|
1
|
Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.
|
J Med Genet
|
2006
|
2.97
|
|
2
|
Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH.
|
Am J Med Genet A
|
2005
|
1.68
|
|
3
|
Face-brain asymmetry in autism spectrum disorders.
|
Mol Psychiatry
|
2008
|
1.45
|
|
4
|
15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
|
Clin Genet
|
2006
|
1.09
|
|
5
|
Autism-associated familial microdeletion of Xp11.22.
|
Clin Genet
|
2008
|
1.03
|
|
6
|
A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
|
Clin Genet
|
2005
|
1.00
|
|
7
|
Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.
|
Hum Genet
|
2010
|
0.97
|
|
8
|
Autism severity is associated with child and maternal MAOA genotypes.
|
Clin Genet
|
2011
|
0.91
|
|
9
|
Phenomic determinants of genomic variation in autism spectrum disorders.
|
J Med Genet
|
2009
|
0.90
|
|
10
|
Parental perspectives on the causes of an autism spectrum disorder in their children.
|
J Genet Couns
|
2006
|
0.84
|
|
11
|
Loud and clear evidence for gene silencing by epigenetic mechanisms in autism spectrum and related neurodevelopmental disorders.
|
Clin Genet
|
2006
|
0.82
|
|
12
|
Prenatally detected trisomy 20 mosaicism.
|
Prenat Diagn
|
2005
|
0.79
|
|
13
|
Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.
|
Cytogenet Genome Res
|
2009
|
0.75
|