| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/GEPI.22344 |
| P698 | PubMed publication ID | 32783248 |
| P50 | author | Celia Greenwood | Q55458850 |
| Lai Jiang | Q91012707 | ||
| Sébastien Jacquemont | Q92881209 | ||
| Guillaume Huguet | Q98387323 | ||
| P2093 | author name string | David Porteous | |
| Gunter Schumann | |||
| Antonio Ciampi | |||
| Catherine Schramm | |||
| Martineau Jean-Louis | |||
| Antoine Main | |||
| Claudine Passo | |||
| Maude Auger | |||
| P2860 | cites work | Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability | Q21261449 |
| FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism | Q24631425 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| 22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features | Q26798055 | ||
| Analysis of protein-coding genetic variation in 60,706 humans | Q26831376 | ||
| The UCSC Genome Browser Database | Q27861125 | ||
| Meta-analysis of the heritability of human traits based on fifty years of twin studies | Q28262090 | ||
| Intraclass correlations: uses in assessing rater reliability | Q28296226 | ||
| PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data | Q29614933 | ||
| STRING v10: protein-protein interaction networks, integrated over the tree of life | Q29615545 | ||
| Optimal tests for rare variant effects in sequencing association studies | Q31065241 | ||
| QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data | Q31104515 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| Convergence of genes and cellular pathways dysregulated in autism spectrum disorders | Q33794546 | ||
| Rare copy number deletions predict individual variation in intelligence | Q33813542 | ||
| Testing for an unusual distribution of rare variants | Q33847792 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors | Q34144319 | ||
| Refining analyses of copy number variation identifies specific genes associated with developmental delay | Q34254472 | ||
| Genetic variability in the regulation of gene expression in ten regions of the human brain | Q34398489 | ||
| Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci | Q34495555 | ||
| Recurrent 16p11.2 microdeletions in autism | Q34729775 | ||
| Copy number variation in schizophrenia in Sweden | Q34742638 | ||
| The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity | Q35059423 | ||
| The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity | Q35762251 | ||
| Assessment of copy number variations in the brain genome of schizophrenia patients. | Q35805267 | ||
| Test review: Wechsler Intelligence Scale for Children-Fourth Edition (WISC-IV). | Q36321414 | ||
| Canonical genetic signatures of the adult human brain | Q36428141 | ||
| A unified mixed-effects model for rare-variant association in sequencing studies | Q37088008 | ||
| Patterns of genic intolerance of rare copy number variation in 59,898 human exomes | Q37297685 | ||
| Statistical analysis strategies for association studies involving rare variants | Q37799723 | ||
| Rare Variant Association Analysis Methods for Complex Traits | Q37806780 | ||
| The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology | Q37811879 | ||
| Intelligence | Q37937739 | ||
| The genetic landscapes of autism spectrum disorders | Q38123219 | ||
| Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects | Q39217627 | ||
| Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects | Q39257462 | ||
| Asymptotic tests of association with multiple SNPs in linkage disequilibrium | Q41854759 | ||
| Characterization of the proteome, diseases and evolution of the human postsynaptic density. | Q42610204 | ||
| Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications. | Q47125495 | ||
| A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. | Q47556706 | ||
| Genomic analysis of family data reveals additional genetic effects on intelligence and personality. | Q48266836 | ||
| Postsynaptic density proteins and their involvement in neurodevelopmental disorders | Q50132951 | ||
| Rare outcomes, common treatments: analytic strategies using propensity scores. | Q52030565 | ||
| Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples. | Q52644870 | ||
| A two stage design for the study of the relationship between a rare exposure and a rare disease. | Q52730190 | ||
| A Mantel-Haenszel statistic for testing the association between a polychotomous exposure and a rare outcome. | Q52741148 | ||
| Monte Carlo sampling methods using Markov chains and their applications | Q55880695 | ||
| Inference from Iterative Simulation Using Multiple Sequences | Q56172083 | ||
| Stan: A Probabilistic Programming Language | Q56551521 | ||
| Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence | Q56967082 | ||
| Association of copy number variation across the genome with neuropsychiatric traits in the general population | Q58462162 | ||
| Genetic and environmental influences on the Verbal-Perceptual-Image Rotation (VPR) model of the structure of mental abilities in the Minnesota study of twins reared apart | Q60018367 | ||
| Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity | Q90597210 | ||
| Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) | Q91130432 | ||
| P577 | publication date | 2020-08-11 | |
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Estimating the effects of copy-number variants on intelligence using hierarchical Bayesian models |
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