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

Detection of Morphological Abnormalities in Schizophrenia: An Important Step to Identify Associated Genetic Disorders or Etiologic Subtypes.

International journal of molecular sciences - 31 Aug 2021

Priol Anne-Clémence, Denis Laure, Boulanger Gaella, Thépaut Mathieu, Geoffray Marie-Maude, Tordjman Sylvie

Abstract excerpt

Current research suggests that alterations in neurodevelopmental processes, involving gene X environment interactions during key stages of brain development (prenatal period and adolescence), are a major risk for schizophrenia. First, epidemiological studies supporting a genetic contribution to schizophrenia are presented in this article, including family, twin, and adoption studies. Then, an extensive literature...

Read the complete abstract on PubMed

Topics

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

Share to DNA Copy Number Variations
Share to Gene-Environment Interaction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genetics

Share to Phenotype

Share to Polymorphism, Single Nucleotide

Share to Schizophrenia

Source

Open in PubMed Open full text

Identifiers

PMID: 34502372
DOI: 10.3390/ijms22179464
PMCID: PMC8430486

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

Detection of Morphological Abnormalities in Schizophrenia: An Important Step to Identify Associated Genetic Disorders or Etiologic Subtypes.PMID 34502372Read ↗

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on GeneticsSemantic proximity Read ↗

Developments in schizophrenia genetics: from linkage to microchips, deletions and duplications.Semantic proximity Read ↗

Schizophrenia genetics: new insights from new approaches.Semantic proximity Read ↗

Schizophrenia in the genetic era: a review from development history, clinical features and genomic research approaches to insights of susceptibility genes.Semantic proximity Read ↗

Physical manifestations of neurodevelopmental disruption: are minor physical anomalies part of the syndrome of schizophrenia?Semantic proximity Read ↗

Genetics of psychiatric disorders in the GWAS era: an update on schizophrenia.Semantic proximity Read ↗

Copy Number Variations and Schizophrenia.Semantic proximity Read ↗

The genetic architecture of schizophrenia: review of large-scale genetic studies.Semantic proximity Read ↗

Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and DiseaseSemantic proximity Read ↗

[An analysis of the relationship between genetic factors and the risk of schizophrenia].Semantic proximity Read ↗

Genetics of Schizophrenia: Overview of Methods, Findings and LimitationsSemantic proximity Read ↗

Genetic insights into the neurodevelopmental origins of schizophrenia.Semantic proximity Read ↗

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