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Michael Hayden
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Year
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
A Brooks-Wilson, M Marcil, SM Clee, LH Zhang, K Roomp, M van Dam, ...
Nature genetics 22 (4), 336-345, 1999
20691999
Unified Huntington's disease rating scale: reliability and consistency
HPH Kremer, Hungtington Study Group
Movement disorders 11, 136-142, 1996
18481996
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato, A Ciammola, D Rigamonti, BR Leavitt, D Goffredo, L Conti, ...
Science 293 (5529), 493-498, 2001
15182001
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
SE Andrew, Y Paul Goldberg, B Kremer, H Telenius, J Theilmann, ...
Nature genetics 4 (4), 398-403, 1993
13861993
Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis
G Papanikolaou, ME Samuels, EH Ludwig, MLE MacDonald, ...
Nature genetics 36 (1), 77-82, 2004
11932004
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines
AV Panov, CA Gutekunst, BR Leavitt, MR Hayden, JR Burke, ...
Nature neuroscience 5 (8), 731-736, 2002
11902002
Huntington disease
GP Bates, R Dorsey, JF Gusella, MR Hayden, C Kay, BR Leavitt, M Nance, ...
Nature reviews Disease primers 1 (1), 1-21, 2015
11022015
Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes
C Zuccato, M Tartari, A Crotti, D Goffredo, M Valenza, L Conti, ...
Nature genetics 35 (1), 76-83, 2003
10752003
Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes
J Nasir, SB Floresco, JR O'Kusky, VM Diewert, JM Richman, J Zeisler, ...
Cell 81 (5), 811-823, 1995
10401995
A YAC mouse model for Huntington’s disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration
JG Hodgson, N Agopyan, CA Gutekunst, BR Leavitt, F LePiane, DJ Smith, ...
Neuron 23 (1), 181-192, 1999
10031999
Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease
EJ Slow, J van Raamsdonk, D Rogers, SH Coleman, RK Graham, Y Deng, ...
Human molecular genetics 12 (13), 1555-1567, 2003
8892003
Detection of Huntington’s disease decades before diagnosis: the Predict-HD study
JS Paulsen, DR Langbehn, JC Stout, E Aylward, CA Ross, M Nance, ...
Journal of Neurology, Neurosurgery & Psychiatry 79 (8), 874-880, 2008
8472008
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
S Hadano, CK Hand, H Osuga, Y Yanagisawa, A Otomo, RS Devon, ...
Nature genetics 29 (2), 166-173, 2001
8342001
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length
DR Langbehn, RR Brinkman, D Falush, JS Paulsen, MR Hayden, ...
Clinical genetics 65 (4), 267-277, 2004
8302004
Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract
YP Goldberg, DW Nicholson, DM Rasper, MA Kalchman, HB Koide, ...
Nature genetics 13 (4), 442-449, 1996
7961996
Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin
RK Graham, Y Deng, EJ Slow, B Haigh, N Bissada, G Lu, J Pearson, ...
Cell 125 (6), 1179-1191, 2006
7822006
A worldwide study of the Huntington's disease mutation: the sensitivity and specificity of measuring CAG repeats
B Kremer, P Goldberg, SE Andrew, J Theilmann, H Telenius, J Zeisler, ...
New England Journal of Medicine 330 (20), 1401-1406, 1994
7581994
Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease
MM Zeron, O Hansson, N Chen, CL Wellington, BR Leavitt, P Brundin, ...
Neuron 33 (6), 849-860, 2002
7182002
Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract
CL Wellington, LM Ellerby, AS Hackam, RL Margolis, MA Trifiro, ...
Journal of Biological Chemistry 273 (15), 9158-9167, 1998
6971998
Phenotypic characterization of individuals with 30–40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals …
DC Rubinsztein, J Leggo, R Coles, E Almqvist, V Biancalana, ...
American journal of human genetics 59 (1), 16, 1996
6641996
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