Pages that link to "Q24654741"
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The following pages link to Large recurrent microdeletions associated with schizophrenia (Q24654741):
Displaying 50 items.
- Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood (Q21144644) (← links)
- Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy (Q21198881) (← links)
- Understanding the impact of 1q21.1 copy number variant (Q21202865) (← links)
- BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1 (Q21261511) (← links)
- Initial impact of the sequencing of the human genome (Q22122172) (← links)
- Finding the missing heritability of complex diseases (Q22122198) (← links)
- The shock of the new: progress in schizophrenia genomics (Q22241409) (← links)
- The Kraepelinian dichotomy - going, going... but still not gone (Q22241683) (← links)
- A review of anti-inflammatory agents for symptoms of schizophrenia (Q22241827) (← links)
- The dopamine hypothesis of schizophrenia: version III--the final common pathway (Q22242827) (← links)
- Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia (Q22248085) (← links)
- Copy-number variations associated with neuropsychiatric conditions (Q22251090) (← links)
- Genetics of psychosis; insights from views across the genome (Q22252693) (← links)
- DUF1220 domains, cognitive disease, and human brain evolution (Q22337096) (← links)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (Q22337245) (← links)
- The chimeric gene CHRFAM7A, a partial duplication of the CHRNA7 gene, is a dominant negative regulator of α7*nAChR function (Q24308763) (← links)
- Structure and control of the actin regulatory WAVE complex (Q24308919) (← links)
- Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling (Q24322974) (← links)
- Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenics (Q24561726) (← links)
- Schizophrenia is associated with an increase in cortical microRNA biogenesis (Q24595592) (← links)
- Common genetic variation and performance on standardized cognitive tests (Q24597954) (← links)
- Diversity of human copy number variation and multicopy genes (Q24600195) (← links)
- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 (Q24603800) (← links)
- Using ERDS to infer copy-number variants in high-coverage genomes (Q24604693) (← links)
- Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Q24605530) (← links)
- The genetic basis of addictive disorders (Q24607129) (← links)
- Common variants conferring risk of schizophrenia (Q24614376) (← links)
- Mapping copy number variation by population-scale genome sequencing (Q24615307) (← links)
- Direct measure of the de novo mutation rate in autism and schizophrenia cohorts (Q24618002) (← links)
- An arrayed human genomic library constructed in the PAC shuttle vector pJCPAC-Mam2 for genome-wide association studies and gene therapy (Q24619270) (← links)
- Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy (Q24620622) (← links)
- De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia (Q24621518) (← links)
- Large, rare chromosomal deletions associated with severe early-onset obesity (Q24623878) (← links)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (Q24628710) (← links)
- Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation (Q24629022) (← links)
- Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus (Q24630434) (← links)
- Strong synaptic transmission impact by copy number variations in schizophrenia (Q24630444) (← links)
- CNV and nervous system diseases--what's new? (Q24632941) (← links)
- Modelling schizophrenia using human induced pluripotent stem cells (Q24633007) (← links)
- Microduplications of 16p11.2 are associated with schizophrenia (Q24634151) (← links)
- Copy number variation at 1q21.1 associated with neuroblastoma (Q24642330) (← links)
- A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB (Q24644827) (← links)
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (Q24645076) (← links)
- Disruption of the neurexin 1 gene is associated with schizophrenia (Q24647095) (← links)
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities (Q24647145) (← links)
- Copy number variation and schizophrenia (Q24651868) (← links)
- Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes (Q24655755) (← links)
- MicroRNAs: Key Regulators in the Central Nervous System and Their Implication in Neurological Diseases (Q26744819) (← links)
- Genetics and genomics of psychiatric disease (Q26781213) (← links)
- The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function (Q26821785) (← links)