E Haan
South Australia Pathology(AU)The University of Adelaide(AU)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Autism Spectrum Disorder Research, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics
Most-Cited Works
- → Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID(2015)206 cited
- → Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes(1992)173 cited
- → Fetal alcohol syndrome: a prospective national surveillance study(2007)130 cited
- → Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome(1995)123 cited
- → Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome(2004)103 cited
- → Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families(2009)79 cited
- → Fetal exposure to herpesviruses may be associated with pregnancy‐induced hypertensive disorders and preterm birth in a Caucasian population*(2008)68 cited
- → A South Australian population‐based study of congenital talipes equinovarus(2005)67 cited
- → FMR2 Expression in Families with Fraxe Mental Retardation(1997)61 cited
- → Linkage studies with the gene for an X‐linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)(1988)58 cited