Browsing by Author Kwok, John

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 20 of 22  next >
Issue DateTitleAuthor(s)Citation
2017Aging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocksKwok, John; Ames, David; Armstrong, Nicola J.; Brodaty, Henry; Mather, Karen A; Sachdev, Perminder; Schofield, P; Thalamuthu, A; Trollor, Julian N; Wright, Margaret; Central Clinical School: MedicineAging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocks, Epigenomics, vol.9, 5, 2017,pp 689-700
2008ATP-binding cassette transporter A7 regulates processing of amyloid precursor protein in vitroGarner, Brett; Rye, Kerry-Anne; Cappai, Roberto; Chan, Sharon; Hill, Andrew; Kim, Woojin; Kwok, John; School of Medical Sciences: School of Medical Sciences; Other or UnknownATP-binding cassette transporter A7 regulates processing of amyloid precursor protein in vitro, Journal of Neurochemistry, vol.106, 2, 2008,pp 793-804
2014Cerebellar Integrity in the Amyotrophic Lateral Sclerosis - Frontotemporal Dementia ContinuumKiernan, Matthew; Devenney, Emma; Dobson-Stone, Carol; Halliday, Glenda M.; Hodges, John R.; Hornberger, Michael; Kwok, John; Tan, Rachel; Central Clinical School: MedicineCerebellar Integrity in the Amyotrophic Lateral Sclerosis - Frontotemporal Dementia Continuum, PLoS One, vol.9, 8, 2014,pp e105632-N/A
2017Clinical and genetic predictors of paclitaxel neurotoxicity based on patient- versus clinicianreported incidence and severity of neurotoxicity in the ICON7 trialAsher, Rebecca; Beale, Philip; Kwok, John; Lee, Chee Khoon; Park, Susanna; Friedlander, Michael; Selle, Frederic; NH&MRC Clinical Trials Centre; Central Clinical School: Medicine; Central Clinical School: Medicine; NH&MRC Clinical Trials Centre; School of Medical Sciences: PhysiologyClinical and genetic predictors of paclitaxel neurotoxicity based on patient- versus clinicianreported incidence and severity of neurotoxicity in the ICON7 trial, Annals of Oncology, vol.28, 11, 2017,pp 2733-2740
2015Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementiaDevenney, Emma; Kiernan, Matthew; Dobson-Stone, Carol; Foxe, David; Hodges, John R.; Kwok, John; Concord Clinical School: Medicine; Central Clinical School: MedicineClinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia, Neurocase, vol.21, 4, 2015,pp 535-541
2017Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosisDobson-Stone, Carol; Halliday, Glenda; Kiernan, Matthew; Kim, Woojin; Kwok, John; Tan, Rachel; Yang, Yue; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: MedicineDistinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis, Acta Neuropathologica Communications, vol.5, 76, 2017,pp 1-7
2016Divergent Network Patterns of Amyloid-b Deposition in Logopenic and Amnestic Alzheimer's Disease PresentationsBallard, Kirrie; Leyton, Cristian; Cassidy, Ben; Hodges, John; Jones, Gareth; Kwok, John; Piquet, O; Rowe, Christopher; Villemagne, Victor; Disability and Community; Disability and CommunityDivergent Network Patterns of Amyloid-b Deposition in Logopenic and Amnestic Alzheimer's Disease Presentations, Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, vol.1, 1, 2016,pp 24-31
2014DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitroArmstrong, Nicola Joy; Brodaty, Henry; Coupland, Kirsten; Dobston-Stone, Carol; Halliday, Glenda; Hallupp, Marianne; Huang, Yue; Kim, Woojin S; Kwok, John; Mather, Karen A; Mellick, George; Sachdev, Perminder; Silburn, Peter A.; Mathematics & StatisticsDNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro, Movement Disorders, vol.29, 13, 2014,pp 1606-1614
2013DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing lossNicholson, Garth; Bird, Thomas; Dyck, Peter; Ertekin-Taner, Nilufer; Hjroth, Robert; Klein, Christopher; Kwok, John; Lincolin, Sarah; Mer, Georges; Wu, Yanhong; Concord Clinical School: ANZAC Research InstituteDNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss, Neurology, vol.80, 9, 2013,pp 824-828
2014Genetics of dementiaLoy, Clement; Kwok, John; Schofield, Peter; Turner, Anne Marie; School of Public Health: Public HealthGenetics of dementia, The Lancet, vol.383, 9919, 2014,pp 828-840
2015Genetics of hand grip strength in mid to late lifeArmstrong, Nicola Joy; Assareh, Amelia; Attia, John; Brodaty, Henry; Chan, Jessica; Hancock, Stephen; Holliday, Elizabeth G; Kwok, John; Mather, Karen A; McEvoy, Mark; Menant, Jasmine C.; Oldmeadow, Christopher; Peel, Rosanne; Reppermund, Simone; Sachdev, Perminder; Schofield, P; Scott, Rodney; Thalamuthu, Anbupalam; Trollor, Julian N; Mathematics & StatisticsGenetics of hand grip strength in mid to late life, Age, vol.37, 3, 2015,pp 1-10
2013GSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individualsKorgaonkar, Mayuresh; Williams, Leanne; Armstrong, Nicola; Dobson-Stone, Carol; Gordon, Evian; Kwok, John; Mather, Karen A; Polly, Patsie; Sachdev, Perminder; Schofield, P. R.; Wen, Wei; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium InstituteGSK3B and MAPT polymorphisms are associated with grey matter and intracranial volume in healthy individuals, PLoS One, vol.8, 8, 2013,pp 1-7
2014Heritability in frontotemporal dementia: more missing pieces?Po, Kieren; Bartley, Lauren; Burrell, James; Gracia, Natalie; Halliday, Glenda; Hodges, John; Kwok, John; Leslie, Felicity; PharmacyHeritability in frontotemporal dementia: more missing pieces?, Journal of Neurology, vol.261, 11, 2014,pp 2170-2177
2015Investigating the Genetics of Hippocampal Volume in Older Adults without DementiaArmstrong, Nicola Joy; Ames, David; Assareh, Amelia; Brodaty, Henry; Duesing, Konsta; Kwok, John; Mather, Karen A; Reppermund, Simone; Sachdev, Perminder; Schofield, P; Thalamuthu, Anbupalam; Trollor, Julian N; Wen, Wei; Wright, Margaret; Mathematics & StatisticsInvestigating the Genetics of Hippocampal Volume in Older Adults without Dementia, PloS One, vol.10, 1, 2015,pp 1-12
2014Paclitaxel-induced neuropathy: potential association of MAPT and GSK3B genotypesKiernan, Matthew; Loy, Clement; Park, Susanna; Friedlander, Michael; Krishnan, Arun V; Kwok, John; Lewis, Craig; Lin, Cindy S.-Y; Central Clinical School: Medicine; School of Public Health: Public Health; School of Medical Sciences: PhysiologyPaclitaxel-induced neuropathy: potential association of MAPT and GSK3B genotypes, BMC Cancer, vol.14, N/A, 2014,pp 1-5
2008Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9Nicholson, Garth; Blumbergs, Peter C.; Brooks, William; Dobson-Stone, Carol; Halliday, Glenda; Hecker, Jane; Kwok, John; Loy, Clement; Luty, Agnes; Panegyres, Peter; Schofield, Peter; Thompson, Elizabeth; Concord Clinical School: ANZAC Research InstitutePedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9, BMC Neurology, vol.8, 32, 2008,pp 1-11
2004Positional Effects Of Presenilin-1 Mutations On Tau Phosphorylation In Cortical Plaques.Kril, Jillian; Shepherd, Claire; Brooks, William S.; Gregory, Gillian C.; Halliday, Glenda M.; Kwok, John; Schofield, Peter R; Vickers, James C.; Concord Clinical School: ANZAC Research Institute; Central Clinical School: MedicinePositional Effects Of Presenilin-1 Mutations On Tau Phosphorylation In Cortical Plaques., Neurobiology of Disease, vol.15,(1),2004,pp 115-119
2015Progression in Behavioral Variant Frontotemporal Dementia: A Longitudinal StudyKiernan, Matthew; Bartley, Lauren; Devenney, Emma; Halliday, Glenda M.; Hodges, John R.; Hoon, Christopher; Hornberger, Michael; Kumfor, Fiona; Kwok, John; O'Callaghan, Claire; Piguet, Oliver; Central Clinical School: MedicineProgression in Behavioral Variant Frontotemporal Dementia: A Longitudinal Study, JAMA Neurology, vol.72, 12, 2015,pp 1501-1509
2010Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron diseaseBlair, Ian; Barcikowsk, Maria; Brooks, William; Coupland, Kirsten; Dobson-Stone, Carol; Halliday, Glenda; Karlstrom, Helena; Kwok, John; Loy, Clement; Luty, Agnes; Maruszak, Aleksandra; Mather, Karen A; Panegyres, Peter; Sachdev, Perminder; Schofield, Peter R.; Sobow, Tomasz; Tchorzewska, Joanna; Williams, Kelly; Zekanowski, Cezary; Concord Clinical School: ANZAC Research InstituteSigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease, Annals of Neurology, vol.68, 5,pp 639-649
2016TDP-43 in the hypoglossal nucleus identifies amyotrophic lateral sclerosis in behavioral variant frontotemporal dementiaKiernan, Matthew; Kril, Jillian; Mito, Remika; Bartley, Lauren; Dobson-Stone, Carol; Halliday, Glenda; Hasegawa, Masato; Hodges, John; Hornberger, Michael; Kwok, John; Masuda-Suzukake, Masami; McCann, Heather; Tan, Rachel; Central Clinical School: Medicine; Central Clinical School: Medicine; School of Medical Sciences: PathologyTDP-43 in the hypoglossal nucleus identifies amyotrophic lateral sclerosis in behavioral variant frontotemporal dementia, Journal of the Neurological Sciences, vol.366, N/A, 2016,pp 197-201