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

Exome array study did not identify novel variants in Alzheimer's disease.

Neurobiology of aging - 1 Aug 2014

Chung Sun Ju, Kim Mi-Jung, Kim Juyeon, Kim Young Jin, You Sooyeoun, Koh Jaeyoung, Kim Seong Yoon, Lee Jae-Hong

Abstract excerpt

Genetic variants so far identified explain a small fraction of the overall inherited risk of Alzheimer's disease (AD). We aimed to identify novel genetic variants in AD using exome array that contains comprehensive panel. We genotyped 295,988 variants in 1005 subjects (400 AD cases and 605 contro...

Read the complete abstract on PubMed

Topics

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

Share to Apolipoprotein C-I
Share to Apolipoproteins E
Share to Exome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotyping Techniques

Share to Logistic Models

Share to Membrane Transport Proteins

Share to Mitochondrial Precursor Protein Import Complex Proteins

Share to Oligonucleotide Array Sequence Analysis

Source

Identifiers

PMID: 24685331
DOI: 10.1016/j.neurobiolaging.2014.03.007

Genes

APOC1
APOE
TOMM40

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24685331-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Exome array study did not identify novel variants in Alzheimer's disease.PMID 24685331Read ↗

Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics data.Semantic proximity Read ↗

PEN2 is not a genetic risk factor for Alzheimer's disease in a large family sample.Semantic proximity Read ↗

Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China.Semantic proximity Read ↗

Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.Semantic proximity Read ↗

Lack of association between rs597668 polymorphism near EXOC3L2 and late-onset Alzheimer's disease in Han Chinese.Semantic proximity Read ↗

Alpha-1 antichymotrypsin and alpha-2 macroglobulin gene polymorphisms are not associated with Korean late-onset Alzheimer's disease.Semantic proximity Read ↗

No replication of genetic association between candidate polymorphisms and Alzheimer's disease.Semantic proximity Read ↗

Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients.Semantic proximity Read ↗

Lack of association of 5 SNPs in the vicinity of the insulin-degrading enzyme (IDE) gene with late-onset Alzheimer's disease.Semantic proximity Read ↗

Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort.Semantic proximity Read ↗

Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts.Semantic proximity Read ↗

No association of the LRRK2 genetic variants with Alzheimer's disease in Han Chinese individuals.Semantic proximity Read ↗

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