Epilepsy Awareness Month: Role of Genomics
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| Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies. Dhindsa Ryan S et al. Current neurology and neuroscience reports 2015 Oct (10) 70 (Time Posted: Nov-05-2015 2PM) |
| Obtaining genetic testing in pediatric epilepsy. Ream Margie A et al. Epilepsia 2015 Oct (10) 1505-14 (Time Posted: Nov-05-2015 2PM) |
| Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications. Torres Fátima et al. Journal of medical genetics 2015 Oct (Time Posted: Nov-05-2015 2PM) |
| Single-Gene Determinants of Epilepsy Comorbidity. Noebels Jeffrey L et al. Cold Spring Harbor perspectives in medicine 2015 (11) (Time Posted: Nov-05-2015 2PM) |
| Genetic testing for pediatric epilepsy can be complicated, but beneficial Medical Xpress, September 9, 2015 (Time Posted: Sep-16-2015 11AM) |
| Identifying clinical correlates for suicide among epilepsy patients in South Korea: A case-control study. Epilepsia 2015 Nov . Park Sung-Jin, Lee Hochang Benjamin, Ahn Myung Hee, Park Subin, Choi Eun Ju, Lee Hoon-Jin, Ryu Han Uk, Kang Joong-Koo, Hong Jin P |
| Association of KEAP1 and NFE2L2 polymorphisms with temporal lobe epilepsy and drug resistant epilepsy. Gene 2015 Oct 571 (2): 231-6. Liu Zhou, Yin Xiaojian, Liu Lingying, Tao Hua, Zhou Haihong, Ma Guoda, Cui Lili, Li You, Zhang Shuyan, Xu Zhi'en, Yao LiFen, Cai Zhiyou, Zhao Bin, Li Kesh |
| Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis. Molecular neurobiology 2015 Oct . Haerian Batoul Sadat, Baum Larry, Kwan Patrick, Cherny Stacey S, Shin Jae-Gook, Kim Sung Eun, Han Bok-Ghee, Tan Hui Jan, Raymond Azman Ali, Tan Chong Tin, Mohamed Zahur |
| Mutations in the mTOR pathway regulators NPRL2 and NPRL3 cause focal epilepsy. Annals of neurology 2015 Oct . Ricos Michael G, Hodgson Bree L, Pippucci Tommaso, Saidin Akzam, Sze Ong Yeh, Heron Sarah E, Licchetta Laura, Bisulli Francesca, Bayly Marta A, Hughes James, Baldassari Sara, Palombo Flavia, , Santucci Margherita, Meletti Stefano, Berkovic Samuel F, Rubboli Guido, Thomas Paul Q, Scheffer Ingrid E, Tinuper Paolo, Geoghegan Joel, Schreiber Andreas W, Dibbens Leanne |
| Prodynorphin gene promoter polymorphism and temporal lobe epilepsy: A meta-analysis. Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2015 Oct 35 (5): 635-9. Zhang Na, Ouyang Tao-Hui, Zhou Qing, Kang Hui-Cong, Zhu Sui-Qia |
| Publication | Product Type |
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| Comorbidity of intellectual disability confounds ascertainment of autism: Implications for genetic diagnosis. Polyak Andrew, et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2015 7 22. | Original Studies |
| Pharmacogenetic testing prior to carbamazepine treatment of epilepsy: patients' and physicians' preferences for testing and service delivery. Powell G, et al. Br J Clin Pharmacol 2015 7 3. | Original Studies |
| "It's good to know": Experiences of gene identification and result disclosure in familial epilepsies. Vears Danya F, et al. Epilepsy Res. 2015 5 0. 64-71 | Original Studies |
| The Clinical Utility of a Single-Nucleotide Polymorphism Microarray in Patients With Epilepsy at a Tertiary Medical Center. Hrabik Sarah A, et al. J. Child Neurol. 2015 4 10. | Original Studies |
| Diagnostic yield of genetic testing in epileptic encephalopathy in childhood. Mercimek-Mahmutoglu Saadet, et al. Epilepsia 2015 3 25. | Original Studies |
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