Martin Robert Turner
Affiliations: | Clinical Neurology | University of Oxford, Oxford, United Kingdom |
Area:
Clinical Neuroscience, amyotrophic lateral sclerosisWebsite:
http://oxfordmnd.clneuro.ox.ac.uk/clinic-staff/dr-martin-turnerGoogle:
"Martin Turner"Mean distance: 19.48 (cluster 51)
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Publications
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| Vahsen BF, Gray E, Thompson AG, et al. (2021) Non-neuronal cells in amyotrophic lateral sclerosis - from pathogenesis to biomarkers. Nature Reviews. Neurology |
| Thompson AG, Gray E, Mäger I, et al. (2020) CSF extracellular vesicle proteomics demonstrates altered protein homeostasis in amyotrophic lateral sclerosis. Clinical Proteomics. 17: 31 |
| Feneberg E, Gordon D, Thompson AG, et al. (2020) An ALS-linked mutation in TDP-43 disrupts normal protein interactions in the motor neuron response to oxidative stress. Neurobiology of Disease. 105050 |
| Feneberg E, Turner MR, Ansorge O, et al. (2020) Amyotrophic lateral sclerosis with a heterozygous D91A SOD1 variant and classical ALS-TDP neuropathology. Neurology |
| Wang C, Foxley S, Ansorge O, et al. (2020) Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T applied to amyotrophic lateral sclerosis. Neuroimage. 117216 |
| Gray E, Thompson AG, Wuu J, et al. (2020) CSF chitinases before and after symptom onset in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology |
| Nolan M, Scott C, Gamarallage MP, et al. (2020) Quantitative patterns of motor cortex proteinopathy across ALS genotypes. Acta Neuropathologica Communications. 8: 98 |
| Kelly M, Lavrov A, Garcia-Gancedo L, et al. (2020) The use of biotelemetry to explore disease progression markers in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-11 |
| Gray E, Oeckl P, Amador MDM, et al. (2020) A multi-center study of neurofilament assay reliability and inter-laboratory variability. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-7 |
| Ababneh NA, Scaber J, Flynn R, et al. (2020) Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair. Human Molecular Genetics |