Risultati della ricerca - Xiaobing Zou

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  1. 1
    A multimodal machine learning system in early screening for toddlers with autism spectrum disorders based on the response to name

    A multimodal machine learning system in early screening for toddlers with autism spectrum disorders based on the response to name di Feng-lei Zhu, Shihuan Wang, Wenbo Liu, Huilin Zhu, Ming Li, Xiaobing Zou

    Pubblicazione 2023
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  2. 2
    Investigating the validation of the Chinese Mandarin version of the Social Responsiveness Scale in a Mainland China child population

    Investigating the validation of the Chinese Mandarin version of the Social Responsiveness Scale in a Mainland China child population di Chaoqun Cen, Yayong Liang, Qiuru Chen, Kai‐Yun Chen, Hong-zhu Deng, Bi-yuan Chen, Xiaobing Zou

    Pubblicazione 2017
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  3. 3
    Phenotype‐to‐genotype approach reveals head‐circumference‐associated genes in an autism spectrum disorder cohort

    Phenotype‐to‐genotype approach reveals head‐circumference‐associated genes in an autism spectrum disorder cohort di Huidan Wu, Honghui Li, Ting Bai, Lin Han, Jianjun Ou, Guanglei Xun, Yu Zhang, Yazhe Wang, Guiqin Duan, Ningxia Zhao, Biyuan Chen, Xiaogang Du, Meiling Yao, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Evan E. Eichler, Hui Guo, Kun Xia

    Pubblicazione 2019
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  4. 4
    Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort

    Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort di Hui Guo, Peng Yu, Zhengmao Hu, Ying Li, Guanglei Xun, Jianjun Ou, Liangdan Sun, Zhimin Xiong, Yanling Liu, Tianyun Wang, Jingjing Chen, Lu Xia, Ting Bai, Yidong Shen, Qi Tian, Yiqiao Hu, Lu Shen, Rongjuan Zhao, Xuejun Zhang, Fengyu Zhang, Jingping Zhao, Xiaobing Zou, Kun Xia

    Pubblicazione 2017
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  5. 5
    Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years

    Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years di Hao Zhou, Xiu Xu, Weili Yan, Xiaobing Zou, Lijie Wu, Xuerong Luo, Tingyu Li, Yi Huang, Hongyan Guan, Xiang Chen, Meng Mao, Kun Xia, Lan Zhang, Erzhen Li, Xiaoling Ge, Lili Zhang, Chunpei Li, Xu Dong Zhang, Yuanfeng Zhou, Ding Ding, Andy Shih, Éric Fombonne, Yi Zheng, Ji‐Sheng Han, Zhong Sheng Sun, Yong‐hui Jiang, Yi Wang

    Pubblicazione 2020
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  6. 6
    De novo genic mutations among a Chinese autism spectrum disorder cohort

    De novo genic mutations among a Chinese autism spectrum disorder cohort di Tianyun Wang, Hui Guo, Bo Xiong, Holly A.F. Stessman, Huidan Wu, Bradley P. Coe, Tychele N. Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Long Min, Janice Lin, Zev Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E. Eichler

    Pubblicazione 2016
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  7. 7
    Common genetic variants on 1p13.2 associate with risk of autism

    Common genetic variants on 1p13.2 associate with risk of autism di Kun Xia, Hui Guo, Zhengmao Hu, Guanglei Xun, Lingjun Zuo, Yu Peng, Keheng Wang, Yijing He, Zhengang Xiong, Linlin Sun, Qian Pan, Z Long, Xiaobing Zou, Xiaoyu Li, Wenjun Li, Xiaojing Xu, Liping Lu, Yukun Liu, Yuantai Hu, Di Tian, Long Liu, Jianjun Ou, Yukun Liu, Xiaoyu Li, Ling Zhang, Yongcheng Pan, Jianxi Chen, Hui Peng, 豊 大根田, Xuerong Luo, Wei Su, Lingqian Wu, Desheng Liang, H Dai, Xin Yan, Yong Feng, Beisha Tang, Jinchen Li, Zosia Miedzybrodzka, Junfeng Xia, Zhiwu Zhang, Xuerong Luo, Xiang Zhang, David St Clair, J. Zhao, Fengyu Zhang

    Pubblicazione 2013
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  8. 8
    Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model

    Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model di Hui Guo, Tianyun Wang, Huidan Wu, Long Min, Bradley P. Coe, Honghui Li, Guanglei Xun, Jianjun Ou, Biyuan Chen, Guiqin Duan, Ting Bai, Ningxia Zhao, Yidong Shen, Yun Li, Yazhe Wang, Yu Zhang, Carl Baker, Yanling Liu, Nan Pang, Li’an Huang, Lin Han, Xiangbin Jia, Cenying Liu, Hailun Ni, Xinyi Yang, Lu Xia, Jingjing Chen, Lu Shen, Ying Li, Rongjuan Zhao, Wenjing Zhao, Jing Peng, Qian Pan, Zhigao Long, Wei Su, Jieqiong Tan, Xiaogang Du, Xiaoyan Ke, Meiling Yao, Zhengmao Hu, Xiaobing Zou, Jingping Zhao, Raphael Bernier, Evan E. Eichler, Kun Xia

    Pubblicazione 2018
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  9. 9
    Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission

    Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission di Hui Guo, Ying Li, Lu Shen, Tianyun Wang, Xiangbin Jia, Lijuan Liu, Tao Xu, Mengzhu Ou, Kendra Hoekzema, Huidan Wu, Madelyn A. Gillentine, Cenying Liu, Hailun Ni, Pengwei Peng, Rongjuan Zhao, Yu Zhang, Chanika Phornphutkul, Alexander P.A. Stegmann, Carlos E. Prada, Robert J. Hopkin, Joseph T.C. Shieh, Kirsty McWalter, Kristin G. Monaghan, Peter M. van Hasselt, Koen L.I. van Gassen, Ting Bai, Long Min, Lin Han, Yingting Quan, Meilin Chen, Yaowen Zhang, Kuokuo Li, Qiumeng Zhang, Jieqiong Tan, Tengfei Zhu, Yaning Liu, Nan Pang, Jing Peng, Daryl A. Scott, Seema R. Lalani, Mahshid S. Azamian, Grazia M.S. Mancini, Darius J. Adams, Malin Kvarnung, Anna Lindstrand, Ann Nordgren, Jonathan Pevsner, Ikeoluwa Osei‐Owusu, Corrado Romano, Giuseppe Calabrese, Ornella Galesi, Jozef Gécz, Eric Haan, Judith D. Ranells, Melissa Racobaldo, Magnus Nordenskjöld, Suneeta Madan‐Khetarpal, Jessica Sebastian, Susie Ball, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Fan Xia, Pengfei Liu, Jill A. Rosenfeld, Bert B.A. de Vries, Raphael Bernier, Qing Xu, Honghui Li, Wei Xie, Robert B. Hufnagel, Evan E. Eichler, Kun Xia

    Pubblicazione 2019
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  10. 10
    Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

    Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders di Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe, Madelyn A. Gillentine, Amy B. Wilfert, Luis A. Pérez‐Jurado, Malin Kvarnung, Yoeri Sleyp, Rachel K. Earl, Jill A. Rosenfeld, Madeleine R. Geisheker, Lin Han, Bing Du, Chris Barnett, E. A. Thompson, Marie Shaw, Renée Carroll, Kathryn Friend, Rachael Catford, Elizabeth E. Palmer, Xiaobing Zou, Jianjun Ou, Honghui Li, Hui Guo, Jennifer Gerdts, Emanuela Avola, Giuseppe Calabrese, Maurizio Elia, Donatella Greco, Anna Lindstrand, Ann Nordgren, Britt‐Marie Anderlid, Geert Vandeweyer, Anke Van Dijck, Nathalie Van der Aa, Brooke G. McKenna, Miroslava Hančárová, Šárka Bendová, Markéta Havlovicová, Giovanni Malerba, Bernardo Dalla Bernardina, Pierandrea Muglia, Arie van Haeringen, Mariëtte J.V. Hoffer, Barbara Franke, Gerarda Cappuccio, Martin B. Delatycki, Paul J. Lockhart, Melanie A. Manning, Pengfei Liu, Ingrid E. Scheffer, Nicola Brunetti‐Pierri, Nanda Rommelse, David G. Amaral, Gijs W.E. Santen, Elisabetta Trabetti, Zdeněk Sedláček, Jacob J. Michaelson, Karen Pierce, Eric Courchesne, R. Frank Kooy, John Acampado, J. Andrea, Alpha Amatya, Irina Astrovskaya, Asif Bashar, Elizabeth Brooks, Martin E. Butler, Lindsey A. Cartner, Wubin Chin, Wendy K. Chung, Amy M. Daniels, Pamela Feliciano, Chris Fleisch, Swami Ganesan, William B. Jensen, Alex E. Lash, Richard P. Marini, Vincent J. Myers, Eirene O’Connor, Chris Rigby, B. E. Robertson, Neelay Shah, Swapnil Shah, Emily Singer, LeeAnne Green Snyder, Alexandra N. Stephens, Jennifer Tjernagel, Brianna M. Vernoia, Natalia Volfovsky, L. Casey White, Alexander Hsieh, Yufeng Shen, Xueya Zhou, Tychele N. Turner, Ethan Bahl, Taylor R. Thomas

    Pubblicazione 2020
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