Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Attention and STS[original query] |
---|
Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Dec 147B (8): 1531-5. Brookes K J, Hawi Z, Kirley A, Barry E, Gill M, Kent |
Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Dec 153B (8): 1417-24. Brookes K J, Hawi Z, Park J, Scott S, Gill M, Kent |
Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes, brain, and behavior 2011 Apr 10 (3): 334-44. Stergiakouli E, Langley K, Williams H, Walters J, Williams N M, Suren S, Giegling I, Wilkinson L S, Owen M J, O'Donovan M C, Rujescu D, Thapar A, Davies |
Variation in the oxytocin receptor gene is associated with behavioral and neural correlates of empathic accuracy. Frontiers in behavioral neuroscience 2014 8 423. Laursen Helle Ruff, Siebner Hartwig Roman, Haren Tina, Madsen Kristoffer, Grønlund Rikke, Hulme Oliver, Henningsson Susan |
Polymorphisms of STS gene and SULT2A1 gene and neurosteroid levels in Han Chinese boys with attention-deficit/hyperactivity disorder: an exploratory investigation. Scientific reports 2017 04 7 45595. Wang Liang-Jen, Chan Wen-Ching, Chou Miao-Chun, Chou Wen-Jiun, Lee Min-Jing, Lee Sheng-Yu, Lin Pao-Yen, Yang Yi-Hsin, Yen Cheng-Fa |
A genetic variant within STS previously associated with inattention in boys with attention deficit hyperactivity disorder is associated with enhanced cognition in healthy adult males. Brain and behavior 2017 Mar 7 (3): e00646. Humby Trevor, Fisher Amelia, Allen Christopher, Reynolds Meghann, Hartman Annette, Giegling Ina, Rujescu Dan, Davies Willi |
Clinical and genetic characteristics of patients with Doose syndrome. Epilepsia open 2020 9 5 (3): 442-450. Hinokuma Nodoka, Nakashima Mitsuko, Asai Hideyuki, Nakamura Kazuyuki, Akaboshi Shinjiro, Fukuoka Masataka, Togawa Masami, Oana Shingo, Ohno Koyo, Kasai Mariko, Ogawa Chikako, Yamamoto Kazuna, Okumiya Kiyohito, Chong Pin Fee, Kira Ryutaro, Uchino Shumpei, Fukuyama Tetsuhiro, Shinagawa Tomoe, Miyata Yohane, Abe Yuichi, Hojo Akira, Kobayashi Kozue, Maegaki Yoshihiro, Ishikawa Nobutsune, Ikeda Hiroko, Amamoto Masano, Mizuguchi Takeshi, Iwama Kazuhiro, Itai Toshiyuki, Miyatake Satoko, Saitsu Hirotomo, Matsumoto Naomichi, Kato Mitsuhi |
Integration analysis based on fatty acid metabolism robustly predicts prognosis, dissecting immunity microenvironment and aiding immunotherapy for soft tissue sarcoma. Frontiers in genetics 2023 4 14 1161791. Liu Binfeng, He Shasha, Li Chenbei, Feng Chengyao, Wang Hua, Zhang Haixia, Tu Chao, Li Zhiho |
- Page last reviewed:Feb 1, 2024
- Content source: