Peter Georgeson

305 Grattan Street
Parkville, VIC 3010, Australia

Last Updated: 09/26/2026

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Found 47 publications

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

Alcohol consumption and molecular subtypes of colorectal cancer: pooled observational and Mendelian randomization analyses.

Alcohol consumption and molecular subtypes of colorectal cancer: pooled observational and Mendelian randomization analyses.

Journal: The American journal of clinical nutrition

Published: August 04, 2025

Germline MLH1 c.-42 C > T is a likely pathogenic variant predisposing to a reduced-penetrance/modified Lynch syndrome phenotype featuring MLH1-methylated cancers.

Germline MLH1 c.-42 C > T is a likely pathogenic variant predisposing to a reduced-penetrance/modified Lynch syndrome phenotype featuring MLH1-methylated cancers.

Journal: Familial cancer

Published: August 03, 2025

Genomic characterization of colorectal tumors: insights into significantly mutated genes, pathways, and survival outcomes.

Genomic characterization of colorectal tumors: insights into significantly mutated genes, pathways, and survival outcomes.

Journal: BMC cancer

Published: July 17, 2025

Association of germline variants with KRAS-mutation status in colorectal cancer.

Association of germline variants with KRAS-mutation status in colorectal cancer.

Journal: Scientific reports

Published: June 18, 2025

The germline POLD1 c.1420 C > A (p.Leu474Ile) variant segregates with endometrial cancer, colorectal cancer and colonic polyps demonstrating hypermutation and defective POLD1 mutational signatures.

The germline POLD1 c.1420 C > A (p.Leu474Ile) variant segregates with endometrial cancer, colorectal cancer and colonic polyps demonstrating hypermutation and defective POLD1 mutational signatures.

Journal: Familial cancer

Published: June 18, 2025

Physical activity and molecular subtypes of colorectal cancer: a pooled observational analysis and Mendelian randomization study.

Physical activity and molecular subtypes of colorectal cancer: a pooled observational analysis and Mendelian randomization study.

Journal: JNCI cancer spectrum

Published: May 15, 2025

Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylation.

Causes of DNA mismatch repair deficiency in sebaceous skin lesions demonstrating loss of MLH1 protein expression: constitutional over somatic MLH1 promoter methylation.

Journal: Familial cancer

Published: January 21, 2025

Intratumoural pks+Escherichia coli is associated with risk of metachronous colorectal cancer and adenoma development in people with Lynch syndrome.

Intratumoural pks+Escherichia coli is associated with risk of metachronous colorectal cancer and adenoma development in people with Lynch syndrome.

Journal: EBioMedicine

Published: October 23, 2024

Waist Circumference, a Body Shape Index, and Molecular Subtypes of Colorectal Cancer: A Pooled Analysis of Four Cohort Studies.

Waist Circumference, a Body Shape Index, and Molecular Subtypes of Colorectal Cancer: A Pooled Analysis of Four Cohort Studies.

Journal: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

Published: October 17, 2024

DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient Cancers.

DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient Cancers.

Journal: Gastroenterology

Published: September 11, 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: Translational oncology

Published: August 31, 2024

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Last Updated: 09/26/2026