Richarda M. De Voer

Nijmegen, GE, Netherlands

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 67 publications

Shallow Whole-Genome Sequencing to Assess Genomic Instability and Predict Treatment Response in Metastatic Castration-Resistant Prostate Cancer.

Shallow Whole-Genome Sequencing to Assess Genomic Instability and Predict Treatment Response in Metastatic Castration-Resistant Prostate Cancer.

Journal: JCO precision oncology
Published: July 08, 2026

Reply.

Reply.

Journal: Gastroenterology
Published: April 24, 2026

Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants.

Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants.

Journal: JCO precision oncology
Published: April 16, 2026

Assessing the Detection Power of Genome-Wide Copy Number Variation Profiles in Prostate Cancer Using Simulated Shallow Whole-Genome Sequencing Data.

Assessing the Detection Power of Genome-Wide Copy Number Variation Profiles in Prostate Cancer Using Simulated Shallow Whole-Genome Sequencing Data.

Journal: JCO clinical cancer informatics
Published: January 23, 2026

Biallelic Germline Inactivation of HROB Causes Primary Gonadal Insufficiency and is Potentially Associated with Colonic Polyposis Predisposition.

Biallelic Germline Inactivation of HROB Causes Primary Gonadal Insufficiency and is Potentially Associated with Colonic Polyposis Predisposition.

Journal: American journal of medical genetics. Part A
Published: November 19, 2025

Integrating germline and tumor sequencing to improve hereditary cancer diagnosis and care.

Integrating germline and tumor sequencing to improve hereditary cancer diagnosis and care.

Journal: European journal of human genetics : EJHG
Published: October 15, 2025

Mapping the genetic landscape of hereditary diffuse-type gastric cancer progression.

Mapping the genetic landscape of hereditary diffuse-type gastric cancer progression.

Journal: Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association
Published: October 05, 2025

Tumour spectrum, distinguishing features and management recommendations for NTHL1-associated tumour syndrome: a systematic review.

Tumour spectrum, distinguishing features and management recommendations for NTHL1-associated tumour syndrome: a systematic review.

Journal: Hereditary cancer in clinical practice
Published: July 01, 2025

Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Journal: Nature medicine
Published: June 19, 2025

Mutational Landscape of Colorectal Tumors From Individuals With Unexplained Adenomatous or Serrated Colorectal Polyposis.

Mutational Landscape of Colorectal Tumors From Individuals With Unexplained Adenomatous or Serrated Colorectal Polyposis.

Journal: Gastroenterology
Published: May 29, 2025

The burden of TTN variants in the genomic era: analysis of 18,462 individuals from the Solve-RD consortium and general recommendations.

The burden of TTN variants in the genomic era: analysis of 18,462 individuals from the Solve-RD consortium and general recommendations.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 17, 2024

The burden of TTN variants in the genomic era: Analysis of 18,462 individuals from the Solve-RD consortium and general recommendations.

The burden of TTN variants in the genomic era: Analysis of 18,462 individuals from the Solve-RD consortium and general recommendations.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 17, 2024
Showing 1-12 of 67

Last Updated: 09/26/2026