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

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.

Psychiatric genetics - 1 Dec 2007

Liu Yu-Li, Fann Cathy Shen-Jang, Liu Chih-Min, Chang Chien Ching, Yang Wei-Chih, Wu Jer-Yuarn, Hung Shuen-Iu, Chan Hung-Yu, Chen Jiahn-Jyh, Hsieh Ming H, Hwang Tzung-Jeng, Faraone Stephen V, Tsuang Ming T, Chen Wei J, Hwu Hai-Gwo

Abstract excerpt

OBJECTIVE: A region at chromosome 22q11.21 has been reported to potentially harbor a candidate gene for schizophrenia, ZDHHC8 (zinc finger, DHHC domain containing 8; also annotated as KIAA1292) in a number of studies. This finding has been replicated in Han Chinese, but not in other ethnicity-specific studies. For further support from within the Han Chinese ethnic group, we selected two single nucleotide...

Read the complete abstract on PubMed

Topics

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

Share to Attention Deficit Disorder with Hyperactivity
Share to Chromosomes, Human, Pair 22

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Introns

Share to Nuclear Family

Share to Proteins

Share to Schizophrenia

Share to Siblings

Share to Taiwan

Source

Identifiers

PMID: 18075473
DOI: 10.1097/YPG.0b013e328133f321

Genes

ZDHHC8

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

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.PMID 18075473Read ↗

RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.Semantic proximity Read ↗

ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function.Semantic proximity Read ↗

NR4A2: effects of an "orphan" receptor on sustained attention in a schizophrenic population.Semantic proximity Read ↗

Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality.Semantic proximity Read ↗

Association of common variants in H2AFZ gene with schizophrenia and cognitive function in patients with schizophrenia.Semantic proximity Read ↗

The DOPA decarboxylase (DDC) gene is associated with alerting attention.Semantic proximity Read ↗

DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan.Semantic proximity Read ↗

Molecular genetics of attention.Semantic proximity Read ↗

Association of Dystrobrevin-Binding Protein 1 Polymorphisms with Sustained Attention and Set-Shifting in Schizophrenia Patients.Semantic proximity Read ↗

Sustained attention in young people at high risk for schizophrenia.Semantic proximity Read ↗

Association between dopamine beta-hydroxylase polymorphism and attention function in suicide attempters with chronic schizophrenia.Semantic proximity Read ↗

Sustained and selective attention deficits as vulnerability markers to psychosis.Semantic proximity Read ↗

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