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Nationwide evaluation of mutation-tailored anti-EGFR therapy selection in patients with colorectal cancer in daily clinical practice
Nationwide evaluation of mutation-tailored treatment of gastrointestinal stromal tumors in daily clinical practice
Multicenter comparison of molecular tumor boards in the Netherlands
"The leading role of pathology in assessing the somatic molecular alterations of cancer: Position Paper of the European Society of Pathology"
ESMO recommendations on microsatellite instability testing for immunotherapy in cancer, and its relationship with PD-1/PD-L1 expression and tumour mutational burden: a systematic review-based approach
Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
Guidance Statement On BRCA1/2 Tumor Testing in Ovarian Cancer Patients
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect
Massive gastric polyposis associated with a germline SMAD4 gene mutation
Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation
Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study