Simone Schröder

FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants

Diana Mitter, Milka Pringsheim, Marc Kaulisch et al. · Genetics in Medicine · 2017 · 108 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +8

Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life

Michael Lingen, Lucia Albers, Matthew Borchers et al. · Clinical Genetics · 2015 · 61 citations

Genetic Testing, Disability, Genetic Epidemiology +16

First Experiences with Laparoscopic Adjustable Gastric Banding (LAGB) in the Treatment of Patients with Childhood Craniopharyngioma and Morbid Obesity

Hermann L. Müller, U Gebhardt, van Wessel et al. · Klinische Pädiatrie · 2007 · 58 citations

Obesity, Childhood Obesity, Bariatric Surgery +11

Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy

Matthias Kettwig, Katharina Ternka, Kristin Wendland et al. · Nature Communications · 2021 · 37 citations · Full text

Quantitative Gel Electrophoresis: Sources of Variation

Simone Schröder, Hui Zhang, Edward S. Yeung et al. · Journal of Proteome Research · 2008 · 36 citations