Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and KCNE2[original query] |
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| Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland. Annals of medicine 2004 36 Suppl 1 (): 53-63. Fodstad Heidi, Swan Heikki, Laitinen Päivi, Piippo Kirsi, Paavonen Kristian, Viitasalo Matti, Toivonen Lauri, Kontula Kim |
| Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice. JAMA 2005 Dec 294 (23): 2975-80. Napolitano Carlo, Priori Silvia G, Schwartz Peter J, Bloise Raffaella, Ronchetti Elena, Nastoli Janni, Bottelli Georgia, Cerrone Marina, Leonardi Serg |
| Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome. Human mutation 2009 Apr 30 (4): 4. Ohno S, Toyoda F, Zankov DP, Yoshida H, Makiyama T, Tsuji K, Honda T, Obayashi K, Ueyama H, Shimizu W, Miyamoto Y, Kamakura S, Matsuura H, Kita T, Horie M |
| Confirmed rare copy number variants implicate novel genes in schizophrenia. Biochemical Society transactions 2010 Apr 38 (2): 445-51. Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G |
| Cardiac ion channel gene mutations in Greek long QT syndrome patients. Journal of applied genetics 2010 51 (4): 515-8. Kotta C-M, Anastasakis A, Gatzoulis K, Papagiannis J, Geleris P, Stefanadis |
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
| Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease. Pacing and clinical electrophysiology : PACE 2011 Jun 34 (6): 742-9. Novotny Tomas, Kadlecova Jitka, Raudenska Martina, Bittnerova Alexandra, Andrsova Irena, Florianova Alena, Vasku Anna, Neugebauer Petr, Kozak Milan, Sepsi Milan, Krivan Lubomir, Gaillyova Renata, Spinar Jindri |
| The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study. Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
| Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing. BMC cardiovascular disorders 2012 12 (1): 95. Stattin Eva-Lena, Boström Ida Maria, Winbo Annika, Cederquist Kristina, Jonasson Jenni, Jonsson Björn-Anders, Diamant Ulla-Britt, Jensen Steen M, Rydberg Annika, Norberg An |
| Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
| Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. PloS one 2014 9 (8): e104082. Sabater-Lleal Maria, Mälarstig Anders, Folkersen Lasse, Soler Artigas María, Baldassarre Damiano, Kavousi Maryam, Almgren Peter, Veglia Fabrizio, Brusselle Guy, Hofman Albert, Engström Gunnar, Franco Oscar H, Melander Olle, Paulsson-Berne Gabrielle, Watkins Hugh, Eriksson Per, Humphries Steve E, Tremoli Elena, de Faire Ulf, Tobin Martin D, Hamsten Ande |
| Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. Biomarkers in medicine 2014 8 (4): 557-70. Nielsen Jonas Bille, Bentzen Bo Hjorth, Olesen Morten Salling, David Jens-Peter, Olesen Søren-Peter, Haunsø Stig, Svendsen Jesper Hastrup, Schmitt Nico |
| Genetic analysis, in silico prediction, and family segregation in long QT syndrome. European journal of human genetics : EJHG 2015 Jan 23 (1): 79-85. Riuró Helena, Campuzano Oscar, Berne Paola, Arbelo Elena, Iglesias Anna, Pérez-Serra Alexandra, Coll-Vidal Mònica, Partemi Sara, Mademont-Soler Irene, Picó Ferran, Allegue Catarina, Oliva Antonio, Gerstenfeld Edward, Sarquella-Brugada Georgia, Castro-Urda Víctor, Fernández-Lozano Ignacio, Mont Lluís, Brugada Josep, Scornik Fabiana S, Brugada Ram |
| Sports Participation in Genotype Positive Children With Long QT Syndrome. JACC. Clinical electrophysiology 0 1 (1-2): 62-70. Aziz Peter F, Sweeten Tammy, Vogel Ramon L, Bonney William J, Henderson Jacqueline, Patel Akash R, Shah Maully |
| A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
Atherosclerosis 2015 Nov 245 62-70. Wakil Salma M, Ram Ramesh, Muiya Nzioka P, Mehta Munish, Andres Editha, Mazhar Nejat, Baz Batoul, Hagos Samya, Alshahid Maie, Meyer Brian F, Morahan Grant, Dzimiri Ndu |
| Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
| The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. Molecular genetics & genomic medicine 2019 Jul e835. Liu Xiumin, Li Yujie, Zhang Huan, Ji Yuqiang, Zhao Zhao, Wang Chang |
- Page last reviewed:Feb 1, 2024
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