Last Posted: Sep 20, 2021
- Impact on the Risk and Severity of Childhood Onset Schizophrenia of Schizophrenia Risk Genetic Variants at the DRD2 and ZNF804A Loci.
Alfimova Margarita V, et al. Child psychiatry and human development 2021 9
- Age Matters: an Atypical Association Between Polymorphism of MTHFR and Clinical Phenotypes in Children with Schizophrenia.
Wan Lin, et al. Journal of molecular neuroscience : MN 2019 7
- Machine Learning
NIH Catalyst, July 2018
- 15q13.3 duplication in two patients with childhood-onset schizophrenia.
Zhou Dale, et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 3
- Common polygenic variation and risk for childhood-onset schizophrenia.
Ahn K, et al. Molecular psychiatry 2014 12
- High rate of disease-related copy number variations in childhood onset schizophrenia.
Ahn K, et al. Molecular psychiatry 2014 5 (5) 568-72
- Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.
Raznahan Armin, et al. NeuroImage 2011 8 (4) 1517-23
- Childhood-Onset Schizophrenia
From NCATS Genetic and Rare Diseases Information Center
- Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Walsh Tom, et al. Science (New York, N.Y.) 2008 4 (5875) 539-43
- Childhood-onset schizophrenia and tryptophan hydroxylase gene polymorphism.
Sekizawa Takahiro, et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 7 (1) 24-6
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
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