Functional Polymorphisms in PRODH Are Associated with Risk and Protection for Schizophrenia and Fronto-Striatal Structure and Function-Reference-Cited by-同舟云学术

Functional Polymorphisms in PRODH Are Associated with Risk and Protection for Schizophrenia and Fronto-Striatal Structure and Function

Published:2008-11-07 Issue:11 Volume:4 Page:e1000252
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Kempf Lucas,Nicodemus Kristin K.,Kolachana Bhaskar,Vakkalanka Radhakrishna,Verchinski Beth A.,Egan Michael F.,Straub Richard E.,Mattay Venkata A.,Callicott Joseph H.,Weinberger Daniel R.,Meyer-Lindenberg Andreas

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference74 articles.

1. Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.;DW Meechan;Mol Cell Neurosci,2006

2. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.;M Karayiorgou;Proc Natl Acad Sci U S A,1995

3. Schizophrenia and chromosomal deletions within 22q11.2.;EA Lindsay;Am J Hum Genet,1995

4. Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives.;AE Pulver;J Nerv Ment Dis,1994

5. High rates of schizophrenia in adults with velo-cardio-facial syndrome.;KC Murphy;Arch Gen Psychiatry,1999

Cited by 85 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia;Translational Psychiatry;2024-06-29

2. Severe Hypocalcemia in the Adolescent as the Only Manifestation of <i>22q11</i> Microdeletion Syndrome: Clinical Case;Current Pediatrics;2023-07-08

3. Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia;Archives of Medical Research;2022-06

4. Learning from atypical development: A systematic review of executive functioning in children and adolescents with the 22q11.2 deletion syndrome;Developmental Review;2021-06

5. Genotypic and phenotypic variability of 22q11.2 microdeletions – an institutional experience;AIMS Molecular Science;2021