Pages that link to "Q33691446"
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The following pages link to Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function (Q33691446):
Displaying 50 items.
- What have we learnt about the causes of ADHD? (Q22242372) (← links)
- Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia (Q28262977) (← links)
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (Q28296286) (← links)
- Evolutionary conservation in genes underlying human psychiatric disorders (Q28657468) (← links)
- Is there a role for endogenous retroviruses to mediate long-term adaptive phenotypic response upon environmental inputs? (Q28710061) (← links)
- Personalized pathway enrichment map of putative cancer genes from next generation sequencing data (Q28729875) (← links)
- Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity (Q28943380) (← links)
- A Fast Multiple-Kernel Method With Applications to Detect Gene-Environment Interaction (Q30279068) (← links)
- Genovar: a detection and visualization tool for genomic variants (Q31061694) (← links)
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. (Q33398247) (← links)
- Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants (Q33818403) (← links)
- Genotype-environment interaction on human cognitive function conditioned on the status of breastfeeding and maternal smoking around birth. (Q33920967) (← links)
- Rare copy number variation in treatment-resistant major depressive disorder (Q33922682) (← links)
- Genetic architectures of psychiatric disorders: the emerging picture and its implications (Q33949729) (← links)
- Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia (Q33960019) (← links)
- Integrating autoimmune risk loci with gene-expression data identifies specific pathogenic immune cell subsets (Q34036705) (← links)
- Networks of neuronal genes affected by common and rare variants in autism spectrum disorders (Q34192901) (← links)
- Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. (Q34255285) (← links)
- INRICH: interval-based enrichment analysis for genome-wide association studies (Q34269233) (← links)
- The genomics of schizophrenia: update and implications. (Q34381708) (← links)
- Rare copy number variants contribute to congenital left-sided heart disease (Q34411873) (← links)
- Disruption of DNA-methylation-dependent long gene repression in Rett syndrome (Q34466731) (← links)
- High-resolution copy number variation analysis of schizophrenia in Japan. (Q34528802) (← links)
- Copy number variation in schizophrenia in Sweden (Q34742638) (← links)
- SNPsnap: a Web-based tool for identification and annotation of matched SNPs (Q35020460) (← links)
- Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder (Q35059381) (← links)
- GPA: a statistical approach to prioritizing GWAS results by integrating pleiotropy and annotation (Q35418401) (← links)
- Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects. (Q35533264) (← links)
- Genome-wide methylation profiling of schizophrenia (Q35549644) (← links)
- Biological interpretation of genome-wide association studies using predicted gene functions (Q35571093) (← links)
- Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism (Q35764564) (← links)
- A New Method for Detecting Associations with Rare Copy-Number Variants (Q35797345) (← links)
- Divergence patterns of genic copy number variation in natural populations of the house mouse (Mus musculus domesticus) reveal three conserved genes with major population-specific expansions (Q35876035) (← links)
- Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants (Q35882608) (← links)
- A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci (Q35885173) (← links)
- Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections (Q35993490) (← links)
- Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways (Q36083120) (← links)
- Epistasis network centrality analysis yields pathway replication across two GWAS cohorts for bipolar disorder (Q36203441) (← links)
- Pervasive pleiotropy between psychiatric disorders and immune disorders revealed by integrative analysis of multiple GWAS. (Q36240270) (← links)
- Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders (Q36275712) (← links)
- Identification and functional characterization of rare SHANK2 variants in schizophrenia (Q36301065) (← links)
- Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders (Q36424672) (← links)
- A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk (Q36559977) (← links)
- Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis (Q36560009) (← links)
- The phenotypic manifestations of rare genic CNVs in autism spectrum disorder (Q36594526) (← links)
- Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. (Q36695747) (← links)
- Psychiatric gene discoveries shape evidence on ADHD's biology (Q36763139) (← links)
- Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. (Q37016817) (← links)
- The genomic psychiatry cohort: partners in discovery (Q37059547) (← links)
- Genome-Wide Association Studies Suggest Limited Immune Gene Enrichment in Schizophrenia Compared to 5 Autoimmune Diseases (Q37183966) (← links)