Petter Strømme
Oslo University Hospital(NO)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Metabolism and Genetic Disorders, Genetic Syndromes and Imprinting, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Prevalence Estimation of Williams Syndrome(2002)770 cited
- → Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy(2002)431 cited
- → GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects(2017)252 cited
- → SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome(2008)235 cited
- → Prevalence of psychiatric diagnoses in children with mental retardation: data from a population-based study(2000)214 cited
- → Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations(2014)205 cited