By Professor Glenda Halliday

Journal articles

Youssef P; Kim WS; Halliday GM; Lewis SJG; Dzamko N, 2021, 'Comparison of Different Platform Immunoassays for the Measurement of Plasma Alpha-Synuclein in Parkinson's Disease Patients', Journal of Parkinson's Disease, 11, pp. 1761 - 1772, http://dx.doi.org/10.3233/jpd-212694

De Boer SCM; Riedl L; Van Der Lee SJ; Otto M; Anderl-Straub S; Landin-Romero R; Sorrentino F; Fieldhouse JLP; Reus LM; Vacaflor B; Halliday G; Galimberti D; Diehl-Schmid J; Ducharme S; Piguet O; Pijnenburg YAL, 2021, 'Differences in Sex Distribution between Genetic and Sporadic Frontotemporal Dementia', Journal of Alzheimer's Disease, 84, pp. 1153 - 1161, http://dx.doi.org/10.3233/JAD-210688

Hughes LP; Pereira MMM; Hammond DA; Kwok JB; Halliday GM; Lewis SJG; Dzamko N, 2021, 'Glucocerebrosidase Activity is Reduced in Cryopreserved Parkinson's Disease Patient Monocytes and Inversely Correlates with Motor Severity', Journal of Parkinson's Disease, 11, pp. 1157 - 1165, http://dx.doi.org/10.3233/JPD-202508

Mestre TA; Fereshtehnejad SM; Berg D; Bohnen NI; Dujardin K; Erro R; Espay AJ; Halliday G; Van Hilten JJ; Hu MT; Jeon B; Klein C; Leentjens AFG; Marinus J; Mollenhauer B; Postuma R; Rajalingam R; Rodríguez-Violante M; Simuni T; Surmeier DJ; Weintraub D; McDermott MP; Lawton M; Marras C, 2021, 'Parkinson's Disease Subtypes: Critical Appraisal and Recommendations', Journal of Parkinson's Disease, 11, pp. 395 - 404, http://dx.doi.org/10.3233/JPD-202472

Ferreira N; Richner M; Van Der Laan A; Bergholdt Jul Christiansen I; Vægter CB; Nyengaard JR; Halliday GM; Weis J; Giasson BI; Mackenzie IR; Jensen PH; Jan A, 2021, 'Prodromal neuroinvasion of pathological α-synuclein in brainstem reticular nuclei and white matter lesions in a model of α-synucleinopathy', Brain Communications, 3, http://dx.doi.org/10.1093/braincomms/fcab104

Ahmed RM; Bocchetta M; Todd EG; Tse NY; Devenney EM; Tu S; Caga J; Hodges JR; Halliday GM; Irish M; Kiernan MC; Piguet O; Rohrer JD, 2021, 'Tackling clinical heterogeneity across the amyotrophic lateral sclerosis-frontotemporal dementia spectrum using a transdiagnostic approach', Brain Communications, 3, http://dx.doi.org/10.1093/braincomms/fcab257

De Boer EMJ; Orie VK; Williams T; Baker MR; De Oliveira HM; Polvikoski T; Silsby M; Menon P; Van Den Bos M; Halliday GM; Van Den Berg LH; Van Den Bosch L; Van Damme P; Kiernan M; Van Es MA; Vucic S, 2021, 'TDP-43 proteinopathies: A new wave of neurodegenerative diseases', Journal of Neurology, Neurosurgery and Psychiatry, 92, pp. 86 - 95, http://dx.doi.org/10.1136/jnnp-2020-322983

de Boer SCM; Van Der Lee SJ; Diehl‐Schmid J; Riedl L; Piguet O; Halliday GM; Galimberti D; Sorrentino F; Ducharme S; Fieldhouse JLP; Reus LM; Pijnenburg YAL, 2021, 'Differences in sex distribution between genetic and sporadic FTD', Alzheimer's & Dementia, 17, http://dx.doi.org/10.1002/alz.052836

Phillips JR; Matar E; Ehgoetz Martens KA; Moustafa AA; Halliday GM; Lewis SJG, 2021, 'Evaluating a novel behavioral paradigm for visual hallucinations in Dementia with Lewy bodies.', Aging Brain, 1, pp. 100011, http://dx.doi.org/10.1016/j.nbas.2021.100011

Stankovic I; Fanciulli A; Kostic VS; Krismer F; Meissner WG; Palma JA; Panicker JN; Seppi K; Wenning GK; MoDiMSA Study Group , 2021, 'Laboratory-Supported Multiple System Atrophy beyond Autonomic Function Testing and Imaging: A Systematic Review by the MoDiMSA Study Group.', Mov Disord Clin Pract, 8, pp. 322 - 340, http://dx.doi.org/10.1002/mdc3.13158

Roudeau S; Trist BG; Carmona A; Davies KM; M. Halliday G; Rufin Y; Claverol S; Van Malderen SJM; Falkenberg G; Double KL; Ortega R, 2020, 'Native Separation and Metallation Analysis of SOD1 Protein from the Human Central Nervous System: A Methodological Workflow', , http://dx.doi.org/10.26434/chemrxiv.13415918

Katzeff JS; Bright F; Lo K; Kril JJ; Connolly A; Crossett B; Ittner LM; Kassiou M; Loy CT; Hodges JR; Piguet O; Kiernan MC; Halliday GM; Kim WS, 2020, 'Altered serum protein levels in frontotemporal dementia and amyotrophic lateral sclerosis indicate calcium and immunity dysregulation', Scientific Reports, 10, http://dx.doi.org/10.1038/s41598-020-70687-7

Vallerga CL; Zhang F; Fowdar J; McRae AF; Qi T; Nabais MF; Zhang Q; Kassam I; Henders AK; Wallace L; Montgomery G; Chuang YH; Horvath S; Ritz B; Halliday G; Hickie I; Kwok JB; Pearson J; Pitcher T; Kennedy M; Bentley SR; Silburn PA; Yang J; Wray NR; Lewis SJG; Anderson T; Dalrymple-Alford J; Mellick GD; Visscher PM; Gratten J, 2020, 'Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease', Nature Communications, 11, http://dx.doi.org/10.1038/s41467-020-15065-7

Szeto JYY; Walton CC; Rizos A; Martinez-Martin P; Halliday GM; Naismith SL; Chaudhuri KR; Lewis SJG, 2020, 'Dementia in long-term Parkinson’s disease patients: a multicentre retrospective study', npj Parkinson's Disease, 6, http://dx.doi.org/10.1038/s41531-019-0106-4

Gao Y; Wang T; Yu X; Ferrari R; 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; 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; George-Hyslop PS; 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; Cruts M; Van Broeckhoven C; Cappa SF; Leber 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, 2020, 'Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis', Scientific Reports, 10, http://dx.doi.org/10.1038/s41598-020-68848-9

Halliday G, 2020, 'Neglected cytotoxic T cell invasion of the brain: How specific for Parkinson's disease?', Brain, 143, pp. 3518 - 3521, http://dx.doi.org/10.1093/brain/awaa390

Phan K; He Y; Pickford R; Bhatia S; Katzeff JS; Hodges JR; Piguet O; Halliday GM; Kim WS, 2020, 'Uncovering pathophysiological changes in frontotemporal dementia using serum lipids', Scientific Reports, 10, http://dx.doi.org/10.1038/s41598-020-60457-w

Phillips JR; Matar E; Martens KAE; Halliday GM; Moustafa AA; Lewis SJG, 2020, 'Evaluating the Sustained Attention Response Task to Quantify Cognitive Fluctuations in Dementia With Lewy Bodies', Journal of Geriatric Psychiatry and Neurology, 33, pp. 333 - 339, http://dx.doi.org/10.1177/0891988719882093

Kwok JB; Loy CT; Dobson-Stone C; Halliday GM, 2020, 'The complex relationship between genotype, pathology and phenotype in familial dementia', Neurobiology of Disease, 145, http://dx.doi.org/10.1016/j.nbd.2020.105082

Raupach AK; Ehgoetz Martens KA; Memarian N; Zhong G; Matar E; Halliday GM; Grunstein R; Lewis SJG, 2020, 'Assessing the role of nocturnal core body temperature dysregulation as a biomarker of neurodegeneration', Journal of Sleep Research, 29, http://dx.doi.org/10.1111/jsr.12939

Gokool A; Loy CT; Halliday GM; Voineagu I, 2020, 'Circular RNAs: The Brain Transcriptome Comes Full Circle', Trends in Neurosciences, 43, pp. 752 - 766, http://dx.doi.org/10.1016/j.tins.2020.07.007

Zhao Y; Keshiya S; Perera G; Schramko L; Halliday GM; Dzamko N, 2020, 'LRRK2 kinase inhibitors reduce alpha-synuclein in human neuronal cell lines with the G2019S mutation', Neurobiology of Disease, 144, http://dx.doi.org/10.1016/j.nbd.2020.105049

Chen Z; Yan Yau W; Jaunmuktane Z; Tucci A; Sivakumar P; Gagliano Taliun SA; Turner C; Efthymiou S; Ibáñez K; Sullivan R; Bibi F; Athanasiou-Fragkouli A; Bourinaris T; Zhang D; Revesz T; Lashley T; DeTure M; Dickson DW; Josephs KA; Gelpi E; Kovacs GG; Halliday G; Rowe DB; Blair I; Tienari PJ; Suomalainen A; Fox NC; Wood NW; Lees AJ; Haltia MJ; Hardy J; Ryten M; Vandrovcova J; Houlden H; Ambrose JC; Arumugam P; Baple EL; Bleda M; Boardman-Pretty F; Boissiere JM; Boustred CR; Brittain H; Caulfield MJ; Chan GC; Craig CEH; Daugherty LC; de Burca A; Devereau A; Elgar G; Foulger RE; Fowler T; Furió-Tarí P; Hackett JM; Halai D; Hamblin A; Henderson S; Holman JE; Hubbard TJP; Jackson R; Jones LJ; Kasperaviciute D; Kayikci M; Lahnstein L; Lawson K; Leigh SEA; Leong IUS; Lopez FJ; Maleady-Crowe F; Mason J; McDonagh EM; Moutsianas L; Mueller M; Murugaesu N; Need AC; Odhams CA; Patch C; Perez-Gil D; Polychronopoulos D; Pullinger J; Rahim T; Rendon A; Riesgo-Ferreiro P; Rogers T; Ryten M; Savage K; Sawant K; Scott RH; Siddiq A; Sieghart A; Smedley D; Smith KR; Sosinsky A; Spooner W; Stevens HE; Stuckey A; Sultana R; Thomas ERA; Thompson SR; Tregidgo C, 2020, 'Neuronal intranuclear inclusion disease is genetically heterogeneous', Annals of Clinical and Translational Neurology, 7, pp. 1716 - 1725, http://dx.doi.org/10.1002/acn3.51151

Ehgoetz Martens KA; Matar E; Shine JM; Phillips JR; Georgiades MJ; Grunstein RR; Halliday GM; Lewis SJG, 2020, 'The Neural Signature of Impaired Dual-Tasking in Idiopathic Rapid Eye Movement Sleep Behavior Disorder Patients', Movement Disorders, 35, pp. 1596 - 1606, http://dx.doi.org/10.1002/mds.28114

Newman M; Nik HM; Sutherland GT; Hin N; Kim WS; Halliday GM; Jayadev S; Smith C; Laird AS; Lucas CW; Kittipassorn T; Peet DJ; Lardelli M, 2020, 'Accelerated loss of hypoxia response in zebrafish with familial Alzheimer's disease-like mutation of presenilin 1', Human Molecular Genetics, 29, pp. 2379 - 2394, http://dx.doi.org/10.1093/hmg/ddaa119

Shepherd CE; Affleck AJ; Bahar AY; Carew-Jones F; Gregory G; Small DH; Halliday GM, 2020, 'Alzheimer's amyloid-β and tau protein accumulation is associated with decreased expression of the LDL receptor-associated protein in human brain tissue', Brain and Behavior, 10, http://dx.doi.org/10.1002/brb3.1672

Piras IS; Bleul C; Schrauwen I; Schrauwen I; Talboom J; Llaci L; De Both MD; Naymik MA; Halliday G; Bettencourt C; Holton JL; Serrano GE; Sue LI; Beach TG; Stefanova N; Huentelman MJ, 2020, 'Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease', Acta Neuropathologica Communications, 8, http://dx.doi.org/10.1186/s40478-020-00950-5

Forrest SL; Halliday GM; Shepherd CE; Kwok JB; Hallupp M; Kril JJ, 2020, 'Are mutations in MAPT associated with GGT type III?', Neuropathology and Applied Neurobiology, 46, pp. 406 - 409, http://dx.doi.org/10.1111/nan.12583

van der Lee SJ; Conway OJ; Jansen I; Carrasquillo MM; Kleineidam L; van den Akker E; Hernández I; van Eijk KR; Stringa N; Chen JA; Zettergren A; Andlauer TFM; Diez-Fairen M; Simon-Sanchez J; Lleó A; Zetterberg H; Nygaard M; Blauwendraat C; Savage JE; Mengel-From J; Moreno-Grau S; Wagner M; Fortea J; Keogh MJ; Blennow K; Skoog I; Friese MA; Pletnikova O; Zulaica M; Lage C; de Rojas I; Riedel-Heller S; Illán-Gala I; Wei W; Jeune B; Orellana A; Then Bergh F; Wang X; Hulsman M; Beker N; Tesi N; Morris CM; Indakoetxea B; Collij LE; Scherer M; Morenas-Rodríguez E; Ironside JW; van Berckel BNM; Alcolea D; Wiendl H; Strickland SL; Pastor P; Rodríguez Rodríguez E; Mead S; Synofzik M; van Swieten JC; Leber I; Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; 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; Blesa R; Landqvist Waldö M; 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, 2020, 'Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)', Acta Neuropathologica, 139, pp. 959 - 962, http://dx.doi.org/10.1007/s00401-019-02107-8

Shepherd CE; Affleck AJ; Bahar AY; Carew-Jones F; Halliday GM, 2020, 'Intracellular and secreted forms of clusterin are elevated early in Alzheimer's disease and associate with both Aβ and tau pathology', Neurobiology of Aging, 89, pp. 129 - 131, http://dx.doi.org/10.1016/j.neurobiolaging.2019.10.025

Hughes LP; Halliday GM; Dzamko N, 2020, 'Flow Cytometry Measurement of Glucocerebrosidase Activity in Human Monocytes', Bio-protocol, 10, http://dx.doi.org/10.21769/BioProtoc.3572

Ling H; Gelpi E; Davey K; Jaunmuktane Z; Mok KY; Jabbari E; Simone R; R’Bibo L; Brandner S; Ellis MJ; Attems J; Mann D; Halliday GM; Al-Sarraj S; Hedreen J; Ironside JW; Kovacs GG; Kovari E; Love S; Vonsattel JPG; Allinson KSJ; Hansen D; Bradshaw T; Setó-Salvia N; Wray S; de Silva R; Morris HR; Warner TT; Hardy J; Holton JL; Revesz T, 2020, 'Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates', Acta Neuropathologica, 139, pp. 717 - 734, http://dx.doi.org/10.1007/s00401-019-02119-4

Piras IS; Bleul C; Talboom JS; De Both MD; Schrauwen I; Halliday G; Myers AJ; Serrano GE; Beach TG; Huentelman MJ, 2020, 'ESHRD: Deconvolution of brain homogenate rna expression data to identify novel cell-type-specific alterations in Alzheimer's disease', Aging, 12, pp. 4124 - 4162, http://dx.doi.org/10.18632/aging.102840

Amadoru S; Doré V; McLean CA; Hinton F; Shepherd CE; Halliday GM; Leyton CE; Yates PA; Hodges JR; Masters CL; Villemagne VL; Rowe CC, 2020, 'Comparison of amyloid PET measured in Centiloid units with neuropathological findings in Alzheimer's disease', Alzheimer's Research and Therapy, 12, http://dx.doi.org/10.1186/s13195-020-00587-5

Dobson-Stone C; Hallupp M; Shahheydari H; Ragagnin AMG; Chatterton Z; Carew-Jones F; Shepherd CE; Stefen H; Paric E; Fath T; Thompson EM; Blumbergs P; Short CL; Field CD; Panegyres PK; Hecker J; Nicholson G; Shaw AD; Fullerton JM; Luty AA; Schofield PR; Brooks WS; Rajan N; Bennett MF; Bahlo M; Shankaracharya ; Landers JE; Piguet O; Hodges JR; Halliday GM; Topp SD; Smith BN; Shaw CE; McCann E; Fifita JA; Williams KL; Atkin JD; Blair IP; Kwok JB, 2020, 'CYLD is a causative gene for frontotemporal dementia - Amyotrophic lateral sclerosis', Brain, 143, pp. 783 - 799, http://dx.doi.org/10.1093/brain/awaa039

Tan RH; Halliday GM, 2020, 'Author response: The underacknowledged PPA-ALS: A unique clinicopathologic subtype with strong heritability', Neurology, 94, pp. 283, http://dx.doi.org/10.1212/WNL.0000000000008921

Moore KM; Nicholas J; Grossman M; McMillan CT; Irwin DJ; Massimo L; Van Deerlin VM; Warren JD; Fox NC; Rossor MN; Mead S; Bocchetta M; Boeve BF; Knopman DS; Graff-Radford NR; Forsberg LK; Rademakers R; Wszolek ZK; van Swieten JC; Jiskoot LC; Meeter LH; Dopper EG; Papma JM; Snowden JS; Saxon J; Jones M; Pickering-Brown S; Le Ber I; Camuzat A; Brice A; Caroppo P; Ghidoni R; Pievani M; Benussi L; Binetti G; Dickerson BC; Lucente D; Krivensky S; Graff C; Öijerstedt L; Fallström M; Thonberg H; Ghoshal N; Morris JC; Borroni B; Benussi A; Padovani A; Galimberti D; Scarpini E; Fumagalli GG; Mackenzie IR; Hsiung GYR; Sengdy P; Boxer AL; Rosen H; Taylor JB; Synofzik M; Wilke C; Sulzer P; Hodges JR; Halliday G; Kwok J; Sanchez-Valle R; Lladó A; Borrego-Ecija S; Santana I; Almeida MR; Tábuas-Pereira M; Moreno F; Barandiaran M; Indakoetxea B; Levin J; Danek A; Rowe JB; Cope TE; Otto M; Anderl-Straub S; de Mendonça A; Maruta C; Masellis M; Black SE; Couratier P; Lautrette G; Huey ED; Sorbi S; Nacmias B; Laforce R; Tremblay MPL; Vandenberghe R; Damme PV; Rogalski EJ; Weintraub S; Gerhard A; Onyike CU; Ducharme S; Papageorgiou SG; Ng ASL; Brodtmann A; Finger E; Guerreiro R, 2020, 'Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study', The Lancet Neurology, 19, pp. 145 - 156, http://dx.doi.org/10.1016/S1474-4422(19)30394-1

Matar E; Ehgoetz Martens KA; Halliday GM; Lewis SJG, 2020, 'Clinical features of Lewy body dementia: insights into diagnosis and pathophysiology', Journal of Neurology, 267, pp. 380 - 389, http://dx.doi.org/10.1007/s00415-019-09583-8

Orme T; Hernandez D; Ross OA; Kun-Rodrigues C; Darwent L; Shepherd CE; Parkkinen L; Ansorge O; Clark L; Honig LS; Marder K; Lemstra A; Rogaeva E; St. George-Hyslop P; Londos E; Zetterberg H; Morgan K; Troakes C; Al-Sarraj S; Lashley T; Holton J; Compta Y; Van Deerlin V; Trojanowski JQ; Serrano GE; Beach TG; Lesage S; Galasko D; Masliah E; Santana I; Pastor P; Tienari PJ; Myllykangas L; Oinas M; Revesz T; Lees A; Boeve BF; Petersen RC; Ferman TJ; Escott-Price V; Graff-Radford N; Cairns NJ; Morris JC; Pickering-Brown S; Mann D; Halliday G; Stone DJ; Dickson DW; Hardy J; Singleton A; Guerreiro R; Bras J, 2020, 'Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies', Acta Neuropathologica Communications, 8, http://dx.doi.org/10.1186/s40478-020-0879-z

Carter A; Richards LJ; Apthorp D; Azghadi MR; Badcock DR; Balleine B; Bekkers JM; Berk M; Bourne JA; Bradley AP; Breakspear M; Brichta A; Carter O; Castles A; Chakli K; Cohen-Woods S; Conn SJ; Cornish J; Cornish K; de Zubicaray G; Egan GF; Enticott PG; Fitzgibbon BM; Forlini C; Fornito A; Griffiths L; Gullifer J; Hall W; Halliday G; Hannan AJ; Harrer S; Harvey A; Hatherly C; Hickie IB; Kennett J; Kiernan M; Kilpatrick T; Kiral-Kornek I; Korgaonkar MS; Lawrence AJ; Leventer R; Levy N; Licinio J; Lovell N; Mackellar G; Malcolm L; Mason A; Mattingley JB; Medland SE; Michie PT; Nithianantharajah J; Parker J; Payne JM; Poole-Warren L; Sah P; Sarnyai Z; Schofield PR; Shimoni O; Shum DHK; Silk T; Slee M; Smith AE; Soulis T; Sriram S; Stuart GJ; Tapson J; Thompson MB; van Schaik A; Vincent NA; Vissel B; Waters A, 2020, 'Erratum: A Neuroethics Framework for the Australian Brain Initiative (Neuron (2019) 101(3) (365–369), (S0896627319300054), (10.1016/j.neuron.2019.01.004))', Neuron, 105, pp. 201, http://dx.doi.org/10.1016/j.neuron.2019.12.019

Szeto JYY; Walton CC; Rizos A; Martinez-Martin P; Halliday GM; Naismith SL; Chaudhuri KR; Lewis SJG, 2020, 'Dementia in long-term Parkinson's disease patients: a multicentre retrospective study.', NPJ Parkinsons Dis, 6, pp. 2, http://dx.doi.org/10.1038/s41531-019-0106-4

Forrest SL; Halliday GM; Sizemova A; van Roijen M; McGinley CV; Bright F; Kapur M; McGeachie AB; McCann H; Shepherd CE; Tan RH; Affleck AJ; Huang Y; Kril JJ, 2020, 'A practical approach to differentiate the frontotemporal tauopathy subtypes', Journal of Neuropathology and Experimental Neurology, 79, pp. 1122 - 1126, http://dx.doi.org/10.1093/jnen/nlaa100

Affleck AJ; Sachdev PS; Stevens J; Halliday GM, 2020, 'Antihypertensive medications ameliorate Alzheimer's disease pathology by slowing its propagation', Alzheimer's and Dementia: Translational Research and Clinical Interventions, 6, http://dx.doi.org/10.1002/trc2.12060

Ehgoetz Martens KA; Matar E; Hall JM; Phillips J; Szeto JYY; Gouelle A; Grunstein RR; Halliday GM; Lewis SJG, 2020, 'Invited Reply to: “Instrumental Analysis of Gait Abnormalities in Idiopathic Rapid Eye Movement Sleep Behavior Disorder”', Movement Disorders, 35, pp. 195 - 196, http://dx.doi.org/10.1002/mds.27939

Amadoru S; Doré V; McLean C; Hinton F; Shepherd C; Halliday G; Leyton C; Yates P; Hodges J; Masters C; Villemagne V; Rowe C, 2020, 'Comparison of amyloid PET measured in Centiloid units with neuropathological findings in Alzheimer’s Disease', , http://dx.doi.org/10.21203/rs.2.17082/v2

Bechara JA; Brooks WS; Kwok JB; Halliday GM; Schofield PR, 2020, 'Familial Alzheimer’s disease in Australia', Alzheimer's & Dementia, 16, http://dx.doi.org/10.1002/alz.040062

Roudeau S; Trist B; Carmona A; Davies K; M. Halliday G; Rufin Y; Claverol S; Van Malderen SJM; Falkenberg G; Double K; Ortega R, 2020, 'Native Separation and Metallation Analysis of SOD1 Protein from the Human Central Nervous System: A Methodological Workflow', , http://dx.doi.org/10.26434/chemrxiv.13415918.v1

Pires G; McElligott S; Drusinsky S; Halliday G; Potier MC; Wisniewski T; Drummond E, 2019, 'Secernin-1 is a novel phosphorylated tau binding protein that accumulates in Alzheimer's disease and not in other tauopathies', Acta Neuropathologica Communications, 7, http://dx.doi.org/10.1186/s40478-019-0848-6

Bonham LW; Steele NZR; Karch CM; Broce I; Geier EG; Wen NL; Momeni P; Hardy J; Miller ZA; Gorno-Tempini ML; Hess CP; Lewis P; Miller BL; Seeley WW; Manzoni C; Desikan RS; Baranzini SE; Ferrari R; Yokoyama JS; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; 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; 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; Cruts M; Van Broeckhoven C; Cappa SF; Leber I; Hannequin D, 2019, 'Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia', Scientific Reports, 9, http://dx.doi.org/10.1038/s41598-019-46415-1

Forrest SL; Halliday GM; McCann H; McGeachie AB; McGinley CV; Hodges JR; Piguet O; Kwok JB; Spillantini MG; Kril JJ, 2019, 'Heritability in frontotemporal tauopathies', Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 11, pp. 115 - 124, http://dx.doi.org/10.1016/j.dadm.2018.12.001

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