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Author Details
Full Name
William T Dauer
Affiliation
Peter O'Donnell Jr. Brain Institute
ORCID
Career Start Year
1988
Papers
101
H Index
39
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
35959901
The Potential for Total Worker Health® Approaches in State and Territorial Health Departments : A National Mixed-Methods Study.
J Occup Environ Med
2023
37547008
Functional interaction of torsinA and its activators in liver lipid metabolism.
bioRxiv
2023
37162852
TorsinA is essential for the timing and localization of neuronal nuclear pore complex biogenesis.
bioRxiv
2023
34686877
A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding.
Hum Mol Genet
2022
35707827
Reply to: "Letter on Discussion of Gait Research".
Mov Disord
2022
36874764
Genetic evidence of aberrant striatal synaptic maturation and secretory pathway alteration in a dystonia mouse model.
Dystonia
2022
36100089
Hepatocytes Deficient in Nuclear Envelope Protein Lamina-associated Polypeptide 1 are an Ideal Mammalian System to Study Intranuclear Lipid Droplets.
J Lipid Res
2022
34939221
Discussion of Research Priorities for Gait Disorders in Parkinson's Disease.
Mov Disord
2022
35304183
A dystonia mouse model with motor and sequencing deficits paralleling human disease.
Behav Brain Res
2022
35266954
The E3 ligase TRIM1 ubiquitinates LRRK2 and controls its localization, degradation, and toxicity.
J Cell Biol
2022
34989453
Oligodendrocyte and Extracellular Matrix Contributions to Central Nervous System Motor Function: Implications for Dystonia.
Mov Disord
2022
34312226
THAP1 modulates oligodendrocyte maturation by regulating ECM degradation in lysosomes.
Proc Natl Acad Sci U S A
2021
33616084
CNS critical periods: implications for dystonia and other neurodevelopmental disorders.
JCI Insight
2021
33529159
TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia.
J Clin Invest
2021
34248567
Heterozygous VPS13A and PARK2 Mutations in a Patient with Parkinsonism and Seizures.
Case Rep Neurol
2021
33977560
α4β2<sup>*</sup> Nicotinic Cholinergic Receptor Target Engagement in Parkinson Disease Gait-Balance Disorders.
Ann Neurol
2021
32202496
TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models.
Elife
2020
30720884
Cholinergic system changes of falls and freezing of gait in Parkinson's disease.
Ann Neurol
2019
31408437
Nuclear envelope-localized torsinA-LAP1 complex regulates hepatic VLDL secretion and steatosis.
J Clin Invest
2019
30938861
Cholinergic interneurons drive maladaptive changes in thalamostriatal circuitry after dopamine depletion.
Mov Disord
2019
29186574
TorsinA dysfunction causes persistent neuronal nuclear pore defects.
Hum Mol Genet
2018
30255936
Regional vesicular acetylcholine transporter distribution in human brain: A [<sup>18</sup> F]fluoroethoxybenzovesamicol positron emission tomography study.
J Comp Neurol
2018
30117805
A cell autonomous torsinA requirement for cholinergic neuron survival and motor control.
Elife
2018
30398673
Targeting the pedunculopontine nucleus in Parkinson's disease: Time to go back to the drawing board.
Mov Disord
2018
29472595
A motif within the armadillo repeat of Parkinson's-linked LRRK2 interacts with FADD to hijack the extrinsic death pathway.
Sci Rep
2018
29740058
Model-based and Model-free Machine Learning Techniques for Diagnostic Prediction and Classification of Clinical Outcomes in Parkinson's Disease.
Sci Rep
2018
29325615
Inherited dystonias: clinical features and molecular pathways.
Handb Clin Neurol
2018
27798115
Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth.
Hum Mol Genet
2017
28224046
Eighth International Chorea-Acanthocytosis Symposium: Summary of Workshop Discussion and Action Points.
Tremor Other Hyperkinet Mov (N Y)
2017
28242745
TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement.
J Cell Biol
2017
28673740
Forebrain knock-out of torsinA reduces striatal free-water and impairs whole-brain functional connectivity in a symptomatic mouse model of DYT1 dystonia.
Neurobiol Dis
2017
28697333
The DYT6 Dystonia Protein THAP1 Regulates Myelination within the Oligodendrocyte Lineage.
Dev Cell
2017
27734238
Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.
Cerebellum
2017
27494614
Predictive Big Data Analytics: A Study of Parkinson's Disease Using Large, Complex, Heterogeneous, Incongruent, Multi-Source and Incomplete Observations.
PLoS One
2016
27653693
Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs.
Cell Rep
2016
27619535
Endolysosomal dysfunction in Parkinson's disease: Recent developments and future challenges.
Mov Disord
2016
25739455
A novel function for the Caenorhabditis elegans torsin OOC-5 in nucleoporin localization and nuclear import.
Mol Biol Cell
2015
26477883
Clinical and scientific perspectives on movement disorders: Stanley Fahn's contributions.
Mov Disord
2015
26370418
A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation.
Hum Mol Genet
2015
26052670
Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons.
Elife
2015
26092934
Access of torsinA to the inner nuclear membrane is activity dependent and regulated in the endoplasmic reticulum.
J Cell Sci
2015
25855184
α-Synuclein-independent histopathological and motor deficits in mice lacking the endolysosomal Parkinsonism protein Atp13a2.
J Neurosci
2015
24725399
Multiplying messages LRRK beneath Parkinson disease.
Cell
2014
28845134
Parkinson's Disease: What role do pedunculopontine nucleus cholinergic neurons play?
Future Neurol
2014
25261113
Neurogenetic disease: genes, mechanisms, and future promise.
Neurotherapeutics
2014
25010278
Nuclear envelope breakdown induced by herpes simplex virus type 1 involves the activity of viral fusion proteins.
Virology
2014
25119890
The nuclear envelope: an intriguing focal point for neurogenetic disease.
Neurotherapeutics
2014
25155315
Inherited isolated dystonia: clinical genetics and gene function.
Neurotherapeutics
2014
24771397
Magic shotgun for Parkinson's disease?
Brain
2014
24895748
Author response.
Neurology
2014
1 - 50 of 101
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Argonne National Laboratory
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