Pages that link to "Q35172094"
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The following pages link to A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes (Q35172094):
Displaying 50 items.
- Human-specific histone methylation signatures at transcription start sites in prefrontal neurons (Q21563522) (← links)
- Genetics of bipolar disorder (Q22241442) (← links)
- Diversity of human copy number variation and multicopy genes (Q24600195) (← links)
- Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological? (Q28283600) (← links)
- Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability (Q28296551) (← links)
- Nuclear RNA-seq of single neurons reveals molecular signatures of activation (Q30276962) (← links)
- Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes. (Q30366287) (← links)
- Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism (Q30717096) (← links)
- Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes (Q33399605) (← links)
- Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies (Q33587483) (← links)
- The genetic variability and commonality of neurodevelopmental disease (Q33965270) (← links)
- CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree. (Q34055765) (← links)
- Cortical parvalbumin GABAergic deficits with α7 nicotinic acetylcholine receptor deletion: implications for schizophrenia (Q34060159) (← links)
- High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy (Q34084054) (← links)
- Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders (Q34162345) (← links)
- Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? (Q34249436) (← links)
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism (Q34273431) (← links)
- Hierarchical clustering of gene expression patterns in the Eomes + lineage of excitatory neurons during early neocortical development (Q34361313) (← links)
- Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems. (Q34381783) (← links)
- Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability (Q34572542) (← links)
- The effects of aging vs. α7 nAChR subunit deficiency on the mouse brain transcriptome: aging beats the deficiency (Q34714815) (← links)
- Genome destabilization by homologous recombination in the germ line (Q34778117) (← links)
- Epilepsy and the new cytogenetics (Q34814385) (← links)
- Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes (Q34873887) (← links)
- Genomic architecture of aggression: rare copy number variants in intermittent explosive disorder (Q35201073) (← links)
- 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain. (Q35389369) (← links)
- Transcriptional repression of the α7 nicotinic acetylcholine receptor subunit gene (CHRNA7) by activating protein-2α (AP-2α). (Q35604900) (← links)
- Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing (Q35877859) (← links)
- Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment (Q35940378) (← links)
- Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways (Q36083120) (← links)
- Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148 (Q36083125) (← links)
- The human clinical phenotypes of altered CHRNA7 copy number (Q36144791) (← links)
- Long-lasting changes in neural networks to compensate for altered nicotinic input (Q36144802) (← links)
- Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era (Q36380279) (← links)
- Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gating (Q36466420) (← links)
- Array comparative genomic hybridization: results from an adult population with drug-resistant epilepsy and co-morbidities (Q36479193) (← links)
- Clinical and Genetic Heterogeneity of the 15q13.3 Microdeletion Syndrome (Q36635250) (← links)
- Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. (Q36695747) (← links)
- Common and specific liability to addiction: approaches to association studies of opioid addiction (Q36946406) (← links)
- Inverted low-copy repeats and genome instability--a genome-wide analysis (Q37081586) (← links)
- NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits (Q37138653) (← links)
- Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome (Q37186050) (← links)
- Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes (Q37460174) (← links)
- Cortical synaptic NMDA receptor deficits in α7 nicotinic acetylcholine receptor gene deletion models: implications for neuropsychiatric diseases. (Q37561567) (← links)
- Small cracks in the dam: rare genetic variants provide opportunities to delve into mechanisms of neuropsychiatric disorders (Q37593443) (← links)
- Genome-wide association analysis of copy number variation in recurrent depressive disorder. (Q37611740) (← links)
- The clinical context of copy number variation in the human genome (Q37704614) (← links)
- Molecular diagnostics: between chips and customized medicine (Q37742118) (← links)
- Phenotypic variability and genetic susceptibility to genomic disorders (Q37784332) (← links)
- Novel genomic techniques open new avenues in the analysis of monogenic disorders (Q37833576) (← links)