HuGE Literature Finder
Records 1-30
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Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy.
BMC cardiovascular disorders 2019 Jul 19 (1): 174. Raju Hariharan, Ware James S, Skinner Jonathan R, Hedley Paula L, Arno Gavin, Love Donald R, van der Werf Christian, Tfelt-Hansen Jacob, Winkel Bo Gregers, Cohen Marta C, Li Xinzhong, John Shibu, Sharma Sanjay, Jeffery Steve, Wilde Arthur A M, Christiansen Michael, Sheppard Mary N, Behr Elijah |
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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 |
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 |
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Exome analysis of a family with Wolff-Parkinson-White syndrome identifies a novel disease locus.
American journal of medical genetics. Part A 2015 Aug . Bowles Neil E, Jou Chuanchau J, Arrington Cammon B, Kennedy Brett J, Earl Aubree, Matsunami Norisada, Meyers Lindsay L, Etheridge Susan P, Saarel Elizabeth V, Bleyl Steven B, Yost H Joseph, Yandell Mark, Leppert Mark F, Tristani-Firouzi Martin, Gruber Peter J, |
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Multiplex ligation-dependent probe amplification copy number variant analysis in patients with acquired long QT syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Apr 17 (4): 635-41. Williams Victoria S, Cresswell Carl J, Ruspi Gerhard, Yang Tao, Atak Thomas C, McLoughlin Matthew, Ingram Christiana D, Ramirez Andrea H, Roden Dan, Armstrong Mart |
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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 |
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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
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The rs9982601 polymorphism of the region between the SLC5A3/MRPS6 and KCNE2 genes associated with a prevalence of myocardial infarction and subsequent long-term mortality.
Polskie Archiwum Medycyny Wewn?trznej 2015 125 (4): 240-8. Szpakowicz Anna, Kiliszek Marek, Pepi?ski Witold, Waszkiewicz Ewa, Franaszczyk Maria, Skawro?ska Ma?gorzata, Dobrzycki S?awomir, Niemcunowicz-Janica Anna, Ploski Rafa?, Opolski Grzegorz, Musia? W?odzimierz J, Kami?ski Karol |
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Evaluation of a new high-throughput next-generation sequencing method based on a custom AmpliSeq™ library and ion torrent PGM™ sequencing for the rapid detection of genetic variations in long QT syndrome.
Molecular diagnosis & therapy 2014 Oct 18 (5): 533-9. Millat Gilles, Chanavat Valérie, Rousson Robe |
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KCNH2 polymorphism and methadone dosage interact to enhance QT duration.
Drug and alcohol dependence 2014 Aug 141 34-8. Hajj Aline, Ksouda Kamilia, Peoc'h Katell, Curis Emmanuel, Messali Anne, Deveaux Laurence Labat, Bloch Vanessa, Prince Nathalie, Mouly Stéphane, Scherrmann Jean-Michel, Lépine Jean-Pierre, Laplanche Jean-Louis, Drici Milou-Daniel, Vorspan Floren |
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Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7. Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan |
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Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2014 Jan 19 (1): 63-9. Mints Yuliya, Zipunnikov Vadim, Khurram Irfan, Calkins Hugh, Nazarian Sam |
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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 |
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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 |
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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 |
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Do LQTS gene single nucleotide polymorphisms alter QTc intervals at rest and during exercise stress testing?
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2013 May 18 (3): 288-93. Aziz Peter F, Wieand Tammy S, Ganley Jamie, Henderson Jacqueline, McBride Michael, Shah Maully |
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Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.
PloS one 2013 8 (7): e69614. Trolle Christian, Mortensen Kristian H, Pedersen Lisbeth N, Berglund Agnethe, Jensen Henrik K, Andersen Niels H, Gravholt Claus |
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Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
Mayo Clinic proceedings 2012 Jun 87 (6): 524-39. Tester David J, Medeiros-Domingo Argelia, Will Melissa L, Haglund Carla M, Ackerman Michael |
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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 |
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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 |
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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 |
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Domperidone treatment for gastroparesis: demographic and pharmacogenetic characterization of clinical efficacy and side-effects.
Digestive diseases and sciences 2011 Jan 56 (1): 115-24. Parkman Henry P, Jacobs Michael R, Mishra Anurag, Hurdle Jessica A, Sachdeva Priyanka, Gaughan John P, Krynetskiy Evge |
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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 |
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Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
The American journal of cardiology 2010 Oct 106 (8): 1124-8. Tester David J, Benton Amber J, Train Laura, Deal Barbara, Baudhuin Linnea M, Ackerman Michael |
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Common variants in cardiac ion channel genes are associated with sudden cardiac death.
Circulation. Arrhythmia and electrophysiology 2010 Jun 3 (3): 222-9. Albert Christine M, MacRae Calum A, Chasman Daniel I, VanDenburgh Martin, Buring Julie E, Manson JoAnn E, Cook Nancy R, Newton-Cheh Christoph |
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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 |
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Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.
The Canadian journal of cardiology 2010 Apr 26 (4): 208-12. Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew |
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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 |
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Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome.
Frontiers of medicine in China 2007 Jul 1 (3): 312-5. Du Rong, Tian Li, Yuan Guohui, Li Jin, Ren Faxin, Gui Le, Li Wei, Zhang Shouyan, Kang Cailian, Yang Jung |
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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 |
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- Page last updated:Feb 24, 2021
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