Björn Schulte

Trio exome sequencing is highly relevant in prenatal diagnostics

Heinz Gabriel, Dirk Korinth, M Ritthaler et al. · Prenatal Diagnosis · 2021 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Marcello Scala, Masashi Nishikawa, Hidenori Ito et al. · Brain · 2022 · 51 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss

Anke Tropitzsch, Thore Schade‐Mann, Philipp Gamerdinger et al. · Ear and Hearing · 2023 · 51 citations · Full text

Medicine, Audiology, Otolaryngology +17

Diagnostic Yield of Targeted Hearing Loss Gene Panel Sequencing in a Large German Cohort With a Balanced Age Distribution from a Single Diagnostic Center: An Eight-year Study

Anke Tropitzsch, Thore Schade‐Mann, Philipp Gamerdinger et al. · Ear and Hearing · 2021 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Aberrant <i>COL11A1</i> splicing causes prelingual autosomal dominant nonsyndromic hearing loss in the DFNA37 locus

Abolfazl Rad, Thore Schade‐Mann, Philipp Gamerdinger et al. · Human Mutation · 2020 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14