Published in Am J Hum Genet on May 01, 2008
The role of redox signaling in epigenetics and cardiovascular disease. Antioxid Redox Signal (2013) 1.03
Epigenetic mechanisms of pulmonary hypertension. Pulm Circ (2011) 0.93
Strong association of de novo copy number mutations with autism. Science (2007) 27.84
UBE3A/E6-AP mutations cause Angelman syndrome. Nat Genet (1997) 5.97
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol Psychiatry (2006) 5.63
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature (1989) 4.72
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nat Genet (1997) 4.65
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. J Med Genet (2006) 4.64
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. N Engl J Med (1981) 4.25
A new genetic concept: uniparental disomy and its potential effect, isodisomy. Am J Med Genet (1980) 4.22
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet (1997) 3.95
Value of a clinical morphology examination in autism. Am J Med Genet (2000) 1.94
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. Am J Med Genet A (2004) 1.79
Autism: highly heritable but not inherited. Nat Med (2007) 1.20
Heritable germline epimutation is not the same as transgenerational epigenetic inheritance. Nat Genet (2007) 1.04