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Author/Creator Stallmeyer, Birgit

1. Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy. (August 2019)

Authors:
Frank, Derk; Yusuf Rangrez, Ashraf; Friedrich, Corinna; Dittmann, Sven; Stallmeyer, Birgit; Yadav, Pankaj; Bernt, Alexander; Schulze-Bahr, Ellen; Borlepawar, Ankush; Zimmermann, Wolfram-Hubertus; Peischard, Stefan; Seebohm, Guiscard; Linke, Wolfgang A.; Baba, Hideo A.; Krüger, Marcus; Unger, Andr...
Journal:
Circulation
Issue:
Volume 12:Number 8(2019)
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Record Type:
Journal Article
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2. Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort. (August 2019)

Authors:
van Lint, Freyja H.M.; Murray, Brittney; Tichnell, Crystal; Zwart, Rob; Amat, Nuria; Lekanne Deprez, Ronald H.; Dittmann, Sven; Stallmeyer, Birgit; Calkins, Hugh; van der Smagt, Jasper J.; van den Wijngaard, Arthur; Dooijes, Dennis; van der Zwaag, Paul A.; Schulze-Bahr, Eric; Judge, Daniel P.; Jo...
Journal:
Circulation
Issue:
Volume 12:Number 8(2019)
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Journal Article
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3. Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography. Issue 4 (1st September 2017)

Authors:
Zumhagen, Sven; Vrachimis, Alexis; Stegger, Lars; Kies, Peter; Wenning, Christian; Ernsting, Marko; Müller, Jovanca; Seebohm, Guiscard; Paul, Matthias; Schäfers, Klaus; Stallmeyer, Birgit; Schäfers, Michael; Schulze-Bahr, Eric
Journal:
Heart
Issue:
Volume 104:Issue 4(2018)
Page Start:
332
Record Type:
Journal Article
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4. Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death. (15th April 2021)

Authors:
Fischer, Björn; Dittmann, Sven; Brodehl, Andreas; Unger, Andreas; Stallmeyer, Birgit; Paul, Matthias; Seebohm, Guiscard; Kayser, Anne; Peischard, Stefan; Linke, Wolfgang A.; Milting, Hendrik; Schulze-Bahr, Eric
Journal:
International journal of cardiology
Issue:
Volume 329(2021)
Page Start:
167
Record Type:
Journal Article
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5. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Issue 4 (28th July 2020)

Authors:
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G.; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L.; Mazzanti, Andrea; Beckmann, Britt M.; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D.; Kucho, Yu; Ro...
Journal:
Circulation
Issue:
Volume 142:Issue 4(2020)
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Journal Article
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6. POPDC2 a novel susceptibility gene for conduction disorders. (August 2020)

Authors:
Rinné, Susanne; Ortiz-Bonnin, Beatriz; Stallmeyer, Birgit; Kiper, Aytug K.; Fortmüller, Lisa; Schindler, Roland F.R.; Herbort-Brand, Ursula; Kabir, Nashitha S.; Dittmann, Sven; Friedrich, Corinna; Zumhagen, Sven; Gualandi, Francesca; Selvatici, Rita; Rapezzi, Claudio; Arbustini, Eloisa; Ferlini, ...
Journal:
Journal of molecular and cellular cardiology
Issue:
Volume 145(2020)
Page Start:
74
Record Type:
Journal Article
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7. Sodium permeable and "hypersensitive" TREK‐1 channels cause ventricular tachycardia. Issue 4 (27th February 2017)

Authors:
Decher, Niels; Ortiz‐Bonnin, Beatriz; Friedrich, Corinna; Schewe, Marcus; Kiper, Aytug K; Rinné, Susanne; Seemann, Gunnar; Peyronnet, Rémi; Zumhagen, Sven; Bustos, Daniel; Kockskämper, Jens; Kohl, Peter; Just, Steffen; González, Wendy; Baukrowitz, Thomas; Stallmeyer, Birgit; Schulze‐Bahr, Eric
Journal:
EMBO molecular medicine
Issue:
Volume 9:Issue 4(2017)
Page Start:
403
Record Type:
Journal Article
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8. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. (March 2015)

Authors:
Wemhöner, Konstantin; Friedrich, Corinna; Stallmeyer, Birgit; Coffey, Alison J.; Grace, Andrew; Zumhagen, Sven; Seebohm, Guiscard; Ortiz-Bonnin, Beatriz; Rinné, Susanne; Sachse, Frank B.; Schulze-Bahr, Eric; Decher, Niels
Journal:
Journal of molecular and cellular cardiology
Issue:
Volume 80(2015:Mar.)
Page Start:
186
Record Type:
Journal Article
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9. A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction. Issue 10 (12th May 2017)

Authors:
Stallmeyer, Birgit; Kuß, Johanna; Kotthoff, Stefan; Zumhagen, Sven; Vowinkel, Kirsty; Rinné, Susanne; Matschke, Lina A.; Friedrich, Corinna; Schulze-Bahr, Ellen; Rust, Stephan; Seebohm, Guiscard; Decher, Niels; Schulze-Bahr, Eric
Journal:
Circulation research
Issue:
Volume 120:Issue 10(2017)
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Journal Article
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10. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome. (March 2015)

Authors:
Wemhöner, Konstantin; Friedrich, Corinna; Stallmeyer, Birgit; Coffey, Alison J.; Grace, Andrew; Zumhagen, Sven; Seebohm, Guiscard; Ortiz-Bonnin, Beatriz; Rinné, Susanne; Sachse, Frank B.; Schulze-Bahr, Eric; Decher, Niels
Journal:
Journal of molecular and cellular cardiology
Issue:
Volume 80(2015:Mar.)
Page Start:
186
Record Type:
Journal Article
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