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Lancet, The, ISSN 0140-6736, 2010, Volume 375, Issue 9725, pp. 1525 - 1535
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2015, Volume 10, Issue 7, p. e0133037
Background The use of next-generation sequencing enables a rapid analysis of many genes associated with sudden cardiac death in diseases like Brugada Syndrome.... 
NA(V)1.5 | ANKYRIN-G | COMMON POLYMORPHISM | MULTIDISCIPLINARY SCIENCES | COMPOUND | SUDDEN CARDIAC DEATH | PHENOTYPE | NOISE | LONG-QT SYNDROME | MUTATIONS | RIGHT-VENTRICULAR CARDIOMYOPATHY/DYSPLASIA | Brugada Syndrome - genetics | Brugada Syndrome - diagnosis | Genetic Testing | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Male | Calsequestrin - genetics | Death, Sudden, Cardiac | Genetic Variation | A Kinase Anchor Proteins - genetics | gamma Catenin | Desmoplakins - genetics | Clinical Decision-Making | Adult | Female | Retrospective Studies | NAV1.5 Voltage-Gated Sodium Channel - genetics | Arrhythmias, Cardiac - genetics | Desmoglein 2 - genetics | Penetrance | Potassium Channels, Inwardly Rectifying - genetics | Sequence Analysis, DNA | Ryanodine Receptor Calcium Release Channel - genetics | Pedigree | Ankyrins - genetics | High-Throughput Nucleotide Sequencing | Cohort Studies | Cardiac arrhythmia | Copy number | Genes | Insertion | Ryanodine receptors | Genetic screening | Gene sequencing | Complexity | Proteins | Clonal deletion | Defibrillators | Genetic analysis | Electrocardiography | Deletion | Potassium channels (voltage-gated) | Heart diseases | Ion channels (cyclic nucleotide-gated) | Potassium channels (inwardly-rectifying) | Decision making | Data processing | Genetic diversity | Patients | Coronary artery disease | Substrates | Diseases | Genetic variance | KCNQ1 protein | Mutation | Variation | Malalties | Heart | Aspectes genètics | Arítmia | Arrhythmia | Cor | Genetic aspects
Journal Article
Journal Article
by Hobbs, Brian D and de Jong, Kim and Lamontagne, Maxime and Bosse, Yohan and Shrine, Nick and Artigas, Maria Soler and Wain, Louise V and Hall, Ian P and Jackson, Victoria E and Wyss, Annah B and London, Stephanie J and North, Kari E and Franceschini, Nora and Strachan, David P and Beaty, Terri H and Hokanson, John E and Crapo, James D and Castaldi, Peter J and Chase, Robert P and Bartz, Traci M and Heckbert, Susan R and Psaty, Bruce M and Gharib, Sina A and Zanen, Pieter and Lammers, Jan W and Oudkerk, Matthijs and Groen, H. J and Locantore, Nicholas and Tal-Singer, Ruth and Rennard, Stephen I and Vestbo, Jurgen and Timens, Wim and Pare, Peter D and Latourelle, Jeanne C and Dupuis, Josee and O'Connor, George T and Wilk, Jemma B and Kim, Woo Jin and Lee, Mi Kyeong and Oh, Yeon-Mok and Vonk, Judith M and de Koning, Harry J and Leng, Shuguang and Belinsky, Steven A and Tesfaigzi, Yohannes and Manichaikul, Ani and Wang, Xin-Qun and Rich, Stephen S and Barr, R. Graham and Sparrow, David and Litonjua, Augusto A and Bakke, Per and Gulsvik, Amund and Lahousse, Lies and Brusselle, Guy G and Stricker, Bruno H and Uitterlinden, Ane G and Ampleford, Elizabeth J and Bleecker, Eugene R and Woouff, Prescott G and Meyers, Deborah A and Qiao, Dandi and Lomas, David A and Yim, Jae-Joon and Kim, Deog Kyeom and Hawrylkiewicz, Iwona and Sliwinski, Pawel and Hardin, Megan and Fingerlin, Tasha E and Schwartz, David A and Postma, Dirkje S and MacNee, William and Tobin, Martin D and Silverman, Edwin K and Boezen, H. Marike and Cho, Michael H and UK BiLEVE Investigators and COPDGene Investigators and ECLIPSE Investigators and SPIROMICS Res Grp and Int COPD Genetics Network and LifeLines Investigators and Int COPD Genetics Consortium and SPIROMICS Research Group and International COPD Genetics Network Investigators and International COPD Genetics Consortium
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 426 - 432
Journal Article
Europace, ISSN 1099-5129, 06/2010, Volume 12, Issue 6, pp. 861 - 868
Journal Article
Journal Article