PubRank

M E S Lewis

Author PubWeight™ 14.35‹?›

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 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