Stegmann JD, Kalanithy JC, Dworschak GC, Ishorst N, Mingardo E, Lopes FM, Ho YM, Grote P, Lindenberg TT, Yilmaz Ö, Channab K, …, Odermatt B, Hilger AC. Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies. NPJ Genom Med. 2024 Mar 1;9(1):18. doi: 10.1038/s41525-024-00398-9. PMID: 38429302; PMCID: PMC10907620.
Florian Reinhardt, Luisa Coen, Mahdi Rivandi, Andrè Franken, Eunike Sawitning Ayu Setyono, Tobias Lindenberg, Jens Eberhardt, Tanja Fehm, Dieter Niederacher, Franziska Knopf, Hans Neubauer (2023) DanioCTC: Analysis of Circulating Tumor Cells from Metastatic Breast Cancer Patients in Zebrafish Xenografts. Cancers PMID: 38001672
Kolvenbach CM, Dworschak GC, Rieke JM, Woolf AS, Reutter H, Odermatt B, Hilger AC. (2023) Modelling human lower urinary tract malformations in zebrafish. Mol Cell Pediatr. PMID: 36977792
Enders M, Weier A, Chunder R, An Y, Bremm F, Feigenspan A, Buettner C, Ekici AB, Mingardo E, Odermatt B, Kuerten S. (2023) Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells. Int J Mol Sci. PMID: 36835129
Kolvenbach CM, Felger T, Schierbaum L, Thiffault I, Pastinen T, Szczepańska M, Zaniew M, Adamczyk P, Bayat A, Yilmaz Ö, Lindenberg TT, Thiele H, Hildebrandt F, Hinderhofer K, Moog U, Hilger AC, Sullivan B, Bartik L, Gnyś P, Grote P, Odermatt B, Reutter H and Dworschak GC. (2022) X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems. J Med Genet. PMID: 36379543
Häberlein F*, Mingardo E*, Merten N, Schulze Köhling NK, Reinoß P, Simon K, Japp A, Nagarajan B, Schrage R, Pegurier C, Gillard M, Monk KR, Odermatt B*, Kostenis E* and Gomeza J*. (2022) Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs. Cell Chem Biol. PMID: 36126653
Harder A, Nagarajan B, Odermatt B and Kubitscheck U. (2022) Automatic detector synchronization for long-term imagingusing confocal light-sheet microscopy. Microsc Res Tech. 1–12; https://doi.org/10.1002/jemt.24223
Wilms C, Lepka K, Häberlein F, Edwards S, Felsberg J, Pudelko L, Lindenberg TT, …. Bräutigam L, Odermatt B and Berndt C. (2021) Glutaredoxin 2 promotes SP-1-dependent CSPG4 transcription and migration of wound healing NG2 glia and glioma cells: Enzymatic Taoism. Redox Biol. Online ahead of print. PMID: 34952462
Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish model. Turan F, Yilmaz Ö, Schünemann L, Lindenberg TT, Kalanithy JC, Harder A, Ahmadi S, Duman T, MacDonald RB, Winter D, Liu C, Odermatt B. J Neurosci Res. 2021 Sep 14. doi: 10.1002/jnr.24940. PMID: 34520578
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies. Genet Med. 2021 May 30. doi: 10.1038/s41436-021-01196-9. 14 September 2021. PMID: 34054129
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. Am J Hum Genet. 2019 May 2;104(5):994-1006
Rieke JM, Zhang R, Braun D, Yilmaz Ö, Japp AS, Lopes FM, Pleschka M, Hilger AC, Schneider S, Newman WG, …. Ludwig M, Schweizer U, Woolf AS, Odermatt B* and Reutter H* (2020) SLC20A1 Is involved in urinary tract and urorectal development. Front. Cell Dev. Biol. 8:567
Trnka D, Engelke AD, Gellert M, Moseler A, Hossain MF, Lindenberg TT, Pedroletti L, Odermatt B, de Souza JV, Bronowska AK, Dick TP, Mühlenhoff U, Meyer AJ, Berndt C and Lillig CH (2020) Molecular basis for the distinct functions of redox-active and FeS-transfering glutaredoxins. Nat Commun. 10;11(1):3445
Nagarajan B, Harder A, Japp A, Häberlein F, Mingardo E, Kleinert H, Yilmaz Ö, Zoons A, Rau B, Christ A, Kubitscheck U, Eiberger B, Sandhoff R, Eckhardt M, Hartmann D, Odermatt B (2019) CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch. Glia 68(3):509-527
Kolvenbach CM, Dworschak GC, …., Odermatt B* and Hilger AC* (2019). Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. Am J Hum Genet. 104:994-1006
Ralser DJ, Basmanav FB, …., Busch M, …., Frank J, Odermatt B* and Betz RC* (2017) Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa. J Clin Invest. doi: 10.1172/JCI90667
Zhang R, Knapp M, …., Schmidt JM, Winkler J, Yilmaz Ö, Pleschka M, …., Yamada G, Odermatt B and Reutter H (2017) ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development. Scientific Reports 7:42170
Baden T,Nikolaev A, Esposti F, Dreosti E, Odermatt B and Lagnado L (2014) A synaptic mechanism for temporal filtering of visual signals. PLoS Biol 21:12
Nikolaev A, Leung K-M, Odermatt B and Lagnado L (2013) Synaptic mechanisms of adaptation and sensitization in the retina. Nat Neurosci 16:934-941
Odermatt B, Nikolaev A and Lagnado L (2012) Encoding of luminance and contrast by linear and non-linear synapses in the retina. Neuron 73:758-773
Hunter PR, Nikolaou N, Odermatt B, Williams PR, Drescher U and Meyer MP (2011) Localization of Cadm2a and Cadm3 proteins during development of the zebrafish nervous system. J Comp Neurol 519:2252-2270