scholarly journals Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study

2008 ◽  
Vol 65 (11) ◽  
pp. 1518 ◽  
Author(s):  
Joseph H. Lee
2011 ◽  
Vol 23 (2) ◽  
pp. 249-255 ◽  
Author(s):  
Robert S. Wilson ◽  
Sandra Barral ◽  
Joseph H. Lee ◽  
Sue E. Leurgans ◽  
Tatiana M. Foroud ◽  
...  

2022 ◽  
Author(s):  
Dolly Reyes‐Dumeyer ◽  
Kelley Faber ◽  
Badri Vardarajan ◽  
Alison Goate ◽  
Alan Renton ◽  
...  

2000 ◽  
Vol 15 (S2) ◽  
pp. 390s-390s
Author(s):  
R. Heun ◽  
A. Papassotiropoulos ◽  
F. Jessen ◽  
W. Maier ◽  
J.C.S. Breitner

Brain ◽  
2019 ◽  
Vol 142 (11) ◽  
pp. 3375-3381 ◽  
Author(s):  
Ming Zhang ◽  
Allison A Dilliott ◽  
Roaa Khallaf ◽  
John F Robinson ◽  
Robert A Hegele ◽  
...  

Zhang, Dilliott et al. examine a unique family with early- and late-onset Alzheimer’s disease phenotypes, as well as disease-discordant monozygotic triplets. The triplets and the patient with early-onset disease are carriers of the APOE ε4-allele plus rare substitutions in other genes. Epigenetic analyses suggest accelerated ageing in the early-onset patient.


2021 ◽  
Author(s):  
Dolly Reyes-Dumeyer ◽  
Kelley Faber ◽  
Badri N. Vardarajan ◽  
Alison Goate ◽  
Alan Renton ◽  
...  

INTRODUCTION: The National Institute on Aging Late-Onset Alzheimers Disease Family Based Study (NIA-LOAD FBS) was established to study the genetic etiology of Alzheimers disease (AD). METHODS: Recruitment focused on families with two living affected siblings and a third first degree relative similar in age with or without dementia. Uniform assessments were completed, DNA was obtained as was neuropathology, when possible. APOE genotypes, genome-wide SNP arrays and sequencing was completed in the majority of families. RESULTS: A wide range in the age-at-onset in many large families was related to APOE genotype, but not in all. Variants typically associated with early-onset AD and frontotemporal dementia were also found. DISCUSSION: The NIA-LOAD FBS is the largest collection of familial AD worldwide, and data or samples have been included in 126 publications addressing the genetic etiology of AD. Genetic heterogeneity and variability in the age-at-onset provides opportunities to investigate the complexity of familial AD.


2014 ◽  
Vol 35 (3) ◽  
pp. 725.e7-725.e10 ◽  
Author(s):  
E. van Exel ◽  
P. Eikelenboom ◽  
H. Comijs ◽  
D.J.H. Deeg ◽  
M.L. Stek ◽  
...  

2003 ◽  
Author(s):  
J. M. Silverman ◽  
C. J. Smith ◽  
D. B. Marin ◽  
R. C. Mohs ◽  
C. B. Propper

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