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

Genomic mapping and cellular expression of human CPG2 transcripts in the SYNE1 gene.

Molecular and cellular neurosciences - 1 Mar 2016

Loebrich Sven, Rathje Mette, Hager Emily, Ataman Bulent, Harmin David A, Greenberg Michael E, Nedivi Elly

Abstract excerpt

Bipolar disorder (BD) is a prevalent and severe mood disorder characterized by recurrent episodes of mania and depression. Both genetic and environmental factors have been implicated in BD etiology, but the biological underpinnings remain elusive. Recent genome-wide association studies (GWAS) for identifying genes conferring risk for schizophrenia, BD, and major depression, identified an association between...

Read the complete abstract on PubMed

Topics

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

Share to Cytoskeletal Proteins
Share to Dendritic Spines

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Endocytosis

Share to Genome, Human

Share to HEK293 Cells

Share to Receptors, Glutamate

Share to Synapses

Share to Transcriptome

Source

Identifiers

PMID: 26704904
DOI: 10.1016/j.mcn.2015.12.007

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

Genomic mapping and cellular expression of human CPG2 transcripts in the SYNE1 gene.PMID 26704904Read ↗

Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder.Semantic proximity Read ↗

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.Semantic proximity Read ↗

Mapping PTBP splicing in human brain identifies targets for therapeutic splice switching including <i>SYNGAP1</i>Semantic proximity Read ↗

Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26.Semantic proximity Read ↗

Association at SYNE1 in both bipolar disorder and recurrent major depression.Semantic proximity Read ↗

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.Semantic proximity Read ↗

Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants.Semantic proximity Read ↗

Integrative analyses prioritize GNL3 as a risk gene for bipolar disorder.Semantic proximity Read ↗

Duplication within 14q32.13 implicates a chimeric <i>CLMN</i> :: <i>SYNE3</i> RNA transcript in cerebellar ataxiaSemantic proximity Read ↗

Decreased CNNM2 expression in prefrontal cortex affects sensorimotor gating function, cognition, dendritic spine morphogenesis and risk of schizophrenia.Semantic proximity Read ↗

Psychiatric risk gene <i>NT5C2</i> regulates protein translation in human neural progenitor cellsSemantic proximity Read ↗

Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing.Semantic proximity Read ↗

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