Veröffentlichungen
2026
MedRxiv [Preprint]. 04. February 2026. doi: 10.64898/2026.01.28.26344748
XPOT Deficiency causes a human disorder through impaired tRNA nuclear export von Hardenberg S, Niehaus I, Wiemers A, Rothoeft T, Huang K, Petree C, Schäffer V, Phillipe C, Bruel AL, Warnatz K, Zamani M, Ahmadi R, Sedaghat A, Bahram S, Sedighzadeh S, Ebrahimi S, Khalilian S, Landwehr-Kenzel S, Schwerk N, Elsayed A, Rösler J, Lin SJ, Sabu S, Strenzke N, Sogkas G, Vona B, Varshney GK, Di Donato N, Auber B
2025
EMBO Mol Med. 09. December 2025. doi: 10.1038/s44321-025-00350-z
Channelrhodopsin variants for high-rate optogenetic neurostimulation at low light intensities Roos L, Garrido-Charles A, Albrecht N, Vavakou A, Alekseev A, Bleyer M, Thirumalai A, Mittring A, Alvanos T, Huet AT, Bamberg E, Kusch K, Wolf BJ, Moser T, Mager T
BioRxiv [Preprint]. 17. November 2025. doi: 10.1101/2025.11.16.688700
CochleaNet: deep learning-based image analysis for cochlear connectomics and gene therapy Roos L, Miraç Diniz A, Koert E, Schilling M, Uhl M, Thirumalai A, Aakhte M, Kusch K, Huisken J, Moser T, Pape C
Sci Adv. 17. October 2025. doi: 10.1126/sciadv.ady8532
Structure and function of otoferlin, a synaptic protein of sensory hair cells essential for hearing Chen H, Cretu C, Trebilcock A, Evdokimova N, Babai N, Feldmann L, Leidner F, Benseler F, Mutschall S, Esch K, Szabo CZK, Pena V, Pape C, Grubmüller H, Strenzke N, Brose N, Wichmann C, Preobraschenski J, Moser T
Med. 01. October 2025. doi: 10.1016/j.medj.2025.100886
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials Fan X, Gao Z, Zhong J, Chen Y, Chen X, Landegger LD, Moser T, Zeng FG, Sun Y, Jin X, Nash R, Chien WW, Jiang D, Greinwald JH, Bance M, Rodríguez MM, Lee SY, Feng G, Yang H, Wu CC, Xu L, Yuan W, Feng Y, Zhao Y, Vona B, Strenzke N, Beutner D, Amin N, Arwyn-Jones J, Chandrasekeharan D, Shi D, Zhang D, Yang J, Qi J, Wang Q, Yin Y, Cheng YF, Tao Y, Yu Y, Wang D, Jiang L, Guo L, Chen L, Cheng X, Cui C, Lv J, Han S, Wang W, Li Y, Gao X, Liu XZ, Zha D, Shi H, Chen B, Wang Q, Yuan H, Yang S, Yin S, Wu H, Wang Z, Li H, Rubinstein JT, Lustig LR, Chai R, Chen ZY, Shu Y
Mol Biol Cell. 28. August 2025. doi: 10.1091/mbc.E24-11-0519
SynapseNet: Deep Learning for Automatic Synapse Reconstruction Muth S, Moschref F, Freckmann L, Mutschall S, Hojas-Garcia-Plaza I, Bahr JN, Petrovic A, Do TT, Schwarze V, Archit A, Weyand K, Michanski S, Maus L, Imig C, Hintze A, Brose N, Wichmann C, Fernandez-Busnadiego R, Moser T, Rizzoli SO, Cooper BH, Pape C
Mol Diagn Ther. 01. July 2025. doi: 10.1007/s40291-025-00782-w
Recurrent and Novel Pathogenic Variants in Genes Involved with Hearing Loss in the Pakistani Population Shadab M, Ben-Mahmoud A, Martínez Völter LN, Abbasi AA, Ku B, Ejaz A, Latif Z, Gupta V, Owrang D, Jang MH, Zhang Z, Mohammad R, Houlden H, Kim HG, Vona B
medRxiv [Preprint]. 28. June 2025. doi: 10.1101/2025.06.26.25330137
Domain specific phenotypic expansion associated with variants in MACF1 Gogate N, Jolly A, Rosenfeld JA, Bahena-Carbajal P, Bernstein JA, Bonner D, Busa T, Cristian I, D'Souza P, Friedman J, Gorokhova S, Haaf T, Herman I, Isin UU, Jhangiani SN, Johnson I, Lenberg J, Macnamara EF, Maroofian R; Undiagnosed Diseases Network, Melissa Racobaldo; Redlich OL, Tifft C, Tos T, Vona B, Zambrano RM, Wentzensen IM, Wigby K, Pehlivan D, Gibbs RA, Lupski JR, Posey JE