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

Investigation of short tandem repeats in major depression using whole-genome sequencing data.

Journal of affective disorders - 1 May 2018

Yu Chenglong, Baune Bernhard T, Wong Ma-Li, Licinio Julio

Abstract excerpt

BACKGROUND: Major depressive disorder (MDD) is a leading contributor to global disease burden. Recent studies have shown that genetic factors play significant roles in the susceptibility to this condition; however, the underlying genetic basis currently remains largely unknown. Short tandem repeat (STR) has been proposed as an explanatory factor in the "missing heritability" of complex diseases or traits....

Read the complete abstract on PubMed

Topics

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

Share to Australia
Share to Depressive Disorder, Major
Share to Genome, Human

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomics

Share to Mexican Americans

Share to Software

Share to White People

Share to Whole Genome Sequencing

Source

Identifiers

PMID: 29501989
DOI: 10.1016/j.jad.2018.02.046

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Investigation of short tandem repeats in major depression using whole-genome sequencing data.PMID 29501989Read ↗

Investigation of copy number variation in subjects with major depression based on whole-genome sequencing data.Semantic proximity Read ↗

A novel strategy for clustering major depression individuals using whole-genome sequencing variant data.Semantic proximity Read ↗

Exome-wide screening identifies novel rare risk variants for major depression disorder.Semantic proximity Read ↗

Single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data.Semantic proximity Read ↗

Sparse whole-genome sequencing identifies two loci for major depressive disorderSemantic proximity Read ↗

Low-frequency and rare variants may contribute to elucidate the genetics of major depressive disorder.Semantic proximity Read ↗

The genetic basis of major depression.Semantic proximity Read ↗

A latent genetic subtype of major depression identified by whole-exome genotyping data in a Mexican-American cohort.Semantic proximity Read ↗

Whole-genome single nucleotide variant distribution on genomic regions and its relationship to major depression.Semantic proximity Read ↗

Overview of the genetics of major depressive disorder.Semantic proximity Read ↗

Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.Semantic proximity Read ↗

Integration of Whole-Exome Sequencing and Structural Neuroimaging Analysis in Major Depressive Disorder: A Joint StudySemantic proximity Read ↗

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