Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Epilepsy[original query] |
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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
Brain : a journal of neurology 2010 Jul 133 (Pt 7): 2136-47. Kasperavici?te Dalia, Catarino Claudia B, Heinzen Erin L, Depondt Chantal, Cavalleri Gianpiero L, Caboclo Luis O, Tate Sarah K, Jamnadas-Khoda Jenny, Chinthapalli Krishna, Clayton Lisa M S, Shianna Kevin V, Radtke Rodney A, Mikati Mohamad A, Gallentine William B, Husain Aatif M, Alhusaini Saud, Leppert David, Middleton Lefkos T, Gibson Rachel A, Johnson Michael R, Matthews Paul M, Hosford David, Heuser Kjell, Amos Leslie, Ortega Marcos, Zumsteg Dominik, Wieser Heinz-Gregor, Steinhoff Bernhard J, Krämer Günter, Hansen Jörg, Dorn Thomas, Kantanen Anne-Mari, Gjerstad Leif, Peuralinna Terhi, Hernandez Dena G, Eriksson Kai J, Kälviäinen Reetta K, Doherty Colin P, Wood Nicholas W, Pandolfo Massimo, Duncan John S, Sander Josemir W, Delanty Norman, Goldstein David B, Sisodiya Sanjay |
| Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
Human molecular genetics 2012 Mar 21 (5): 1184-9. Guo Youling, Baum Larry W, Sham Pak Chung, Wong Virginia, Ng Ping Wing, Lui Colin Hiu Tung, Sin Ngai Chuen, Tsoi Tak Hong, Tang Clara S M, Kwan Johnny S H, Yip Benjamin H K, Xiao Su-Mei, Thomas G Neil, Lau Yu Lung, Yang Wanling, Cherny Stacey S, Kwan Patri |
| Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Human molecular genetics 2012 Dec 21 (24): 5359-72. , , Steffens Michael, Leu Costin, Ruppert Ann-Kathrin, Zara Federico, Striano Pasquale, Robbiano Angela, Capovilla Giuseppe, Tinuper Paolo, Gambardella Antonio, Bianchi Amedeo, La Neve Angela, Crichiutti Giovanni, de Kovel Carolien G F, Kasteleijn-Nolst Trenité Dorothée, de Haan Gerrit-Jan, Lindhout Dick, Gaus Verena, Schmitz Bettina, Janz Dieter, Weber Yvonne G, Becker Felicitas, Lerche Holger, Steinhoff Bernhard J, Kleefuß-Lie Ailing A, Kunz Wolfram S, Surges Rainer, Elger Christian E, Muhle Hiltrud, von Spiczak Sarah, Ostertag Philipp, Helbig Ingo, Stephani Ulrich, Møller Rikke S, Hjalgrim Helle, Dibbens Leanne M, Bellows Susannah, Oliver Karen, Mullen Saul, Scheffer Ingrid E, Berkovic Samuel F, Everett Kate V, Gardiner Mark R, Marini Carla, Guerrini Renzo, Lehesjoki Anna-Elina, Siren Auli, Guipponi Michel, Malafosse Alain, Thomas Pierre, Nabbout Rima, Baulac Stephanie, Leguern Eric, Guerrero Rosa, Serratosa Jose M, Reif Philipp S, Rosenow Felix, Mörzinger Martina, Feucht Martha, Zimprich Fritz, Kapser Claudia, Schankin Christoph J, Suls Arvid, Smets Katrin, De Jonghe Peter, Jordanova Albena, Caglayan Hande, Yapici Zuhal, Yalcin Destina A, Baykan Betul, Bebek Nerses, Ozbek Ugur, Gieger Christian, Wichmann Heinz-Erich, Balschun Tobias, Ellinghaus David, Franke Andre, Meesters Christian, Becker Tim, Wienker Thomas F, Hempelmann Anne, Schulz Herbert, Rüschendorf Franz, Leber Markus, Pauck Steffen M, Trucks Holger, Toliat Mohammad R, Nürnberg Peter, Avanzini Giuliano, Koeleman Bobby P C, Sander Thom |
| Identification of common variants associated with human hippocampal and intracranial volumes.
Nature genetics 2012 May 44 (5): 552-61. Stein Jason L, Medland Sarah E, Vasquez Alejandro Arias, Hibar Derrek P, Senstad Rudy E, Winkler Anderson M, Toro Roberto, Appel Katja, Bartecek Richard, Bergmann Ørjan, Bernard Manon, Brown Andrew A, Cannon Dara M, Chakravarty M Mallar, Christoforou Andrea, Domin Martin, Grimm Oliver, Hollinshead Marisa, Holmes Avram J, Homuth Georg, Hottenga Jouke-Jan, Langan Camilla, Lopez Lorna M, Hansell Narelle K, Hwang Kristy S, Kim Sungeun, Laje Gonzalo, Lee Phil H, Liu Xinmin, Loth Eva, Lourdusamy Anbarasu, Mattingsdal Morten, Mohnke Sebastian, Maniega Susana Muñoz, Nho Kwangsik, Nugent Allison C, O'Brien Carol, Papmeyer Martina, Pütz Benno, Ramasamy Adaikalavan, Rasmussen Jerod, Rijpkema Mark, Risacher Shannon L, Roddey J Cooper, Rose Emma J, Ryten Mina, Shen Li, Sprooten Emma, Strengman Eric, Teumer Alexander, Trabzuni Daniah, Turner Jessica, van Eijk Kristel, van Erp Theo G M, van Tol Marie-Jose, Wittfeld Katharina, Wolf Christiane, Woudstra Saskia, Aleman Andre, Alhusaini Saud, Almasy Laura, Binder Elisabeth B, Brohawn David G, Cantor Rita M, Carless Melanie A, Corvin Aiden, Czisch Michael, Curran Joanne E, Davies Gail, de Almeida Marcio A A, Delanty Norman, Depondt Chantal, Duggirala Ravi, Dyer Thomas D, Erk Susanne, Fagerness Jesen, Fox Peter T, Freimer Nelson B, Gill Michael, Göring Harald H H, Hagler Donald J, Hoehn David, Holsboer Florian, Hoogman Martine, Hosten Norbert, Jahanshad Neda, Johnson Matthew P, Kasperaviciute Dalia, Kent Jack W, Kochunov Peter, Lancaster Jack L, Lawrie Stephen M, Liewald David C, Mandl René, Matarin Mar, Mattheisen Manuel, Meisenzahl Eva, Melle Ingrid, Moses Eric K, Mühleisen Thomas W, Nauck Matthias, Nöthen Markus M, Olvera Rene L, Pandolfo Massimo, Pike G Bruce, Puls Ralf, Reinvang Ivar, Rentería Miguel E, Rietschel Marcella, Roffman Joshua L, Royle Natalie A, Rujescu Dan, Savitz Jonathan, Schnack Hugo G, Schnell Knut, Seiferth Nina, Smith Colin, Steen Vidar M, Valdés Hernández Maria C, Van den Heuvel Martijn, van der Wee Nic J, Van Haren Neeltje E M, Veltman Joris A, Völzke Henry, Walker Robert, Westlye Lars T, Whelan Christopher D, Agartz Ingrid, Boomsma Dorret I, Cavalleri Gianpiero L, Dale Anders M, Djurovic Srdjan, Drevets Wayne C, Hagoort Peter, Hall Jeremy, Heinz Andreas, Jack Clifford R, Foroud Tatiana M, Le Hellard Stephanie, Macciardi Fabio, Montgomery Grant W, Poline Jean Baptiste, Porteous David J, Sisodiya Sanjay M, Starr John M, Sussmann Jessika, Toga Arthur W, Veltman Dick J, Walter Henrik, Weiner Michael W, , , , , Bis Joshua C, Ikram M Arfan, Smith Albert V, Gudnason Vilmundur, Tzourio Christophe, Vernooij Meike W, Launer Lenore J, DeCarli Charles, Seshadri Sudha, , Andreassen Ole A, Apostolova Liana G, Bastin Mark E, Blangero John, Brunner Han G, Buckner Randy L, Cichon Sven, Coppola Giovanni, de Zubicaray Greig I, Deary Ian J, Donohoe Gary, de Geus Eco J C, Espeseth Thomas, Fernández Guillén, Glahn David C, Grabe Hans J, Hardy John, Hulshoff Pol Hilleke E, Jenkinson Mark, Kahn René S, McDonald Colm, McIntosh Andrew M, McMahon Francis J, McMahon Katie L, Meyer-Lindenberg Andreas, Morris Derek W, Müller-Myhsok Bertram, Nichols Thomas E, Ophoff Roel A, Paus Tomas, Pausova Zdenka, Penninx Brenda W, Potkin Steven G, Sämann Philipp G, Saykin Andrew J, Schumann Gunter, Smoller Jordan W, Wardlaw Joanna M, Weale Michael E, Martin Nicholas G, Franke Barbara, Wright Margaret J, Thompson Paul M, |
| Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain : a journal of neurology 2013 Oct 136 (Pt 10): 3140-50. Kasperaviciute Dalia, Catarino Claudia B, Matarin Mar, Leu Costin, Novy Jan, Tostevin Anna, Leal Bárbara, Hessel Ellen V S, Hallmann Kerstin, Hildebrand Michael S, Dahl Hans-Henrik M, Ryten Mina, Trabzuni Daniah, Ramasamy Adaikalavan, Alhusaini Saud, Doherty Colin P, Dorn Thomas, Hansen Jörg, Krämer Günter, Steinhoff Bernhard J, Zumsteg Dominik, Duncan Susan, Kälviäinen Reetta K, Eriksson Kai J, Kantanen Anne-Mari, Pandolfo Massimo, Gruber-Sedlmayr Ursula, Schlachter Kurt, Reinthaler Eva M, Stogmann Elisabeth, Zimprich Fritz, Théâtre Emilie, Smith Colin, O'Brien Terence J, Meng Tan K, Petrovski Slave, Robbiano Angela, Paravidino Roberta, Zara Federico, Striano Pasquale, Sperling Michael R, Buono Russell J, Hakonarson Hakon, Chaves João, Costa Paulo P, Silva Berta M, da Silva António M, de Graan Pierre N E, Koeleman Bobby P C, Becker Albert, Schoch Susanne, von Lehe Marec, Reif Philipp S, Rosenow Felix, Becker Felicitas, Weber Yvonne, Lerche Holger, Rössler Karl, Buchfelder Michael, Hamer Hajo M, Kobow Katja, Coras Roland, Blumcke Ingmar, Scheffer Ingrid E, Berkovic Samuel F, Weale Michael E, , Delanty Norman, Depondt Chantal, Cavalleri Gianpiero L, Kunz Wolfram S, Sisodiya Sanjay |
| A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
Human molecular genetics 2014 Jan 23 (1): 247-58. Speed Doug, Hoggart Clive, Petrovski Slave, Tachmazidou Ioanna, Coffey Alison, Jorgensen Andrea, Eleftherohorinou Hariklia, De Iorio Maria, Todaro Marian, De Tisham, Smith David, Smith Philip E, Jackson Margaret, Cooper Paul, Kellett Mark, Howell Stephen, Newton Mark, Yerra Raju, Tan Meng, French Chris, Reuber Markus, Sills Graeme E, Chadwick David, Pirmohamed Munir, Bentley David, Scheffer Ingrid, Berkovic Samuel, Balding David, Palotie Aarno, Marson Anthony, O'Brien Terence J, Johnson Michael |
| Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2014 Sep 13 (9): 893-903. Authors are not available |
| GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy.
Epilepsy research 2015 Sep 115 88-94. Jang Hui Won, Kim So Won, Cho Yang-Je, Heo Kyoung, Lee Byung In, Lee Sang Kun, Jang In-Jin, Lee Min Goo, Kim Won-Joo, Lee Ji Hy |
| Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Neurology 2017 Dec . McCormack Mark, Gui Hongsheng, Ingason Andrés, Speed Doug, Wright Galen E B, Zhang Eunice J, Secolin Rodrigo, Yasuda Clarissa, Kwok Maxwell, Wolking Stefan, Becker Felicitas, Rau Sarah, Avbersek Andreja, Heggeli Kristin, Leu Costin, Depondt Chantal, Sills Graeme J, Marson Anthony G, Auce Pauls, Brodie Martin J, Francis Ben, Johnson Michael R, Koeleman Bobby P C, Striano Pasquale, Coppola Antonietta, Zara Federico, Kunz Wolfram S, Sander Josemir W, Lerche Holger, Klein Karl Martin, Weckhuysen Sarah, Krenn Martin, Gudmundsson Lárus J, Stefánsson Kári, Krause Roland, Shear Neil, Ross Colin J D, Delanty Norman, , Pirmohamed Munir, Carleton Bruce C, , Cendes Fernando, Lopes-Cendes Iscia, Liao Wei-Ping, O'Brien Terence J, Sisodiya Sanjay M, , Cherny Stacey, Kwan Patrick, Baum Larry, , Cavalleri Gianpiero |
| Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy.
Epilepsia 2018 Aug 59 (8): 1557-1566. Schoeler Natasha E, Leu Costin, Balestrini Simona, Mudge Jonathan M, Steward Charles A, Frankish Adam, Leung Mary-Anne, Mackay Mark, Scheffer Ingrid, Williams Ruth, Sander Josemir W, Cross J Helen, Sisodiya Sanjay |
| Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity.
Human brain mapping 2018 Jun . Smit Dirk J A, Wright Margaret J, Meyers Jacquelyn L, Martin Nicholas G, Ho Yvonne Y W, Malone Stephen M, Zhang Jian, Burwell Scott J, Chorlian David B, de Geus Eco J C, Denys Damiaan, Hansell Narelle K, Hottenga Jouke-Jan, McGue Matt, van Beijsterveldt Catharina E M, Jahanshad Neda, Thompson Paul M, Whelan Christopher D, Medland Sarah E, Porjesz Bernice, Lacono William G, Boomsma Dorret |
| Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Nature communications 2018 12 9 (1): 5269. Authors are not available |
| A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
Epilepsia open 2019 Mar 4 (1): 102-109. Berghuis Bianca, Stapleton Caragh, Sonsma Anja C M, Hulst Janic, de Haan Gerrit-Jan, Lindhout Dick, Demurtas Rita, , Krause Roland, Depondt Chantal, Kunz Wolfram S, Zara Federico, Striano Pasquale, Craig John, Auce Pauls, Marson Anthony G, Stefansson Hreinn, O'Brien Terence J, Johnson Michael R, Sills Graeme J, Wolking Stefan, Lerche Holger, Sisodiya Sanjay M, Sander Josemir W, Cavalleri Gianpiero L, Koeleman Bobby P C, McCormack Ma |
| Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.
Molecular genetics and metabolism reports 2019 Dec 21 100518. Stevelink Remi, Pangilinan Faith, Jansen Floor E, Braun Kees P J, , Molloy Anne M, Brody Lawrence C, Koeleman Bobby P |
| Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population.
EBioMedicine 2020 Jul 57 102840. Shi Xiu-Yu, Wang Geng, Li Ting, Li Zhixiu, Leo Paul, Liu Zhisheng, Wu Gefei, Zhu Hongmin, Zhang Yuqin, Li Dong, Gao Li, Yang Liu, Wang Wei, Liao Jianxiang, Wang Jiwen, Zhou Shuizhen, Wang Hua, Li Xiaojing, Gao Jingyun, Zhang Li, Shu Xiaomei, Li Dan, Li Yan, Chen Chunhong, Zhang Xiuju, Partida Gabriel Cuellar, Lundberg Mischa, Reutens David, Bartlett Perry, Brown Matthew A, Zou Li-Ping, Xu Hu |
| Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
Pharmacogenomics 2020 Apr 21 (5): 325-335. Wolking Stefan, Schulz Herbert, Nies Anne T, McCormack Mark, Schaeffeler Elke, Auce Pauls, Avbersek Andreja, Becker Felicitas, Klein Karl M, Krenn Martin, Møller Rikke S, Nikanorova Marina, Weckhuysen Sarah, Consortium EpiPGx, Cavalleri Gianpiero L, Delanty Norman, Depondt Chantal, Johnson Michael R, Koeleman Bobby Pc, Kunz Wolfram S, Marson Anthony G, Sander Josemir W, Sills Graeme J, Striano Pasquale, Zara Federico, Zimprich Fritz, Weber Yvonne G, Krause Roland, Sisodiya Sanjay, Schwab Matthias, Sander Thomas, Lerche Holg |
| Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy.
Genes 2021 Sep 12 (9): . Buono Russell J, Bradfield Jonathan P, Wei Zhi, Sperling Michael R, Dlugos Dennis J, Privitera Michael D, French Jacqueline A, Lo Warren, Cossette Patrick, Schachter Steven C, Basehore Heather, Lohoff Falk W, Grant Struan F A, Ferraro Thomas N, Hakonarson Hak |
| Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy.
Frontiers in neuroscience 2021 8 15 722592. Song Meng, Liu Jiewei, Yang Yongfeng, Lv Luxian, Li Wenqiang, Luo Xiong-Ji |
| Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications.
Frontiers in pharmacology 2021 6 12 688386. Wolking Stefan, Campbell Ciarán, Stapleton Caragh, McCormack Mark, Delanty Norman, Depondt Chantal, Johnson Michael R, Koeleman Bobby P C, Krause Roland, Kunz Wolfram S, Marson Anthony G, Sander Josemir W, Sills Graeme J, Striano Pasquale, Zara Federico, Sisodiya Sanjay M, Cavalleri Gianpiero L, Lerche Holg |
| Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.
Epilepsia 2021 Apr . Suzuki Toshimitsu, Koike Yoshinao, Ashikawa Kyota, Otomo Nao, Takahashi Atsushi, Aoi Tomomi, Kamatani Naoyuki, Nakamura Yusuke, Kubo Michiaki, Kamatani Yoichiro, Momozawa Yukihide, Terao Chikashi, Yamakawa Kazuhi |
| A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies.
Brain : a journal of neurology 2022 3 . Strippel Christine, Herrera-Rivero Marisol, Wendorff Mareike, Tietz Anja K, Degenhardt Frauke, Witten Anika, Schroeter Christina, Nelke Christopher, Golombeck Kristin S, Madlener Marie, Rüber Theodor, Ernst Leon, Racz Attila, Baumgartner Tobias, Widman Guido, Doppler Kathrin, Thaler Franziska, Siebenbrodt Kai, Dik Andre, Kerin Constanze, Räuber Saskia, Gallus Marco, Kovac Stjepana, Grauer Oliver M, Grimm Alexander, Prüss Harald, Wickel Jonathan, Geis Christian, Lewerenz Jan, Goebels Norbert, Ringelstein Marius, Menge Til, Tackenberg Björn, Kellinghaus Christoph, Bien Christian G, Kraft Andrea, Zettl Uwe, Ismail Fatme Seval, Ayzenberg Ilya, Urbanek Christian, Sühs Kurt-Wolfram, Tauber Simone C, Mues Sigrid, Körtvélyessy Peter, Markewitz Robert, Paliantonis Asterios, Elger Christian E, Surges Rainer, Sommer Claudia, Kümpfel Tania, Gross Catharina C, Lerche Holger, Wellmer Jörg, Quesada Carlos M, Then Bergh Florian, Wandinger Klaus-Peter, Becker Albert J, Kunz Wolfram S, Meyer Zu Hörste Gerd, Malter Michael P, Rosenow Felix, Wiendl Heinz, Kuhlenbäumer Gregor, Leypoldt Frank, Lieb Wolfgang, Franke Andre, Meuth Sven G, Stoll Monika, Melzer Nico, |
| Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications.
Epilepsia 2022 Feb . Mullan Kerry A, Anderson Alison, Shi Yi-Wu, Ding Jia-Hong, Ng Ching-Ching, Chen Zhibin, Baum Larry, Cherny Stacey, Petrovski Slave, Sham Pak C, Lim Kheng-Seang, Liao Wei-Ping, Kwan Patri |
| Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes.
Brain : a journal of neurology 2022 1 145 (2): 555-568. Skotte Line, Fadista João, Bybjerg-Grauholm Jonas, Appadurai Vivek, Hildebrand Michael S, Hansen Thomas F, Banasik Karina, Grove Jakob, Albiñana Clara, Geller Frank, Bjurström Carmen F, Vilhjálmsson Bjarni J, Coleman Matthew, Damiano John A, Burgess Rosemary, Scheffer Ingrid E, Pedersen Ole Birger Vesterager, Erikstrup Christian, Westergaard David, Nielsen Kaspar René, Sørensen Erik, Bruun Mie Topholm, Liu Xueping, Hjalgrim Henrik, Pers Tune H, Mortensen Preben Bo, Mors Ole, Nordentoft Merete, Dreier Julie W, Børglum Anders D, Christensen Jakob, Hougaard David M, Buil Alfonso, Hviid Anders, Melbye Mads, Ullum Henrik, Berkovic Samuel F, Werge Thomas, Feenstra Bjar |
| The genetic and phenotypic correlates of mtDNA copy number in a multi-ancestry cohort.
HGG advances 2023 5 4 (3): 100202. Arslan A Zaidi, Anurag Verma, Colleen Morse, , Marylyn D Ritchie, Iain Mathies |
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