Published in J Autism Dev Disord on November 16, 2016
Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy. Neurosci Bull (2017) 0.76
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet (2009) 6.21
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet (2010) 5.78
Phenotypic heterogeneity of genomic disorders and rare copy-number variants. N Engl J Med (2012) 4.36
CNVs conferring risk of autism or schizophrenia affect cognition in controls. Nature (2013) 2.96
Phenotypic variability and genetic susceptibility to genomic disorders. Hum Mol Genet (2010) 2.57
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry (2012) 2.48
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nat Genet (2009) 1.98
Association study of CHRFAM7A copy number and 2 bp deletion polymorphisms with schizophrenia and bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet (2006) 1.80
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological? Hum Mutat (2010) 1.66
Cognitive and behavioral characterization of 16p11.2 deletion syndrome. J Dev Behav Pediatr (2010) 1.20
Assortative mating in the affective disorders: a systematic review and meta-analysis. Compr Psychiatry (2001) 1.10
Copy number variations and cognitive phenotypes in unselected populations. JAMA (2015) 1.09
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Genet Med (2014) 1.01
The human clinical phenotypes of altered CHRNA7 copy number. Biochem Pharmacol (2015) 0.95
The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function. Neuropharmacology (2015) 0.90
CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree. Eur J Hum Genet (2014) 0.89
Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med (2015) 0.84
Association study of the 2-bp deletion polymorphism in exon 6 of the CHRFAM7A gene with idiopathic generalized epilepsy. DNA Cell Biol (2013) 0.79
The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med (2016) 0.75
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genet Med (2016) 0.79
The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations. Genet Med (2016) 0.76
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nat Genet (2017) 0.75
Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome. J Autism Dev Disord (2016) 0.75
The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med (2016) 0.75
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations. Nat Genet (2017) 0.75
Erratum to: The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. J Autism Dev Disord (2017) 0.75
Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty. Genes Brain Behav (2017) 0.75
Quantitative real-time imaging of glutathione. Nat Commun (2017) 0.75