Differences in genomic structure between individuals are ubiquitous features of human genetic variation. Specific copy number variants (CNVs) have been associated with susceptibility to numerous complex psychiatric disorders, including attention-deficit-hyperactivity disorder, autism-spectrum disorders and schizophrenia. These disorders often display co-morbidity with low intelligence. Rare chromosomal deletions and duplications are associated with these disorders, so it has been suggested that these deletions or duplications may be associated with differences in intelligence. Here we investigate associations between large (≥500kb), rare (<1% population frequency) CNVs and both fluid and crystallized intelligence in community-dwelling older...
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predispo...
International audienceGenomic copy number variants (CNVs) are routinely identified and reported back...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
<div><p>Differences in genomic structure between individuals are ubiquitous features of human geneti...
Differences in genomic structure between individuals are ubiquitous features of human genetic variat...
There is increasing evidence for the role of rare copy-number variation (CNV) in the development of ...
Abstract There is increasing evidence for the role of rare copy-number variation (CNV) in the develo...
Variation in human intelligence is approximately 50% heritable, but understanding of the genes invol...
Variation in human intelligence is approximately 50% heritable, but understanding of the genes invol...
IMPORTANCE The association of copy number variations (CNVs), differing numbers of copies of genetic ...
Phenotypic variation in human intellectual functioning shows substantial heritability, as demonstrat...
Copy number variants (CNVs) are associated with psychiatric conditions in clinical populations. The ...
International audienceIMPORTANCE:Copy number variants (CNVs) classified as pathogenic are identified...
Background: Rare copy number variants (CNVs) are associated with risk of neurodevelopmental disorder...
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predispo...
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predispo...
International audienceGenomic copy number variants (CNVs) are routinely identified and reported back...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
<div><p>Differences in genomic structure between individuals are ubiquitous features of human geneti...
Differences in genomic structure between individuals are ubiquitous features of human genetic variat...
There is increasing evidence for the role of rare copy-number variation (CNV) in the development of ...
Abstract There is increasing evidence for the role of rare copy-number variation (CNV) in the develo...
Variation in human intelligence is approximately 50% heritable, but understanding of the genes invol...
Variation in human intelligence is approximately 50% heritable, but understanding of the genes invol...
IMPORTANCE The association of copy number variations (CNVs), differing numbers of copies of genetic ...
Phenotypic variation in human intellectual functioning shows substantial heritability, as demonstrat...
Copy number variants (CNVs) are associated with psychiatric conditions in clinical populations. The ...
International audienceIMPORTANCE:Copy number variants (CNVs) classified as pathogenic are identified...
Background: Rare copy number variants (CNVs) are associated with risk of neurodevelopmental disorder...
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predispo...
Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predispo...
International audienceGenomic copy number variants (CNVs) are routinely identified and reported back...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...