Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: SLC6A1[original query] |
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Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Dec 147B (8): 1345-54. Lasky-Su Jessica, Neale Benjamin M, Franke Barbara, Anney Richard J L, Zhou Kaixin, Maller Julian B, Vasquez Alejandro Arias, Chen Wai, Asherson Philip, Buitelaar Jan, Banaschewski Tobias, Ebstein Richard, Gill Michael, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Sonuga-Barke Edmund, Steinhausen Hans Christoph, Taylor Eric, Daly Mark, Laird Nan, Lange Christoph, Faraone Stephen |
The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders. Journal of neural transmission (Vienna, Austria : 1996) 2009 Jun 116 (6): 649-57. Thoeringer C K, Ripke S, Unschuld P G, Lucae S, Ising M, Bettecken T, Uhr M, Keck M E, Mueller-Myhsok B, Holsboer F, Binder E B, Erhardt |
Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2013 Apr 16 (2): 560-74. Ebejer Jane L, Duffy David L, van der Werf Julius, Wright Margaret J, Montgomery Grant, Gillespie Nathan A, Hickie Ian B, Martin Nicholas G, Medland Sarah |
Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2015 Aug 18 (4): 335-47. Adkins Daniel E, Clark Shaunna L, Copeland William E, Kennedy Martin, Conway Kevin, Angold Adrian, Maes Hermine, Liu Youfang, Kumar Gaurav, Erkanli Alaattin, Patkar Ashwin A, Silberg Judy, Brown Tyson H, Fergusson David M, Horwood L John, Eaves Lindon, van den Oord Edwin J C G, Sullivan Patrick F, Costello E |
Associations Between Neurotransmitter Genes and Fatigue and Energy Levels in Women After Breast Cancer Surgery. Journal of pain and symptom management 2017 Jan 53 (1): 67-84.e7. Eshragh Jasmine, Dhruva Anand, Paul Steven M, Cooper Bruce A, Mastick Judy, Hamolsky Deborah, Levine Jon D, Miaskowski Christine, Kober Kord |
GABBR1 and SLC6A1, Two Genes Involved in Modulation of GABA Synaptic Transmission, Influence Risk for Alcoholism: Results from Three Ethnically Diverse Populations. Alcoholism, clinical and experimental research 2016 Jan 40 (1): 93-101. Enoch Mary-Anne, Hodgkinson Colin A, Shen Pei-Hong, Gorodetsky Elena, Marietta Cheryl A, Roy Alec, Goldman Dav |
SLC6A1 gene involvement in susceptibility to attention-deficit/hyperactivity disorder: A case-control study and gene-environment interaction. Progress in neuro-psychopharmacology & biological psychiatry 2017 Apr 77 202-208. Yuan Fang-Fen, Gu Xue, Huang Xin, Zhong Yan, Wu Ji |
Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia 2018 1 59 (2): 389-402. Johannesen Katrine M, Gardella Elena, Linnankivi Tarja, Courage Carolina, de Saint Martin Anne, Lehesjoki Anna-Elina, Mignot Cyril, Afenjar Alexandra, Lesca Gaetan, Abi-Warde Marie-Thérèse, Chelly Jamel, Piton Amélie, Merritt J Lawrence, Rodan Lance H, Tan Wen-Hann, Bird Lynne M, Nespeca Mark, Gleeson Joseph G, Yoo Yongjin, Choi Murim, Chae Jong-Hee, Czapansky-Beilman Desiree, Reichert Sara Chadwick, Pendziwiat Manuela, Verhoeven Judith S, Schelhaas Helenius J, Devinsky Orrin, Christensen Jakob, Specchio Nicola, Trivisano Marina, Weber Yvonne G, Nava Caroline, Keren Boris, Doummar Diane, Schaefer Elise, Hopkins Sarah, Dubbs Holly, Shaw Jessica E, Pisani Laura, Myers Candace T, Tang Sha, Tang Shan, Pal Deb K, Millichap John J, Carvill Gemma L, Helbig Kathrine L, Mecarelli Oriano, Striano Pasquale, Helbig Ingo, Rubboli Guido, Mefford Heather C, Møller Rikke |
Dissecting the phenotypic and genetic spectrum of early childhood-onset generalized epilepsies. Seizure 2019 8 71 222-228. Kim Soo Yeon, Jang Se Song, Kim Jong-Il, Kim Hunmin, Hwang Hee, Choi Ji Eun, Chae Jong-Hee, Kim Ki Joong, Lim Byung Ch |
Kava for generalised anxiety disorder: A 16-week double-blind, randomised, placebo-controlled study. The Australian and New Zealand journal of psychiatry 2019 12 54 (3): 288-297. Sarris Jerome, Byrne Gerard J, Bousman Chad A, Cribb Lachlan, Savage Karen M, Holmes Oliver, Murphy Jenifer, Macdonald Patricia, Short Anika, Nazareth Sonia, Jennings Emma, Thomas Stuart R, Ogden Edward, Chamoli Suneel, Scholey Andrew, Stough C |
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 |
GAT-1 (rs2697153) and GAT-3 (rs2272400) polymorphisms are associated with febrile seizures and temporal lobe epilepsy. Epileptic disorders : international epilepsy journal with videotape 2020 4 22 (2): 176-182. Schijns Olaf Emg, Bisschop Jeroen, Rijkers Kim, Dings Jim, Vanherle Sabina, Lindsey Patrick, Smeets Hubert Jm, Hoogland Gove |
Genetic Association of Epilepsy and Anti-Epileptic Drugs Treatment in Jordanian Patients. Pharmacogenomics and personalized medicine 2020 10 13 503-510. Al-Eitan Laith N, Al-Dalala Islam M, Elshammari Afrah K, Khreisat Wael H, Nimiri Aseel F, Alnaamneh Adan H, Aljamal Hanan A, Alghamdi Mansour |
De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature neuroscience 2020 1 23 (2): 179-184. Rees Elliott, Han Jun, Morgan Joanne, Carrera Noa, Escott-Price Valentina, Pocklington Andrew J, Duffield Madeleine, Hall Lynsey S, Legge Sophie E, Pardiñas Antonio F, Richards Alexander L, Roth Julian, Lezheiko Tatyana, Kondratyev Nikolay, Kaleda Vasilii, Golimbet Vera, Parellada Mara, González-Peñas Javier, Arango Celso, , Gawlik Micha, Kirov George, Walters James T R, Holmans Peter, O'Donovan Michael C, Owen Michael |
New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PloS one 2021 16 (10): e0258766. Aguilera Cinthia, Gabau Elisabeth, Ramirez-Mallafré Ariadna, Brun-Gasca Carme, Dominguez-Carral Jana, Delgadillo Veronica, Laurie Steve, Derdak Sophia, Padilla Natàlia, de la Cruz Xavier, Capdevila Núria, Spataro Nino, Baena Neus, Guitart Miriam, Ruiz An |
SLC6A1 variant pathogenicity, molecular function, and phenotype: a genetic and clinical analysis. Brain : a journal of neurology 2023 8 . Arthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner, Katrine M Johannesen, Kimberly Goodspeed, Marie Macnee, Alexander T Deng, Ángel Aledo-Serrano, Artem Borovikov, Maina Kava, Arjan M Bouman, M J Hajianpour, Deb K Pal, Marc Engelen, Eveline E O Hagebeuk, Marwan Shinawi, Alexis R Heidlebaugh, Kathryn Oetjens, Trevor L Hoffman, Pasquale Striano, Amanda S Freed, Line Futtrup, Thomas Balslev, Anna Abulí, Leslie Danvoye, Damien Lederer, Tugce Balci, Maryam Nabavi Nouri, Elizabeth Butler, Sarah Drewes, Kalene van Engelen, Katherine B Howell, Jean Khoury, Patrick May, Marena Trinidad, Steven Froelich, Johannes R Lemke, Jacob Tiller, Amber N Freed, Jing-Qiong Kang, Arthur Wuster, Rikke S Møller, Dennis L |
Neurotransmitter Gene Polymorphisms Are Associated with Symptom Clusters in Patients Undergoing Radiation Therapy. Seminars in oncology nursing 2023 7 151461. Carolyn Harris, Kord M Kober, Steven M Paul, Bruce A Cooper, Joosun Shin, Kate Oppegaard, Lisa Morse, Alejandra Calvo-Schimmel, Yvette Conley, Jon D Levine, Christine Miaskows |
Prognostic analysis of hepatocellular carcinoma based on cuproptosis -associated lncRNAs. BMC gastroenterology 2024 4 24 (1): 142. Mingwei Wei, Libai Lu, Zongjiang Luo, Jiasheng Ma, Jianchu Wa |
Next-generation sequencing testing in children with epilepsy reveals novel clinical, diagnostic and therapeutic implications. Frontiers in genetics 2024 1 14 1300952. Magdalena Krygier, Marta Pietruszka, Marta Zawadzka, Agnieszka Sawicka, Anna Lemska, Monika Limanówka, Jan ?urek, Weronika Tala?ka-Liczbik, Maria Mazurkiewicz-Be?dzi?s |
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- Page last updated:Apr 29, 2024
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