18 results on '"Helthuis, Marinka"'
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2. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia
3. Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data
4. Mediation and Longitudinal Analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count
5. A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia
6. Rare Variants in Pharmacogenes Influence Clozapine Metabolism in Individuals with Schizophrenia
7. Genomic Stratification of Clozapine Prescription Patterns Using Schizophrenia Polygenic Scores
8. 86. RARE VARIANTS IN PHARMACOGENES IMPACT CLOZAPINE METABOLISM IN INDIVIDUALS WITH TREATMENT-RESISTANT SCHIZOPHRENIA
9. Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: A longitudinal analysis and GWAS using clinical monitoring data from the UK
10. Genomic stratification of clozapine prescription patterns using schizophrenia polygenic scores
11. Clozapine Metabolism is Associated With Absolute Neutrophil Count in Individuals With Treatment-Resistant Schizophrenia
12. There Is Life After the UK Clozapine Central Non-Rechallenge Database
13. Clozapine metabolism is associated with Absolute Neutrophil Count in individuals with treatment-resistant schizophrenia
14. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
15. Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism
16. PHARMACOGENOMIC ARCHITECTURE OF CLOZAPINE PLASMA CONCENTRATIONS
17. THE IMPACT OF THE DUFFY-NULL GENOTYPE IN CLOZAPINE-ASSOCIATED NEUTROPENIA: A GENOME-WIDE ASSOCIATION STUDY IN INDIVIDUALS OF AFRICAN ANCESTRY
18. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
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