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Journal articles | 2023
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Journal articles | 2023
Luckett PH; Chen C; Gordon BA; Wisch J; Berman SB; Chhatwal JP; Cruchaga C; Fagan AM; Farlow MR; Fox NC; Jucker M; Levin J; Masters CL; Mori H; Noble JM; Salloway S; Schofield PR; Brickman AM; Brooks WS; Cash DM; Fulham MJ; Ghetti B; Jack CR; Vöglein J; Klunk WE; Koeppe R; Su Y; Weiner M; Wang Q; Marcus D; Koudelis D; Joseph-Mathurin N; Cash L; Hornbeck R; Xiong C; Perrin RJ; Karch CM; Hassenstab J; McDade E; Morris JC; Benzinger TLS; Bateman RJ; Ances BM, 2023, 'Biomarker clustering in autosomal dominant Alzheimer's disease', Alzheimer's and Dementia, 19, pp. 274 - 284, http://dx.doi.org/10.1002/alz.12661
Journal articles | 2023
McKay NS; Gordon BA; Hornbeck RC; Dincer A; Flores S; Keefe SJ; Joseph-Mathurin N; Jack CR; Koeppe R; Millar PR; Ances BM; Chen CD; Daniels A; Hobbs DA; Jackson K; Koudelis D; Massoumzadeh P; McCullough A; Nickels ML; Rahmani F; Swisher L; Wang Q; Allegri RF; Berman SB; Brickman AM; Brooks WS; Cash DM; Chhatwal JP; Day GS; Farlow MR; la Fougère C; Fox NC; Fulham M; Ghetti B; Graff-Radford N; Ikeuchi T; Klunk W; Lee JH; Levin J; Martins R; Masters CL; McConathy J; Mori H; Noble JM; Reischl G; Rowe C; Salloway S; Sanchez-Valle R; Schofield PR; Shimada H; Shoji M; Su Y; Suzuki K; Vöglein J; Yakushev I; Cruchaga C; Hassenstab J; Karch C; McDade E; Perrin RJ; Xiong C; Morris JC; Bateman RJ; Benzinger TLS; Brickman AM; la Fougère C, 2023, 'Positron emission tomography and magnetic resonance imaging methods and datasets within the Dominantly Inherited Alzheimer Network (DIAN)', Nature Neuroscience, 26, pp. 1449 - 1460, http://dx.doi.org/10.1038/s41593-023-01359-8
Journal articles | 2023
Xu Y; Aung HL; Bateman RJ; Brooks WS; Chhatwal J; Day GS; Fagan AM; Farlow MR; Gordon B; Kehoe PG; Levin J; Mori H; Morris JC; Wharton W; Humburg P; Schofield PR; Peters R, 2023, 'Higher systolic blood pressure in early-mid adulthood is associated with poorer cognitive performance in those with a dominantly inherited Alzheimer's disease mutation but not in non-carriers. Results from the DIAN study', Alzheimer's and Dementia, http://dx.doi.org/10.1002/alz.13082
Journal articles | 2022
Aschenbrenner AJ; Hassenstab J; Wang G; Li Y; Xiong C; McDade E; Clifford DB; Salloway S; Farlow M; Yaari R; Cheng EYJ; Holdridge KC; Mummery CJ; Masters CL; Hsiung GY; Surti G; Day GS; Weintraub S; Honig LS; Galvin JE; Ringman JM; Brooks WS; Fox NC; Snyder PJ; Suzuki K; Shimada H; Gräber S; Bateman RJ, 2022, 'Avoid or Embrace? Practice Effects in Alzheimer’s Disease Prevention Trials', Frontiers in Aging Neuroscience, 14, http://dx.doi.org/10.3389/fnagi.2022.883131
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Journal articles | 2022
Joseph-Mathurin N; Llibre-Guerra JJ; Li Y; McCullough AA; Hofmann C; Wojtowicz J; Park E; Wang G; Preboske GM; Wang Q; Gordon BA; Chen CD; Flores S; Aggarwal NT; Berman SB; Bird TD; Black SE; Borowski B; Brooks WS; Chhatwal JP; Clarnette R; Cruchaga C; Fagan AM; Farlow M; Fox NC; Gauthier S; Hassenstab J; Hobbs DA; Holdridge KC; Honig LS; Hornbeck RC; Hsiung GYR; Jack CR; Jimenez-Velazquez IZ; Jucker M; Klein G; Levin J; Mancini M; Masellis M; McKay NS; Mummery CJ; Ringman JM; Shimada H; Snider BJ; Suzuki K; Wallon D; Xiong C; Yaari R; McDade E; Perrin RJ; Bateman RJ; Salloway SP; Benzinger TLS; Clifford DB, 2022, 'Amyloid-Related Imaging Abnormalities in the DIAN-TU-001 Trial of Gantenerumab and Solanezumab: Lessons from a Trial in Dominantly Inherited Alzheimer Disease', Annals of Neurology, 92, pp. 729 - 744, http://dx.doi.org/10.1002/ana.26511
Journal articles | 2022
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Journal articles | 2022
Morenas-Rodríguez E; Li Y; Nuscher B; Franzmeier N; Xiong C; Suárez-Calvet M; Fagan AM; Schultz S; Gordon BA; Benzinger TLS; Hassenstab J; McDade E; Feederle R; Karch CM; Schlepckow K; Morris JC; Kleinberger G; Nellgard B; Vöglein J; Blennow K; Zetterberg H; Ewers M; Jucker M; Levin J; Bateman RJ; Haass C; Adams S; Allegri R; Araki A; Barthelemy N; Bechara J; Berman S; Bodge C; Brandon S; Brooks W; Brosch J; Buck J; Buckles V; Carter K; Cash L; Chen C; Chhatwal J; Chrem P; Chua J; Chui H; Cruchaga C; Day GS; De La Cruz C; Denner D; Diffenbacher A; Dincer A; Donahue T; Douglas J; Duong D; Egido N; Esposito B; Farlow M; Feldman B; Fitzpatrick C; Flores S; Fox N; Franklin E; Friedrichsen N; Fujii H; Gardener S; Ghetti B; Goate A; Goldberg S; Goldman J; Gonzalez A; Gräber-Sultan S; Graff-Radford N; Graham M; Gray J; Gremminger E; Grilo M; Groves A; Häsler L; Hellm C; Herries E; Hoechst-Swisher L; Hofmann A; Holtzman D; Hornbeck R; Igor Y; Ihara R; Ikeuchi T; Ikonomovic S; Ishii K; Jack C; Jerome G; Johnson E; Käser S; Kasuga K; Keefe S; Klunk W; Koeppe R; Koudelis D; Kuder-Buletta E; Laske C, 2022, 'Soluble TREM2 in CSF and its association with other biomarkers and cognition in autosomal-dominant Alzheimer's disease: a longitudinal observational study', The Lancet Neurology, 21, pp. 329 - 341, http://dx.doi.org/10.1016/S1474-4422(22)00027-8
Journal articles | 2021
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Journal articles | 2021
Joseph-Mathurin N; Llibre-Guerra JJ; McCullough AA; Li Y; Hofmann C; Wojtowicz J; Wang Q; Wang G; Gordon BA; Chen CD; Brooks WS; Gauthier S; Holdridge KC; Hsiung G-YR; Jack CR; Klein G; Masellis M; Mummery CJ; Preboske GM; Santacruz A; Wallon D; Xiong C; Yaari R; McDade E; Bateman RJ; Salloway SP; Benzinger TLS; Clifford DB, 2021, 'Characterization of amyloid-related imaging abnormality in the DIAN-TU-001 trial', ALZHEIMERS & DEMENTIA, 17, http://dx.doi.org/10.1002/alz.056393
Journal articles | 2021
Joseph-Mathurin N; Wang G; Kantarci K; Jack CR; Mcdade E; Hassenstab J; Blazey TM; Gordon BA; Su Y; Chen G; Massoumzadeh P; Hornbeck RC; Allegri RF; Ances BM; Berman SB; Brickman AM; Brooks WS; Cash DM; Chhatwal JP; Chui HC; Correia S; Cruchaga C; Farlow MR; Fox NC; Fulham M; Ghetti B; Graff-Radford NR; Johnson KA; Karch CM; Laske C; Lee AKW; Levin J; Masters CL; Noble JM; O'connor A; Perrin RJ; Preboske GM; Ringman JM; Rowe CC; Salloway S; Saykin AJ; Schofield PR; Shimada H; Shoji M; Suzuki K; Villemagne VL; Xiong C; Yakushev I; Morris JC; Bateman RJ; Benzinger TLS, 2021, 'Longitudinal Accumulation of Cerebral Microhemorrhages in Dominantly Inherited Alzheimer Disease', Neurology, 96, pp. E1632 - E1645, http://dx.doi.org/10.1212/WNL.0000000000011542
Journal articles | 2021
Keret O; Staffaroni AM; Ringman JM; Cobigo Y; Goh SYM; Wolf A; Allen IE; Salloway S; Chhatwal J; Brickman AM; Reyes-Dumeyer D; Bateman RJ; Benzinger TLS; Morris JC; Ances BM; Joseph-Mathurin N; Perrin RJ; Gordon BA; Levin J; Vöglein J; Jucker M; la Fougère C; Martins RN; Sohrabi HR; Taddei K; Villemagne VL; Schofield PR; Brooks WS; Fulham M; Masters CL; Ghetti B; Saykin AJ; Jack CR; Graff-Radford NR; Weiner M; Cash DM; Allegri RF; Chrem P; Yi S; Miller BL; Rabinovici GD; Rosen HJ, 2021, 'Pattern and degree of individual brain atrophy predicts dementia onset in dominantly inherited Alzheimer's disease', Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 13, http://dx.doi.org/10.1002/dad2.12197
Journal articles | 2021
Luckett PH; McCullough A; Gordon BA; Strain J; Flores S; Dincer A; McCarthy J; Kuffner T; Stern A; Meeker KL; Berman SB; Chhatwal JP; Cruchaga C; Fagan AM; Farlow MR; Fox NC; Jucker M; Levin J; Masters CL; Mori H; Noble JM; Salloway S; Schofield PR; Brickman AM; Brooks WS; Cash DM; Fulham MJ; Ghetti B; Jack CR; Vöglein J; Klunk W; Koeppe R; Oh H; Su Y; Weiner M; Wang Q; Swisher L; Marcus D; Koudelis D; Joseph-Mathurin N; Cash L; Hornbeck R; Xiong C; Perrin RJ; Karch CM; Hassenstab J; McDade E; Morris JC; Benzinger TLS; Bateman RJ; Ances BM, 2021, 'Modeling autosomal dominant Alzheimer's disease with machine learning', Alzheimer's and Dementia, 17, pp. 1005 - 1016, http://dx.doi.org/10.1002/alz.12259
Journal articles | 2021
Pichet Binette A; Vachon-Presseau É; Morris JC; Bateman RJ; Benzinger T; Collins DL; Poirier J; Breitner JCS; Villeneuve S; Allegri R; Amtashar F; Berman S; Bodge C; Brandon S; Brooks W; Buck J; Buckles V; Chea S; Chhatwal J; Chrem P; Chui H; Cinco J; Clifford J; Cruchaga C; D‘Mello M; Donahue T; Douglas J; Edigo N; Erekin-Taner N; Fagan A; Farlow M; Farrar A; Feldman H; Flynn G; Fox N; Franklin E; Fujii H; Gant C; Gardener S; Ghetti B; Goate A; Goldman J; Gordon B; Graff-Radford N; Gray J; Gurney J; Hassenstab J; Hirohara M; Holtzman D; Hornbeck R; DiBari SH; Ikeuchi T; Ikonomovic S; Jerome G; Jucker M; Karch C; Kasuga K; Kawarabayashi T; Klunk W; Koeppe R; Kuder-Buletta E; Laske C; Lee JH; Levin J; Marcus D; Martins R; Mason NS; Masters C; Maue-Dreyfus D; McDade E; Montoya L; Mori H; Nagamatsu A; Neimeyer K; Noble J; Norton J; Perrin R; Raichle M; Ringman J; Roh JH; Salloway S; Schofield P; Shimada H; Shiroto T; Shoji M; Sigurdson W; Sohrabi H; Sparks P; Suzuki K; Swisher L; Taddei K; Wang J; Wang P; Weiner M; Wolfsberger M; Xiong C; Xu X; Tam A; Labonté A; Faubert AM, 2021, 'Amyloid and Tau Pathology Associations With Personality Traits, Neuropsychiatric Symptoms, and Cognitive Lifestyle in the Preclinical Phases of Sporadic and Autosomal Dominant Alzheimer's Disease', Biological Psychiatry, 89, pp. 776 - 785, http://dx.doi.org/10.1016/j.biopsych.2020.01.023
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Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Brooks William S. BS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Waldö ML; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; Van der Zee J; Deschamps W; Van Langenhove T; Cruts M; Van Broeckhoven C; Cappa SF; Le Ber I; Hannequin D; Golfier V; Vercelletto M; Brice A; Nacmias B; Sorbi S; Bagnoli S; Piaceri I; Nielsen JE; Hjermind LE; Riemenschneider M; Mayhaus M; Ibach B; Gasparoni G; Pichler S; Gu W; Rossor MN, 2014, 'Frontotemporal dementia and its subtypes: A genome-wide association study', The Lancet Neurology, 13, pp. 686 - 699, http://dx.doi.org/10.1016/S1474-4422(14)70065-1
Journal articles | 2014
Gallagher MD; Suh E; Grossman M; Elman L; McCluskey L; Van Swieten JC; Al-Sarraj S; Neumann M; Gelpi E; Ghetti B; Rohrer JD; Halliday G; Van Broeckhoven C; Seilhean D; Shaw PJ; Frosch MP; Alafuzoff I; Antonell A; Bogdanovic N; Brooks W; Cairns NJ; Cooper-Knock J; Cotman C; Cras P; Cruts M; De Deyn PP; Decarli C; Dobson-Stone C; Engelborghs S; Fox N; Galasko D; Gearing M; Gijselinck I; Grafman J; Hartikainen P; Hatanpaa KJ; Highley JR; Hodges J; Hulette C; Ince PG; Jin LW; Kirby J; Kofler J; Kril J; Kwok JBJ; Levey A; Lieberman A; Llado A; Martin JJ; Masliah E; McDermott CJ; McKee A; McLean C; Mead S; Miller CA; Miller J; Munoz DG; Murrell J; Paulson H; Piguet O; Rossor M; Sanchez-Valle R; Sano M; Schneider J; Silbert LC; Spina S; Van Der Zee J; Van Langenhove T; Warren J; Wharton SB; White CL; Woltjer RL; Trojanowski JQ; Lee VMY; Van Deerlin V; Chen-Plotkin AS, 2014, 'TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions', Acta Neuropathologica, 127, pp. 407 - 418, http://dx.doi.org/10.1007/s00401-013-1239-x
Journal articles | 2013
Dobson-Stone C; Hallupp M; Loy CT; Thompson EJ; Haan E; Sue C; Panegyres P; Razquin C; Seijo-Martínez M; Rene R; Gascon J; Campdelacreu J; Schmoll B; Volk AE; Brooks WS; Schofield PR; Pastor P; Kwok J, 2013, 'C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients', PLoS ONE, 8, pp. e56899, http://dx.doi.org/10.1371/journal.pone.0056899
Journal articles | 2013
Dobson-Stone C; Luty A; Thompson EM; Blumbergs P; Brooks WS; Short CL; Field C; Panegyres P; Hecker J; Solski JA; Blair I; Fullerton JM; Halliday GM; Schofield PR; Kwok J, 2013, 'Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: Genetic, clinical and neuropathological analysis', ACTA Neuropathologica, 125, pp. 523 - 533, http://dx.doi.org/10.1007/s00401-013-1078-9
Journal articles | 2013
Mills SM; Mallmann J; Santacruz AM; Fuqua A; Carril M; Aisen PS; Althage MC; Belyew S; Benzinger TL; Brooks WS; Buckles VD; Cairns NJ; Clifford D; Danek A; Fagan AM; Farlow M; Fox N; Ghetti B; Goate AM; Heinrichs D; Hornbeck R; Jack C; Jucker M; Klunk WE; Marcus DS; Martins RN; Masters CM; Mayeux R; McDade E; Morris JC; Oliver A; Ringman JM; Rossor MN; Salloway S; Schofield PR; Snider J; Snyder P; Sperling RA; Stewart C; Thomas RG; Xiong C; Bateman RJ, 2013, 'Erratum: Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial (Rev. Neurol. (2013) 169 (10) (737-743))', Revue Neurologique, 169, pp. 1018, http://dx.doi.org/10.1016/j.neurol.2013.10.005
Journal articles | 2013
Mills SM; Mallmann J; Santacruz AM; Fuqua A; Carril M; Aisen PS; Althage MC; Belyew S; Benzinger TL; Brooks WS; Buckles VD; Cairns NJ; Clifford D; Danek A; Fagan AM; Farlow M; Fox N; Ghetti B; Goate AM; Heinrichs D; Hornbeck R; Jack C; Jucker M; Klunk WE; Marcus DS; Martins RN; Masters CM; Mayeux R; McDade E; Morris JC; Oliver A; Ringman JM; Rossor MN; Salloway S; Schofield PR; Snider J; Snyder P; Sperling RA; Stewart C; Thomas RG; Xiong C; Bateman RJ, 2013, 'Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial', Revue Neurologique, 169, pp. 737 - 743, http://dx.doi.org/10.1016/j.neurol.2013.07.017
Journal articles | 2011
Chen-Plotkin A; Martinez-Lage M; Sleiman PMA; Hu W; Greene R; Wood EF; Bing S; Grossman M; Schellenberg GD; Hatanpaa K; Weiner M; White III CL; Brooks WS; Halliday GM; Kril JJ; Gearing M; Beach T; Graff-radford N; Dickson D; Rademakers R; Boeve B; Pickering-Brown SM; Snowden J; Van Swieten JC; Heutink P; Seelaar H; Murrell J; Ghetti B; Spina S; Grafman J; Kaye JA; Woltjer RL; Mesulam M; Bigio EH; Llado A; Miller B; Alzualde A; Moreno FS; Rohrer JD; Mackenzie IRA; Feldman H; Hamilton RL; Cruts M; Engelborghs ; De Deyn PP; Van Broeckhoven C; Bird T; Cairns NJ; Goate A; Frosch MP; Riederer PF; Bogdanovic N; Lee VM; Trojanowski JQ; Van deerlin VM, 2011, 'Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration', Archives of Neurology, 68, pp. 488 - 497, http://dx.doi.org/10.1001/archneurol.2011.53
Journal articles | 2011
Dobson‐Stone C; Luty A; Hallupp M; Coupland K; Brooks W; Panegyres P; Piguet O; Broe GA; Sobow T; Zekanowski C; Halliday G; Schofield P; Kwok J, 2011, 'P1‐285: Sigma non‐opioid intracellular receptor 1 and neurodegeneration: prevalence of mutations and therapeutic implications', Alzheimer's & Dementia, 7, pp. S201 - S202, http://dx.doi.org/10.1016/j.jalz.2011.05.566
Journal articles | 2011
Kwok J; Luty A; Dobson‐Stone C; Loy C; Brooks W; Karlström H; Halliday G; Schofield P, 2011, 'P1‐287: Positional cloning identifies SIGMAR1 gene as a causative locus for FTLD‐MND in a large Australian pedigree', Alzheimer's & Dementia, 7, pp. S202 - S202, http://dx.doi.org/10.1016/j.jalz.2011.05.568
Journal articles | 2010
Loy C; McCusker E; Kril J; Kwok J; Brooks WS; Mccann H; Isaacs A; Halliday GM, 2010, 'Very early onset frontotemporal dementia with no family history preducts underlying fused in sarcoma pathology', Brain, 133, pp. e158, http://dx.doi.org/10.1093/brain/awq186
Villemagne V; Ataka S; Mizuno T; Brooks WS; Wada Y; Kondo M; Jones G; Watanabe Y; Mulligan R; Nakagawa M; Miki T; Shimada H; O''keefe G; Masters CL; Mori H; Rowe C, 2009, 'high striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types', Archives of Neurology, 66, pp. 1537 - 1544, http://dx.doi.org/10.1001/archneurol.2009.285
Journal articles | 2008
Brooks WS; Helton ES; Banerjee S; Venable M; Johnson L; Schoeb TR; Kesterson RA; Crawford DF, 2008, 'G2E3 is a dual function ubiquitin ligase required for early embryonic development', Journal of Biological Chemistry, 283, pp. 22304 - 22315, http://dx.doi.org/10.1074/jbc.M803238200
Journal articles | 2008
Gnjec A; D Costa K; Laws SM; Hedley R; Balakrishnan K; Taddei K; Martins G; Paton A; Verdile G; Gandy SE; Broe G; Brooks WS; Bennett HP; Piguet O; Price P; Miklossy J; Hallmayer J; McGeer P; Martins RN, 2008, 'Association of alleles carried at TNFA-850 and BAT1-22 with Alzheimer`s disease', Journal of Neuroinflammation, 5, pp. 36, http://dx.doi.org/10.1186/1742-2094-5-36
Journal articles | 2008
Karlstrom H; Brooks WS; Kwok JB; Broe T; Kril J; Mccann H; Halliday GM; Schofield PR, 2008, 'Variable phenotype of Alzheimer's disease with spastic paraparesis', Journal of Neurochemistry, 104, pp. 573 - 583, http://dx.doi.org/10.1111/j.1471-4159.2007.05038.x
Journal articles | 2008
Luty A; Kwok JB; Thompson E; Blumbergs PC; Brooks WS; Loy CT; Dobson-Stone C; Panegyres P; Hecker J; Nicholson GA; Halliday GM; Schofield PR, 2008, 'Pedigree with frontotemporal lobar degeneration - motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9', BMC NEUROLOGY, 8, http://dx.doi.org/10.1186/1471-2377-8-32
Journal articles | 2008
Mori H; Rowe CC; Shimada H; Brooks W; Ataka S; Jones G; Wada Y; O'Keefe G; Yoshioka E; Watanabe Y; Masters CL; Villemagne VL, 2008, 'P2‐054: Pattern of Aβ deposition in familial Alzheimer's disease is not related to mutation type or cognitive status', Alzheimer's & Dementia, 4, pp. T382 - T382, http://dx.doi.org/10.1016/j.jalz.2008.05.1127
Journal articles | 2007
Banerjee S; Brooks WS; Crawford DF, 2007, 'Inactivation of the ubiquitin conjugating enzyme UBE2Q2 causes a prophase arrest and enhanced apoptosis in response to microtubule inhibiting agents', Oncogene, 26, pp. 6509 - 6517, http://dx.doi.org/10.1038/sj.onc.1210471
Journal articles | 2007
Brooks WS; Banerjee S; Crawford DF, 2007, 'G2E3 is a nucleo-cytoplasmic shuttling protein with DNA damage responsive localization', Experimental Cell Research, 313, pp. 665 - 676, http://dx.doi.org/10.1016/j.yexcr.2006.11.020
Journal articles | 2007
Karlstrom H; Kwok JB; Gregory GC; Hallupp M; Brooks WS; Schofield PR, 2007, 'No association of spastic paraparesis genes in PSENI Alzheimer`s disease with spastic paraparesis', Neuroreport, 18, pp. 1267 - 1269, http://dx.doi.org/10.1097/WNR.0b013e3282405209
Journal articles | 2007
Rademakers R; Baker M; Gass J; Adamson J; Huey ED; Momeni P; Spina S; Coppola G; Karydas AM; Stewart H; Johnson N; Hsiung G-Y; Kelley B; Kuntz K; Steinbart E; Wood EM; Yu C-E; Josephs K; Sorenson E; Womack KB; Weintraub S; Pickering-Brown SM; Schopeld PR; Brooks WS; van Deerlin VM; Snowden J; Clark CM; Kertesz A; Boylan K; Ghetti B; Neary D; Schellenberg GD; Beach TG; Mesulam M; Mann D; Grafman J; Mackenzie IR; Feldman H; Bird T; Petersen R; Knopman D; Boeve B; Geschwind DH; Miller B; Wszolek Z; Lippa C; Bigio EH; Dickson D; Graff-Radford N; Hutton M, 2007, 'Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C -> T (Arg493X) mutation: an international initiative', LANCET NEUROLOGY, 6, pp. 857 - 868, http://dx.doi.org/10.1016/S1474-4422(07)70221-1
Journal articles | 2007
Rademakers R; Baker M; Gass J; adamson J; Huey ED; Momeni P; Spina S; Coppola G; Karydas AM; Stewart H; Johnson NA; Hsiung G; Kelley B; Kuntz K; Steinbart E; Wood EF; Yu C; Josephs K; Sorenson E; Womack KB; Weintraub S; Pickering-Brown S; Schofield PR; Brooks WS; Van Deerlin VM; Snowden J; Clark C; Kertesz A; boylan K; Ghetti B; Neary D; Schellenberg G; Beach T; Mesulam M; Mann D; Grafman J; McKenzie IR; Feldman H; Bird T; Petersen RC; Knopman D; Boeve B; Geschwind DH; Miller B; Wszolek Z; Lippa C; Bigio E; Dickson D; Graff-radford N; Hutton M, 2007, 'Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-T (Arg493X) mutation: an international initiative', Lancet Neurology, 6, pp. 857 - 868, http://dx.doi.org/10.1016/S1474-4422(07)70221-1
Journal articles | 2006
Halliday GM; Song YC; Creasey H; Morris JC; Brooks WS; Kril J, 2006, 'Neuropathology in the S305S tau gene mutation', Brain, 129, pp. E40 - E40, http://dx.doi.org/10.1093/brain/awh720
Journal articles | 2006
Huang Y; Hayes M; Harding AJ; Brooks WS; Fung VS; Rowe DB; Joffe R; Crimmins D; Hely MA; Halliday GM, 2006, 'Anticipation of onset age in familial Parkinson`s disease without SCA gene mutations', Parkinsonism and Related Disorders, 12, pp. 309 - 313, http://dx.doi.org/10.1016/j.parkreldis.2006.01.002
Journal articles | 2006
Luty AA; Kwok JB; Thompson E; Blumbergs PC; Brooks W; Schofield PR, 2006, 'P1–318: A novel Alzheimer's disease locus associated with atypical ‘plaque–predominant’ neuropathology', Alzheimer's & Dementia, 2, pp. S190 - S190, http://dx.doi.org/10.1016/j.jalz.2006.05.696
Journal articles | 2006
Pickering-Brown S; Baker M; Gass J; Boeve B; Loy CT; Brooks WS; Mackenzie IR; Martins RN; Kwok JB; Halliday GM; Kril J; Schofield PR; Mann DM; Hutton M, 2006, 'Mutations in progranulin explain atypical phenotypes with variants in MAPT', Brain, 129, pp. 3124 - 3126, http://dx.doi.org/10.1093/brain/awl289
Journal articles | 2005
Halliday GM; Song YC; Lepar GS; Brooks WS; Kwok JB; Kersaitis C; Gregory GC; Shepherd CE; Rahimi F; Schofield PR; Kril J, 2005, 'Pick bodies in a family with presenilin-1 Alzheimer's disease', Annals of Neurology, 57, pp. 139 - 143, http://dx.doi.org/10.1002/ana.20366
Journal articles | 2005
Piguet O; Grayson DA; Tate RL; Bennett HP; Lye TC; Creasey H; Brooks WS; Broe T, 2005, 'A model of executive functions in very old community dwellers: Evidence from the Sydney older persons study', Cortex, 41, pp. 27 - 37, http://dx.doi.org/10.1016/S0010-9452(08)70175-8
Journal articles | 2004
Brooks WS; Kwok JB; Halliday GM; Godbolt AK; Rossor MN; Creasey H; Jones A; Schofield PR, 2004, 'Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation', Neurology, 63, pp. 1613 - 1617, http://dx.doi.org/10.1212/01.WNL.0000142965.10778.C7
Journal articles | 2004
Harding AJ; Das A; Kril J; Brooks WS; Duffy DL; Halliday GM, 2004, 'Identification of families with cortical Lewy body disease', American Journal of Medical Genetics Part A, 128B, pp. 118 - 122
Journal articles | 2004
Piguet O; Brooks WS; Halliday GM; Schofield PR; Stanford PM; Kwok JB; Spillantini M; Yancopoulou D; Nestor PJ; Broe G; Hodges JR, 2004, 'Similar early clinical presentations in familial and non-familial frontotemporal dementia', Journal of Neurosurgery, 75, pp. 1743 - 1745, http://dx.doi.org/10.1136/jnnp.2003.031948
Journal articles | 2004
Shepherd CE; Gregory GC; Vickers J; Brooks WS; Kwok J; Schofield PR; Kril J; Halliday GM, 2004, 'Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques', Neurobiology of Disease, 15, pp. 115 - 119, http://dx.doi.org/10.1016/j.nbd.2003.10.008
Journal articles | 2004
Shepherd CE; Piguet O; Broe G; Creasey H; Waite LM; Brooks WS; Kril J, 2004, 'Histocompatibility antigens, aspirin use and cognitive performance in non-demented elderly subjects', Journal of Neuroimmunology, 148, pp. 178 - 182, http://dx.doi.org/10.1016/j.jneuroim.2003.11.007
Journal articles | 2004
Stanford PM; Brooks WS; Teber E; Hallupp M; McLean CA; Halliday GM; Martins RN; Kwok JB; Schofield PR, 2004, 'Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies', Journal of Neurology, 251, pp. 1098 - 1104, http://dx.doi.org/10.1007/s00415-004-0489-x
Journal articles | 2003
Brooks WS; Kwok JB; Kril J; Broe T; Blumbergs P; Tannenberg T; Lamont P; Hedges P; Schofield PR, 2003, 'Alzheimer`s disease with spastic paraparesis and `cotton wool` plaques: two pedigrees with PS-1 exon 9 deletions', Brain, 126, pp. 783 - 791, http://dx.doi.org/10.1093/brain/awg084
Journal articles | 2003
Janu MR; Creasey H; Grayson DA; Cullen J; Whyte S; Brooks WS; Waite LM; Broe T, 2003, 'Laboratory results in the elderly: the Sydney Older Persons Study', Annals of Clinical Biochemistry, 40, pp. 273 - 279
Journal articles | 2003
Janu MR; Creasey H; Grayson DA; Cullen JS; Whyte S; Brooks WS; Waite LM; Broe GA, 2003, 'Laboratory results in the elderly: The Sydney older persons study', Annals of Clinical Biochemistry, 40, pp. 274 - 279, http://dx.doi.org/10.1258/000456303321610600
Journal articles | 2003
Kwok JB; Halliday GM; Brooks WS; Dolios G; Laudon H; Murayama O; Hallupp M; Vickers J; Wang R; Naslund J; Takashima A; Gandy SE; Badenhop RF; Schofield PR, 2003, 'Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy', The Journal of Biological Chemistry, 278, pp. 6748 - 6754, http://dx.doi.org/10.1074/jbc.M211827200
Journal articles | 2003
Miklossy J; Taddei K; Suva D; Verdile G; Fonte J; Fisher C; Ghika JA; Suard F; Mehta PD; McLean CA; Masters CL; Brooks WS; Martins RN, 2003, 'Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer`s disease', Neurobiology of Aging, 24, pp. 655 - 662, http://dx.doi.org/10.1016/S0197-4580(02)00192-6
Journal articles | 2003
Piguet O; Grayson DA; Creasey H; Bennett HP; Brooks WS; Waite LM; Broe T, 2003, 'Vascular risk factors, cognition and dementia incidence over 6 years in the Sydney Older Persons Study', Neuroepidemiology, 22, pp. 165 - 171, http://dx.doi.org/10.1159/000069886
Journal articles | 2003
Stanford PM; Shepherd CE; Halliday GM; Brooks WS; Schofield PR, 2003, 'Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia', Brain, 126, pp. 814 - 826, http://dx.doi.org/10.1093/brain/awg090
Journal articles | 2002
Broe T; Grayson DA; Waite LM; Creasey H; Edelbrock D; Bennett HP; Brooks WS, 2002, 'Determinants of service use among the elderly:the Sydney older persons study', Australasian Journal on Ageing, 21, pp. 61 - 66, http://dx.doi.org/10.1111/j.1741-6612.2002.tb00419.x
Waite LM; Creasey H; Grayson DA; Edelbrock D; Cullen J; Brooks WS; Casey B; Bennett HP; Broe T, 2001, 'Clinical diagnosis and disability among community dwellers aged 75 and over: The Sydney older persons study.', Australasian Journal on Ageing, 20, pp. 67 - 72, http://dx.doi.org/10.1111/j.1741-6612.2001.tb00356.x
Journal articles | 2000
Broe T; Grayson DA; Creasey H; Waite LM; Casey B; Bennett HP; Brooks WS; Halliday GM, 2000, 'Anti-inflammatory drugs protect against Alzheimer's disease at low doses', Archives of Neurology, 57, pp. 1586 - 1591, http://dx.doi.org/10.1001/archneur.57.11.1586
Journal articles | 2000
Kwok JBJ; Smith MJ; Brooks WS; Kril J; Mclean C; Hallupp M; Schofield PR, 2000, 'Variable presentation of Alzheimer's disease and/or spastic paraparesis phenotypes in pedigrees with a novel PS-1 exon 9 gene deletion or exon 9 splice acceptor mutations', Neurobiology of Aging, 21, pp. 25 - 25, http://dx.doi.org/10.1016/s0197-4580(00)82789-x
Stanford PM; Halliday GM; Brooks WS; Kwok JB; Storey CE; Creasey H; Morris J; Fulham MJ; Schofield PR, 2000, 'Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations', Brain, 123, pp. 880 - 893, http://dx.doi.org/10.1093/brain/123.5.880
Journal articles | 2000
Stanford PM; Halliday GM; Brooks WS; Kwok JB; Storey CE; Creasey H; Morris JG; Fulham MJ, 2000, 'Tau gene mutations are pleiotropic: Identification of two novel mutations in the tau gene', Neurobiology of Aging, 21, pp. 36 - 36, http://dx.doi.org/10.1016/s0197-4580(00)82837-7
Journal articles | 1999
Laws SM; Taddei K; Fisher C; Small D; Clarnette R; Hallmayer J; Brooks WS; Kwok JB; Schofield PR; Gandy SE; Martins RN, 1999, 'Evidence that the butyrylcholinesterase K variant can protect against late-onset Alzheimer`s disease', Alzheimers Reports, 2, pp. 219 - 223
Journal articles | 1999
Laws SM; Taddei K; Martins G; Paton A; Fisher C; Clarnette R; Hallmayer J; Brooks WS; Gandy SE; Martins RN, 1999, 'The -491AA polymorphism in the APOE gene is associated with increased plasma apoE levels in Alzheimer's disease', NeuroReport, 10, pp. 879 - 882, http://dx.doi.org/10.1097/00001756-199903170-00038
Journal articles | 1999
Mcritchie DA; Reid WG; Halliday GM; Hely MA; Brooks WS; Morris J, 1999, 'Neuropathology of three clinical cases prospectively diagnosed with diffuse Lewy body disease', Journal of Clinical Neuroscience, 6, pp. 149 - 154, http://dx.doi.org/10.1016/S0967-5868(99)90082-6
Journal articles | 1999
Milward EA; Grayson DA; Creasey H; Janu MR; Brooks WS; Broe GA, 1999, 'Evidence for association of anaemia with vascular dementia', NeuroReport, 10, pp. 2377 - 2381, http://dx.doi.org/10.1097/00001756-199908020-00029
Journal articles | 1998
Taddei K; Kwok JB; Kril J; Halliday GM; Creasey H; Hallupp M; Fisher C; Brooks WS; Chung C; Andrews C; Masters C; Schofield PR; Martins RN, 1998, 'Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease.', Neuroreport, 9, pp. 3335 - 3339, http://dx.doi.org/10.1097/00001756-199810050-00034
Journal articles | 1998
Taddei K; Yang D; Fisher C; Clarnette R; Hallmayer J; Barnetson R; Maller R; Brooks WS; Whyte S; Nicholson GA; Masters CL; Broe GA; Gandy SE; Martins RN, 1998, 'No association of presenilin-1 intronic polymorphism and Alzheimer's disease in Australia', Neuroscience Letters, 246, pp. 178 - 180, http://dx.doi.org/10.1016/S0304-3940(98)00248-1
Journal articles | 1997
Cullen K; Halliday GM; Double KL; Brooks WS; Creasey H; Broe T, 1997, 'Nucleus basalis cell loss is related to regional volumetric brain changes in Alzheimer's disease', Neuroscience, pp. 641 - 652
Journal articles | 1997
Cullen KM; Halliday GM; Double KL; Brooks WS; Creasey H; Broe GA, 1997, 'Cell loss in the nucleus basalis is related to regional cortical atrophy in Alzheimer's disease', Neuroscience, 78, pp. 641 - 652, http://dx.doi.org/10.1016/S0306-4522(96)00569-6
Journal articles | 1997
Halliday GM; Brooks WS; Arthur HA; Creasey H; Broe T, 1997, 'Further evidence for an association between a mutation in the APP gene and Lewy body formation', Neuroscience Letters, 227, pp. 49 - 52, http://dx.doi.org/10.1016/S0304-3940(97)00294-2
Journal articles | 1997
Kwok JB; Taddei K; Hallupp M; Fisher C; Brooks WS; Broe T; Hardy J; Fulham MJ; Nicholson GA; Stell R; St George-Hyslop PH; Fraser PE; Kakulas B; Clarnette R; Relkin N; Gandy SE; Schofield PR; Martins RN, 1997, 'Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer`s disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype', Neuroreport, 8, pp. 1537 - 1542, http://dx.doi.org/10.1097/00001756-199704140-00043
Journal articles | 1996
Double KL; Halliday GM; Kril J; Harasty JA; Cullen K; Brooks WS; Creasey H; Broe T, 1996, 'Topography of brain atrophy during normal aging and Alzheimer's disease', Neurobiology of Aging, 17, pp. 513 - 521, http://dx.doi.org/10.1016/0197-4580(96)00005-X
Journal articles | 1996
Harasty JA; Halliday GM; Code C; Brooks WS, 1996, 'Quantification of cortical atrophy in a case of progressive fluent asphsia', Brain, 119, pp. 181 - 190, http://dx.doi.org/10.1093/brain/119.1.181
Journal articles | 1996
Hely MA; Reid WG; Halliday GM; Mcritchie DA; Leicester J; Joffe R; Brooks WS; Broe T; Morris J, 1996, 'Diffuse Lewy body disease: Clinical features in nine cases without co-existent Alzheimer's disease', Journal of Neurology Neurosurgery and Psychiatry, 60, pp. 532 - 538, http://dx.doi.org/10.1136/jnnp.60.5.531
Journal articles | 1996
Yang JG; Poropat RA; Brooks WS; Broe GA; Nicholson GA, 1996, 'Apolipoprotein E genotyping in Alzheimer's disease in an Australian sample', Australian and New Zealand Journal of Medicine, 26, pp. 658 - 661, http://dx.doi.org/10.1111/j.1445-5994.1996.tb02936.x
Journal articles | 1995
Brooks WS; Martins RN; De Voecht J; Nicholson GA; Schofield PR; Kwok JBJ; Fisher C; Yeung LU; Van Broeckhoven C, 1995, 'A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's disease', Neuroscience Letters, 199, pp. 183 - 186, http://dx.doi.org/10.1016/0304-3940(95)12046-7
Journal articles | 1995
Martins RN; Clarnette R; Fisher C; Broe GA; Brooks WS; Montgomery P; Gandy SE, 1995, 'ApoE genotypes in australia: Roles in early and late onset alzheimer’s disease and down’s syndrome', NeuroReport, 6, pp. 1513 - 1516, http://dx.doi.org/10.1097/00001756-199507310-00012
Journal articles | 1994
Maltby N; Broe GA; Creasey H; Jorm AF; Christensen H; Brooks WS, 1994, 'Efficacy of tacrine and lecithin in mild to moderate Alzheimer's disease: Double blind trial', BMJ, 308, pp. 879, http://dx.doi.org/10.1136/bmj.308.6933.879
Journal articles | 1993
Martins RN; Muir J; Brooks WS; Creasey H; Montgomery P; Sellers P; Broe GA, 1993, 'Plasma amyloid precursor protein is decreased in alzheimer’s disease', NeuroReport, 4, pp. 757 - 759, http://dx.doi.org/10.1097/00001756-199306000-00040
McKay NS; Gordon BA; Hornbeck RC; Jack CR; Koeppe R; Flores S; Keefe S; Hobbs DA; Joseph-Mathurin N; Wang Q; Rahmani F; Chen CD; McCullough A; Koudelis D; Chua J; Ances BM; Millar PR; Nickels M; Perrin RJ; Allegri RF; Berman SB; Brooks WS; Cash DM; Chhatwal JP; Farlow MR; Fox NC; Fulham M; Ghetti B; Graff-Radford N; Ikeuchi T; Day G; Klunk W; Levin J; Lee J-H; Martins R; Masters CL; McConathy J; Mori H; Noble JM; Rowe C; Salloway S; Sanchez-Valle R; Schofield PR; Shimada H; Shoji M; Su Y; Suzuki K; Vöglein J; Yakushev I; Swisher L; Cruchaga C; Hassenstab J; Karch C; McDade E; Xiong C; Morris JC; Bateman RJ; Benzinger TLS, 2022, Neuroimaging within the Dominantly Inherited Alzheimer’s Network (DIAN): PET and MRI, , http://dx.doi.org/10.1101/2022.03.25.485799
Conference Abstracts | 2020
Bateman R; Aschenbrenner A; Benzinger T; Clifford D; Cruchaga C; Fagan A; Farlow M; Goate A; Gordon B; Hassenstab J; Jack C; Koeppe R; McDade E; Mills S; Morris JC; Salloway S; Santacruz A; Snyder P; Wang G; Xiong C; Snider BJ; Mummery C; Surti G; Didier H; Wallon D; Berman S; Lah J; Jimenez-Velazquez IZ; Roberson E; Van Dyck C; Honig LS; Valle RS; Brooks WS; Gauthier S; Masters C; Galasko D; Brosch J; Hsiung R; Jayadev S; Formaglio M; Masellis M; Clarnette R; Pariente J; Dubois B; Pasquier F; Andersen S; Holdridge K; Mintun M; Sims J; Yaari R; Baudler M; Delmar P; Doody R; Fountouro P; Kerchner G, 2020, 'DIAN-TU Alzheimer's Disease Prevention Trial of Solanezumab and Gantenerumab: Amyloid, Tau and Neurodegeneration Outcomes', in ANNALS OF NEUROLOGY, WILEY, ELECTR NETWORK, Vol. 88, pp. S103 - S103, presented at 145th Annual Meeting American-Neurological-Association, ELECTR NETWORK, 04 October 2020 - 09 October 2020, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000572509100139&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
Conference Abstracts | 2019
Weickert T; Jacomb I; Lenroot R; Lappin J; Weinberg D; Brooks W; Brown D; Pellen D; Kindler J; Mohan A; Wakefield D; Lloyd A; Stanton C; O'Donnell M; Liu D; Galletly C; Weickert CS, 2019, 'REDUCTION IN PERIPHERAL C-REACTIVE PROTEIN LEVELS WITH CANAKINUMAB ADMINISTRATION IS RELATED TO REDUCED POSITIVE SYMPTOM SEVERITY IN PATIENTS WITH SCHIZOPHRENIA AND INFLAMMATION', in SCHIZOPHRENIA BULLETIN, OXFORD UNIV PRESS, FL, Orlando, Vol. 45, pp. S318 - S318, presented at Congress of the Schizophrenia-International-Research-Society (SRIS), FL, Orlando, 10 April 2019 - 14 April 2019, http://dx.doi.org/10.1093/schbul/sbz020.578
Conference Abstracts | 2019
Weickert T; Jacomb I; Lenroot R; Lappin J; Weinberg D; Brooks W; Brown D; Pellen D; Kindler J; Mohan A; Wakefield D; Lloyd A; Stanton C; O'Donnell M; Liu D; Galletly C; Weickert CS, 2019, 'Reduction in Peripheral C-Reactive Protein Levels With Canakinumab Administration is Related to Reduced Positive Symptom Severity in Patients With Schizophrenia and Inflammation', in BIOLOGICAL PSYCHIATRY, ELSEVIER SCIENCE INC, IL, Chicago, Vol. 85, pp. S44 - S45, presented at 74th Annual Meeting of the Society-of-Biological-Psychiatry (SOBP), IL, Chicago, 16 May 2019 - 18 May 2019, http://dx.doi.org/10.1016/j.biopsych.2019.03.121
Dobson-Stone C; Shaw A; Brooks W; Loy C; Schofield P; Mather K; Kochan N; Sachdev P; Halliday G; Piguet O; Hodges J; Kwok J, 2015, 'Utility and challenges of whole-exome sequencing in the hunt for neurodegeneration genes [Abstract MTU02-05]', in Journal of Neurochemistry, Wiley: 12 months, Cairns, Australia, Vol. 134, pp. 111 - 111, presented at 25th Biennial Meeting of the International Society for Neurochemistry Jointly with the 13th Meeting of the Asian Pacific Society for Neurochemistry in Conjunction with the 35th Meeting of the Australasian Neuroscience Society, Cairns, Australia, 23 August 2015 - 27 August 2015, http://dx.doi.org/10.1111/jnc.13188
Schofield PR; Luty A; Kwok JB; Thompson E; Blumbergs P; Brooks WS; Loy CT; Dobson-Stone C; Panegyres P; Hecker J; Nicholson GA; Halliday GM, 2008, 'Linkage to chromosome 9 and examination of candidate genes in a pedigree with FTLD-MND and TDP-43 positive neuropathology', in Dementia and Geriatric Cognitive Disorders, Karger, Basel, Switzerland, pp. 9 - 9, presented at 6th International Conference on Frontotemporal Dementias, Rotterdam, Netherlands, 03 September 2008 - 05 September 2008
Conference Papers | 2005
Huang Y; Hayes M; Harding AJ; Brooks WS; Fung VS; Rowe DB; Hely MA; Halliday GM, 2005, 'Genetic anticipation in familial Lewy body disease', in Parkinsonism and Related Disorders, Elsevier Sci Ltd, Kidlington, Oxford, England, pp. 254 - 254, presented at 16th International Congress on Parkinson`s Disease and Related Disorders, Berlin, Germany, 05 June 2005 - 09 June 2005
Conference Papers | 2005
Song YC; Halliday GM; Creasey H; Morris JG; Brooks WS; Kril J, 2005, 'Neuropathology in the S305S tau gene mutation', in Journal of the Neurological Sciences, Elsevier Science BV, Amsterdam, Netherlands, pp. S302 - S302, presented at XVIIIth World Congress of Neurology, Sydney, 05 November 2005 - 11 November 2005
Conference Posters | 2005
Song YE; Halliday GM; Creasey H; Morris J; Brooks WS; Kril J, 2005, 'Neuropathology in the S305S Tau gene mutation', Vol. 238, pp. S302 - S302, http://dx.doi.org/10.1093/brain/awh720
Conference Papers | 2004
Brooks WS; Kwok JB; Halliday GM; Godbolt AK; Rossor MN; Creasey H; Jones A; Schofield PR, 2004, 'Familial Alzheimer's disease and cerebral haemorrhage: A second family with the Flemish APP ALA692GLY mutation', in Neurobiology of Aging, Elsevier Science Inc, New York, NY, USA, pp. S499 - S499, presented at 9th International Conference on Alzheimer's Disease and Related Disorders, Philadelphia, Pennsylvania, 17 July 2004 - 22 July 2004, http://dx.doi.org/10.1016/S0197-4580(04)81645-2
Conference Papers | 2004
Brooks WS; Stanford PM; Teber ET; Hallupp M; Mclean C; Halliday GM; Martins RN; Kwok JB; Schofield PR, 2004, 'Screening for tau mutations: an Australian series', in Internal Medicine Journal, Blackwell Publishing Asia, Carlton, VIC, pp. A59 - A59, presented at Annual Scientific Meeting of the Australian Society for Geriatric Medicine, Fremantle, WA, 27 April 2004 - 30 April 2004
Conference Papers | 2004
Gregory GC; Kwok JB; Shepherd CE; Brooks WS; Xuereb J; Schofield PR; Halliday GM, 2004, 'Beta-amyloid toxicity in Alzheimer's disease', in Proceedings of Aust Neuroscience Society, 24th Annual Meeting of the Australian Neuroscience Society, Melbourne Convention Centre, pp. 42 - 42, presented at 24th Annual Meeting of the Australian Neuroscience Society, Melbourne Convention Centre, 27 January 2004 - 30 January 2004
Conference Papers | 2003
Gregory GC; Kril J; Macdonald V; Png F; Patel S; Brooks WS; Schofield PR; Halliday GM, 2003, 'Familial Alzheimer's disease differs from sporadic in the severity of degeneration', in Proceedings of Aust Neuroscience Society, 23rd Annual Meeting of the Australian Neuroscience Society, Adelaide, Sth Aust, pp. 376 - 376, presented at 23rd Annual Meeting of the Australian Neuroscience Society, Adelaide, Sth Aust, 28 January 2003 - 31 January 2003
Conference Papers | 2003
Shepherd CE; Stanford PM; Brooks WS; Kwok JB; Schofield PR; Brodaty H; Martins RN; Halliday GM, 2003, 'Absence of tau pathology in a familial frontotemporal dementia case with a mutation in the tau gene', in Proceedings of Aust Neuroscience Society, 23rd Annual Meeting of the Australian Neuroscience Society, Adelaide, Sth Aust, pp. 375 - 375, presented at 23rd Annual Meeting of the Australian Neuroscience Society, Adelaide, Sth Aust, 28 January 2003 - 31 January 2003
Conference Papers | 2002
Harding AJ; Das A; Kril J; Brooks WS; Halliday GM, 2002, 'Frequency of familial Lewy body diseases', in Australian New Zealand Society of Neuropathology Annual General Meeting, Australian New Zealand Society of Neuropathology Annual General Meeting, presented at Australian New Zealand Society of Neuropathology Annual General Meeting
Conference Papers | 2002
Harding AJ; Das A; Kril J; Brooks WS; Halliday GM, 2002, 'The frequency of familial lewy body diseases', in Proceedings of Aust Neuroscience Society, 22nd Annual meeting of the Australian Neuroscience Society, Darling Harbour, Sydney, pp. 134 - 134, presented at 22nd Annual meeting of the Australian Neuroscience Society, Darling Harbour, Sydney, 04 February 2002 - 06 February 2002
Conference Papers | 1998
Broe T; Corbett AD; Bennett HP; Brooks WS; Kril J; Halliday GM; Grayson DA, 1998, 'White matter lesions, cognitive decline and dementia: A 6 year follow-up', in Neurobiology of Aging, Elsevier Science Inc, New York, NY, USA, pp. S243, presented at 6th International Conference on Alzheimer`s Disease and Related Disorders, Amsterdam, Netherlands, 18 July 1998 - 23 July 1998
Conference Papers | 1997
Aguzzi A; Barbara J; Brown P; Budka H; Diringer H; Dormont D; Flanagan P; Heeschen W; Hope J; Hornlimann B; Kenney K; Masters C; Macnaughton MR; Pocchiari M; Rohwer RG; Safar J; Somogyi A; Tateishi J; Taylor D; Van Duijn CM; Wilesmith JW; Will R; Wisher M; Asher D; De Pedro J; Feek C; Hasebe K; Horaud F; Lower J; Minor P; Nandapalan P; Pavlov A; Perez AC; Ricketts M; Vicari G; Van Aken WG; Beal R; Menache-Aronson D; Bradley R; Bailey A; Chalumeau HP; Garland A; Brooks W; Schrieber R; Sprengers E; Andjaparidze AG; Bolis CL; Emmanuel JC; Griffiths E; Heymann DL; Kaboyo W; Meslin FX; Miyagawa S; Marroquin AP; Schudel A; Zeidler M, 1997, 'Medicinal and other products and human and animal transmissible spongiform encephalopathies: Memorandum from a WHO meeting', in Bulletin of the World Health Organization, pp. 505 - 513
Halliday GM; Brooks WS; Arthur HA; Nicholson GA; Yeung LM, 1997, 'Familial Alzheimer's disease, chromosome 21 and Parkinson's disease', in Journal of Clinical Neuroscience, Churchill Livingstone, Edinburgh, Midlothian, Scotland, pp. 386 - 387, presented at Australian Association of Neurologists Annual Scientific Meeting 1997, Sydney, 30 April 1997 - 02 May 1997
Conference Papers | 1997
Halliday GM; Mccann H; Brooks WS; Broe T, 1997, 'Inflammation in Alzheimer's disease: anti-inflammatory medications increase post-mortem neuropathology', in Brain Pathology, Int Society Neuropathology, Los Angeles, CA, USA, pp. 1054 - 1054, presented at XIIIth International Congress of Neuropathology, Perth, WA, 07 September 1997 - 12 September 1997
Conference Papers | 1997
Halliday GM; Mccann H; Brooks WS; Broe T, 1997, 'Inflammation in Alzheimer's disease: anti-inflammatory medications increase post-mortem neuropathology', in Andrews GR; Mykyta LJ; Andrews MM; Pearson SA; Gregory AJ; Hagger JC(eds.), 16th Congress of the International Association of Gerontology, 16th Congress of the International Association of Gerontology, Adelaide, Sth Aust, pp. 398 - 398, presented at 16th Congress of the International Association of Gerontology, Adelaide, Sth Aust, 19 August 1997 - 23 August 1997