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John Hardy, PhD, Imperial College 1979

Affiliations: 
University College London, London, United Kingdom 
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=13
Website:
http://www.ucl.ac.uk/rlweston-inst/people/john
Google:
"John Hardy"
Bio:

http://neuroscience.nih.gov/Lab.asp?Org_ID=436

http://www.nature.com/nm/journal/v10/n10/full/nm1004-1009.html

http://en.wikipedia.org/wiki/John_Hardy_(geneticist)

http://www.ucl.ac.uk/news/news-articles/0905/09051504/

Mean distance: 17.28 (cluster 28)
 
Cross-listing: Alzheimer's Tree

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Publications

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Bracher-Smith M, Leonenko G, Baker E, et al. (2022) Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis. Neurobiology of Aging. 119: 67-76
Stolp Andersen M, Tan M, Holtman IR, et al. (2022) Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease. Annals of Clinical and Translational Neurology
Escott-Price V, Hardy J. (2022) Genome-wide association studies for Alzheimer's disease: bigger is not always better. Brain Communications. 4: fcac125
Wong HY, Zhong H, Zhong M, et al. (2022) Demographics and Medication Use of Patients with Late-Onset Alzheimer's Disease in Hong Kong. Journal of Alzheimer's Disease : Jad
Stevenson-Hoare J, Heslegrave A, Leonenko G, et al. (2022) Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Brain : a Journal of Neurology
Bellenguez C, Küçükali F, Jansen IE, et al. (2022) New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics
Makarious MB, Leonard HL, Vitale D, et al. (2022) Multi-modality machine learning predicting Parkinson's disease. Npj Parkinson's Disease. 8: 35
Karlsson IK, Escott-Price V, Gatz M, et al. (2022) Measuring heritable contributions to Alzheimer's disease: polygenic risk score analysis with twins. Brain Communications. 4: fcab308
van Rheenen W, van der Spek RAA, Bakker MK, et al. (2022) Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics
van Rheenen W, van der Spek RAA, Bakker MK, et al. (2021) Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. 53: 1636-1648
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