Sarah J. Brockmann
Albert Einstein Allee 11
Ulm, BW 89081, Germany
Ulm, BW 89081, Germany
Last Updated: 09/26/2026
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Found 8 publications
Multi-modal dissection of cell-type specific TDP-43 pathology in the motor cortex.
Journal: Nature communications
Published: December 10, 2024
Mitochondrial genome study in blood of maternally inherited ALS cases.
Journal: Human genomics
Published: March 01, 2023
Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease Serum.
Journal: Cells
Published: February 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis.
Journal: Brain : a journal of neurology
Published: June 24, 2019
Heterozygous Tbk1 loss has opposing effects in early and late stages of ALS in mice.
Journal: The Journal of experimental medicine
Published: April 18, 2018
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS.
Journal: Cellular and molecular life sciences : CMLS
Published: March 06, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.
Journal: Human molecular genetics
Published: October 17, 2017
Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant.
Journal: Brain : a journal of neurology
Published: September 13, 2015
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Last Updated: 09/26/2026