Bobby P C Koeleman
Universiteit Utrecht
H-index: 85
Europe-Netherlands
Top articles of Bobby P C Koeleman
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Corrigendum to ‘Oral microbiota analyses of Saudi sickle cell anemics with dental caries’ International Dental Journal, 73/1, February 2023, Pages 144-150 | International Dental Journal | Yousef M Alyousef Faisal A Alonaizan Ahmed A Alsulaiman Halima Abukabbos Mohammed I Aldarwish | 2023/6 |
Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin | Frontiers in Neuroscience | Isabelle Boothman Lisa M Clayton Mark McCormack Alexandra McKibben Driscoll Remi Stevelink | 2023/9/8 |
Distinct genetic basis of common epilepsies and structural magnetic resonance imaging measures | Epilepsia | Remi Stevelink Bobby PC Koeleman Sanjay M Sisodiya International League Against Epilepsy Consortium on Complex Epilepsies | 2023/5 |
Identification of candidate genes for developmental colour agnosia in a single unique family | Plos one | Tanja CW Nijboer Ellen VS Hessel Gijs W van Haaften Martine J van Zandvoort Peter J van der Spek | 2023/9/6 |
Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls | Frontiers in Molecular Neuroscience | Mahdi S Abumadini Kholoud S Al Ghamdi Abdullah H Alqahtani Dana K Almedallah Lauren Callans | 2023/2/10 |
Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’condition | Brain | Helena Martins Custodio Lisa M Clayton Ravishankara Bellampalli Susanna Pagni Katri Silvennoinen | 2023/9 |
Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts | Scientific Reports | Amein K Al-Ali Abdullah M Al-Rubaish Rudaynah A Alali Mohammed S Almansori Mohammed A Al-Jumaan | 2023/12/10 |
Oral microbiota analyses of Saudi sickle cell anemics with dental caries | international dental journal | Yousef M Alyousef Faisal A Alonaizan Ahmed A Alsulaiman Mohammed I Aldarwish Ali A Alali | 2023/2/1 |
Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids | BMC biology | N Dirkx Wout J Weuring E De Vriendt N Smal J Van De Vondervoort | 2023/7/13 |
GWAS in two Saudi Myocardial Infarction Cohorts and European based studies reveal dozens of concordant signals | Amein AlAli Abdullah Al-Rubaish Rudaynah Alali Mohammed Almansori Mohammed Aljumaan | 2023/7/5 | |
KBTBD13 is a novel cardiomyopathy gene | Human mutation | Josine M de Winter Karlijn Bouman Joshua Strom Mei Methawasin Jan DH Jongbloed | 2022/12 |
Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study | Epilepsia | Mahmoud Koko Joshua E Motelow Kate E Stanley Dheeraj R Bobbili Ryan S Dhindsa | 2022/3 |
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: a systematic review and individual … | Remi Stevelink Dania Al-Toma Floor E Jansen Herm J Lamberink Ali A Asadi-Pooya | 2022/11/1 | |
Genetic and Functional Differences between Duplicated Zebrafish Genes for Human SCN1A | Cells | Wout J Weuring Jos W Hoekman Kees PJ Braun Bobby PC Koeleman | 2022/1/28 |
Genome-wide meta-analysis of over 29,000 people with epilepsy reveals 26 loci and subtype-specific genetic architecture | MedRxiv | International League Against Epilepsy Consortium on Complex Epilepsies Samuel F Berkovic Gianpiero L Cavalleri Bobby PC Koeleman | 2022/6/14 |
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam | Epilepsia | Ciarán Campbell Mark McCormack Sonn Patel Caragh Stapleton Dheeraj Bobbili | 2022/6 |
Genetische therapie voor epilepsie | Epilepsie, periodiek voor professionals | Bobby Koeleman Eva Brilstra | 2022/12/15 |
Efficient and accurate prime editing strategy to correct genetic alterations in hiPSC using single EF-1alpha driven all-in-one plasmids | bioRxiv | Wout J Weuring N Dirkx E De Vriendt N Smal J van de Vondervoort | 2022/5/4 |
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns | Genetics in Medicine | Hannah Stamberger Trine B Hammer Elena Gardella Danique RM Vlaskamp Birgitte Bertelsen | 2021/2 |
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations | Epilepsia | Remi Stevelink Jurjen J Luykx Bochao D Lin Costin Leu Dennis Lal | 2021/7 |
