Kun Xia

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 17

Top Venues

Molecular genetics & genomic medicine

Science advances

Nature communications

Cancer medicine

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

Publications

Wanjing Lai, Yingying Zhao, Yalan Chen, Zhenzhu Dai, Ruhai Chen, Yimei Niu, Xiaoxia Chen, Shuting Chen, Guanqun Huang, Ziyun Shan, Jiajun Zheng, Yu Hu, Qingpei Chen, Siyi Gong, Sai Kang, Hui Guo, Xiaokuang Ma, Youqiang Song, Kun Xia, Jie Wang, Libing Zhou, Kowk-Fai So, Kai Wang, Shenfeng Qiu, Li Zhang, Jie-Kai Chen, Lingling Shi
Autism patient-derived SHANK2B Y29X mutation affects the development of ALDH1A1 negative dopamine neuron. Molecular psychiatry (2024)
Ying Han, Ying Peng, Haofeng Xiong, Liujun Zeng, Tianyi Zhang, Kun Xia, Xin Hu, Tong Su
XPO1 serves as a prognostic marker involving AKT/MAPK/TGFBR1 pathway in OSCC. Cancer medicine 13 (16) (2024)
Shiyu Zhang, Zheng Wang, Yijing Wang, Yixiao Zhu, Qiao Zhou, Xingxing Jian, Guihu Zhao, Jian Qiu, Kun Xia, Bei-Sha Tang, Julian Mutz, Jinchen Li, Bin Li
A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank. Nature communications 15 (1) (2024)
Ying Han, Ying Peng, Haofeng Xiong, Liujun Zeng, Tianyi Zhang, Kun Xia, Xin Hu, Tong Su
XPO1 serves as a prognostic marker involving AKT/MAPK/TGFBR1 pathway in OSCC. Cancer medicine 13 (16) (2024)
Zheng Wang, Guihu Zhao, Zhaopo Zhu, Yijing Wang, Xudong Xiang, Shiyu Zhang, Tengfei Luo, Qiao Zhou, Jian Qiu, Bei-Sha Tang, Kun Xia, Bin Li, Jin-Chen Li
VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome. Nucleic acids research (2023)
Xiangbin Jia, Shujie Zhang, Senwei Tan, Bing Du, Mei He, Haisong Qin, Jia Chen, Xinyu Duan, Jingsi Luo, Fei Chen, Luping Ouyang, Jian Wang, Guodong Chen, Bin Yu, Ge Zhang, Zimin Zhang, Yongqing Lyu, Yi Huang, Jian Jiao, Jin Yun Helen Chen, Kathryn J Swoboda, Emanuele Agolini, Antonio Novelli, Chiara Leoni, Giuseppe Zampino, Gerarda Cappuccio, Nicola Brunetti-Pierri, Bénédicte Gérard, Emmanuelle Ginglinger, Julie Richer, Hugh J Mcmillan, Alexandre White-Brown, Kendra Hoekzema, Raphael A Bernier, Evangeline C Kurtz-Nelson, Rachel K Earl, Claartje Meddens, Marielle Alders, Meredith Fuchs, Roseline Caumes, Perrine Brunelle, Thomas Smol, Ryan Kuehl, Debra-Lynn Day-Salvatore, Kristin G Monaghan, Michelle M Morrow, Evan E Eichler, Zhengmao Hu, Ling Yuan, Jieqiong Tan, Kun Xia, Yiping Shen, Hui Guo
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders. Science advances 8 (33) (2022)
Kuokuo Li, Tengfei Luo, Yan Zhu, Yuanfeng Huang, An Wang, Di Zhang, Lijie Dong, Yujian Wang, Rui Wang, Dongdong Tang, Zhen Yu, Qunshan Shen, Mingrong Lv, Zhengbao Ling, Zhenghuan Fang, Jing Yuan, Bin Li, Kun Xia, Xiaojin He, Jin-Chen Li, Guihu Zhao
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction. Nucleic acids research 50 (16) (2022)
Qiong Liu, Kailin Zhang, Yunhee Kang, Yangping Li, Penghui Deng, Yujing Li, Yun Tian, Qiying Sun, Yu Tang, Keqin Xu, Yao Zhou, Jun-Ling Wang, Jifeng Guo, Jia-Da Li, Kun Xia, Qingtuan Meng, Emily Graves Allen, Zhexing Wen, Ziyi Li, Jiang Hong, Lu Shen, Ranhui Duan, Bing Yao, Bei-Sha Tang, Peng Jin, Yongcheng Pan
Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease. Science advances 8 (47) (2022)
Fei Gao, Wen Huang, Yanjun You, Jie Huang, Juan Zhao, Jin Xue, Huaixing Kang, Yingbao Zhu, Zhengmao Hu, Emily G Allen, Peng Jin, Kun Xia, Ranhui Duan
Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy. Molecular genetics & genomic medicine 8 (6) (2020)
Ting Mao, Haofeng Xiong, Xin Hu, Yue Hu, Can Wang, Liudi Yang, Danni Huang, Kun Xia, Tong Su
DEC1: a potential biomarker of malignant transformation in oral leukoplakia. Brazilian oral research 34 (2020)
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P Coe, Madelyn A Gillentine, Amy B Wilfert, Luis A Perez-Jurado, Malin Kvarnung, Yoeri Sleyp, Rachel K Earl, Jill Anne Rosenfeld, Madeleine R Geisheker, Lin Han, Bing Du, Chris Barnett, Elizabeth Thompson, Marie Shaw, Renee 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 McKenna, Miroslava Hancarova, Sarka Bendova, Marketa Havlovicova, Giovanni Malerba, Bernardo Dalla Bernardina, Pierandrea Muglia, Arie van Haeringen, Mariette J V Hoffer, Barbara Franke, Gerarda Cappuccio, Martin 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, null null, Magnus Nordenskjöld, Corrado Romano, Hilde Peeters, Raphael A Bernier, Jozef Gecz, Kun Xia, Evan E Eichler
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature communications 11 (1) (2020)
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P Coe, Madelyn A Gillentine, Amy B Wilfert, Luis A Perez-Jurado, Malin Kvarnung, Yoeri Sleyp, Rachel K Earl, Jill Anne Rosenfeld, Madeleine R Geisheker, Lin Han, Bing Du, Chris Barnett, Elizabeth Thompson, Marie Shaw, Renee 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 McKenna, Miroslava Hancarova, Sarka Bendova, Marketa Havlovicova, Giovanni Malerba, Bernardo Dalla Bernardina, Pierandrea Muglia, Arie van Haeringen, Mariette J V Hoffer, Barbara Franke, Gerarda Cappuccio, Martin 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, null null, Magnus Nordenskjöld, Corrado Romano, Hilde Peeters, Raphael A Bernier, Jozef Gecz, Kun Xia, Evan E Eichler
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature communications 11 (1) (2020)
Lin Wang, Yi Zhang, Kuokuo Li, Zheng Wang, Xiaomeng Wang, Bin Li, Guihu Zhao, Zhenghuan Fang, Zhengbao Ling, Tengfei Luo, Lu Xia, Yanping Li, Hui Guo, Zhengmao Hu, Jinchen Li, Zhongsheng Sun, Kun Xia
Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder. Molecular autism 11 (1) (2020)
Wenjing Zhao, Yingting Quan, Huidan Wu, Lin Han, Ting Bai, Linya Ma, Bin Li, Guanglei Xun, Jianjun Ou, Jingping Zhao, Zhengmao Hu, Hui Guo, Kun Xia
POGZ de novo missense variants in neuropsychiatric disorders. Molecular genetics & genomic medicine 7 (9) (2019)
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 Shieh, Kirsty McWalter, Kristin G Monaghan, Peter M van Hasselt, Koen van Gassen, Ting Bai, Min Long, 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 A Osei-Owusu, Corrado Romano, Giuseppe Calabrese, Ornella Galesi, Jozef Gecz, Eric A Haan, Judith Ranells, Melissa Racobaldo, Magnus Nordenskjold, Suneeta Madan-Khetarpal, Jessica Sebastian, Susie Ball, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Fan Xia, Pengfei Liu, Jill Anne Rosenfeld, Bert B A de Vries, Raphael A Bernier, Zhi-Qing David Xu, Honghui Li, Wei Xie, Robert B Hufnagel, Evan E Eichler, Kun Xia
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission. Science advances 5 (9) (2019)
Lu Xia, Jianjun Ou, Kuokuo Li, Hui Guo, Zhengmao Hu, Ting Bai, Jingping Zhao, Kun Xia, Fengyu Zhang
Genome-wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders. Autism research : official journal of the International Society for Autism Research 13 (3) (2019)
Lin Han, Meilin Chen, Yazhe Wang, Huidan Wu, Yingting Quan, Ting Bai, Kuokuo Li, Guiqin Duan, Yan Gao, Zhengmao Hu, Kun Xia, Hui Guo
Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders. Molecular genetics & genomic medicine 7 (7) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Kun Xia