Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A diffusion model analysis of episodic recognition in preclinical individuals with a family history for Alzheimer's disease: The adult children study.

Neuropsychology - 1 Feb 2016

Aschenbrenner Andrew J, Balota David A, Gordon Brian A, Ratcliff Roger, Morris John C

Abstract excerpt

OBJECTIVE: A family history of Alzheimer's disease (AD) increases the risk of developing AD and can influence the accumulation of well-established AD biomarkers. There is some evidence that family history can influence episodic memory performance even in cognitively normal individuals. We attempted to replicate the effect of family history on episodic memory and used a specific computational model of binary...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adult Children
Share to Apolipoprotein E4

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Apolipoproteins E

Share to Cognition

Share to Cognition Disorders

Share to Memory, Episodic

Share to Reaction Time

Source

Open in PubMed Open full text

Identifiers

PMID: 26192539
DOI: 10.1037/neu0000222
PMCID: PMC4720576

Genes

APOE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A diffusion model analysis of episodic recognition in preclinical individuals with a family history for Alzheimer's disease: The adult children study.PMID 26192539Read ↗

Influence of Alzheimer disease family history and genetic risk on cognitive performance in healthy middle-aged and older people.Semantic proximity Read ↗

Computational modeling of the N-Back task in the ABCD study: associations of drift diffusion model parameters to polygenic scores of mental disorders and cardiometabolic diseasesSemantic proximity Read ↗

Impairment of memory generalization in preclinical autosomal dominant Alzheimer's disease mutation carriers.Semantic proximity Read ↗

Computational Modeling of the n-Back Task in the ABCD Study: Associations of Drift Diffusion Model Parameters to Polygenic Scores of Mental Disorders and Cardiometabolic Diseases.Semantic proximity Read ↗

Predicting Alzheimer's disease with practice effects, APOE genotype and brain metabolism.Semantic proximity Read ↗

APOE4 status is related to differences in memory-related brain function in asymptomatic older adults: Baseline analysis of the PREVENT-AD task fMRI datasetSemantic proximity Read ↗

Family history and APOE4 risk for Alzheimer’s Disease impact the neural correlates of episodic memory by early midlifeSemantic proximity Read ↗

Episodic memory retrieval with increasing task demand: Associations with age, <i>APOE4</i> genotype, and Alzheimer’s disease pathologySemantic proximity Read ↗

A Three-Factor Structure of Cognitive Functioning Among Unimpaired Carriers and Non-Carriers of Autosomal-Dominant Alzheimer's Disease.Semantic proximity Read ↗

Reaction time and response inhibition in autosomal dominant Alzheimer's disease.Semantic proximity Read ↗

Past and future episodic detail retrieval is reduced among clinically normal older adults at higher genetic risk for late-onset Alzheimer’s diseaseSemantic proximity Read ↗

Reduced expression of fMRI subsequent memory effects with increasing severity across the Alzheimer’s disease risk spectrumSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.