison, Merry-Lynn N McDonald, Mina K Chung, Myriam Fornage, Nathalie Chami, Nicholas L Smith, Patrick T Ellinor, Ramachandran S Vasan, Rasika A Mathias, Ruth J F Loos, Stephen S Rich, Steven A Lubitz, Susan R Heckbert, Susan Redline, Xiuqing Guo, Y -D Ida Chen, Cecelia A Laurie, Ryan D Hernandez, Stephen T McGarvey, Michael E Goddard, Cathy C Laurie, Kari E North, Leslie A Lange, Bruce S Weir, Loic Yengo, Jian Yang, Peter M Visscher
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nature genetics 54 (3) (2022)
Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik, Alex Stuckey, Christopher A Odhams, Susan Walker, Clark D Russell, Tomas Malinauskas, Yang Wu, Jonathan Millar, Xia Shen, Katherine S Elliott, Fiona Griffiths, Wilna Oosthuyzen, Kirstie Morrice, Sean Keating, Bo Wang, Daniel Rhodes, Lucija Klarić, Marie Zechner, Nicholas J Parkinson, Afshan Siddiq, Peter Goddard, Sally Donovan, David Maslove, Alistair Nichol, Malcolm Gracie Semple, Tala Zainy, Fiona Maleady-Crowe, Linda Todd, Shahla Salehi, Julian C Knight, Greg Elgar, Georgia Chan, Prabhu Arumugam, Christine Patch, Augusto Rendon, David Bentley, Clare Kingsley, Jack A Kosmicki, Julie E Horowitz, Aris Baras, Gonçalo R Abecasis, Manuel A R Ferreira, Anne Justice, Tooraj Mirshahi, Matthew Oetjens, Daniel James Rader, Marylyn DeRiggi Ritchie, Anurag Verma, Tom A Fowler, Manu Shankar-Hari, Charlotte Summers, Charles J Hinds, Peter Horby, Lowell Ling, Daniel Francis McAuley, Hugh E Montgomery, Peter J M Openshaw, Paul Elliott, Timothy Walsh, Albert Tenesa, null null, null null, null null, Angie Fawkes, Lee Murphy, Kathryn M Rowan, Chris Paul Ponting, Veronique Vitart, James F Wilson, Jian Yang, Andrew D Bretherick, Richard H Scott, Sara Clohisey Hendry, Loukas Moutsianas, Andrew Law, Mark J Caulfield, John Kenneth Baillie
Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature 607 (7917) (2022)
Xiwei Sun, Jian Yang
Towards the understanding of the genetics of somatic mutations. British journal of cancer 125 (5) (2021)
Jian Zeng, Angli Xue, Longda Jiang, Luke R Lloyd-Jones, Yang Wu, Huanwei Wang, Zhili Zheng, Loic Yengo, Kathryn E Kemper, Michael E Goddard, Naomi R Wray, Peter M Visscher, Jian Yang
Widespread signatures of natural selection across human complex traits and functional genomic categories. Nature communications 12 (1) (2021)
Urmo Võsa, Annique A J Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng, Holger Kirsten, Ashis Saha, Roman Kreuzhuber, Seyhan Yazar, Harm Brugge, Roy Oelen, Dylan H de Vries, Monique G P van der Wijst, Silva Kasela, Natalia Pervjakova, Isabel Alves, Marie-Julie Favé, Mawussé Agbessi, Mark W Christiansen, Rick Jansen, Ilkka Seppälä, Lin Tong, Alexander Teumer, Katharina Schramm, Gibran Hemani, Joost A M Verlouw, Hanieh Yaghootkar, Reyhan Sönmez Flitman, Andrew Anand Brown, Viktorija Kukushkina, Anette Kalnapenkis, Sina Rueger, Eleonora Porcu, Jaanika Kronberg, Johannes Kettunen, Bernett Lee, Futao Zhang, Ting Qi, Jose Alquicira Hernandez, Wibowo Arindrarto, Frank Beutner, null null, null null, Julia Dmitrieva, Mahmoud Elansary, Benjamin P Fairfax, Michel Georges, Bastiaan T Heijmans, Alex W Hewitt, Mika Kähönen, Yungil Kim, Julian C Knight, Peter Kovacs, Knut Krohn, Shuang Li, Markus Loeffler, Urko M Marigorta, Hailang Mei, Yukihide Momozawa, Martina Müller-Nuraysid, Matthias Nauck, Michel G Nivard, Brenda W J H Penninx, Jonathan K Pritchard, Olli T Raitakari, Olaf Rotzschke, Pieternella Eline Slagboom, Coen D A Stehouwer, Michael Stumvoll, Patrick Sullivan, Peter A C 't Hoen, Joachim Thiery, Anke Tönjes, Jenny Van Dongen, Maarten van Iterson, Jan Herman Veldink, Linus Völker, C A Robert Warmerdam, Cisca Wijmenga, Morris A Swertz, Anand Kumar Andiappan, Grant W Montgomery, Samuli Ripatti, Markus Perola, Zoltan Kutalik, Emmanouil T Dermitzakis, Sven Bergmann, Timothy M Frayling, Joyce van Meurs, Holger Prokisch, Habibul Ahsan, Brandon L Pierce, Terho Lehtimäki, Dorret I Boomsma, Bruce M Psaty, Sina A Gharib, Philip Awadalla, Lili A Milani, Willem Hendrik Ouwehand, Kate Downes, Oliver Stegle, Alexis Battle, Peter M Visscher, Jian Yang, Markus Scholz, Joseph Powell, Greg Gibson, Tõnu Esko, Lude H Franke
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nature genetics 53 (9) (2021)
Longda Jiang, Zhili Zheng, Hailing Fang, Jian Yang
A generalized linear mixed model association tool for biobank-scale data. Nature genetics 53 (11) (2021)
Wenhan Chen, Yang Wu, Zhili Zheng, Ting Qi, Peter M Visscher, Zhihong Zhu, Jian Yang
Improved analyses of GWAS summary statistics by reducing data heterogeneity and errors. Nature communications 12 (1) (2021)
Kathryn E Kemper, Loic Yengo, Zhili Zheng, Abdel Abdellaoui, Matthew C Keller, Michael E Goddard, Naomi R Wray, Jian Yang, Peter M Visscher
Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. Nature communications 12 (1) (2021)
Xiwei Sun, Angli Xue, Ting Qi, Dan Chen, Dandan Shi, Yang Wu, Zhili Zheng, Jian Zeng, Jian Yang
Tumor Mutational Burden Is Polygenic and Genetically Associated with Complex Traits and Diseases. Cancer research 81 (5) (2021)
H C Palmer Rohan, Chelsie E Benca-Bachman, Spencer B Huggett, Jason A Bubier, John E McGeary, Nikhil Ramgiri, Jenani Srijeyanthan, Jingjing Yang, Peter M Visscher, Jian Yang, Valerie S Knopik, Elissa J Chesler
Multi-omic and multi-species meta-analyses of nicotine consumption. Translational psychiatry 11 (1) (2021)
Gibran Hemani, Joseph E Powell, Huanwei Wang, Konstantin Shakhbazov, Harm-Jan Westra, Tonu Esko, Anjali K Henders, Allan F McRae, Nicholas G Martin, Andres Metspalu, Lude H Franke, Grant W Montgomery, Michael E Goddard, Greg Gibson, Jian Yang, Peter M Visscher
Phantom epistasis between unlinked loci. Nature 596 (7871) (2021)
Yang Wu, Ting Qi, Huanwei Wang, Futao Zhang, Zhili Zheng, Jennifer E Phillips-Cremins, Ian J Deary, Allan F McRae, Naomi R Wray, Jian Zeng, Jian Yang
Promoter-anchored chromatin interactions predicted from genetic analysis of epigenomic data. Nature communications 11 (1) (2020)
Joana A Revez, Tian Lin, Zhen Qiao, Angli Xue, Yan Holtz, Zhihong Zhu, Jian Zeng, Huanwei Wang, Julia Sidorenko, Kathryn E Kemper, Anna A E Vinkhuyzen, Julanne Frater, Darryl Eyles, Thomas H J Burne, Brittany L Mitchell, Nicholas G Martin, Gu Zhu, Peter M Visscher, Jian Yang, Naomi R Wray, John G McGrath
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nature communications 11 (1) (2020)
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Guo-Bo Chen, Sang Hong Lee, Matthew R Robinson, Maciej Trzaskowski, Zhi-Xiang Zhu, Thomas W Winkler, Felix R Day, Damien C Croteau-Chonka, Andrew R Wood, Adam E Locke, Zoltán Kutalik, Ruth J F Loos, Timothy M Frayling, Joel N Hirschhorn, Jian Yang, Naomi R Wray, null null, Peter M Visscher
Across-cohort QC analyses of GWAS summary statistics from complex traits. European journal of human genetics : EJHG 25 (1) (2016)
Aysu Okbay, Bart M L Baselmans, Jan-Emmanuel De Neve, Patrick Turley, Michel G Nivard, Mark Alan Fontana, S Fleur W Meddens, Richard Karlsson Linnér, Cornelius A Rietveld, Jaime Derringer, Jacob Gratten, James J Lee, Jimmy Z Liu, Ronald de Vlaming, Tarunveer S Ahluwalia, Jadwiga Buchwald, Alana Cavadino, Alexis C Frazier-Wood, Nicholas A Furlotte, Victoria Garfield, Marie Henrike Geisel, Juan R Gonzalez, Saskia Haitjema, Robert Karlsson, Sander W van der Laan, Karl-Heinz Ladwig, Jari Lahti, Sven J Van der Lee, Penelope A Lind, Tian Liu, Lindsay Matteson, Evelin Mihailov, Michael B Miller, Camelia C Minica, Ilja M Nolte, Dennis Mook-Kanamori, Peter J van der Most, Christopher Oldmeadow, Yong Qian, Olli Raitakari, Rajesh Rawal, Anu Realo, Rico Rueedi, Börge Schmidt, Albert Vernon Smith, Evie Stergiakouli, Toshiko Tanaka, Kent Taylor, Gudmar Thorleifsson, Juho Wedenoja, Juergen Wellmann, Harm-Jan Westra, Sara M Willems, Wei Zhao, null null, Najaf Amin, Andrew Bakshi, Sven Bergmann, Gyda Bjornsdottir, Patricia A Boyle, Samantha Cherney, Simon R Cox, Gail Davies, Oliver S P Davis, Jun Ding, Nese Direk, Peter Eibich, Rebecca T Emeny, Ghazaleh Fatemifar, Jessica D Faul, Luigi Ferrucci, Andreas J Forstner, Christian Gieger, Richa Gupta, Tamara B Harris, Juliette M Harris, Elizabeth G Holliday, Jouke-Jan Hottenga, Philip L De Jager, Marika A Kaakinen, Eero Kajantie, Ville Karhunen, Ivana Kolcic, Meena Kumari, Lenore J Launer, Lude H Franke, Ruifang Li-Gao, David C Liewald, Marisa Koini, Anu Loukola, Pedro Marques-Vidal, Grant W Montgomery, Miriam A Mosing, Lavinia Paternoster, Alison Pattie, Katja E Petrovic, Laura Pulkki-Råback, Lydia Quaye, Katri Räikkönen, Igor Rudan, Rodney J Scott, Jennifer A Smith, Angelina R Sutin, Maciej Trzaskowski, Anna E Vinkhuyzen, Lei Yu, Delilah Zabaneh, John Richard Attia, David A Bennett, Klaus Berger, Lars Bertram, Dorret I Boomsma, Harold Snieder, Shun-Chiao Chang, Francesco Cucca, Ian J Deary, Cornelia M van Duijn, Johan G Eriksson, Ute Bültmann, Eco J C N de Geus, Patrick J F Groenen, Vilmundur Gudnason, Torben Hansen, Catharine A Hartman, Claire M A Haworth, Caroline Hayward, Andrew C Heath, David A Hinds, Elina Hyppönen, William G Iacono, Marjo-Riitta Järvelin, Karl-Heinz Jöckel, Jaakko A Kaprio, Sharon L R Kardia, Liisa Keltikangas-Järvinen, Peter Kraft, Laura D Kubzansky, Terho Lehtimäki, Patrik K E Magnusson, Nicholas G Martin, Matt McGue, Andres Metspalu, Melinda Mills, Renée de Mutsert, Albertine J Oldehinkel, Gerard Pasterkamp, Nancy L Pedersen, Robert Plomin, Ozren Polasek, Christine Power, Stephen S Rich, Frits R Rosendaal, Hester M den Ruijter, David Schlessinger, Helena Schmidt, Rauli Svento, Reinhold Schmidt, Behrooz Z Alizadeh, Thorkild I A Sørensen, Tim D Spector, John M Starr, Kari Stefansson, Andrew Steptoe, Antonio Terracciano, Unnur Thorsteinsdottir, A Roy Thurik, Nicholas J Timpson, Henning Tiemeier, André G Uitterlinden, Peter Vollenweider, Gert G Wagner, David R Weir, Jian Yang, Dalton C Conley, George Davey Smith, Albert Hofman, Magnus Johannesson, David I Laibson, Sarah E Medland, Michelle N Meyer, Joseph K Pickrell, Tõnu Esko, Robert F Krueger, Jonathan P Beauchamp, Philipp D Koellinger, Daniel J Benjamin, Meike Bartels, David Cesarini
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature genetics 48 (6) (2016)
Jennifer M Whitehead Pavlides, Zhihong Zhu, Jacob Gratten, Allan F McRae, Naomi R Wray, Jian Yang
Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits. Genome medicine 8 (1) (2016)
Wouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, Russell L McLaughlin, Frank P Diekstra, Sara L Pulit, Rick A A van der Spek, Urmo Võsa, Simone de Jong, Matthew R Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs H P Tazelaar, Max Koppers, Anna M Blokhuis, William Sproviero, Ashley R Jones, Kevin P Kenna, Kristel R van Eijk, Oliver Harschnitz, Raymond D Schellevis, William J Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik-Glavač, Blaz Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesus S Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen E Morrison, Pamela J Shaw, John Hardy, Richard W Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon D Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A Ophoff, Kim A Staats, Martina Wiedau-Pazos, Catherine Lomen-Hoerth, Vivanna M Van Deerlin, John Q Trojanowski, Lauren Elman, Leo McCluskey, A Nazli Basak, Ceren Tunca, Hamid Hamzeiy, Yesim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov-Blagojevic, Christian R Andres, Cindy Maurel, Gilbert Bensimon, Bernhard Landwehrmeyer, Alexis Brice, Christine A M Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas W Wood, Lukas Tittmann, Wolfgang Lieb, Andre Franke, Marcella Rietschel, Sven Cichon, Markus M Nöthen, Phillippe Amouyel, Christophe Tzourio, Jean-François Dartigues, Andre G Uitterlinden, Fernando Rivadeneira, Karol Estrada, Albert Hofman, Charles Curtis, Hylke M Blauw, Anneke J van der Kooi, Marianne de Visser, An Goris, Markus Weber, Christopher E Shaw, Bradley N Smith, Orietta Pansarasa, Cristina Cereda, Roberto Del Bo, Giacomo P Comi, Sandra D'Alfonso, Cinzia Bertolin, Gianni Sorarù, Letizia Mazzini, Viviana Pensato, Cinzia Gellera, Cinzia Tiloca, Antonia Ratti, Andrea Calvo, Cristina Moglia, Maura Brunetti, Simona Arcuti, Rosa Capozzo, Chiara Zecca, Christian Lunetta, Silvana Penco, Nilo Riva, Alessandro Padovani, Massimiliano Filosto, Bernard Muller, Robbert Jan Stuit, null null, null null, null null, null null, null null, null null, Ian Blair, Katharine Zhang, Emily P McCann, Jennifer A Fifita, Garth A Nicholson, Dominic B Rowe, Roger Pamphlett, Matthew C Kiernan, Julian Grosskreutz, Otto W Witte, Thomas Ringer, Tino Prell, Beatrice Stubendorff, Ingo Kurth, Christian A Hübner, P Nigel Leigh, Federico Casale, Adriano Chio, Ettore Beghi, Elisabetta Pupillo, Rosanna Tortelli, Giancarlo Logroscino, John Powell, Albert C Ludolph, Jochen H Weishaupt, Wim Robberecht, Philip Van Damme, Lude H Franke, Tune H Pers, Robert H Brown, Jonathan D Glass, John E Landers, Orla Hardiman, Peter M Andersen, Philippe Corcia, Patrick Vourc'h, Vincenzo Silani, Naomi R Wray, Peter M Visscher, Paul I W de Bakker, Michael A van Es, Ronald Jeroen Pasterkamp, Cathryn M Lewis, Gerome Breen, Ammar Al-Chalabi, Leonard H van den Berg, Jan H Veldink
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature genetics 48 (9) (2016)
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, null null, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature genetics 47 (3) (2015)
Jian Yang, Andrew Bakshi, Zhihong Zhu, Gibran Hemani, Anna A E Vinkhuyzen, Sang Hong Lee, Matthew R Robinson, John R B Perry, Ilja M Nolte, Jana V van Vliet-Ostaptchouk, Harold Snieder, null null, Tõnu Esko, Lili Milani, Reedik Mägi, Andres Metspalu, Anders Hamsten, Patrik K E Magnusson, Nancy L Pedersen, Erik Ingelsson, Nicole Soranzo, Matthew C Keller, Naomi R Wray, Michael E Goddard, Peter M Visscher
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Nature genetics 47 (10) (2015)

Jian Yang.css-eqlu8i{font-size:small;padding-left:4px;} (J Yang)

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Jian Yang (J Yang)