Identification of a functional 339 bp <i>Alu</i> insertion polymorphism in the schizophrenia-associated
locus at 10q24.32 Back Article [1] Barešić A, Nash AJ, Dahoun T, Howes O, Lenhard B. 2020 …

Recently discovered genome-wide rare copy number variants (CNVs) have unprecedented
levels of statistical association with many developmental neuropsychiatric disorders …

15q25. 2 or generally 15q25 copy number variations are rare genetic disorders that cause
neuropsychiatric disorders, developmental delay and cardiac abnormalities. The exact …

Defects in genetic and developmental processes are thought to contribute susceptibility to
autism and schizophrenia. Presumably, owing to etiological complexity identifying …

Psychiatric diagnoses are valuable for clinical communication and decision making but have
proved less useful as entry points for unraveling the biological bases of mental disorders …

22q11. 2 Deletion Syndrome (22q11. 2DS) is a genetic disorder caused by a hemizygous
deletion at chromosome 22q11. 2. It is the most common chromosomal microdeletion and …

目的: 在中国北方汉族精神分裂症患者和其健康父母组成的105 个核心家系中探讨
13q33LOCl22330 位点与精神分裂症的关系. 方法: 从全血中提取基因组DNA, 应用PCR …

The 16p11. 2 locus is a pericentromeric region found in chromosome 16, one of the most
gene-rich chromosomes in our genome, for which 10% of its sequence consists of …

Genome-wide association studies (GWAS) have identified multiple single nucleotide
polymorphisms (SNPs) or small indels robustly associated with schizophrenia; however, the …

Anatomical structures and mechanisms linking genes to neuropsychiatric disorders are not
deciphered. Reciprocal copy number variants at the 16p11. 2 BP4-BP5 locus offer a unique …