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Annals of Neurology|August 4, 2026
Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease RiskAndrés Peña-Tauber, Ricardo Hernández Arriaza, Dylan Reil, et al.
JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.
Brain : a Journal of Neurology|October 23, 2015
Common polygenic variation enhances risk prediction for Alzheimer's diseaseValentina Escott-Price, Rebecca Sims, Christian Bannister, et al.
Neurobiology of Aging|February 17, 2009
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degenerationSara Rollinson, Patrizia Rizzu, Stephen Sikkink, et al.
American Journal of Human Genetics|February 26, 2013
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK populationJon Beck, Mark Poulter, Davina Hensman, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|August 28, 2014
R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementiaCatherine F Slattery, Jonathan A Beck, Lorna Harper, et al.
Neurology|June 8, 2019
Age at onset in genetic prion disease and the design of preventive clinical trialsEric Vallabh Minikel, Sonia M Vallabh, Margaret C Orseth, et al.
Age and Ageing|July 19, 2026
Multidisciplinary recommendations for palliative and supportive care in Creutzfeldt-Jakob disease and related disordersMelissa Ng, Anna Grundy, Brian Appleby, et al.
Plos One|July 9, 2019
Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's diseaseEmily Baker, Rebecca Sims, Ganna Leonenko, et al.
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