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Literature DB >> 18439401

Schizophrenia: genome, interrupted.

Abstract

Structural chromosomal variation is increasingly recognized as an important contributor to human diseases, particularly those of neurodevelopment, such as autism. A current paper makes a significant advance to schizophrenia genetics by establishing an association with rare copy number variants (CNV), which are over-represented in neurodevelopmental genes.

Entities: Disease Species

Mesh：

Year: 2008 PMID： 18439401 DOI： 10.1016/j.neuron.2008.04.007

Source DB: PubMed Journal: Neuron ISSN： 0896-6273 Impact factor: 17.173

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Cited

14 in total

Review 1. Molecular genetics of autism.

Authors: Rita M Cantor
Journal: Curr Psychiatry Rep Date: 2009-04 Impact factor: 5.285

2. The association of child mental health conditions and parent mental health status among U.S. Children, 2007.

Authors: Amanda C Bennett; Katherine C Brewer; Kristin M Rankin
Journal: Matern Child Health J Date: 2012-08

3. Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Authors: Daniel Moreno-De-Luca; Jennifer G Mulle; Erin B Kaminsky; Stephan J Sanders; Scott M Myers; Margaret P Adam; Amy T Pakula; Nancy J Eisenhauer; Kim Uhas; LuAnn Weik; Lisa Guy; Melanie E Care; Chantal F Morel; Charlotte Boni; Bonnie Anne Salbert; Ashadeep Chandrareddy; Laurie A Demmer; Eva W C Chow; Urvashi Surti; Swaroop Aradhya; Diane L Pickering; Denae M Golden; Warren G Sanger; Emily Aston; Arthur R Brothman; Troy J Gliem; Erik C Thorland; Todd Ackley; Ram Iyer; Shuwen Huang; John C Barber; John A Crolla; Stephen T Warren; Christa L Martin; David H Ledbetter
Journal: Am J Hum Genet Date: 2010-11-04 Impact factor: 11.025

Review 4. The Role of the Immune System in Autism Spectrum Disorder.

Authors: Amory Meltzer; Judy Van de Water
Journal: Neuropsychopharmacology Date: 2016-08-18 Impact factor: 7.853

5. Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.

Authors: J Alexander Bodkin; Michael J Coleman; Laura J Godfrey; Claudia M B Carvalho; Charity J Morgan; Raymond F Suckow; Thea Anderson; Dost Öngür; Marc J Kaufman; Kathryn E Lewandowski; Arthur J Siegel; Elliot Waldstreicher; Christopher M Grochowski; Daniel C Javitt; Dan Rujescu; Scott Hebbring; Richard Weinshilboum; Stephanie Burgos Rodriguez; Colette Kirchhoff; Timothy Visscher; Alexander Vuckovic; Allison Fialkowski; Shane McCarthy; Dheeraj Malhotra; Jonathan Sebat; Donald C Goff; James I Hudson; James R Lupski; Joseph T Coyle; Uwe Rudolph; Deborah L Levy
Journal: Biol Psychiatry Date: 2019-05-09 Impact factor: 13.382

6. Copy number variation of the SELENBP1 gene in schizophrenia.

Authors: Shirly Amar; Ofer Ovadia; Wolfgang Maier; Richard Ebstein; R H Belmaker; Dan Mishmar; Galila Agam
Journal: Behav Brain Funct Date: 2010-07-08 Impact factor: 3.759

Review 7. Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus.

Authors: Y L Wu; Y Yang; E K Chung; B Zhou; K J Kitzmiller; S L Savelli; H N Nagaraja; D J Birmingham; B P Tsao; B H Rovin; L A Hebert; C Y Yu
Journal: Cytogenet Genome Res Date: 2009-03-11 Impact factor: 1.636