Genetics of dementia
Loy, Clement T, FRACP, Schofield, Peter R, Prof, Turner, Anne M, FRACP, Kwok, John BJ, Dr
Published in The Lancet (British edition) (01.03.2014)
Published in The Lancet (British edition) (01.03.2014)
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Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease
Coupland, Kirsten G, Kim, Woojin S, Halliday, Glenda M, Hallupp, Marianne, Dobson-Stone, Carol, Kwok, John B J
Published in PloS one (23.06.2016)
Published in PloS one (23.06.2016)
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DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro
Coupland, Kirsten G., Mellick, George D., Silburn, Peter A., Mather, Karen, Armstrong, Nicola J., Sachdev, Perminder S., Brodaty, Henry, Huang, Yue, Halliday, Glenda M., Hallupp, Marianne, Kim, Woojin S., Dobson-Stone, Carol, Kwok, John B.J.
Published in Movement disorders (01.11.2014)
Published in Movement disorders (01.11.2014)
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The underacknowledged PPA-ALS: A unique clinicopathologic subtype with strong heritability
Tan, Rachel H, Guennewig, Boris, Dobson-Stone, Carol, Kwok, John B J, Kril, Jillian J, Kiernan, Matthew C, Hodges, John R, Piguet, Olivier, Halliday, Glenda M
Published in Neurology (19.03.2019)
Published in Neurology (19.03.2019)
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C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts
Dobson-Stone, Carol, Hallupp, Marianne, Bartley, Lauren, Shepherd, Claire E, Halliday, Glenda M, Schofield, Peter R, Hodges, John R, Kwok, John B J
Published in Neurology (04.09.2012)
Published in Neurology (04.09.2012)
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Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies
Forrest, Shelley L, Kril, Jillian J, Stevens, Claire H, Kwok, John B, Hallupp, Marianne, Kim, Woojin S, Huang, Yue, McGinley, Ciara V, Werka, Hellen, Kiernan, Matthew C, Götz, Jürgen, Spillantini, Maria Grazia, Hodges, John R, Ittner, Lars M, Halliday, Glenda M
Published in Brain (London, England : 1878) (01.02.2018)
Published in Brain (London, England : 1878) (01.02.2018)
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TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes
Tan, Rachel H, Kril, Jillian J, Fatima, Manaal, McGeachie, Andrew, McCann, Heather, Shepherd, Claire, Forrest, Shelley L, Affleck, Andrew, Kwok, John B J, Hodges, John R, Kiernan, Matthew C, Halliday, Glenda M
Published in Brain (London, England : 1878) (01.10.2015)
Published in Brain (London, England : 1878) (01.10.2015)
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C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients
Dobson-Stone, Carol, Hallupp, Marianne, Loy, Clement T, Thompson, Elizabeth M, Haan, Eric, Sue, Carolyn M, Panegyres, Peter K, Razquin, Cristina, Seijo-Martínez, Manuel, Rene, Ramon, Gascon, Jordi, Campdelacreu, Jaume, Schmoll, Birgit, Volk, Alexander E, Brooks, William S, Schofield, Peter R, Pastor, Pau, Kwok, John B J
Published in PloS one (20.02.2013)
Published in PloS one (20.02.2013)
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Reduced glucocerebrosidase activity in monocytes from patients with Parkinson’s disease
Atashrazm, Farzaneh, Hammond, Deborah, Perera, Gayathri, Dobson-Stone, Carol, Mueller, Nicole, Pickford, Russell, Kim, Woojin Scott, Kwok, John B., Lewis, Simon J. G., Halliday, Glenda M., Dzamko, Nicolas
Published in Scientific reports (18.10.2018)
Published in Scientific reports (18.10.2018)
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A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome
Porter, Melanie A, Dobson-Stone, Carol, Kwok, John B J, Schofield, Peter R, Beckett, William, Tassabehji, May
Published in PloS one (31.10.2012)
Published in PloS one (31.10.2012)
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GSK3B polymorphisms alter transcription and splicing in Parkinson's disease
Kwok, John B. J., Hallupp, Marianne, Loy, Clement T., Chan, Daniel K. Y., Woo, Jean, Mellick, George D., Buchanan, Daniel D., Silburn, Peter A., Halliday, Glenda M., Schofield, Peter R.
Published in Annals of neurology (01.12.2005)
Published in Annals of neurology (01.12.2005)
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Heritability in frontotemporal dementia: more missing pieces?
Po, Kieren, Leslie, Felicity V. C., Gracia, Natalie, Bartley, Lauren, Kwok, John B. J., Halliday, Glenda M., Hodges, John R., Burrell, James R.
Published in Journal of neurology (01.11.2014)
Published in Journal of neurology (01.11.2014)
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The complex relationship between genotype, pathology and phenotype in familial dementia
Kwok, John B., Loy, Clement T., Dobson-Stone, Carol, Halliday, Glenda M.
Published in Neurobiology of disease (01.11.2020)
Published in Neurobiology of disease (01.11.2020)
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Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease
Luty, Agnes A., Kwok, John B.J., Dobson-Stone, Carol, Loy, Clement T., Coupland, Kirsten G., Karlström, Helena, Sobow, Tomasz, Tchorzewska, Joanna, Maruszak, Aleksandra, Barcikowska, Maria, Panegyres, Peter K., Zekanowski, Cezary, Brooks, William S., Williams, Kelly L., Blair, Ian P., Mather, Karen A., Sachdev, Perminder S., Halliday, Glenda M., Schofield, Peter R.
Published in Annals of neurology (01.11.2010)
Published in Annals of neurology (01.11.2010)
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