1. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Issue 9 (24th July 2015) Authors: Xu, Xiaojing; Yang, Xiaoxu; Wu, Qixi; Liu, Aijie; Yang, Xiaoling; Ye, Adam Yongxin; Huang, August Yue; Li, Jiarui; Wang, Meng; Yu, Zhe; Wang, Sheng; Zhang, Zhichao; Wu, Xiru; Wei, Liping; Zhang, Yuehua Journal: Human mutation Issue: Volume 36:Issue 9(2015:Sep.) Page Start: 861 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. (18th October 2018) Authors: Yang, Changhong; Li, Jiarui; Wu, Qixi; Yang, Xiaoxu; Huang, August Yue; Zhang, Jie; Ye, Adam Yongxin; Dou, Yanmei; Yan, Linlin; Zhou, Wei-zhen; Kong, Lei; Wang, Meng; Ai, Chen; Yang, Dechang; Wei, Liping Journal: Database Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cover Image, Volume 38, Issue 8. Issue 8 (11th July 2017) Authors: Dou, Yanmei; Yang, Xiaoxu; Li, Ziyi; Wang, Sheng; Zhang, Zheng; Ye, Adam Yongxin; Yan, Linlin; Yang, Changhong; Wu, Qixi; Li, Jiarui; Zhao, Boxun; Huang, August Yue; Wei, Liping Journal: Human mutation Issue: Volume 38:Issue 8(2017) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples. Issue 10 (28th January 2017) Authors: Huang, August Yue; Zhang, Zheng; Ye, Adam Yongxin; Dou, Yanmei; Yan, Linlin; Yang, Xiaoxu; Zhang, Yuehua; Wei, Liping Journal: Nucleic acids research Issue: Volume 45:Issue 10(2017) Page Start: e76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mycobacterial and Plasmodium ovale‐associated destruction of the jaw bones. (29th December 2020) Authors: Yang, Xianrui; Ye, Adam Yongxin; Katebi, Negin; Volloch, Vladimir; Khullar, Shelley M.; Patel, Vinod; Olsen, Bjorn R. Journal: Oral diseases Issue: Volume 28:Number 2(2022) Page Start: 452 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Issue 8 (30th May 2017) Authors: Dou, Yanmei; Yang, Xiaoxu; Li, Ziyi; Wang, Sheng; Zhang, Zheng; Ye, Adam Yongxin; Yan, Linlin; Yang, Changhong; Wu, Qixi; Li, Jiarui; Zhao, Boxun; Huang, August Yue; Wei, Liping Journal: Human mutation Issue: Volume 38:Issue 8(2017) Page Start: 1002 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype–phenotype correlations. Issue 6 (29th April 2019) Authors: Zhou, Wei‐Zhen; Zhang, Jie; Li, Ziyi; Lin, Xiaojing; Li, Jiarui; Wang, Sheng; Yang, Changhong; Wu, Qixi; Ye, Adam Yongxin; Wang, Meng; Wang, Dandan; Pu, Tad Zhengzhang; Wu, Yu‐Yu; Wei, Liping Journal: Human mutation Issue: Volume 40:Issue 6(2019) Page Start: 801 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗