Pages that link to "Q29308426"

The following pages link to CNVs conferring risk of autism or schizophrenia affect cognition in controls (Q29308426):

Displaying 50 items.

• Genetics and genomics of psychiatric disease (Q26781213) (← links)
• Human molecular cytogenetics: From cells to nucleotides (Q27024633) (← links)
• Brain-specific Crmp2 deletion leads to neuronal development deficits and behavioural impairments in mice (Q27314818) (← links)
• Investigating the effects of copy number variants on reading and language performance (Q27320217) (← links)
• A mouse model of the 15q13.3 microdeletion syndrome shows prefrontal neurophysiological dysfunctions and attentional impairment (Q27324628) (← links)
• A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? (Q27326701) (← links)
• Perspective-taking abilities in the balance between autism tendencies and psychosis proneness (Q27330208) (← links)
• The role of sex-differential biology in risk for autism spectrum disorder (Q28077103) (← links)
• The 15q11.2 BP1-BP2 microdeletion syndrome: a review (Q28081580) (← links)
• CNVs in neuropsychiatric disorders (Q28083143) (← links)
• Autism As a Disorder of High Intelligence (Q28277283) (← links)
• Cyfip1 Regulates Presynaptic Activity during Development (Q28566588) (← links)
• Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals (Q28607995) (← links)
• Directional dominance on stature and cognition in diverse human populations (Q28646221) (← links)
• Extracting research-quality phenotypes from electronic health records to support precision medicine (Q28648163) (← links)
• Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Q28655079) (← links)
• Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate (Q28657831) (← links)
• Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders (Q30241067) (← links)
• Dissecting the genetics of complex traits using summary association statistics (Q30241340) (← links)
• Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice. (Q30359319) (← links)
• Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. (Q30381277) (← links)
• 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks (Q30390740) (← links)
• Periventricular white matter abnormalities and restricted repetitive behavior in autism spectrum disorder (Q30488710) (← links)
• State-dependent architecture of thalamic reticular subnetworks (Q30594812) (← links)
• Cognitive Effort and Schizophrenia Modulate Large-Scale Functional Brain Connectivity (Q30667666) (← links)
• A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. (Q30699408) (← links)
• Prenatal sonographic diagnosis of urorectal septum malformation sequence and chromosomal microarray analysis: A case report and review of the literature (Q30828384) (← links)
• Neurobiology of schizophrenia: new findings from the structure to the molecules (Q30842754) (← links)
• The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population (Q30847370) (← links)
• 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia (Q30847754) (← links)
• Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data (Q30849515) (← links)
• Structural MRI biomarkers of shared pathogenesis in autism spectrum disorder and epilepsy (Q30917098) (← links)
• NMDA receptor-deficient mice display sexual dimorphism in the onset and severity of behavioural abnormalities. (Q33359313) (← links)
• Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes. (Q33619538) (← links)
• "Gestaltomics": Systems Biology Schemes for the Study of Neuropsychiatric Diseases (Q33651168) (← links)
• Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. (Q33772616) (← links)
• Reproductive fitness and genetic risk of psychiatric disorders in the general population (Q33810169) (← links)
• Prioritization of neurodevelopmental disease genes by discovery of new mutations (Q33830995) (← links)
• Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 (Q33837115) (← links)
• ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data. (Q33862491) (← links)
• The importance of copy number variation in congenital heart disease (Q33894532) (← links)
• Psychiatric disorders: diagnosis to therapy (Q33922884) (← links)
• Most genetic risk for autism resides with common variation (Q34063817) (← links)
• The clinical significance of small copy number variants in neurodevelopmental disorders (Q34238113) (← links)
• Refining analyses of copy number variation identifies specific genes associated with developmental delay (Q34254472) (← links)
• Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy (Q34257185) (← links)
• Substantial SNP-based heritability estimates for working memory performance (Q34370486) (← links)
• Multivariate neuroanatomical classification of cognitive subtypes in schizophrenia: a support vector machine learning approach (Q34432031) (← links)
• Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (Q34495555) (← links)
• Modeling a genetic risk for schizophrenia in iPSCs and mice reveals neural stem cell deficits associated with adherens junctions and polarity (Q34540416) (← links)