By Dr William Brooks

Journal articles

Pottier C; Zhou X; Perkerson RB; Baker M; Jenkins GD; Serie DJ; Ghidoni R; Benussi L; Binetti G; López de Munain A; Zulaica M; Moreno F; Le Ber I; Pasquier F; Hannequin D; Sánchez-Valle R; Antonell A; Lladó A; Parsons TM; Finch NCA; Finger EC; Lippa CF; Huey ED; Neumann M; Heutink P; Synofzik M; Wilke C; Rissman RA; Slawek J; Sitek E; Johannsen P; Nielsen JE; Ren Y; van Blitterswijk M; DeJesus-Hernandez M; Christopher E; Murray ME; Bieniek KF; Evers BM; Ferrari C; Rollinson S; Richardson A; Scarpini E; Fumagalli GG; Padovani A; Hardy J; Momeni P; Ferrari R; Frangipane F; Maletta R; Anfossi M; Gallo M; Petrucelli L; Suh ER; Lopez OL; Wong TH; van Rooij JGJ; Seelaar H; Mead S; Caselli RJ; Reiman EM; Noel Sabbagh M; Kjolby M; Nykjaer A; Karydas AM; Boxer AL; Grinberg LT; Grafman J; Spina S; Oblak A; Mesulam MM; Weintraub S; Geula C; Hodges JR; Piguet O; Brooks WS; Irwin DJ; Trojanowski JQ; Lee EB; Josephs KA; Parisi JE; Ertekin-Taner N; Knopman DS; Nacmias B; Piaceri I; Bagnoli S; Sorbi S; Gearing M; Glass J; Beach TG; Black SE; Masellis M; Rogaeva E; Vonsattel JP; Honig LS; Kofler J; Bruni AC; Snowden J; Mann D; Pickering-Brown S, 2018, 'Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study', The Lancet Neurology, 17, pp. 548 - 558, http://dx.doi.org/10.1016/S1474-4422(18)30126-1

Broce I; Karch CM; Wen N; Fan CC; Wang Y; Hong Tan C; Kouri N; Ross OA; Höglinger GU; Muller U; Hardy J; Momeni P; Hess CP; Dillon WP; Miller ZA; Bonham LW; Rabinovici GD; Rosen HJ; Schellenberg GD; Franke A; Karlsen TH; Veldink JH; Ferrari R; Yokoyama JS; Miller BL; Andreassen OA; Dale AM; Desikan RS; Sugrue LP; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Brooks WS; 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; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Landqvist Waldö M; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; G McKeith I; 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; Schofield P, 2018, 'Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies', PLoS Medicine, 15, pp. e1002487, http://dx.doi.org/10.1371/journal.pmed.1002487

Williams KL; Topp S; Yang S; Smith B; Fifita JA; Warraich ST; Zhang KY; Farrawell N; Vance C; Hu X; Chesi A; Leblond CS; Lee A; Rayner SL; Sundaramoorthy V; Dobson-Stone C; Molloy MP; Van Blitterswijk M; Dickson DW; Petersen RC; Graff-Radford NR; Boeve BF; Murray ME; Pottier C; Don E; Winnick C; McCann EP; Hogan A; Daoud H; Levert A; Dion PA; Mitsui J; Ishiura H; Takahashi Y; Goto J; Kost J; Gellera C; Gkazi AS; Miller J; Stockton J; Brooks WS; Boundy K; Polak M; Muñoz-Blanco JL; Esteban-Pérez J; Rábano A; Hardiman O; Morrison KE; Ticozzi N; Silani V; De Belleroche J; Glass JD; Kwok JBJ; Guillemin GJ; Chung RS; Tsuji S; Brown RH; García-Redondo A; Rademakers R; Landers JE; Gitler AD; Rouleau GA; Cole NJ; Yerbury JJ; Atkin JD; Shaw CE; Nicholson GA; Blair IP, 2016, 'CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia', Nature Communications, 7, pp. 11253, http://dx.doi.org/10.1038/ncomms11253

Dobson-Stone C; Shaw AD; Hallupp M; Bartley L; McCann H; Brooks WS; Loy CT; Schofield PR; Mather KA; Kochan NA; Sachdev PS; Halliday GM; Piguet O; Hodges JR; Kwok JBJ; Schofield P, 2015, 'Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?', Brain, 138, pp. e385, http://dx.doi.org/10.1093/brain/awv115

Cairns NJ; Perrin RJ; Franklin EE; Carter D; Vincent B; Xie M; Bateman RJ; Benzinger T; Friedrichsen K; Brooks WS; Halliday GM; Mclean C; Ghetti B; Morris JC, 2015, 'Neuropathologic assessment of participants in two multi-center longitudinal observational studies: The Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)', Neuropathology, 35, pp. 390 - 400, http://dx.doi.org/10.1111/neup.12205

Monserrate AE; Ryman DC; Ma S; Xiong C; Noble JM; Ringman JM; Morris JC; Danek A; Müller-Sarnowski F; Clifford DB; McDade EM; Brooks WS; Darby DG; Masters CL; Weston PSJ; Farlow MR; Graff-Radford NR; Salloway SP; Fagan AM; Oliver A; Bateman RJ; Dominantly Inherited Alzheimer Network , 2015, 'Factors associated with the onset and persistence of post-lumbar puncture headache', JAMA Neurology, 72, pp. 325 - 332, http://dx.doi.org/10.1001/jamaneurol.2014.3974

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; Brooks W; Schofield P, 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

Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Brooks WS; Eld PRS; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernandez 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; Clarimon J; Lleo A; Blesa R; Waldoe ML; Nilsson K; Nilsson C; Mackenzie IRA; Hsiung G; Mann DMA; Grafman J; Morris CM; Attems J; Ths TDG; 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; Rubino IRE; 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; Fox NC; Warren JD; Spillantini MG; Morris HR; Rizzu P; Heutink P; Snowden JS; Rollinson S; Richardson A; Gerhard A; Bruni AC; Maletta R; Frangipane F; Cupidi C; Bernardi L; Anfossi M; Gallo M; Conidi ME; Smirne N; Rademakers R; Baker M; Dickson DW; Graff-Radford NR; Petersen RC; Knopman D; Josephs KA; Boeve BF; Parisi JE; Seeley WW; Miller BL; Karydas AM; Rosen H; van Swieten JC; Dopper EGP; Seelaar H; Pijnenburg YA; Scheltens P; Logroscino G; Capozzo R; Novelli V; Puca AA; Franceschi M; Postiglione A; Milan G; Sorrentino P; Kristiansen M; Chiang HH; Graff C; Pasquier F; Rollin A; Deramecourt V; Lebert F; Kapogiannis D; Ferrucci L; Pickering-Brown S; Hardy J; Momeni P; Singleton AB, 2014, 'Genetic analysis suggests lysosomal and immune system involvement in frontotemporal dementia', JOURNAL OF ALZHEIMERS DISEASE, 41, pp. S25 - S26, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000337049200051&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

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

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

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

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; Schofield P, 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

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; Schofield P, 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

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

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, http://dx.doi.org/10.1016/j.jalz.2011.05.566

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, http://dx.doi.org/10.1016/j.jalz.2011.05.568

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

Schofield PR; Kwok JBJ; Brooks WS; Loy CT, 2009, 'The genetics of familial dementias', Pathology, 41, pp. 30 - 30, http://dx.doi.org/10.1097/01268031-200941001-00064

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

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

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, http://dx.doi.org/10.1016/j.jalz.2008.05.1127

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

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

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

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

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

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

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

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

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

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

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, http://dx.doi.org/10.1016/j.jalz.2006.05.696

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Brooks WS; Broe GA; Kwok JBJ; Schofield PR; Kril JJ, 2002, 'Familial Alzheimer's disease with spastic paraparesis: Two pedigrees with PS-1 exon 9 deletion due to splice acceptor mutations', NEUROBIOLOGY OF AGING, 23, pp. S313 - S313, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000177465301145&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Kwok J; Hallupp M; Badenhop RF; Schofield PR; Halliday GM; Brooks WS; Dolois G; Wang R; Murayama O; Takashima A; Vickers J; Gandy SE, 2002, 'Presenilin-1 mutation (L271V) results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy', NEUROBIOLOGY OF AGING, 23, pp. S277 - S277, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000177465301016&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

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