Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: KCNQ3[original query] |
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A high-density association screen of 155 ion transport genes for involvement with common migraine. Human molecular genetics 2008 Nov 17 (21): 3318-31. Nyholt Dale R, LaForge K Steven, Kallela Mikko, Alakurtti Kirsi, Anttila Verneri, Färkkilä Markus, Hämaläinen Eija, Kaprio Jaakko, Kaunisto Mari A, Heath Andrew C, Montgomery Grant W, Göbel Hartmut, Todt Unda, Ferrari Michel D, Launer Lenore J, Frants Rune R, Terwindt Gisela M, de Vries Boukje, Verschuren W M Monique, Brand Jan, Freilinger Tobias, Pfaffenrath Volker, Straube Andreas, Ballinger Dennis G, Zhan Yiping, Daly Mark J, Cox David R, Dichgans Martin, van den Maagdenberg Arn M J M, Kubisch Christian, Martin Nicholas G, Wessman Maija, Peltonen Leena, Palotie Aar |
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes. Neurology 2008 Jul 71 (3): 177-83. Neubauer B A, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander |
Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs. Bipolar disorders 2010 Dec 12 (8): 786-92. Zhang Peng, Xiang Nan, Chen Yi, Sliwerska El?bieta, McInnis Melvin G, Burmeister Margit, Zöllner Sebasti |
Targeted next generation sequencing as a diagnostic tool in epileptic disorders. Epilepsia 2012 Aug 53 (8): 1387-98. Lemke Johannes R, Riesch Erik, Scheurenbrand Tim, Schubach Max, Wilhelm Christian, Steiner Isabelle, Hansen Jörg, Courage Carolina, Gallati Sabina, Bürki Sarah, Strozzi Susi, Simonetti Barbara Goeggel, Grunt Sebastian, Steinlin Maja, Alber Michael, Wolff Markus, Klopstock Thomas, Prott Eva C, Lorenz Rüdiger, Spaich Christiane, Rona Sabine, Lakshminarasimhan Maya, Kröll Judith, Dorn Thomas, Krämer Günter, Synofzik Matthis, Becker Felicitas, Weber Yvonne G, Lerche Holger, Böhm Detlef, Biskup Sask |
Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis. Brain & development 2012 Oct . Ishii A, Yasumoto S, Ihara Y, Inoue T, Fujita T, Nakamura N, Ohfu M, Yamashita Y, Takatsuka H, Taga T, Miyata R, Ito M, Tsuchiya H, Matsuoka T, Kitao T, Murakami K, Lee WT, Kaneko S, Hirose S |
KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. Annals of neurology 2012 Jan 71 (1): 15-25. Weckhuysen Sarah, Mandelstam Simone, Suls Arvid, Audenaert Dominique, Deconinck Tine, Claes Lieve R F, Deprez Liesbet, Smets Katrien, Hristova Dimitrina, Yordanova Iglika, Jordanova Albena, Ceulemans Berten, Jansen An, Hasaerts Danièle, Roelens Filip, Lagae Lieven, Yendle Simone, Stanley Thorsten, Heron Sarah E, Mulley John C, Berkovic Samuel F, Scheffer Ingrid E, de Jonghe Pet |
Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Frontiers in genetics 2013 4 87. Judy Jennifer Toolan, Seifuddin Fayaz, Pirooznia Mehdi, Mahon Pamela Belmonte, , Jancic Dubravka, Goes Fernando S, Schulze Thomas, Cichon Sven, Noethen Markus, Rietschel Marcella, Depaulo J Raymond, Potash James B, Zandi Peter |
Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance. Epilepsia 2013 Jan . Zara F, Specchio N, Striano P, Robbiano A, Gennaro E, Paravidino R, Vanni N, Beccaria F, Capovilla G, Bianchi A, Caffi L, Cardilli V, Darra F, Bernardina BD, Fusco L, Gaggero R, Giordano L, Guerrini R, Incorpora G, Mastrangelo M, Spaccini L, Laverda AM, Vecchi M, Vanadia F, Veggiotti P, Viri M, Occhi G, Budetta M, Taglilatela M, Coviello DA, Vigevano F, Minetti C |
Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.
Journal of nutrigenetics and nutrigenomics 2015 8 (1): 44-53. Rudkowska Iwona, Pérusse Louis, Bellis Claire, Blangero John, Després Jean-Pierre, Bouchard Claude, Vohl Marie-Clau |
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology. The pharmacogenomics journal 2017 Jul . Seyerle A A, Sitlani C M, Noordam R, Gogarten S M, Li J, Li X, Evans D S, Sun F, Laaksonen M A, Isaacs A, Kristiansson K, Highland H M, Stewart J D, Harris T B, Trompet S, Bis J C, Peloso G M, Brody J A, Broer L, Busch E L, Duan Q, Stilp A M, O'Donnell C J, Macfarlane P W, Floyd J S, Kors J A, Lin H J, Li-Gao R, Sofer T, Méndez-Giráldez R, Cummings S R, Heckbert S R, Hofman A, Ford I, Li Y, Launer L J, Porthan K, Newton-Cheh C, Napier M D, Kerr K F, Reiner A P, Rice K M, Roach J, Buckley B M, Soliman E Z, de Mutsert R, Sotoodehnia N, Uitterlinden A G, North K E, Lee C R, Gudnason V, Stürmer T, Rosendaal F R, Taylor K D, Wiggins K L, Wilson J G, Chen Y-DI, Kaplan R C, Wilhelmsen K, Cupples L A, Salomaa V, van Duijn C, Jukema J W, Liu Y, Mook-Kanamori D O, Lange L A, Vasan R S, Smith A V, Stricker B H, Laurie C C, Rotter J I, Whitsel E A, Psaty B M, Avery C |
Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy. Seizure 2018 6 59 132-140. Kothur Kavitha, Holman Katherine, Farnsworth Elizabeth, Ho Gladys, Lorentzos Michelle, Troedson Christopher, Gupta Sachin, Webster Richard, Procopis Peter G, Menezes Manoj P, Antony Jayne, Ardern-Holmes Simone, Dale Russell C, Christodoulou John, Gill Deepak, Bennetts Bru |
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature communications 2020 10 11 (1): 4932. Wang Tianyun, Hoekzema Kendra, Vecchio Davide, Wu Huidan, Sulovari Arvis, Coe Bradley P, Gillentine Madelyn A, Wilfert Amy B, Perez-Jurado Luis A, Kvarnung Malin, Sleyp Yoeri, Earl Rachel K, Rosenfeld Jill A, Geisheker Madeleine R, Han Lin, Du Bing, Barnett Chris, Thompson Elizabeth, Shaw Marie, Carroll Renee, Friend Kathryn, Catford Rachael, Palmer Elizabeth E, Zou Xiaobing, Ou Jianjun, Li Honghui, Guo Hui, Gerdts Jennifer, Avola Emanuela, Calabrese Giuseppe, Elia Maurizio, Greco Donatella, Lindstrand Anna, Nordgren Ann, Anderlid Britt-Marie, Vandeweyer Geert, Van Dijck Anke, Van der Aa Nathalie, McKenna Brooke, Hancarova Miroslava, Bendova Sarka, Havlovicova Marketa, Malerba Giovanni, Bernardina Bernardo Dalla, Muglia Pierandrea, van Haeringen Arie, Hoffer Mariette J V, Franke Barbara, Cappuccio Gerarda, Delatycki Martin, Lockhart Paul J, Manning Melanie A, Liu Pengfei, Scheffer Ingrid E, Brunetti-Pierri Nicola, Rommelse Nanda, Amaral David G, Santen Gijs W E, Trabetti Elisabetta, Sedlá?ek Zden?k, Michaelson Jacob J, Pierce Karen, Courchesne Eric, Kooy R Frank, , Nordenskjöld Magnus, Romano Corrado, Peeters Hilde, Bernier Raphael A, Gecz Jozef, Xia Kun, Eichler Evan |
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 |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability. Archives of Iranian medicine 2023 8 25 (12): 788-797. Naeim Ehtesham, Meysam Mosallaei, Maryam Beheshtian, Shahrouz Khoshbakht, Mahsa Fadaee, Raheleh Vazehan, Mehrshid Faraji Zonooz, Parvaneh Karimzadeh, Kimia Kahrizi, Hossein Najmaba |
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