Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: EEF1A2[original query] |
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Array-comparative genomic hybridization analysis of a cohort of Saudi patients with epilepsy. CNS & neurological disorders drug targets 2015 14 (4): 468-75. Faheem Muhammad, Naseer Muhammad I, Chaudhary Adeel G, Kumosani Taha A, Rasool Mahmood, Algahtani Hussein A, Bibi Fehmida, Kamal Mohammad A, Al-Qahtani Mohammad |
The EEF1A2 gene expression as risk predictor in localized prostate cancer. BMC urology 2017 9 17 (1): 86. Worst Thomas Stefan, Waldbillig Frank, Abdelhadi Abdallah, Weis Cleo-Aron, Gottschalt Maria, Steidler Annette, von Hardenberg Jost, Michel Maurice Stephan, Erben Phili |
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. American journal of human genetics 2019 Jul . , |
EEF1A2 mutations in epileptic encephalopathy/intellectual disability: Understanding the potential mechanism of phenotypic variation. Epilepsy & behavior : E&B 2020 2 105 106955. Long Kexin, Wang Hua, Song Zhanyi, Yin Xiaomeng, Wang Yaq |
Development of RNA binding proteins expression signature for prognosis prediction in gastric cancer patients. American journal of translational research 2020 11 12 (10): 6775-6792. Zhou Liqiang, Wu You, Xin Lin, Zhou Qi, Li Shihao, Yuan Yiwu, Wang Jinliang, Wu Dengzho |
Whole exome sequencing reveals a de novo missense variant in EEF1A2 in a Rett syndrome-like patient. Clinical case reports 2020 1 7 (12): 2476-2482. Kaur Simranpreet, Van Bergen Nicole J, Gold Wendy Anne, Eggers Stefanie, Lunke Sebastian, White Susan M, Ellaway Carolyn, Christodoulou Jo |
Vagus nerve stimulation in children with drug-resistant epilepsy of monogenic etiology. Frontiers in neurology 2022 9 13 951850. Xie Han, Ma Jiayi, Ji Taoyun, Liu Qingzhu, Cai Lixin, Wu |
Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2-Related Disorders. Frontiers in molecular neuroscience 2022 5 15 809810. Xiao Tiantian, Chen Xiang, Xu Yan, Chen Huiyao, Dong Xinran, Yang Lin, Wu Bingbing, Chen Liping, Li Long, Zhuang Deyi, Chen Dongmei, Zhou Yuanfeng, Wang Huijun, Zhou Wenh |
Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. The Journal of molecular diagnostics : JMD 2023 4 . Se Hee Kim, Soon Sung Kwon, Mi Ri Park, Hyeon Ah Lee, Ji Hun Kim, JiHoon Cha, Sangwoo Kim, Seung Tae Baek, Se Hoon Kim, Joon Soo Lee, Heung Dong Kim, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Ka |
Analysis of eEF1A2 gene expression and copy number in cervical carcinoma. Medicine 2023 1 102 (2): e32559. Zheng Weinan, Jin Fuyuan, Wang Fang, Wang Luyue, Fu Shaowei, Pan Zemin, Long Haich |
Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study. European journal of human genetics : EJHG 2024 4 . Alix Paulet, Cavan Bennett-Ness, Faustine Ageorges, Detlef Trost, Andrew Green, David Goudie, Rosalyn Jewell, Minna Kraatari-Tiri, Juliette Piard, Christine Coubes, Wayne Lam, Sally Ann Lynch, Samuel Groeschel, Francis Ramond, Joël Fluss, Christina Fagerberg, Charlotte Brasch Andersen, Konstantinos Varvagiannis, Tjitske Kleefstra, Bénédicte Gérard, Mélanie Fradin, Antonio Vitobello, Romano Tenconi, Anne-Sophie Denommé-Pichon, Aline Vincent-Devulder, Tobias Haack, Joseph A Marsh, Lone Walentin Laulund, Mona Grimmel, Angelika Riess, Elke de Boer, Sergio Padilla-Lopez, Somayeh Bakhtiari, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink, Michael C Kruer, Jonathan Levy, Alain Verloes, Catherine M Abbott, Lyse Rua |
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- Page last updated:Apr 16, 2024
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