Petter Strømme

Prevalence Estimation of Williams Syndrome

Petter Strømme, Per G. Bjømstad, Kjersti Ramstad · Journal of Child Neurology · 2002 · 766 citations

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 · 431 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +7

<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 · 249 citations · Full text

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 · 235 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5

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 · 213 citations

Psychiatric Disorders, Mental Health, Mild Mental Retardation +21