Bobby P. Koeleman

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 219 publications

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Journal: Epilepsia

Published: February 25, 2026

Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity.

Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity.

Journal: Neurology

Published: January 14, 2026

Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.

Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.

Journal: Clinical genetics

Published: November 28, 2025

Monogenic no more: are all epilepsies polygenic?

Monogenic no more: are all epilepsies polygenic?

Journal: Trends in genetics : TIG

Published: October 14, 2025

Penetrance of pathogenic epilepsy variants is low and shaped by common genetic background.

Penetrance of pathogenic epilepsy variants is low and shaped by common genetic background.

Journal: Epilepsia

Published: June 23, 2025

KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndrome.

KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndrome.

Journal: Human molecular genetics

Published: April 08, 2025

Genome-wide association meta-analyses of drug-resistant epilepsy.

Genome-wide association meta-analyses of drug-resistant epilepsy.

Journal: EBioMedicine

Published: August 12, 2024

Somatic variant analysis of resected brain tissue in epilepsy surgery patients.

Somatic variant analysis of resected brain tissue in epilepsy surgery patients.

Journal: Epilepsia

Published: March 05, 2024

Identification of candidate genes for developmental colour agnosia in a single unique family.

Identification of candidate genes for developmental colour agnosia in a single unique family.

Journal: PloS one

Published: June 30, 2023

Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts.

Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts.

Journal: Scientific reports

Published: June 27, 2023

Corrigendum to 'Oral microbiota analyses of Saudi sickle cell anemics with dental caries' International Dental Journal, 73/1, February 2023, Pages 144-150.

Corrigendum to 'Oral microbiota analyses of Saudi sickle cell anemics with dental caries' International Dental Journal, 73/1, February 2023, Pages 144-150.

Journal: International dental journal

Published: May 18, 2023

Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

Journal: Frontiers in neuroscience

Published: April 25, 2023

Showing 1-12 of 219

Last Updated: 09/26/2026