Torthaí cuardaigh - Arne Pfeufer
- 1 - 20 toradh as 40 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Toll-like receptor 4 gene polymorphisms and myocardial infarction: no association in a Caucasian population de réir Werner Koch, Petra Hoppmann, Arne Pfeufer, Albert Schömig, A. Kastrati
Foilsithe / Cruthaithe 2006Artigo -
2
<i>SNiPA</i>: an interactive, genetic variant-centered annotation browser de réir Matthias Arnold, Johannes Raffler, Arne Pfeufer, Karsten Suhre, Gabi Kastenmüller
Foilsithe / Cruthaithe 2014Artigo -
3
Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: a case control pilot study de réir Martin Hinterseer, Morten B. Thomsen, Britt-Maria Beckmann, Arne Pfeufer, Rainer Schimpf, H.‐Erich Wichmann, G. Steinbeck, MA Vos, Stefan Kääb
Foilsithe / Cruthaithe 2007Artigo -
4
Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21 de réir Katja Grohmann, Thomas F. Wienker, Kathrin Saar, Sabine Rudnik–Schöneborn, Gisela Stoltenburg‐Didinger, Rainer Rossi, Giuseppe Novelli, Gudrun Nürnberg, Arne Pfeufer, Brunhilde Wirth, André Reis, Klaus Zerres, Christoph Hübner
Foilsithe / Cruthaithe 1999Carta -
5
The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG) de réir Moritz F. Sinner, Arne Pfeufer, Mahmut Akyol, Britt-Maria Beckmann, Martin Hinterseer, Annette Wacker, Siegfried Perz, Wiebke Sauter, Thomas Illig, Michael Näbauer, Claus Schmitt, Hans Wichmann, Albert Schömig, Gerhard Steinbeck, Thomas Meitinger, Stefan Kääb
Foilsithe / Cruthaithe 2008Artigo -
6
Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA) de réir Moritz F. Sinner, Wibke Reinhard, Martina Müller‐Nurasyid, Britt-Maria Beckmann, Eimo Martens, Siegfried Perz, Arne Pfeufer, Janina Winogradow, Klaus Stark, Christa Meisinger, H.‐Erich Wichmann, Annette Peters, Günter A.J. Riegger, Gerhard Steinbeck, Christian Hengstenberg, Stefan Kääb
Foilsithe / Cruthaithe 2010Artigo -
7
Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations de réir Jakob C. Mueller, Elin Lõhmussaar, Reedik Mägi, Maido Remm, Thomas Bettecken, Peter Lichtner, Saskia Biskup, Thomas Illig, Arne Pfeufer, Jan Luedemann, Stefan Schreiber, Peter P. Pramstaller, Irene Pichler, Giovanni Romeo, Anthony Gaddi, A. Testa, Heinz‐Erich Wichmann, Andres Metspalu, Thomas Meitinger
Foilsithe / Cruthaithe 2005Artigo -
8
Drug-Sensitized Zebrafish Screen Identifies Multiple Genes, Including <i>GINS3</i> , as Regulators of Myocardial Repolarization de réir David J. Milan, Albert M. Kim, Jeffrey R. Winterfield, Ian L. Jones, Arne Pfeufer, Serena Sanna, Dan E. Arking, Adam Amsterdam, Khaled Sabeh, John D. Mably, David Rosenbaum, Randall T. Peterson, Aravinda Chakravarti, Stefan Kääb, Dan M. Roden, Calum A. MacRae
Foilsithe / Cruthaithe 2009Artigo -
9
Regulation of Endocytic Recycling of KCNQ1/KCNE1 Potassium Channels de réir Guiscard Seebohm, Nathalie Strutz‐Seebohm, Ria Birkin, Ghislaine Dell, Cecilia Bucci, Maria Rita Spinosa, Ravshan Baltaev, Andreas F. Mack, Ganna Korniychuk, Amit Choudhury, David L. Marks, Richard E. Pagano, Bernard Attali, Arne Pfeufer, Robert S. Kass, Michael C. Sanguinetti, Jeremy M. Tavaré, Florian Läng
Foilsithe / Cruthaithe 2007Artigo -
10
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans de réir Hiroshi Watanabe, Tamara T. Koopmann, Solena Le Scouarnec, Tao Yang, Christiana R. Ingram, Jean‐Jacques Schott, Sophie Demolombe, Vincent Probst, Frédéric Anselme, Denis Escande, Ans C.P. Wiesfeld, Arne Pfeufer, Stefan Kääb, Hans Wichmann, Can Hasdemir, Yoshifusa Aizawa, Arthur A.M. Wilde, Dan M. Roden, Connie R. Bezzina
Foilsithe / Cruthaithe 2008Artigo -
11
A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations de réir Fabio Marroni, Arne Pfeufer, Yurii S. Aulchenko, Christopher S. Franklin, Aaron Isaacs, Irene Pichler, Philipp S. Wild, Ben A. Oostra, Alan F. Wright, Harry Campbell, Jacqueline C.M. Witteman, Stefan Kääb, Andrew A. Hicks, Ulf Gyllensten, Igor Rudan, Thomas Meitinger, Cristian Pattaro, Cornelia M. van Duijn, James F. Wilson, Peter P. Pramstaller
Foilsithe / Cruthaithe 2009Revisão -
12
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy de réir Dirk Sibbing, Arne Pfeufer, Tamara Perisic, Alexander M. Mannes, Karin Fritz‐Wolf, Sarah Unwin, Moritz F. Sinner, Christian Gieger, Christian Johannes Gloeckner, Heinz‐Erich Wichmann, Elisabeth Kremmer, Zasie Schäfer, Axel Walch, Martin Hinterseer, Michael Näbauer, Stefan Kääb, Adnan Kastrati, Albert Schömig, Thomas Meitinger, Georg W. Bornkamm, Marcus Conrad, Nicolas von Beckerath
Foilsithe / Cruthaithe 2011Artigo -
13
An Enhancer Polymorphism at the Cardiomyocyte Intercalated Disc Protein NOS1AP Locus Is a Major Regulator of the QT Interval de réir Ashish Kapoor, Rajesh B. Sekar, Nancy F. Hansen, Karen Fox-Talbot, Michael P. Morley, Vasyl Pihur, Sumantra Chatterjee, Jeffrey Brandimarto, Christine S. Moravec, Sara L. Pulit, Arne Pfeufer, Jim Mullikin, Mark T. Ross, Eric D. Green, David Bentley, Christopher Newton‐Cheh, Eric Boerwinkle, Gordon F. Tomaselli, Thomas P. Cappola, Dan E. Arking, Marc K. Halushka, Aravinda Chakravarti
Foilsithe / Cruthaithe 2014Artigo -
14
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2 de réir I. Kolder, Michael W.T. Tanck, Pieter G. Postema, Julien Barc, Moritz F. Sinner, Sven Zumhagen, Anja Husemann, Birgit Stallmeyer, Tamara T. Koopmann, Nynke Hofman, Arne Pfeufer, Peter Lichtner, Thomas Meitinger, Britt Maria Beckmann, Robert J. Myerburg, Nanette H. Bishopric, Dan M. Roden, Stefan Kääb, Arthur A.M. Wilde, Jean‐Jacques Schott, Eric Schulze‐Bahr, Connie R. Bezzina
Foilsithe / Cruthaithe 2015Artigo -
15
Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction de réir Connie R. Bezzina, Raha Pazoki, Abdennasser Bardai, Roos F. Marsman, Jonas S.S.G. de Jong, Marieke T. Blom, Brendon P. Scicluna, J. Wouter Jukema, Navin R. Bindraban, Peter Lichtner, Arne Pfeufer, Nanette H. Bishopric, Dan M. Roden, Thomas Meitinger, Sumeet S. Chugh, Robert J. Myerburg, Xavier Jouven, Stefan Kääb, Henk L. Dekker, Hanno L. Tan, Michael W.T. Tanck, Arthur A.M. Wilde
Foilsithe / Cruthaithe 2010Artigo -
16
Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery de réir Simon C. Body, Charles D. Collard, Stanton K. Shernan, Amanda A. Fox, Kuang-Yu Liu, Marylyn D. Ritchie, Tjörvi E. Perry, Jochen D. Muehlschlegel, Sary F. Aranki, Brian S. Donahue, Mias Pretorius, Juan-Carlos Estrada, Patrick T. Ellinor, Christopher Newton‐Cheh, Christine E. Seidman, Jonathan G. Seidman, Daniel S. Herman, Peter Lichtner, Thomas Meitinger, Arne Pfeufer, Stefan Kääb, Nancy J. Brown, Dan M. Roden, Dawood Darbar
Foilsithe / Cruthaithe 2009Artigo -
17
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics de réir Alicia Lundby, Elizabeth J. Rossin, Annette Buur Steffensen, Moshe Rav, Christopher Newton‐Cheh, Arne Pfeufer, Stacey N. Lynch, Søren‐Peter Olesen, Søren Brunak, Patrick T. Ellinor, J. Wouter Jukema, Stella Trompet, Ian Ford, Peter W. Macfarlane, Bouwe P. Krijthe, Albert Hofman, André G. Uitterlinden, Bruno H. Stricker, Hendrik M. Nathoe, Wilko Spiering, Mark J. Daly, Folkert W. Asselbergs, Pim van der Harst, David J. Milan, Paul I. W. de Bakker, Kasper Lage, Jesper V. Olsen
Foilsithe / Cruthaithe 2014Artigo -
18
Genome-Wide Association Studies of the PR Interval in African Americans de réir J. G. Smith, Jared W. Magnani, Colin N. A. Palmer, Yan Meng, Elsayed Z. Soliman, Solomon K. Musani, Kathleen F. Kerr, Renate B. Schnabel, Steven A. Lubitz, Nona Sotoodehnia, Susan Redline, Arne Pfeufer, Martina Müller‐Nurasyid, Daniel S. Evans, Michael A. Nalls, Yongmei Liu, Anne B. Newman, Alan B. Zonderman, Michele K. Evans, Rajat Deo, Patrick T. Ellinor, Dina N. Paltoo, Christopher Newton‐Cheh, Emelia J. Benjamin, Reena Mehra, Álvaro Alonso, Susan R. Heckbert, Ervin R. Fox
Foilsithe / Cruthaithe 2011Revisão -
19
A Global In Vivo Drosophila RNAi Screen Identifies NOT3 as a Conserved Regulator of Heart Function de réir G. Gregory Neely, Keiji Kuba, Anthony Cammarato, Kazuya Isobe, Sabine Amann, Liyong Zhang, Mitsushige Murata, Lisa Elmeń, Vaijayanti Gupta, Suchir Arora, Rinku Sarangi, Debasis Dan, Susumu Fujisawa, Takako Usami, Cui-ping Xia, Alex C. Keene, Nakissa N. Alayari, Hiroyuki Yamakawa, Ulrich Elling, Christian Berger, Maria Novatchkova, Rubina Koglgruber, Keiichi Fukuda, Hiroshi Nishina, Mitsuaki Isobe, J. Andrew Pospisilik, Yumiko Imai, Arne Pfeufer, Andrew A. Hicks, Peter P. Pramstaller, Sai Subramaniam, Akinori Kimura, Karen Ocorr, Rolf Bodmer, Josef Penninger
Foilsithe / Cruthaithe 2010Artigo -
20
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation de réir Stefan Kääb, Dawood Darbar, Charlotte van Noord, Josée Dupuis, Arne Pfeufer, Chris Newton-Cheh, Renate B. Schnabel, S Makino, Moritz F. Sinner, Prince J. Kannankeril, Britt Maria Beckmann, Subbarao Choudry, Brian S. Donahue, Jan Heeringa, Siegfried Perz, Kathryn L. Lunetta, Martin G. Larson, Daniel Levy, Calum A. MacRae, Jeremy N. Ruskin, A. Wacker, Albert Schömig, H.‐Erich Wichmann, Gerhard Steinbeck, Thomas Meitinger, André G. Uitterlinden, Jacqueline C.M. Witteman, D M Roden, Emelia J. Benjamin, Patrick T. Ellinor
Foilsithe / Cruthaithe 2008Revisão
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Medicine
Gene
Internal medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Cardiology
Genetic association
Population
Environmental health
Atrial fibrillation
Odds ratio
QT interval
Endocrinology
Allele
SNP
Sudden cardiac death
Bioinformatics
Blood pressure
Genotyping
Long QT syndrome
Confidence interval
Disease
Heart rate
Locus (genetics)
Mathematics
Allele frequency
Cohort