Brett A. McCray

University of Michigan–Ann Arbor — United States

Neuroscience · Life Sciences

19h-index2.3kcitations47works4.52yr avg
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Research Topics

Ion Channels and Receptors(15), Hereditary Neurological Disorders(12), Ion channel regulation and function(7), Neurological diseases and metabolism(5), Hearing, Cochlea, Tinnitus, Genetics(4)

Publications47 total

Profiling the TRPV4 ankyrin repeat domain interactome and its disruption by neuromuscular disease-causing mutations
Journal of Biological Chemistry·2025Open Access
Association of the Recurrent <i>ATP1</i> <i>A1</i> Variant p.Gly549Arg With Intermediate CMT and Loss of Na,K-ATPase Function
Neurology Genetics·2025Open Access
Atypical diabetic neuropathies
BMJ·2025· 1 citedOpen Access
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of <i>PMP22</i> variants
Brain·2025· 1 cited
Clinical Outcome Assessments and Biomarkers in Charcot-Marie-Tooth Disease
Neurology·2024· 4 citedOpen Access
Exploring P2X7 receptor antagonism as a therapeutic target for neuroprotection in an hiPSC motor neuron model
Stem Cells Translational Medicine·2024· 7 citedOpen Access
Clinical Characteristics of Charcot-Marie-Tooth Disease Type 4J
Neurology·2024· 6 citedOpen Access
Combined clinical, structural and cellular studies discriminate pathogenic and benign TRPV4 variants
Brain·2024· 6 citedOpen Access
TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations
Brain·2024· 5 citedOpen Access
Gain-of-function mutations of TRPV4 acting in endothelial cells drive blood-CNS barrier breakdown and motor neuron degeneration in mice
Science Translational Medicine·2024· 20 citedOpen Access
Functional evaluation of a CMT2DD-causing ATP1A1 variant
Biophysical Journal·2024
Crosstalk between regulatory elements in disordered TRPV4 N-terminus modulates lipid-dependent channel activity
Nature Communications·2023· 44 citedOpen Access
TRPV4-Rho GTPase complex structures reveal mechanisms of gating and disease
Nature Communications·2023· 72 citedOpen Access
Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to <i>GJB1</i> variants
Brain·2023· 31 citedOpen Access
MD simulations for "TRPV4-Rho GTPase complex structures reveal mechanisms of gating and disease"
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Natural History of TRPV4-Associated Neuromuscular Disease (S7.009)
Neurology·2023
Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history
Brain·2023· 20 cited
Structural insights into TRPV4-Rho GTPase signaling complex function and disease
2023· 3 citedOpen Access
Crosstalk between regulatory elements in the disordered TRPV4 N-terminus modulates lipid-dependent channel activity
2022· 6 citedOpen Access
TRPV4: A trigger of pathological RhoA activation in neurological disease
BioEssays·2022· 31 citedOpen Access
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Frequent Co-authors

Charlotte J. Sumner(17), Steven S. Scherer(9), Michael E. Shy(9), Jeremy M. Sullivan(9), Mary M. Reilly(8), J. Paul Taylor(7), Reza Sadjadi(7), Richard S. Finkel(7), Sabrina W. Yum(7), Simone Thomas(7), Thomas E. Lloyd(7), Davide Pareyson(7), David N. Herrmann(7), Ute A. Hellmich(7), David Walk(6), Joshua Burns(6), Alexander M. Rossor(6), Jack K. Donohue(6), John Q. Trojanowski(6), Gyula Acsádi(5)