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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 9, 2023. (Total: 217811Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Epilepsy and GABRB2[original query]
Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures.
Neuroscience letters 2005 Aug 383 (3): 220-4.
Ito Minako, Ohmori Iori, Nakahori Tomoyuki, Ouchida Mamoru, Ohtsuka Yo
Potential role of GABAA receptor subunit; GABRA6, GABRB2 and GABRR2 gene polymorphisms in epilepsy susceptibility and pharmacotherapy in North Indian population.
Clinica chimica acta; international journal of clinical chemistry 2011 Jun 412 (13-14): 1244-8.
Kumari Ritu, Lakhan Ram, Kalita J, Garg R K, Misra U K, Mittal Balr
GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures.
Pharmacogenetics and genomics 2013 Nov 23 (11): 605-10.
Balan Shabeesh, Sathyan Sanish, Radha Saradalekshmi K, Joseph Vijai, Radhakrishnan Kurupath, Banerjee Moin
Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.
The Lancet. Neurology 2018 Aug 17 (8): 699-708.
May Patrick, Girard Simon, Harrer Merle, Bobbili Dheeraj R, Schubert Julian, Wolking Stefan, Becker Felicitas, Lachance-Touchette Pamela, Meloche Caroline, Gravel Micheline, Niturad Cristina E, Knaus Julia, De Kovel Carolien, Toliat Mohamad, Polvi Anne, Iacomino Michele, Guerrero-López Rosa, Baulac Stéphanie, Marini Carla, Thiele Holger, Altmüller Janine, Jabbari Kamel, Ruppert Ann-Kathrin, Jurkowski Wiktor, Lal Dennis, Rusconi Raffaella, Cestèle Sandrine, Terragni Benedetta, Coombs Ian D, Reid Christopher A, Striano Pasquale, Caglayan Hande, Siren Auli, Everett Kate, Møller Rikke S, Hjalgrim Helle, Muhle Hiltrud, Helbig Ingo, Kunz Wolfram S, Weber Yvonne G, Weckhuysen Sarah, Jonghe Peter De, Sisodiya Sanjay M, Nabbout Rima, Franceschetti Silvana, Coppola Antonietta, Vari Maria S, Kasteleijn-Nolst Trenité Dorothée, Baykan Betul, Ozbek Ugur, Bebek Nerses, Klein Karl M, Rosenow Felix, Nguyen Dang K, Dubeau François, Carmant Lionel, Lortie Anne, Desbiens Richard, Clément Jean-François, Cieuta-Walti Cécile, Sills Graeme J, Auce Pauls, Francis Ben, Johnson Michael R, Marson Anthony G, Berghuis Bianca, Sander Josemir W, Avbersek Andreja, McCormack Mark, Cavalleri Gianpiero L, Delanty Norman, Depondt Chantal, Krenn Martin, Zimprich Fritz, Peter Sarah, Nikanorova Marina, Kraaij Robert, van Rooij Jeroen, Balling Rudi, Ikram M Arfan, Uitterlinden André G, Avanzini Giuliano, Schorge Stephanie, Petrou Steven, Mantegazza Massimo, Sander Thomas, LeGuern Eric, Serratosa Jose M, Koeleman Bobby P C, Palotie Aarno, Lehesjoki Anna-Elina, Nothnagel Michael, Nürnberg Peter, Maljevic Snezana, Zara Federico, Cossette Patrick, Krause Roland, Lerche Holger, , ,
De novo variants in neurodevelopmental disorders with epilepsy.
Nature genetics 2018 6 50 (7): 1048-1053.
Heyne Henrike O, Singh Tarjinder, Stamberger Hannah, Abou Jamra Rami, Caglayan Hande, Craiu Dana, De Jonghe Peter, Guerrini Renzo, Helbig Katherine L, Koeleman Bobby P C, Kosmicki Jack A, Linnankivi Tarja, May Patrick, Muhle Hiltrud, Møller Rikke S, Neubauer Bernd A, Palotie Aarno, Pendziwiat Manuela, Striano Pasquale, Tang Sha, Wu Sitao, , Poduri Annapurna, Weber Yvonne G, Weckhuysen Sarah, Sisodiya Sanjay M, Daly Mark J, Helbig Ingo, Lal Dennis, Lemke Johannes
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