Michelle K Lupton
Michelle K Lupton
Genetic Epidemiology, QIMR Berghofer Medical Research Institute, Queensland, Australia.
Підтверджена електронна адреса в QIMRberghofer.edu.au
НазваПосиланняРік
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ...
Nature genetics 41 (10), 1088, 2009
22652009
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452, 2013
19212013
TREM2 variants in Alzheimer's disease
R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ...
New England Journal of Medicine 368 (2), 117-127, 2013
15042013
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429, 2011
13722011
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nat Genet 46 (9), 989-93, 2014
9512014
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550, 2014
3262014
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
2972018
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
L Jones, PA Holmans, ML Hamshere, D Harold, V Moskvina, D Ivanov, ...
PloS one 5 (11), e13950, 2010
2762010
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373, 2017
2322017
The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
BN Smith, S Newhouse, A Shatunov, C Vance, S Topp, L Johnson, ...
European Journal of Human Genetics 21 (1), 102, 2013
1622013
The HdhQ150/Q150 knock-in mouse model of HD and the R6/2 exon 1 model develop comparable and widespread molecular phenotypes
B Woodman, R Butler, C Landles, MK Lupton, J Tse, E Hockly, H Moffitt, ...
Brain research bulletin 72 (2-3), 83-97, 2007
1552007
Plasma proteins predict conversion to dementia from prodromal disease
A Hye, J Riddoch-Contreras, AL Baird, NJ Ashton, C Bazenet, R Leung, ...
Alzheimer's & Dementia 10 (6), 799-807. e2, 2014
1532014
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
G Coppola, S Chinnathambi, JJY Lee, BA Dombroski, MC Baker, ...
Human molecular genetics 21 (15), 3500-3512, 2012
1492012
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis
SH Lee, D Harold, DR Nyholt, ME Goddard, KT Zondervan, J Williams, ...
Human molecular genetics 22 (4), 832-841, 2012
1282012
A novel Alzheimer disease locus located near the gene encoding tau protein
G Jun, CA Ibrahim-Verbaas, M Vronskaya, JC Lambert, J Chung, AC Naj, ...
Molecular psychiatry 21 (1), 108, 2016
1082016
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population
IJDAMMI T-K Clarke, MK Lupton, AM Fernandez-Pujals, J Starr, G Davies, S Cox ...
Molecular Psychiatry, 2015
95*2015
Missense variant in TREML2 protects against Alzheimer's disease
BA Benitez, SC Jin, R Guerreiro, R Graham, J Lord, D Harold, R Sims, ...
Neurobiology of aging 35 (6), 1510. e19-1510. e26, 2014
852014
A paired RNAi and RabGAP overexpression screen identifies Rab11 as a regulator of β-amyloid production
V Udayar, V Buggia-Prévot, RL Guerreiro, G Siegel, N Rambabu, ...
Cell reports 5 (6), 1536-1551, 2013
792013
Genome-wide association study of Alzheimer's disease with psychotic symptoms
P Hollingworth, R Sweet, R Sims, D Harold, G Russo, R Abraham, ...
Molecular psychiatry 17 (12), 1316, 2012
702012
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases.
IPDGC IPDGC), PD consortium.
Neurobiol Aging 36 (3), 1605.e7-12, 2015
64*2015
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