MicroRNAs: key regulators in the central nervous system and their implication in neurological diseases

DD Cao, L Li, WY Chan - International journal of molecular sciences, 2016 - mdpi.com
MicroRNAs (miRNAs) are a class of small, well-conserved noncoding RNAs that regulate
gene expression post-transcriptionally. They have been demonstrated to regulate a lot of …

Human copy number variation and complex genetic disease

S Girirajan, CD Campbell… - Annual review of genetics, 2011 - annualreviews.org
Copy number variants (CNVs) play an important role in human disease and population
diversity. Advancements in technology have allowed for the analysis of CNVs in thousands …

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

SC Greenway, AC Pereira, JC Lin, SR DePalma… - Nature …, 2009 - nature.com
Tetralogy of Fallot (TOF), the most common severe congenital heart malformation, occurs
sporadically, without other anomaly, and from unknown cause in 70% of cases. Through a …

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

D Malhotra, S McCarthy, JJ Michaelson, V Vacic… - Neuron, 2011 - cell.com
While it is known that rare copy-number variants (CNVs) contribute to risk for some
neuropsychiatric disorders, the role of CNVs in bipolar disorder is unclear. Here, we …

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

J Gauthier, N Champagne… - Proceedings of the …, 2010 - National Acad Sciences
Schizophrenia likely results from poorly understood genetic and environmental factors. We
studied the gene encoding the synaptic protein SHANK3 in 285 controls and 185 …

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

A Guilmatre, C Dubourg, AL Mosca… - Archives of general …, 2009 - jamanetwork.com
Context Results of comparative genomic hybridization studies have suggested that rare
copy number variations (CNVs) at numerous loci are involved in the cause of mental …

Genomewide association studies: history, rationale, and prospects for psychiatric disorders

Psychiatric GWAS Consortium … - American Journal of …, 2009 - Am Psychiatric Assoc
Objective: The authors conducted a review of the history and empirical basis of genomewide
association studies (GWAS), the rationale for GWAS of psychiatric disorders, results to date …

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice

JL Doherty, MJ Owen - Genome medicine, 2014 - Springer
Psychiatric disorders such as schizophrenia, bipolar disorder, major depressive disorder,
attention-deficit/hyperactivity disorder and autism spectrum disorder are common and result …

Disruption of the neurexin 1 gene is associated with schizophrenia

D Rujescu, A Ingason, S Cichon… - Human molecular …, 2009 - academic.oup.com
Deletions within the neurexin 1 gene (NRXN1; 2p16. 3) are associated with autism and have
also been reported in two families with schizophrenia. We examined NRXN1, and the …

Genetic overlap between autism, schizophrenia and bipolar disorder

LS Carroll, MJ Owen - Genome medicine, 2009 - Springer
There is strong evidence that genetic factors make substantial contributions to the etiology of
autism, schizophrenia and bipolar disorders, with heritability estimates being at least 80 …