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

Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population.

PloS one - 27 Oct 2010

Wang Ti, Zeng Zhen, Li Tao, Liu Jie, Li Junyan, Li You, Zhao Qian, Wei Zhiyun, Wang Yang, Li Baojie, Feng Guoyin, He Lin, Shi Yongyong

Abstract excerpt

BACKGROUND: Myelin transcription factor 1-like (MYT1L) is a member of the myelin transcription factor 1 (MYT1) gene family, and the neural specific, zinc-finger-containing, DNA-binding protein that it encodes plays a role in the development of the nervous system. On the basis of a recent copy num...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to China
Share to Depressive Disorder, Major

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-Binding Proteins

Share to Ethnicity

Share to Gene Dosage

Share to Polymorphism, Single Nucleotide

Share to Transcription Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 21048971
DOI: 10.1371/journal.pone.0013662
PMCID: PMC2965102

Genes

MYT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21048971-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Common SNPs in myelin transcription factor 1-like (MYT1L): association with major depressive disorder in the Chinese Han population.PMID 21048971Read ↗

Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population.Semantic proximity Read ↗

Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci.Semantic proximity Read ↗

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample.Semantic proximity Read ↗

Associations of the Intellectual Disability Gene MYT1L with Helix-Loop-Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval.Semantic proximity Read ↗

Genome-wide copy number variation-, validation- and screening study implicates a novel copy number polymorphism associated with suicide attempts in major depressive disorderSemantic proximity Read ↗

Association Analysis Between Common Variants of the TRPM1 Gene and Three Mental Disorders in the Han Chinese Population.Semantic proximity Read ↗

Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder.Semantic proximity Read ↗

Copy number variations in multiple sclerosis and neuromyelitis optica.Semantic proximity Read ↗

Lack of association between dendritic cell nuclear protein-1 gene and major depressive disorder in the Han Chinese population.Semantic proximity Read ↗

Identification of TNFA influencing MDD risk and clinical features in Han Chinese.Semantic proximity Read ↗

A haplotype in the 5'-upstream region of the NDUFV2 gene is associated with major depressive disorder in Han Chinese.Semantic proximity Read ↗

Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population.Semantic proximity Read ↗

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