Sample Tracking and Use in Published Genome-wide Association StudiesHARDY, John.Archives of neurology (Chicago). 2010, Vol 67, Num 10, pp 1267-1268, issn 0003-9942, 2 p.Article

The amyloid hypothesis for Alzheimer's disease: a critical reappraisalHARDY, John.Journal of neurochemistry. 2009, Vol 110, Num 4, pp 1129-1134, issn 0022-3042, 6 p.Article

Reporting and interpretation of genetic variants in cases and controlsHARDY, John; SINGLETON, Andrew.Neurology. 2007, Vol 69, Num 1, pp 111-112, issn 0028-3878, 2 p.Article

Presenilin mutations line up along transmembrane α-helicesHARDY, John; CROOK, Richard.Neuroscience letters. 2001, Vol 306, Num 3, pp 203-205, issn 0304-3940Article

Impact of Genetic analysis on Parkinson's disease researchHARDY, John.Movement disorders. 2003, Vol 18, Num 6, pp S96-S98, issn 0885-3185, SUPConference Paper

The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeuticsHARDY, John; SELKOE, Dennis J.Science (Washington, D.C.). 2002, Vol 297, Num 5580, pp 353-356, issn 0036-8075Article

Clusterin as an Alzheimer BiomarkerHARDY, John; GUERREIRO, Rita; LOVESTONE, Simon et al.Archives of neurology (Chicago). 2011, Vol 68, Num 11, pp 1459-1460, issn 0003-9942, 2 p.Article

Milestones in PD GeneticsGASSER, Thomas; HARDY, John; MIZUNO, Yoshikuni et al.Movement disorders. 2011, Vol 26, Num 6, pp 1042-1048, issn 0885-3185, 7 p.Article

Ag-Al based air braze for high temperature electrochemical devicesKIM, Jinyong; HARDY, John S; WEIL, K. Scott et al.International journal of hydrogen energy. 2007, Vol 32, Num 16, pp 3754-3762, issn 0360-3199, 9 p.Conference Paper

The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseasesSINGLETON, Andrew; MYERS, Amanda; HARDY, John et al.Human molecular genetics (Print). 2004, Vol 13, pp R123-R126, issn 0964-6906, NS1Article

Epigenetic mechanisms in Alzheimer's disease: progress but much to doBALAZS, Robert; VERNON, Jeffrey; HARDY, John et al.Neurobiology of aging. 2011, Vol 32, Num 7, pp 1181-1187, issn 0197-4580, 7 p.Article

Complicated Recessive Dystonia Parkinsonism SyndromesSCHNEIDER, Susanne A; BHATIA, Kailash P; HARDY, John et al.Movement disorders. 2009, Vol 24, Num 4, pp 490-499, issn 0885-3185, 10 p.Article

Parkinson's diseaseLEES, Andrew J; HARDY, John; REVESZ, Tamas et al.Lancet (British edition). 2009, Vol 373, Num 9680, pp 2055-2066, issn 0140-6736, 12 p.Article

Dual-atmosphere tolerance of Ag-CuO-based air brazeKIM, Jinyong; HARDY, John S; WEIL, Scott et al.International journal of hydrogen energy. 2007, Vol 32, Num 16, pp 3655-3663, issn 0360-3199, 9 p.Conference Paper

Twenty years of Alzheimer's disease-causing mutationsGOATE, Alison; HARDY, John.Journal of neurochemistry. 2012, Vol 120, pp 3-8, issn 0022-3042, 6 p., SUP1Article

Production and Processing of Spider Silk ProteinsHARDY, John G; SCHEIBEL, Thomas R.Journal of polymer science. Part A. Polymer chemistry. 2009, Vol 47, Num 16, pp 3957-3963, issn 0887-624X, 7 p.Article

Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA): an Update on Clinical Presentations, Histological and Genetic Underpinnings, and Treatment ConsiderationsSCHNEIDER, Susanne A; HARDY, John; BHATIA, Kailash P et al.Movement disorders. 2012, Vol 27, Num 1, pp 42-53, issn 0885-3185, 12 p.Article

Apolipoprotein E genotype, cardiovascular biomarkers and risk of stroke: Systematic review and meta-analysis of 14015 stroke cases and pooled analysis of primary biomarker data from up to 60883 individualsKHAN, Tauseef A; SHAH, Tina; HUBACEK, Jaroslav A et al.International journal of epidemiology. 2013, Vol 42, Num 2, pp 475-492, issn 0300-5771, 18 p.Article

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72COOPER-KNOCK, Johnathan; HEWITT, Christopher; BAXTER, Lynne et al.Brain. 2012, Vol 135, pp 751-764, issn 0006-8950, 14 p., 3Article

Glucocerebrosidase Deficiency in Substantia Nigra of Parkinson Disease BrainsGEGG, Matthew E; BURKE, Derek; HEALES, Simon J. R et al.Annals of neurology. 2012, Vol 72, Num 3, pp 455-463, issn 0364-5134, 9 p.Article

Siblings With Ischemic Stroke Study: Results of a Genome-Wide Scan for Stroke LociMESCHIA, James F; NALLS, Michael; FERRUCCI, Luigi et al.Stroke (1970). 2011, Vol 42, Num 10, pp 2726-2732, issn 0039-2499, 7 p.Article

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseHAROLD, Denise; ABRAHAM, Richard; JONES, Nicola et al.Nature genetics. 2009, Vol 41, Num 10, pp 1088-1093, issn 1061-4036, 6 p.Article

Novel Progranulin Mutation : Screening for PGRN Mutations in a Portuguese Series of FTD/CBS CasesJOAO GUERREIRO, Rita; SANTANA, Isabel; BRAS, Jose Miguel et al.Movement disorders. 2008, Vol 23, Num 9, pp 1269-1273, issn 0885-3185, 5 p.Article

The etiopathogenesis of parkinson disease and suggestions for future research. Part IILITVAN, Irene; CHESSELET, Marie-Francoise; HALLETT, Mark et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 5, pp 329-336, issn 0022-3069, 8 p.Article

Correlations between apolipoprotein E ε4 gene dose and whole brain atrophy ratesCHEN, Kewei; REIMAN, Eric M; SAUNDERS, Ann M et al.The American journal of psychiatry. 2007, Vol 164, Num 6, pp 916-921, issn 0002-953X, 6 p.Article