Genetic Influences on Atrophy Patterns in Familial Alzheimer's Disease: A Comparison of APP and PSEN1 Mutations-Reference-Cited by-同舟云学术

Genetic Influences on Atrophy Patterns in Familial Alzheimer's Disease: A Comparison of APP and PSEN1 Mutations

Published:2013-03-29 Issue:1 Volume:35 Page:199-212
ISSN:1875-8908
Container-title:Journal of Alzheimer's Disease
language:
Short-container-title:JAD

Author:

Scahill Rachael I.¹,Ridgway Gerard R.¹²,Bartlett Jonathan W.³,Barnes Josephine¹,Ryan Natalie S.¹,Mead Simon⁴,Beck Jonathan⁴,Clarkson Matthew J.¹⁵,Crutch Sebastian J.¹,Schott Jonathan M.¹,Ourselin Sebastien¹⁵,Warren Jason D.¹,Hardy John⁶,Rossor Martin N.¹,Fox Nick C.¹

Affiliation:

1. Dementia Research Centre, Department of Neurodegeneration, UCL Institute of Neurology, London, UK

2. Wellcome Trust Centre for Neuroimaging, UCL Institute of Neurology, London, UK

3. Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK

4. MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK

5. Centre for Medical Image Computing, University College London, London, UK

6. Reta Lila Weston Institute and Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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1. Shared and unique effects of ApoEε4 and pathogenic gene mutation on cognition and imaging in preclinical familial Alzheimer’s disease;Alzheimer's Research & Therapy;2023-02-28

2. Distribution of Cortical Atrophy Associated with Cognitive Decline in Alzheimer’s Disease: A Cross-Sectional Quantitative Structural MRI Study from PUMCH Dementia Cohort;Current Alzheimer Research;2022-07

3. The APOE ε4 Allele Affects Cognitive Functions Differently in Carriers of APP Mutations Compared to Carriers of PSEN1 Mutations in Autosomal-Dominant Alzheimer’s Disease;Genes;2021-12-07

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