Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: KCND3[original query] |
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Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome. Clinica chimica acta; international journal of clinical chemistry 2005 Jan 351 (1-2): 95-100. Frank-Hansen Rune, Larsen Lars Allan, Andersen Paal, Jespersgaard Cathrine, Christiansen Micha |
Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2011 Jul 8 (7): 1024-32. Giudicessi John R, Ye Dan, Tester David J, Crotti Lia, Mugione Alessandra, Nesterenko Vladislav V, Albertson Richard M, Antzelevitch Charles, Schwartz Peter J, Ackerman Michael |
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Oct 9 (10): 1627-34. Sinner Moritz F, Porthan Kimmo, Noseworthy Peter A, Havulinna Aki S, Tikkanen Jani T, Müller-Nurasyid Martina, Peloso Gina, Ulivi Sheila, Beckmann Britt Maria, Brockhaus A Catharina, Cooper Rebecca R, Gasparini Paolo, Hengstenberg Christian, Hwang Shih-Jen, Iorio Annamaria, Junttila M Juhani, Klopp Norman, Kähönen Mika, Laaksonen Maarit A, Lehtimäki Terho, Lichtner Peter, Lyytikäinen Leo-Pekka, Martens Eimo, Meisinger Christa, Meitinger Thomas, Merchant Faisal M, Nieminen Markku S, Peters Annette, Pietilä Arto, Perz Siegfried, Oikarinen Lasse, Raitakari Olli, Reinhard Wibke, Silander Kaisa, Thorand Barbara, Wichmann H-Erich, Sinagra Gianfranco, Viikari Jorma, O'Donnell Christopher J, Ellinor Patrick T, Huikuri Heikki V, Kääb Stefan, Newton-Cheh Christopher, Salomaa Veik |
Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death. Human mutation 2012 Feb . Giudicessi JR, Ye D, Kritzberger CJ, Nesterenko VV, Tester DJ, Antzelevitch C, Ackerman MJ |
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
Replication and meta-analysis of candidate loci identified variation at RAB3GAP1 associated with keratoconus. Investigative ophthalmology & visual science 2013 Jul 54 (7): 5132-5. Bae Ha Ae, Mills Richard A D, Lindsay Richard G, Phillips Tony, Coster Douglas J, Mitchell Paul, Wang Jie Jin, Craig Jamie E, Burdon Kathryn |
Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation. Heart rhythm : the official journal of the Heart Rhythm Society 2014 Feb 11 (2): 246-51. Olesen Morten S, Andreasen Laura, Jabbari Javad, Refsgaard Lena, Haunsø Stig, Olesen Søren-Peter, Nielsen Jonas B, Schmitt Nicole, Svendsen Jesper |
Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death. Circulation. Cardiovascular genetics 2014 Dec 7 (6): 782-9. Perrin Mark J, Adler Arnon, Green Sharon, Al-Zoughool Foad, Doroshenko Petro, Orr Nathan, Uppal Shaheen, Healey Jeff S, Birnie David, Sanatani Shubhayan, Gardner Martin, Champagne Jean, Simpson Chris, Ahmad Kamran, van den Berg Maarten P, Chauhan Vijay, Backx Peter H, van Tintelen J Peter, Krahn Andrew D, Gollob Michael |
Genetic determinants of P wave duration and PR segment.
Circulation. Cardiovascular genetics 2014 Aug 7 (4): 475-81. Verweij Niek, Mateo Leach Irene, van den Boogaard Malou, van Veldhuisen Dirk J, Christoffels Vincent M, , Hillege Hans L, van Gilst Wiek H, Barnett Phil, de Boer Rudolf A, van der Harst P |
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies. Brain : a journal of neurology 2017 Jun 140 (6): 1579-1594. Coutelier Marie, Coarelli Giulia, Monin Marie-Lorraine, Konop Juliette, Davoine Claire-Sophie, Tesson Christelle, Valter Rémi, Anheim Mathieu, Behin Anthony, Castelnovo Giovanni, Charles Perrine, David Albert, Ewenczyk Claire, Fradin Mélanie, Goizet Cyril, Hannequin Didier, Labauge Pierre, Riant Florence, Sarda Pierre, Sznajer Yves, Tison François, Ullmann Urielle, Van Maldergem Lionel, Mochel Fanny, Brice Alexis, Stevanin Giovanni, Durr Alexandra, |
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nature genetics 2017 Apr . Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, , Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihi |
Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis. Scientific reports 2017 Jan 7 41653. Pasanen Anu, Karjalainen Minna K, Bont Louis, Piippo-Savolainen Eija, Ruotsalainen Marja, Goksör Emma, Kumawat Kuldeep, Hodemaekers Hennie, Nuolivirta Kirsi, Jartti Tuomas, Wennergren Göran, Hallman Mikko, Rämet Mika, Korppi Mat |
Genetic Variants Associated with Episodic Ataxia in Korea. Scientific reports 2017 10 7 (1): 13855. Choi Kwang-Dong, Kim Ji-Soo, Kim Hyo-Jung, Jung Ileok, Jeong Seong-Hae, Lee Seung-Han, Kim Dong Uk, Kim Sang-Ho, Choi Seo Young, Shin Jin-Hong, Kim Dae-Seong, Park Kyung-Pil, Kim Hyang-Sook, Choi Jae-Hw |
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern.
JCI insight 2019 Dec 4 (23): . Teumer Alexander, Trenkwalder Teresa, Kessler Thorsten, Jamshidi Yalda, van den Berg Marten E, Kaess Bernhard, Nelson Christopher P, Bastiaenen Rachel, De Bortoli Marzia, Rossini Alessandra, Deisenhofer Isabel, Stark Klaus, Assa Solmaz, Braund Peter S, Cabrera Claudia, Dominiczak Anna F, Gögele Martin, Hall Leanne M, Ikram M Arfan, Kavousi Maryam, Lackner Karl J, , Müller Christian, Münzel Thomas, Nauck Matthias, Padmanabhan Sandosh, Pfeiffer Norbert, Spector Tim D, Uitterlinden Andre G, Verweij Niek, Völker Uwe, Warren Helen R, Zafar Mobeen, Felix Stephan B, Kors Jan A, Snieder Harold, Munroe Patricia B, Pattaro Cristian, Fuchsberger Christian, Schmidt Georg, Nolte Ilja M, Schunkert Heribert, Pramstaller Peter P, Wild Philipp S, van der Harst Pim, Stricker Bruno H, Schnabel Renate B, Samani Nilesh J, Hengstenberg Christian, Dörr Marcus, Behr Elijah R, Reinhard Wib |
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
European journal of human genetics : EJHG 2019 Jan . van Setten Jessica, Verweij Niek, Mbarek Hamdi, Niemeijer Maartje N, Trompet Stella, Arking Dan E, Brody Jennifer A, Gandin Ilaria, Grarup Niels, Hall Leanne M, Hemerich Daiane, Lyytikäinen Leo-Pekka, Mei Hao, Müller-Nurasyid Martina, Prins Bram P, Robino Antonietta, Smith Albert V, Warren Helen R, Asselbergs Folkert W, Boomsma Dorret I, Caulfield Mark J, Eijgelsheim Mark, Ford Ian, Hansen Torben, Harris Tamara B, Heckbert Susan R, Hottenga Jouke-Jan, Iorio Annamaria, Kors Jan A, Linneberg Allan, MacFarlane Peter W, Meitinger Thomas, Nelson Christopher P, Raitakari Olli T, Silva Aldana Claudia T, Sinagra Gianfranco, Sinner Moritz, Soliman Elsayed Z, Stoll Monika, Uitterlinden Andre, van Duijn Cornelia M, Waldenberger Melanie, Alonso Alvaro, Gasparini Paolo, Gudnason Vilmundur, Jamshidi Yalda, Kääb Stefan, Kanters Jørgen K, Lehtimäki Terho, Munroe Patricia B, Peters Annette, Samani Nilesh J, Sotoodehnia Nona, Ulivi Sheila, Wilson James G, de Geus Eco J C, Jukema J Wouter, Stricker Bruno, van der Harst Pim, de Bakker Paul I W, Isaacs Aar |
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes. Stem cells international 2020 9 2020 8842398. Barajas-Martinez Hector, Smith Maya, Hu Dan, Goodrow Robert J, Puleo Colleen, Hasdemir Can, Antzelevitch Charles, Pfeiffer Ryan, Treat Jacqueline A, Cordeiro Jonathan |
Host genetics influences the relationship between the gut microbiome and psychiatric disorders. Progress in neuro-psychopharmacology & biological psychiatry 2020 11 106 110153. Martins-Silva Thais, Salatino-Oliveira Angélica, Genro Júlia Pasqualini, Meyer Fernando D T, Li Yan, Rohde Luís Augusto, Hutz Mara Helena, Tovo-Rodrigues Lucia |
V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations. Neurology. Genetics 2021 Feb 7 (1): e546. Paucar Martin, Ågren Richard, Li Tianyi, Lissmats Simon, Bergendal Åsa, Weinberg Jan, Nilsson Daniel, Savichetva Irina, Sahlholm Kristoffer, Nilsson Johanna, Svenningsson P |
Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain. Neurology. Genetics 2022 12 8 (6): e200038. Baviera-Muñoz Raquel, Carretero-Vilarroig Lidón, Vázquez-Costa Juan Francisco, Morata-Martínez Carlos, Campins-Romeu Marina, Muelas Nuria, Sastre-Bataller Isabel, Martínez-Torres Irene, Pérez-García Julia, Sivera Rafael, Sevilla Teresa, Vilchez Juan J, Jaijo Teresa, Espinós Carmen, Millán Jose M, Bataller Luis, Aller Ele |
Genetic Determinants of Atherogenic Indexes. Genes 2023 6 14 (6): . Tomas Texis, Susana Rivera-Mancía, Eloisa Colín-Ramírez, Raul Cartas-Rosado, David Koepsell, Kenneth Rubio-Carrasco, Mauricio Rodríguez-Dorantes, Vanessa Gonzalez-Covarrubi |
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- Page last updated:Apr 16, 2024
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