Bernard J. Pope

Grattan Street
Parkville, VIC 3050, Australia

Last Updated: 09/26/2026

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Found 72 publications

Immune Suppression and Somatic Mutation in Endometriosis - An Opportunity for Personalized Immunotherapy.

Immune Suppression and Somatic Mutation in Endometriosis - An Opportunity for Personalized Immunotherapy.

Journal: International journal of women's health

Published: June 02, 2026

Lynch syndrome caused by a pathogenic SINE-VNTR-Alu (SVA) insertion in MSH2 gene identified by long-read DNA sequencing.

Lynch syndrome caused by a pathogenic SINE-VNTR-Alu (SVA) insertion in MSH2 gene identified by long-read DNA sequencing.

Journal: Familial cancer

Published: May 07, 2026

The Landscape of Prostate Tumour Methylation.

The Landscape of Prostate Tumour Methylation.

Journal: Cancer discovery

Published: April 30, 2025

Causes of evolutionary divergence in prostate cancer.

Causes of evolutionary divergence in prostate cancer.

Journal: ArXiv

Published: April 01, 2025

The Landscape of Prostate Tumour Methylation.

The Landscape of Prostate Tumour Methylation.

Journal: bioRxiv : the preprint server for biology

Published: February 24, 2025

Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications.

Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications.

Journal: Translational oncology

Published: August 31, 2024

Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications.

Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications.

Journal: medRxiv : the preprint server for health sciences

Published: August 16, 2024

Prevalence of Germline Pathogenic Variants in Renal Cancer Predisposition Genes in a Population-Based Study of Renal Cell Carcinoma.

Prevalence of Germline Pathogenic Variants in Renal Cancer Predisposition Genes in a Population-Based Study of Renal Cell Carcinoma.

Journal: Cancers

Published: June 18, 2024

A Family-Based Study of Inherited Genetic Risk in Lipedema.

A Family-Based Study of Inherited Genetic Risk in Lipedema.

Journal: Lymphatic research and biology

Published: February 26, 2024

DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands.

DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands.

Journal: Cancers

Published: September 06, 2023

Ultrasensitive Detection of Circulating Tumour DNA enriches for Patients with a Greater Risk of Recurrence of Clinically Localised Prostate Cancer.

Ultrasensitive Detection of Circulating Tumour DNA enriches for Patients with a Greater Risk of Recurrence of Clinically Localised Prostate Cancer.

Journal: European urology

Published: August 06, 2023

The Germline and Somatic Origins of Prostate Cancer Heterogeneity.

The Germline and Somatic Origins of Prostate Cancer Heterogeneity.

Journal: Cancer discovery

Published: August 03, 2023

Showing 1-12 of 72

Last Updated: 09/26/2026