Sarah Fehr

Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders

Björn Fischer‐Zirnsak, Lara Segebrecht, Max Schubach et al. · The American Journal of Human Genetics · 2019 · 68 citations · Full text

Neurodevelopmental Disorders, Developmental Anomaly, Developmental Biology +8

A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort

Kathrin Klein, Roman Tremmel, Stefan Winter et al. · Frontiers in Genetics · 2019 · 53 citations · Full text

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews et al. · Cell Reports · 2022 · 51 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Syndromic Autism +10

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 · 49 citations · Full text

Cell-mediated reduction of human β-defensin 1: a major role for mucosal thioredoxin

Simon U. Jaeger, Bjoern O. Schroeder, Ulf Meyer‐Hoffert et al. · Mucosal Immunology · 2013 · 47 citations · Full text