| HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS UB Pandey, Z Nie, Y Batlevi, BA McCray, GP Ritson, NB Nedelsky, ... Nature 447 (7146), 860-864, 2007 | 1467 | 2007 |
| Disease mutations in Rab7 result in unregulated nucleotide exchange and inappropriate activation BA McCray, E Skordalakes, JP Taylor Human molecular genetics 19 (6), 1033-1047, 2010 | 142 | 2010 |
| Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes A Cortese, Y Zhu, AP Rebelo, S Negri, S Courel, L Abreu, CJ Bacon, ... Nature genetics 52 (5), 473-481, 2020 | 140 | 2020 |
| The role of autophagy in age-related neurodegeneration BA McCray, JP Taylor Neurosignals 16 (1), 75-84, 2007 | 107 | 2007 |
| Selective accumulation of aggregation-prone proteasome substrates in response to proteotoxic stress FA Salomons, V Menéndez-Benito, C Böttcher, BA McCray, JP Taylor, ... Molecular and cellular biology 29 (7), 1774-1785, 2009 | 76 | 2009 |
| Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study M Pipis, SME Feely, JM Polke, M Skorupinska, L Perez, RR Shy, M Laura, ... Brain 143 (12), 3589-3602, 2020 | 66 | 2020 |
| Network analyses reveal novel aspects of ALS pathogenesis M Sanhueza, A Chai, C Smith, BA McCray, TI Simpson, JP Taylor, ... PLoS genetics 11 (3), e1005107, 2015 | 63 | 2015 |
| TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2+ BM Woolums, BA McCray, H Sung, M Tabuchi, JM Sullivan, KT Ruppell, ... Nature communications 11 (1), 2679, 2020 | 59 | 2020 |
| Axonal Charcot-Marie-Tooth disease: from common pathogenic mechanisms to emerging treatment opportunities BA McCray, SS Scherer Neurotherapeutics 18 (4), 2269-2285, 2021 | 58 | 2021 |
| Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension BA McCray, E Diehl, JM Sullivan, WH Aisenberg, NW Zaccor, AR Lau, ... Nature communications 12 (1), 1444, 2021 | 41 | 2021 |
| TRPV4-Rho GTPase complex structures reveal mechanisms of gating and disease DH Kwon, F Zhang, BA McCray, S Feng, M Kumar, JM Sullivan, W Im, ... Nature communications 14 (1), 3732, 2023 | 38 | 2023 |
| Isolated cerebral mucormycosis of the basal ganglia AN Malik, WL Bi, B McCray, M Abedalthagafi, H Vaitkevicius, IF Dunn Clinical neurology and neurosurgery 124, 102-105, 2014 | 34 | 2014 |
| Crosstalk between regulatory elements in disordered TRPV4 N-terminus modulates lipid-dependent channel activity B Goretzki, C Wiedemann, BA McCray, SL Schäfer, J Jansen, F Tebbe, ... Nature communications 14 (1), 4165, 2023 | 28 | 2023 |
| TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of function A Taga, MA Peyton, B Goretzki, TQ Gallagher, A Ritter, A Harper, ... Annals of Clinical and Translational Neurology 9 (3), 375-391, 2022 | 24 | 2022 |
| Assessing non-Mendelian inheritance in inherited axonopathies DM Bis-Brewer, Z Gan-Or, P Sleiman, H Hakonarson, S Fazal, S Courel, ... Genetics in medicine 22 (12), 2114-2119, 2020 | 24 | 2020 |
| TRPV4: A trigger of pathological RhoA activation in neurological disease AM Bagnell, CJ Sumner, BA McCray BioEssays 44 (6), 2100288, 2022 | 21 | 2022 |
| Autosomal dominant TRPV4 disorders BA McCray, A Schindler, JE Hoover-Fong, CJ Sumner | 20 | 2020 |
| Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants CJ Record, M Skorupinska, M Laura, AM Rossor, D Pareyson, C Pisciotta, ... Brain 146 (10), 4336-4349, 2023 | 15 | 2023 |
| Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history T Rehbein, TT Wu, S Treidler, D Pareyson, R Lewis, SW Yum, BA McCray, ... Brain 146 (9), 3826-3835, 2023 | 12 | 2023 |
| Multiubiquitination of TRPV4 reduces channel activity independent of surface localization WH Aisenberg, BA McCray, JM Sullivan, E Diehl, LR DeVine, J Alevy, ... Journal of biological chemistry 298 (4), 101826, 2022 | 12 | 2022 |