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

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Archives of general psychiatry - 1 Oct 2009

Holliday Elizabeth G, McLean Duncan E, Nyholt Dale R, Mowry Bryan J

Abstract excerpt

CONTEXT: Identifying susceptibility genes for schizophrenia may be complicated by phenotypic heterogeneity, with some evidence suggesting that phenotypic heterogeneity reflects genetic heterogeneity. OBJECTIVE: To evaluate the heritability and conduct genetic linkage analyses of empirically derived, clinically homogeneous schizophrenia subtypes. DESIGN: Latent class and linkage analysis. SETTING: Taiwanese field...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 1
Share to Diagnostic and Statistical Manual of Mental Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Heterogeneity

Share to Models, Statistical

Share to Multivariate Analysis

Share to Psychiatric Status Rating Scales

Share to Schizophrenia

Share to Taiwan

Source

Identifiers

PMID: 19805696
DOI: 10.1001/archgenpsychiatry.2009.136

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.PMID 19805696Read ↗

Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.Semantic proximity Read ↗

Genetic Architecture of Schizophrenia Clinical SubtypesSemantic proximity Read ↗

Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families.Semantic proximity Read ↗

Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective.Semantic proximity Read ↗

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families.Semantic proximity Read ↗

Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.Semantic proximity Read ↗

Heterogeneity of schizophrenia: Genetic and symptomatic factors.Semantic proximity Read ↗

Sibling correlation of deficit syndrome in the Irish study of high-density schizophrenia families.Semantic proximity Read ↗

Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families.Semantic proximity Read ↗

Using disease symptoms to improve detection of linkage under genetic heterogeneity.Semantic proximity Read ↗

Symptom dimensions as alternative phenotypes to address genetic heterogeneity in schizophrenia and bipolar disorder.Semantic proximity Read ↗

Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework.Semantic proximity Read ↗

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