Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: ASXL3[original query] |
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Clonal architectures and driver mutations in metastatic melanomas. PloS one 2014 9 (11): e111153. Ding Li, Kim Minjung, Kanchi Krishna L, Dees Nathan D, Lu Charles, Griffith Malachi, Fenstermacher David, Sung Hyeran, Miller Christopher A, Goetz Brian, Wendl Michael C, Griffith Obi, Cornelius Lynn A, Linette Gerald P, McMichael Joshua F, Sondak Vernon K, Fields Ryan C, Ley Timothy J, Mulé James J, Wilson Richard K, Weber Jeffrey |
Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma. Nature genetics 2015 Sep 47 (9): 1061-6. Jiang Lu, Gu Zhao-Hui, Yan Zi-Xun, Zhao Xia, Xie Yin-Yin, Zhang Zi-Guan, Pan Chun-Ming, Hu Yuan, Cai Chang-Ping, Dong Ying, Huang Jin-Yan, Wang Li, Shen Yang, Meng Guoyu, Zhou Jian-Feng, Hu Jian-Da, Wang Jin-Fen, Liu Yuan-Hua, Yang Lin-Hua, Zhang Feng, Wang Jian-Min, Wang Zhao, Peng Zhi-Gang, Chen Fang-Yuan, Sun Zi-Min, Ding Hao, Shi Ju-Mei, Hou Jian, Yan Jin-Song, Shi Jing-Yi, Xu Lan, Li Yang, Lu Jing, Zheng Zhong, Xue Wen, Zhao Wei-Li, Chen Zhu, Chen Sai-Ju |
Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas. Endocrinology 2018 Jul . Wei Zhe, Sun Bin, Wang Zong-Ping, He Jin-Wei, Fu Wen-Zhen, Fan You-Ben, Zhang Zhen-L |
Mild prominence of the Sylvian fissure in a Bainbridge-Ropers syndrome patient with a novel frameshift variant in ASXL3. Clinical case reports 2018 2 6 (2): 330-336. Chinen Yasutsugu, Nakamura Sadao, Ganaha Akira, Hayashi Shin, Inazawa Johji, Yanagi Kumiko, Nakanishi Koichi, Kaname Tadashi, Naritomi Ken |
Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations. Clinica chimica acta; international journal of clinical chemistry 2018 12 489 103-108. Fu Chunyun, Luo Shiyu, Zhang Yue, Fan Xin, D'Gama Alissa M, Zhang Xiaofei, Zheng Haiyang, Su Jiasun, Li Chuan, Luo Jingsi, Agrawal Pankaj B, Li Qifei, Chen Shao |
Further expanding the clinical phenotype in Bainbridge-Ropers syndrome and dissecting genotype-phenotype correlation in the ASXL3 mutational cluster regions. European journal of medical genetics 2020 11 64 (1): 104107. Yu Kris Pui-Tak, Luk Ho-Ming, Fung Jasmine L F, Chung Brian Hon-Yin, Lo Ivan Fai-M |
New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PloS one 2021 16 (10): e0258766. Aguilera Cinthia, Gabau Elisabeth, Ramirez-Mallafré Ariadna, Brun-Gasca Carme, Dominguez-Carral Jana, Delgadillo Veronica, Laurie Steve, Derdak Sophia, Padilla Natàlia, de la Cruz Xavier, Capdevila Núria, Spataro Nino, Baena Neus, Guitart Miriam, Ruiz An |
Identification of genetic mutations of cutaneous squamous cell carcinoma using whole exome sequencing in non-Caucasian population. Journal of dermatological science 2022 4 106 (2): 70-77. Lee Soo Young, Lee Minho, Yu Dong Soo, Lee Young B |
De novo mutations identified by whole-genome sequencing implicate chromatin modifications in obsessive-compulsive disorder. Science advances 2022 1 8 (2): eabi6180. Lin Guan Ning, Song Weichen, Wang Weidi, Wang Pei, Yu Huan, Cai Wenxiang, Jiang Xue, Huang Wu, Qian Wei, Chen Yucan, Chen Miao, Yu Shunying, Xu Tingting, Jiao Yumei, Liu Qiang, Zhang Chen, Yi Zhenghui, Fan Qing, Chen Jue, Wang Zh |
Sex-Specific Genetic and Transcriptomic Liability to Neuroticism.
Biological psychiatry 2022 10 93 (3): 243-252. Wendt Frank R, Pathak Gita A, Singh Kritika, Stein Murray B, Koenen Karestan C, Krystal John H, Gelernter Joel, Davis Lea K, Polimanti Rena |
Genomic profiling reveals the variant landscape of sporadic parathyroid adenomas in Chinese population. The Journal of clinical endocrinology and metabolism 2023 1 . Tao Xiaohui, Xu Tian, Lin Xiaoyun, Xu Shuqin, Fan Youben, Guo Bomin, Deng Xianzhao, Jiao Qiong, Chen Lihui, Wei Zhe, Chen Chengkun, Yang Wendi, Zhang Zhenlin, Yu Xiangtian, Yue H |
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- Page last updated:Apr 22, 2024
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