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Stepwise ABC system for classification of any type of genetic variant
Genotype-Guided Thiopurine Dosing Does not Lead to Additional Costs in Patients With Inflammatory Bowel Disease
Patients' beliefs about medicine are associated with early thiopurine discontinuation in patients with inflammatory bowel diseases
The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine
Risk factors for thiopurine-induced myelosuppression and infections in inflammatory bowel disease patients with a normal TPMT genotype
More Dose-dependent Side Effects with Mercaptopurine over Azathioprine in IBD Treatment Due to Relatively Higher Dosing
Critical points for an accurate human genome analysis
European registration process for Clinical Laboratory Geneticists in genetic healthcare
Diagnostic exome sequencing in 266 Dutch patients with visual impairment
Early Assessment of Thiopurine Metabolites Identifies Patients at Risk of Thiopurine-induced Leukopenia in Inflammatory Bowel Disease
Early prediction of thiopurine-induced hepatotoxicity in inflammatory bowel disease
Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene-disease associations and unanticipated rare disorders
Guidelines for diagnostic next-generation sequencing
Identification of Patients With Variants in TPMT and Dose Reduction Reduces Hematologic Events During Thiopurine Treatment of Inflammatory Bowel Disease
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood
Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis
Mutational analysis of TARDBP in Parkinson's disease
Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Genome-Wide Association Analysis of Rheumatoid Arthritis Patients Treated with Anti-TNF Medication
Genome-wide association study confirms extant PD risk loci among the Dutch
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies