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

Assessing the impact of the de novo SLC6A1 mutation in schizophrenia through a comprehensive case study.

Psychiatry research - 1 Sept 2023

Kondratyev N V, Alfimova M V, Kaleda V G, Lezheiko T V, Mikhailova V A, Karpov D S, Ublinsky M V, Ushakov V L, Lebedeva I S, Golimbet V E

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to GABA Plasma Membrane Transport Proteins
Share to Genetic Predisposition to Disease
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Schizophrenia

Source

Identifiers

PMID: 37540943
DOI: 10.1016/j.psychres.2023.115399

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Assessing the impact of the de novo SLC6A1 mutation in schizophrenia through a comprehensive case study.PMID 37540943Read ↗

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia.Semantic proximity Read ↗

Pathogenic mechanisms underlying SLC6A1 variant-mediated neurodevelopmental disorders.Semantic proximity Read ↗

Rare variants are common in schizophrenia.Semantic proximity Read ↗

Exome sequencing supports a de novo mutational paradigm for schizophrenia.Semantic proximity Read ↗

Analysis of association between common variants in the SLCO6A1 gene with schizophrenia, bipolar disorder and major depressive disorder in the Han Chinese population.Semantic proximity Read ↗

De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample.Semantic proximity Read ↗

Increased exonic de novo mutation rate in individuals with schizophrenia.Semantic proximity Read ↗

De novo mutation in schizophrenia.Semantic proximity Read ↗

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis.Semantic proximity Read ↗

SLC6A4 polymorphism, population genetics, and psychiatric traitsSemantic proximity Read ↗

Phenotypic features of patients with schizophrenia carrying de novo gene mutations: a pilot study.Semantic proximity Read ↗

Darier's Disease Complicated by Schizophrenia Caused by a Novel ATP2A2 Mutation.Semantic proximity Read ↗

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