Torthaí cuardaigh - Javad Jabbari
- 1 - 6 toradh as 6 á dtaispeáint
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1
New Exome Data Question the Pathogenicity of Genetic Variants Previously Associated With Catecholaminergic Polymorphic Ventricular Tachycardia de réir Javad Jabbari, Reza Jabbari, Morten W. Nielsen, Anders G. Holst, Jonas B. Nielsen, Stig Haunsø, Jacob Tfelt‐Hansen, Jesper Hastrup Svendsen, Morten S. Olesen
Foilsithe / Cruthaithe 2013Artigo -
2
Stability of Circulating Blood-Based MicroRNAs – Pre-Analytic Methodological Considerations de réir Charlotte Glinge, Sebastian Clauß, Kim Boddum, Reza Jabbari, Javad Jabbari, Bjarke Risgaard, Philipp Tomsits, Bianca Hildebrand, Stefan Kääb, Reza Wakili, Thomas Jespersen, Jacob Tfelt‐Hansen
Foilsithe / Cruthaithe 2017Artigo -
3
Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation de réir Morten S. Olesen, Bo Hjorth Bentzen, Jonas B. Nielsen, Annette Buur Steffensen, Jens‐Peter David, Javad Jabbari, Henrik Kjærulf Jensen, Stig Haunsø, Jesper Hastrup Svendsen, Nicole Schmitt
Foilsithe / Cruthaithe 2012Artigo -
4
Common and Rare Variants in <i>SCN10A</i> Modulate the Risk of Atrial Fibrillation de réir Javad Jabbari, Morten S. Olesen, Lei Yuan, Jonas B. Nielsen, Bo Liang, Vincenzo Macri, Ingrid E. Christophersen, Nikolaj Nielsen, Ahmad Sajadieh, Patrick T. Ellinor, Morten Grunnet, Stig Haunsø, Anders G. Holst, Jesper Hastrup Svendsen, Thomas Jespersen
Foilsithe / Cruthaithe 2014Artigo -
5
Incidence and Risk Factors of Ventricular Fibrillation Before Primary Angioplasty in Patients With First ST‐Elevation Myocardial Infarction: A Nationwide Study in Denmark de réir Reza Jabbari, Thomas Engstrøm, Charlotte Glinge, Bjarke Risgaard, Javad Jabbari, Bo Gregers Winkel, Christian Juhl Terkelsen, Hans‐Henrik Tilsted, Lisette Okkels Jensen, Mikkel Hougaard, Stephanie E. Chiuve, Frants Pedersen, Jesper Hastrup Svendsen, Stig Haunsø, Christine M. Albert, Jacob Tfelt‐Hansen
Foilsithe / Cruthaithe 2015Artigo -
6
Role of common and rare variants in <i>SCN10A</i>: results from the Brugada syndrome QRS locus gene discovery collaborative study de réir Elijah R. Behr, Eleonora Savio‐Galimberti, Julien Barc, Anders G. Holst, Evmorfia Petropoulou, Bram P. Prins, Javad Jabbari, Margherita Torchio, Myriam Berthet, Yuka Mizusawa, Tao Yang, Eline A. Nannenberg, Federica Dagradi, Peter Weeke, Rachel Bastiaenan, Michael J. Ackerman, Stig Haunsø, Antoine Leenhardt, Stefan Kääb, Vincent Probst, Richard Redon, Sanjay Sharma, Arthur A.M. Wilde, Jacob Tfelt‐Hansen, Peter J. Schwartz, D M Roden, Connie R. Bezzina, Morten S. Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi
Foilsithe / Cruthaithe 2015Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Medicine
Biology
Genetics
Gene
Internal medicine
Atrial fibrillation
Cardiology
Mutation
Allele
Allele frequency
Exome sequencing
Angioplasty
Bioinformatics
Brugada syndrome
Candidate gene
Catecholaminergic polymorphic ventricular tachycardia
Chromosome
Computational biology
Cytogenetics
Environmental health
Exome
Human genetics
Incidence (geometry)
Intracellular
Locus (genetics)
Minor allele frequency
Missense mutation
Myocardial infarction
Neuroscience
Optics