Publications by authors named "Simon Sumer"

6Publications

Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection.

Authors:
Simon Alexander Sumer Sandra Hoffmann Svenja Laue Birgit Campbell Kristin Raedecke Viktoria Frajs Sebastian Clauss Stefan Kääb Johannes W G Janssen Anna Jauch Karl-Ludwig Laugwitz Tatjana Dorn Alessandra Moretti Gudrun A Rappold

Stem Cell Reports 2020 10 24;15(4):999-1013. Epub 2020 Sep 24.

Department of Human Molecular Genetics, Institute of Human Genetics, University of Heidelberg, 69120 Heidelberg, Baden-Wuerttemberg, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Heidelberg/Mannheim, Heidelberg, Germany. Electronic address:

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October 2020

Functional Characterization of Rare Variants in the Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation.

Authors:
Sandra Hoffmann Christoph Paone Simon A Sumer Sabrina Diebold Birgit Weiss Ralph Roeth Sebastian Clauss Ina Klier Stefan Kääb Andreas Schulz Philipp S Wild Adil Ghrib Tanja Zeller Renate B Schnabel Steffen Just Gudrun A Rappold

Front Genet 2019 11;10:648. Epub 2019 Jul 11.

Department of Human Molecular Genetics, Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany.

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July 2019

Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathways.

Authors:
Stefanie Schmitteckert Anne Griesbeck Simon Sumer Anna Jauch Alexandra Rolletschek Beate Niesler Gudrun A Rappold Sandra Hoffmann

Stem Cell Res 2017 12 11;25:278-282. Epub 2017 Jul 11.

Institute of Human Genetics, University Heidelberg, Germany; DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Germany. Electronic address:

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December 2017

Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells.

Authors:
Sandra Hoffmann Stefanie Schmitteckert Anne Griesbeck Hannes Preiss Simon Sumer Alexandra Rolletschek Martin Granzow Volker Eckstein Beate Niesler Gudrun A Rappold

Stem Cell Res 2017 05 29;21:51-57. Epub 2017 Mar 29.

Department of Human Molecular Genetics, Institute of Human Genetics, University Heidelberg, Germany; DZHK, German Centre for Cardiovascular Research, Partner site Heidelberg/Mannheim, Germany. Electronic address:

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May 2017

A large-scale functional screen identifies Nova1 and Ncoa3 as regulators of neuronal miRNA function.

Authors:
Peter H Störchel Juliane Thümmler Gabriele Siegel Ayla Aksoy-Aksel Federico Zampa Simon Sumer Gerhard Schratt

EMBO J 2015 Sep 23;34(17):2237-54. Epub 2015 Jun 23.

Institute for Physiological Chemistry Biochemical-Pharmacological Center Marburg Philipps-University Marburg, Marburg, Germany

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September 2015

A coding-independent function of an alternative Ube3a transcript during neuronal development.

Authors:
Jeremy Valluy Silvia Bicker Ayla Aksoy-Aksel Martin Lackinger Simon Sumer Roberto Fiore Tatjana Wüst Dominik Seffer Franziska Metge Christoph Dieterich Markus Wöhr Rainer Schwarting Gerhard Schratt

Nat Neurosci 2015 May 13;18(5):666-73. Epub 2015 Apr 13.

Institute of Physiological Chemistry, Biochemical-Pharmacological Center Marburg, Philipps University Marburg, Marburg, Germany.

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May 2015