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Sebastian Rösch

15PUBLICATIONS

43CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Memory and attentionGene expression (incl. microarray and other genome-wide approaches)Optical technologyLinguistic structures (incl. phonology, morphology and syntax)

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Publications (15)

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|Mar 23, 2025

Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct.

Emanuele Bernardinelli, Raffaella Liuni, Rapolas Jamontas

|May 01, 2024

Eye movements track prioritized auditory features in selective attention to natural speech.

Quirin Gehmacher, Juliane Schubert, Fabian Schmidt

|Feb 24, 2024

Mutational spectrum in patients with dominant non-syndromic hearing loss in Austria.

Alexandra Frohne, Sybille Vrabel, Franco Laccone

|Jun 28, 2023

Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.

Emanuele Bernardinelli, Florian Huber, Sebastian Roesch

|Jun 23, 2023

Neural speech tracking shifts from the syllabic to the modulation rate of speech as intelligibility decreases.

Fabian Schmidt, Ya-Ping Chen, Anne Keitel

|May 23, 2023

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

Laurence Jonard, Davide Brotto, Miguel A Moreno-Pelayo

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Frequent Collaborators

6 joint publications

Silvia Dossena

2 joint publications

Nina Suess

2 joint publications

Fabian Schmidt

2 joint publications

Emanuele Bernardinelli

2 joint publications

Patrick Reisinger

2 joint publications

Quirin Gehmacher

2 joint publications

Nathan Weisz

1 joint publications

Gerd Rasp

1 joint publications

Zippora Brownstein

1 joint publications

Miguel A Moreno-Pelayo

Frequent Collaborators

6 joint publications

Silvia Dossena

2 joint publications

Nina Suess

2 joint publications

Fabian Schmidt

2 joint publications

Emanuele Bernardinelli

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