Petter Strømme

Prevalence Estimation of Williams Syndrome

Petter Strømme, Per G. Bjømstad, Kjersti Ramstad · Journal of Child Neurology · 2002 · 779 citations

Life Sciences, Genetics, Pediatrics +15

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

Petter Strømme, Marie Mangelsdorf, Marie Shaw et al. · Nature Genetics · 2002 · 432 citations

Life Sciences, Genetics, Molecular Genetics +14

<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects

Konrad Platzer, Hongjie Yuan, Hannah M. Schutz et al. · Journal of Medical Genetics · 2017 · 256 citations · Full text

Life Sciences, Neurology, Neuroscience +17

SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome

Gregor D. Gilfillan, Kaja Kristine Selmer, Ingrid Roxrud et al. · The American Journal of Human Genetics · 2008 · 236 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Prevalence of psychiatric diagnoses in children with mental retardation: data from a population-based study

Petter Strømme, Trond H. Diseth · Developmental Medicine & Child Neurology · 2000 · 214 citations

Medicine, Pediatrics, Psychiatry +15