Publications by authors named "Benjamin Odermatt"

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Haploinsufficiency of is associated with dominant isolated omphalocele.
Caroline M Kolvenbach, Öznur Yilmaz, Filipa M Lopes, Jeshurun C Kalanithy, Katharina Lemberg, Benjamin Odermatt

Front Cell Dev Biol· September 2025

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Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models.
Nina Ishorst, Selina Hölzel, Carola Greve, Öznur Yilmaz, Tobias Lindenberg, Benjamin Odermatt

Eur J Hum Genet· May 2025

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is implicated in central nervous system, orofacial and maxillofacial anomalies.
Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann, Ramgopal Dhakar, Tikam Chand Dakal, Benjamin Odermatt

J Med Genet· January 2025

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EZH2 specifically regulates ISL1 during embryonic urinary tract formation.
Enrico Mingardo, Jeshurun C Kalanithy, Gabriel Dworschak, Nina Ishorst, Öznur Yilmaz, Benjamin Odermatt

Sci Rep· October 2024

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Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.
Jil D Stegmann, Jeshurun C Kalanithy, Gabriel C Dworschak, Nina Ishorst, Enrico Mingardo, Benjamin Odermatt

NPJ Genom Med· March 2024

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X-linked variations in are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.
Caroline M Kolvenbach, Tim Felger, Luca Schierbaum, Isabelle Thiffault, Tomi Pastinen, Benjamin Odermatt

J Med Genet· June 2023

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Modelling human lower urinary tract malformations in zebrafish.
Caroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, Adrian S Woolf, Heiko Reutter, Benjamin Odermatt

Mol Cell Pediatr· March 2023

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Automatic detector synchronization for long-term imaging using confocal light-sheet microscopy.
Alexander Harder, Bhuvaneswari Nagarajan, Benjamin Odermatt, Ulrich Kubitscheck

Microsc Res Tech· February 2023

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Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells.
Michael Enders, Alicia Weier, Rittika Chunder, Young An, Franziska Bremm, Benjamin Odermatt

Int J Mol Sci· February 2023

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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Enrico Mingardo, Glenda Beaman, Philip Grote, Agneta Nordenskjöld, William Newman, Benjamin Odermatt

Commun Biol· November 2022

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Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs.
Felix Häberlein, Enrico Mingardo, Nicole Merten, Nina-Katharina Schulze Köhling, Philip Reinoß, Benjamin Odermatt

Cell Chem Biol· October 2022

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Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism.
Christina Wilms, Klaudia Lepka, Felix Häberlein, Steven Edwards, Jörg Felsberg, Benjamin Odermatt

Redox Biol· February 2022

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Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish model.
Funda Turan, Öznur Yilmaz, Lena Schünemann, Tobias T Lindenberg, Jeshurun C Kalanithy, Benjamin Odermatt

J Neurosci Res· November 2021

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Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, Enrico Mingardo, Haktan B Erdem, Benjamin Odermatt

Genet Med· September 2021

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Is Involved in Urinary Tract and Urorectal Development.
Johanna Magdalena Rieke, Rong Zhang, Doreen Braun, Öznur Yilmaz, Anna S Japp, Benjamin Odermatt

Front Cell Dev Biol· August 2020

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Molecular basis for the distinct functions of redox-active and FeS-transfering glutaredoxins.
Daniel Trnka, Anna D Engelke, Manuela Gellert, Anna Moseler, Md Faruq Hossain, Benjamin Odermatt

Nat Commun· July 2020

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CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch.
Bhuvaneswari Nagarajan, Alexander Harder, Anna Japp, Felix Häberlein, Enrico Mingardo, Benjamin Odermatt

Glia· March 2020

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Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.
Caroline M Kolvenbach, Gabriel C Dworschak, Sandra Frese, Anna S Japp, Peggy Schuster, Benjamin Odermatt

Am J Hum Genet· May 2019

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Dynamic assembly of ribbon synapses and circuit maintenance in a vertebrate sensory system.
Haruhisa Okawa, Wan-Qing Yu, Ulf Matti, Karin Schwarz, Benjamin Odermatt

Nat Commun· May 2019

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Synaptic Convergence Patterns onto Retinal Ganglion Cells Are Preserved despite Topographic Variation in Pre- and Postsynaptic Territories.
Wan-Qing Yu, Rana N El-Danaf, Haruhisa Okawa, Justin M Pacholec, Ulf Matti, Benjamin Odermatt

Cell Rep· November 2018

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Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene.
Valerie Weitensteiner, Rong Zhang, Julia Bungenberg, Matthias Marks, Jan Gehlen, Benjamin Odermatt

Birth Defects Res· April 2018

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Uncoupling of neurogenesis and differentiation during retinal development.
Peter Engerer, Sachihiro C Suzuki, Takeshi Yoshimatsu, Prisca Chapouton, Nancy Obeng, Benjamin Odermatt

EMBO J· May 2017

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Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa.
Damian J Ralser, F Buket Ü Basmanav, Aylar Tafazzoli, Jade Wititsuwannakul, Sarah Delker, Benjamin Odermatt

J Clin Invest· April 2017

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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.
Rong Zhang, Michael Knapp, Kentaro Suzuki, Daiki Kajioka, Johanna M Schmidt, Benjamin Odermatt

Sci Rep· February 2017

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Synaptic vesicles are "primed" for fast clathrin-mediated endocytosis at the ribbon synapse.
Ilaria Pelassa, CongJian Zhao, Mathias Pasche, Benjamin Odermatt, Leon Lagnado

Front Mol Neurosci· December 2014

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