Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Attention and TRIO[original query] |
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Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2012 Jan 18 (1): 16-22. Cox Mathew B, Ban Maria, Bowden Nikola A, Baker Amie, Scott Rodney J, Lechner-Scott Jeannet |
Genome-wide association study of the child behavior checklist dysregulation profile.
Journal of the American Academy of Child and Adolescent Psychiatry 2011 Aug 50 (8): 807-17.e8. Mick Eric, McGough James, Loo Sandra, Doyle Alysa E, Wozniak Janet, Wilens Timothy E, Smalley Susan, McCracken James, Biederman Joseph, Faraone Stephen |
The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits. Journal of neural transmission (Vienna, Austria : 1996) 2016 Apr . Freitag Christine M, Lempp Thomas, Nguyen T Trang, Jacob Christian P, Weissflog Lena, Romanos Marcel, Renner Tobias J, Walitza Susanne, Warnke Andreas, Rujescu Dan, Lesch Klaus-Peter, Reif Andre |
An Investigation of Brain Functional Connectivity by Form of Craniosynostosis. The Journal of craniofacial surgery 2019 4 30 (6): 1719-1723. Sun Alexander H, Eilbott Jeffrey, Chuang Carolyn, Yang Jenny F, Brooks Eric D, Beckett Joel, Steinbacher Derek M, Pelphrey Kevin, Persing John |
A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational psychiatry 2020 5 10 (1): 135. Martin Joanna, Hosking Grace, Wadon Megan, Agha Sharifah Shameem, Langley Kate, Rees Elliott, Owen Michael J, O'Donovan Michael, Kirov George, Thapar Ani |
Clinical and genetic findings in patients with congenital cataract and heart diseases. Orphanet journal of rare diseases 2021 6 16 (1): 242. Li Xinru, Si Nuo, Song Zixun, Ren Yaqiong, Xiao W |
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia. Frontiers in neuroscience 2021 4 15 629610. Ma Mei-Gang, Liu Xiao-Rong, Wu Yuan, Wang Jie, Li Bing-Mei, Shi Yi-Wu, Su Tao, Li Bin, Liu De-Tian, Yi Yong-Hong, Liao Wei-Pi |
Investigating Direct and Indirect Genetic Effects in Attention-Deficit/Hyperactivity Disorder Using Parent-Offspring Trios. Biological psychiatry 2022 Jun . Martin Joanna, Wray Matthew, Agha Sharifah Shameem, Lewis Katie J S, Anney Richard J L, O'Donovan Michael C, Thapar Anita, Langley Ka |
Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations. Molecular genetics & genomic medicine 2023 8 e2269. Liangliang Jiang, Shaohua Bi, Li Lin, Fan He, Fang De |
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- Page last updated:Apr 22, 2024
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