Bobby P C Koeleman
Overview
Explore the profile of Bobby P C Koeleman including associated specialties, affiliations and a list of published articles.
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Articles
147
Citations
4019
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Recent Articles
1.
Sanders M, Koeleman B, Brilstra E, Jansen F, Baldassari S, Chipaux M, et al.
Epilepsia
. 2024 Oct;
65(12):e209-e215.
PMID: 39460693
We studied the distribution of germline and somatic variants in epilepsy surgery patients with (suspected) malformations of cortical development (MCD) who underwent surgery between 2015 and 2020 at University Medical...
2.
Al-Ali A, Al-Rubaish A, Alali R, Almansori M, Al-Jumaan M, Alshehri A, et al.
Sci Rep
. 2023 Dec;
13(1):21866.
PMID: 38072966
Genome-wide association studies (GWAS) have yielded significant insights into the genetic architecture of myocardial infarction (MI), although studies in non-European populations are still lacking. Saudi Arabian cohorts offer an opportunity...
3.
Nijboer T, Hessel E, van Haaften G, van Zandvoort M, van der Spek P, Troelstra C, et al.
PLoS One
. 2023 Sep;
18(9):e0290013.
PMID: 37672513
Colour agnosia is a disorder that impairs colour knowledge (naming, recognition) despite intact colour perception. Previously, we have identified the first and only-known family with hereditary developmental colour agnosia. The...
4.
Alyousef Y, Alonaizan F, Alsulaiman A, Abukabbos H, Aldarwish M, Alali A, et al.
Int Dent J
. 2023 May;
73(3):470.
PMID: 37201962
No abstract available.
5.
Martins Custodio H, Clayton L, Bellampalli R, Pagni S, Silvennoinen K, Caswell R, et al.
Brain
. 2023 Apr;
146(9):3885-3897.
PMID: 37006128
Dravet syndrome is an archetypal rare severe epilepsy, considered 'monogenic', typically caused by loss-of-function SCN1A variants. Despite a recognizable core phenotype, its marked phenotypic heterogeneity is incompletely explained by differences...
6.
Abumadini M, Al Ghamdi K, Alqahtani A, Almedallah D, Callans L, Jarad J, et al.
Front Mol Neurosci
. 2023 Feb;
16:1069375.
PMID: 36846569
Introduction: Genome-wide association studies have discovered common polymorphisms in regions associated with schizophrenia. No genome-wide analyses have been performed in Saudi schizophrenia subjects. Methods: Genome-wide genotyping data from 136 Saudi...
7.
Stevelink R, Koeleman B, Sisodiya S
Epilepsia
. 2023 Feb;
64(5):e82-e86.
PMID: 36799507
Focal and generalized epilepsies are associated with robust differences in magnetic resonance imaging (MRI) measures of subcortical structures, gray matter, and white matter. However, it is unknown whether such structural...
8.
Stevelink R, Al-Toma D, Jansen F, Lamberink H, Asadi-Pooya A, Farazdaghi M, et al.
EClinicalMedicine
. 2022 Dec;
53:101732.
PMID: 36467455
Background: A third of people with juvenile myoclonic epilepsy (JME) are drug-resistant. Three-quarters have a seizure relapse when attempting to withdraw anti-seizure medication (ASM) after achieving seizure-freedom. It is currently...
9.
Alyousef Y, Alonaizan F, Alsulaiman A, Aldarwish M, Alali A, Almasood N, et al.
Int Dent J
. 2022 Sep;
73(1):144-150.
PMID: 36180284
Objectives: The objectives of this study were to identify the composition of oral microbiota in a cohort of patients with sickle cell anemia (SCA) and a high mean number of...
10.
Weuring W, Hoekman J, Braun K, Koeleman B
Cells
. 2022 Feb;
11(3).
PMID: 35159264
There are currently seven different zebrafish strains that model Dravet Syndrome, a severe childhood form of epilepsy. These models are based on a set of duplicated genes, and , which...