Application of targeted next generation sequencing (NGS) in clinical genetic diagnostics of cardiomyopathies

被引：0
|
作者：
Van Tintelen, P. [1 ]
Posafalvi, A. [1 ]
Hoedemaekers, Y. M. [1 ]
Van der Zwaag, P. A. [1 ]
Barge-Schaapveld, D. Q. C. M. [2 ]
Piers, S. [2 ]
Zeppenfeld, K. [2 ]
De Boer, R. A. [1 ]
Van den Berg, M. P. [1 ]
Jongbloed, J. D. H. [1 ]
机构：
[1] Univ Med Ctr Groningen, NL-9713 AV Groningen, Netherlands
[2] Leiden Univ, Med Ctr, Leiden, Netherlands
来源：
EUROPEAN HEART JOURNAL | 2014年 / 35卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P621
引用
收藏
页码：109 / 110
页数：2
相关论文
共 50 条
  • [1] Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies
    Meder, Benjamin
    Haas, Jan
    Keller, Andreas
    Heid, Christiane
    Just, Steffen
    Borries, Anne
    Boisguerin, Valesca
    Scharfenberger-Schmeer, Maren
    Staehler, Peer
    Beier, Markus
    Weichenhan, Dieter
    Strom, Tim M.
    Pfeufer, Arne
    Korn, Bernhard
    Katus, Hugo A.
    Rottbauer, Wolfgang
    [J]. CIRCULATION-CARDIOVASCULAR GENETICS, 2011, 4 (02) : 110 - 122
  • [2] Gene-Panel Based Next Generation Sequencing (NGS) Greatly Improves Clinical Genetic Diagnostics in Inherited Cardiomyopathies
    Jongbloed, Jan D.
    Posafalvi, Anna
    Niessen, Renee C.
    Hoedemaekers, Yvonne M.
    van der Zwaag, Paul A.
    Barge-Schaapveld, Daniela Q.
    Piers, Sebastiaan R.
    van der Smagt, Jasper J.
    Asselbergs, Folkert W.
    de Boer, Rudolf A.
    van den Berg, Maarten P.
    Almomani, Rowida
    Sinke, Richard J.
    van Tintelen, J. P.
    [J]. CIRCULATION, 2014, 130
  • [3] Next-generation sequencing (NGS)-based diagnostics in heritable cardiomyopathies and channelopathies
    De Backer, Julie
    Marjolijn, Renard
    Steyaert, Wouter
    Mosquera, Laura Muino
    Steijns, Felke
    Symoens, Sofie
    Callewaert, Bert
    [J]. ACTA CARDIOLOGICA, 2017, 72 (01) : 117 - 117
  • [4] Diagnostic Yield of Three Years Next Generation Sequencing in Clinical Genetic Diagnostics of Cardiomyopathies
    van der Zwaag, Paul A.
    Niessen, Renee C.
    Boven, Ludolf G.
    Hoedemaekers, Yvonne M.
    Sinke, Richard J.
    Jongbloed, Jan D.
    [J]. CIRCULATION, 2016, 134
  • [5] Diagnostic yield of three years next generation sequencing in clinical genetic diagnostics of cardiomyopathies
    Vos, Y. J.
    van der Zwaag, P. A.
    Boven, L. G.
    Niessen, R. C.
    Hoedemaekers, Y. M.
    Sikkema-Raddatz, B.
    Sinke, R. J.
    Jongbloed, J. D. H.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 265 - 265
  • [6] Next generation sequencing analysis in clinical practice of cardiomyopathies diagnostics
    Boronova, Iveta
    Bernasovska, Jarmila
    Petrejcikova, Eva
    Zigova, Michaela
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 578 - 578
  • [7] TARGETED NEXT GENERATION SEQUENCING IN GENETIC DIAGNOSTICS OF OSTEOGENESIS IMPERFECTA
    Schweiger, Darja Smigoc
    Bertok, Sara
    Debeljak, Marusa
    Kovac, Jernej
    Tesovnik, Tine
    Battelino, Tadej
    Podkrajsek, Katarina Trebusak
    [J]. HORMONE RESEARCH IN PAEDIATRICS, 2017, 88 : 86 - 86
  • [8] Translation of next-generation sequencing (NGS) into molecular diagnostics
    Kotschote, Stefan
    Wagner, Carola
    Marschall, Christoph
    Mayer, Karin
    Hirv, Kaimo
    Kerick, Martin
    Timmermann, Bernd
    Klein, Harms-Georg
    [J]. LABORATORIUMSMEDIZIN-JOURNAL OF LABORATORY MEDICINE, 2010, 34 (06): : 311 - 318
  • [9] Application of Next-generation Sequencing in Clinical Molecular Diagnostics
    Seifi, Morteza
    Ghasemi, Asghar
    Raeisi, Sina
    Heidarzadeh, Siamak
    [J]. BRAZILIAN ARCHIVES OF BIOLOGY AND TECHNOLOGY, 2017, 60
  • [10] Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics
    Sikkema-Raddatz, Birgit
    Johansson, Lennart F.
    de Boer, Eddy N.
    Almomani, Rowida
    Boven, Ludolf G.
    van den Berg, Maarten P.
    van Spaendonck-Zwarts, Karin Y.
    van Tintelen, J. Peter
    Sijmons, Rolf H.
    Jongbloed, Jan D. H.
    Sinke, Richard J.
    [J]. HUMAN MUTATION, 2013, 34 (07) : 1035 - 1042
12345