PubRank

J J A Holden

Author PubWeight™ 17.20‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1. J Med Genet 2006 2.97
2 Reelin gene alleles and susceptibility to autism spectrum disorders. Mol Psychiatry 2002 2.05
3 Face-brain asymmetry in autism spectrum disorders. Mol Psychiatry 2008 1.45
4 Association of autism severity with a monoamine oxidase A functional polymorphism. Clin Genet 2003 1.11
5 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
6 Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions. Mol Psychiatry 2005 1.08
7 Autism-associated familial microdeletion of Xp11.22. Clin Genet 2008 1.03
8 FMR1 alleles in Tasmania: a screening study of the special educational needs population. Clin Genet 2005 1.01
9 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
10 Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics. Hum Genet 2010 0.97
11 Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability. Clin Genet 2012 0.97
12 Autism severity is associated with child and maternal MAOA genotypes. Clin Genet 2011 0.91
13 Phenomic determinants of genomic variation in autism spectrum disorders. J Med Genet 2009 0.90
14 Parental perspectives on the causes of an autism spectrum disorder in their children. J Genet Couns 2006 0.84
15 Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability. Cytogenet Genome Res 2009 0.75