Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: ARHGAP32[original query] |
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Analysis of functional variants reveals new candidate genes associated with alexithymia. Psychiatry research 2015 Jun 227 (2-3): 363-5. Mezzavilla Massimo, Ulivi Sheila, Bianca Martina La, Carlino Davide, Gasparini Paolo, Robino Antoniet |
De novo genic mutations among a Chinese autism spectrum disorder cohort. Nature communications 2016 Nov 7 13316. Wang Tianyun, Guo Hui, Xiong Bo, Stessman Holly A F, Wu Huidan, Coe Bradley P, Turner Tychele N, Liu Yanling, Zhao Wenjing, Hoekzema Kendra, Vives Laura, Xia Lu, Tang Meina, Ou Jianjun, Chen Biyuan, Shen Yidong, Xun Guanglei, Long Min, Lin Janice, Kronenberg Zev N, Peng Yu, Bai Ting, Li Honghui, Ke Xiaoyan, Hu Zhengmao, Zhao Jingping, Zou Xiaobing, Xia Kun, Eichler Evan |
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population.
Journal of clinical medicine 2019 Feb 8 (2): . Hong Eun Pyo, Kim Bong Jun, Cho Steve S, Yang Jin Seo, Choi Hyuk Jai, Kang Suk Hyung, Jeon Jin Pyeo |
Fine-mapping of intracranial aneurysm susceptibility based on a genome-wide association study. Scientific reports 2022 02 12 (1): 2717. Hong Eun Pyo, Youn Dong Hyuk, Kim Bong Jun, Ahn Jun Hyong, Park Jeong Jin, Rhim Jong Kook, Kim Heung Cheol, Hwang Gyojun, Jeon Hong Jun, Jeon Jin Pyeo |
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