Letter to the editorsMutation analysis of ARVCF gene on chromosome 22q11 as a candidate for a schizophrenia gene
Section snippets
Acknowledgements
This project was supported by the grant NSC 92-3112-B-320-001 from the National Science Council of Taiwan.
References (12)
- et al.
Identification of sequence variants and analysis of the role of the catechol-O-methyl-transferase gene in schizophrenia susceptibility
Biol. Psychiatry
(1998) - et al.
Identification of a new human catenin gene family member (ARVCF) from region deleted in velo-cardio-facial syndrome
Genomics
(1997) - et al.
Velocardiofacial syndrome in childhood-onset schizophrenia
J. Am. Acad. Child Adolesc. Psych
(1999) - et al.
The p120catenin family: complex roles in adhesion, signaling and cancer
J. Cell Sci
(2000) - et al.
22q11 Deletion syndrome in adults with schizophrenia
Am. J. Med. Genet
(1998) - et al.
Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders
Am. J. Hum. Genet
(1997)
Cited by (12)
Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development
2015, Progress in NeurobiologyCitation Excerpt :Our analysis showing a lack of imprinting or parent of origin bias on any of the genes in the mouse equivalent of the 22q11.2 minimal critical deleted region (Maynard et al., 2006) amplifies the conclusion that 22q11 deletion pathology likely reflects dosage change. Genetic association studies in human patients and control subjects implicate several individual 22q11 genes, including PRODH2, COMT, ZDHHC8, and ARVCF in SCZ (Chen et al., 2005; Fan et al., 2002; Li et al., 2004; Liu et al., 2002b; Mas et al., 2009; Mukai et al., 2004; Sanders et al., 2005) and there are some indications of independent association (single gene polymorphisms without deletion) of individual 22q11 genes with ASD (Chen et al., 2012). Nevertheless, the strongest genetic association between SCZ, ASD, or ADHD remains between these disorders and deletion across the 22q11 minimal or typically deleted region (Schneider et al., 2014).
ARVCF single marker and haplotypic association with schizophrenia
2009, Progress in Neuro-Psychopharmacology and Biological PsychiatryPlacental dna methylation related to both infant toenail mercury and adverse neurobehavioral outcomes
2015, Environmental Health PerspectivesARVCF expression is significantly correlated with the malignant phenotype of non-small cell lung cancer
2015, Molecular Carcinogenesis