Sandrina Weber

Monogenic variants in dystonia: an exome-wide sequencing study

Michael Zech, Robert Jech, Sylvia Boesch et al. · The Lancet Neurology · 2020 · 206 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

<i>De novo</i> variants in neurodevelopmental disorders—experiences from a tertiary care center

Theresa Brunet, Robert Jech, Melanie Brügger et al. · Clinical Genetics · 2021 · 111 citations · Full text

Neurogenomics, Brain Development, Genetics +28

Clinical exome sequencing in early‐onset generalized dystonia and large‐scale resequencing follow‐up

Michael Zech, Sylvia Boesch, Angela Jochim et al. · Movement Disorders · 2016 · 110 citations

Accurate Detection of <scp>α‐Synuclein</scp> Seeds in Cerebrospinal Fluid from Isolated Rapid Eye Movement Sleep Behavior Disorder and Patients with Parkinson's Disease in the DeNovo Parkinson (DeNoPa) Cohort

Luis Concha‐Marambio, Sandrina Weber, Carly M. Farris et al. · Movement Disorders · 2023 · 96 citations · Full text

Plasma proteomics identify biomarkers predicting Parkinson’s disease up to 7 years before symptom onset

Jenny Hällqvist, Michael Bartl, Mohammed Dakna et al. · Nature Communications · 2024 · 81 citations · Full text