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Stephan Sonntag

Observed names: Sonntag S, Sonntag, Stephan
OpenAlex ID: A5113969195
The neuronal connexin36 interacts with and is phosphorylated by CaMKII in a way similar to CaMKII interaction with glutamate receptors
2008 · Cantas Alev, Stephanie Urschel, et al. · Proceedings of the National Academy of Sciences · 131
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice
2010 · Melanie Schütz, Pietro Scimemi, et al. · Human Molecular Genetics · 77
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SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects
2018 · Johanne Dubail, Céline Huber, et al. · Nature Communications · 67
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A new conditional mouse mutant reveals specific expression and functions of connexin36 in neurons and pancreatic beta-cells
2008 · Kerstin Wellershaus, Joachim Degen, et al. · Experimental Cell Research · 65
Cardiac-specific ablation of synapse-associated protein SAP97 in mice decreases potassium currents but not sodium current
2014 · Ludovic Gillet, Jean-Sébastien Rougier, et al. · Heart Rhythm · 61
Gating, permselectivity and pH‐dependent modulation of channels formed by connexin57, a major connexin of horizontal cells in the mouse retina
2009 · Nicolas Palacios‐Prado, Stephan Sonntag, et al. · The Journal of Physiology · 60
Mouse lens connexin23 (Gje1) does not form functional gap junction channels but causes enhanced ATP release from HeLa cells
2008 · Stephan Sonntag, Goran Söhl, et al. · European Journal of Cell Biology · 58
Expression of connexin30.2 in interneurons of the central nervous system in the mouse
2007 · Maria M. Kreuzberg, Jim Deuchars, et al. · Molecular and Cellular Neuroscience · 58
Epigenetic regulation of promiscuous gene expression in thymic medullary epithelial cells
2010 · Lars-Oliver Tykocinski, Anna Sinemus, et al. · Proceedings of the National Academy of Sciences · 55
Connexin57 is expressed in dendro‐dendritic and axo‐axonal gap junctions of mouse horizontal cells and its distribution is modulated by light
2009 · Ulrike Janssen‐Bienhold, Jennifer Trümpler, et al. · The Journal of Comparative Neurology · 51
Gap Junctions between Neuronal Inputs But Not Gonadotropin-Releasing Hormone Neurons Control Estrous Cycles in the Mouse
2011 · Rebecca E. Campbell, Eric Ducret, et al. · Endocrinology · 41
The TSG101 protein binds to connexins and is involved in connexin degradation
2009 · Tanja Auth, Sharazad Schlüter, et al. · Experimental Cell Research · 39
The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans
2017 · Eveline Boudin, Timur Yorgan, et al. · Journal of Bone and Mineral Research · 33
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Carbamazepine reduces disease severity in a mouse model of metaphyseal chondrodysplasia type Schmid caused by a premature stop codon (Y632X) in the Col10a1 gene
2018 · Mitra Forouhan, Stephan Sonntag, et al. · Human Molecular Genetics · 27
The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV
2021 · Nele Vollersen, Wenbo Zhao, et al. · Bone Research · 25
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Cell-Specific Cre Recombinase Expression Allows Selective Ablation of Glutamate Receptors from Mouse Horizontal Cells
2013 · Sebastian Ströh, Stephan Sonntag, et al. · PLoS ONE · 22
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A Distinct Pool of Nav1.5 Channels at the Lateral Membrane of Murine Ventricular Cardiomyocytes
2019 · Jean-Sébastien Rougier, Maria C. Essers, et al. · Frontiers in Physiology · 21
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Impaired calcium homeostasis is associated with sudden cardiac death and arrhythmias in a genetic equivalent mouse model of the human HRC-Ser96Ala variant
2017 · Christos Tzimas, Daniel M Johnson, et al. · Cardiovascular Research · 18
CaMKII inhibition due to TRIC-B loss-of-function dysregulates SMAD signaling in osteogenesis imperfecta
2023 · Roberta Besio, Barbara M. Contento, et al. · Matrix Biology · 13
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Testing the Cre-mediated genetic switch for the generation of conditional knock-in mice
2019 · Mattia Capulli, Rossella Costantini, et al. · PLoS ONE · 8
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Gnathodiaphyseal dysplasia is not recapitulated in a respective mouse model carrying a mutation of the Ano5 gene
2020 · Tim Rolvien, Osman Avci, et al. · Bone Reports · 6
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A distinct pool of Nav1.5 channels at the lateral membrane of murine ventricular cardiomyocytes
2019 · Jean-Sébastien Rougier, Maria C. Essers, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 3
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Tmem38b osteoblast specific knock out mouse resembles osteogenesis imperfecta type XIV
2022 · Barbara Maria Contento, Nadia Garibaldi, et al. · Bone Reports
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Investigating the role of KIF22 in musculoskeletal development
2021 · Pearson RD, Kalamajski S, et al. · Newcastle University ePrints (Newcastle Univesity)
Abstract 18492: Cardiac-specific Ablation of Synapse-Associated Protein SAP97 in Mice Decreases Potassium Currents but Not Sodium Current
2014 · Ludovic Gillet, Jean‐Sébastien Rougier, et al. · Circulation
Works count: 27
Citation count: 939
H-index: 18
I10-index: 19
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