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 Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders.

Current Alzheimer research - 1 Jan 2020

El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Nada

Abstract excerpt

BACKGROUND: Copy number variations (CNVs) play an important role in the genetic etiology of various neurological disorders, including Alzheimer's disease (AD). Type 2 diabetes mellitus (T2DM) and major depressive disorder (MDD) were shown to have share mechanisms and signaling pathways with AD. OBJECTIVE: We aimed to assess CNVs regions that may harbor genes contributing to AD, T2DM, and MDD in 67 Saudi familial...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Alzheimer Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Amyloid beta-Protein Precursor

Share to Cohort Studies

Share to Depressive Disorder, Major

Share to Diabetes Mellitus, Type 2

Share to DNA Copy Number Variations

Share to Nerve Tissue Proteins

Source

Identifiers

PMID: 33256577
DOI: 10.2174/1567205017666201130111424

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders.PMID 33256577Read ↗

Whole genome sequencing–based copy number variations reveal novel pathways and targets in Alzheimer's diseaseSemantic proximity Read ↗

A comprehensive analysis of copy number variation in a Turkish dementia cohort.Semantic proximity Read ↗

Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study.Semantic proximity Read ↗

Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.Semantic proximity Read ↗

Landscape of copy number variants in Spanish People with DementiaSemantic proximity Read ↗

Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.Semantic proximity Read ↗

Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease.Semantic proximity Read ↗

Extremely rare CNVs contributing to Alzheimer disease risk: a case-control association analysis of exome sequencing data from 22,319 individualsSemantic proximity Read ↗

Genomic Copy Number Analysis in Alzheimer′s Disease and Mild Cognitive Impairment: An ADNI StudySemantic proximity Read ↗

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.Semantic proximity Read ↗

The genetic effect of copy number variations on the risk of type 2 diabetes in a Korean population.Semantic proximity Read ↗

Targeted copy number variant identification across the neurodegenerative disease spectrum.Semantic proximity Read ↗

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