Voreak Suybeng

Paris, France

Last Updated: 09/26/2026

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Found 12 publications

Author Correction: A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript.

Author Correction: A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript.

Journal: NPJ genomic medicine

Published: September 02, 2025

A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript.

A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript.

Journal: NPJ genomic medicine

Published: February 14, 2025

Expanding the spectrum of FUS::CREM-rearranged neoplasms: a case of mesenchymal malignant tumor with neuroendocrine differentiation.

Expanding the spectrum of FUS::CREM-rearranged neoplasms: a case of mesenchymal malignant tumor with neuroendocrine differentiation.

Journal: Virchows Archiv : an international journal of pathology

Published: January 28, 2025

MSH3: a confirmed predisposing gene for adenomatous polyposis.

MSH3: a confirmed predisposing gene for adenomatous polyposis.

Journal: Journal of medical genetics

Published: April 25, 2023

Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees.

Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees.

Journal: Journal of medical genetics

Published: April 07, 2023

Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh-frozen breast/ovarian tumor versus blood.

Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh-frozen breast/ovarian tumor versus blood.

Journal: Clinical genetics

Published: January 19, 2023

First report of medulloblastoma in a patient with MUTYH-associated polyposis.

First report of medulloblastoma in a patient with MUTYH-associated polyposis.

Journal: Neuropathology and applied neurobiology

Published: December 13, 2022

APC germline pathogenic variants and epithelial ovarian cancer: causal or coincidental findings?

APC germline pathogenic variants and epithelial ovarian cancer: causal or coincidental findings?

Journal: Journal of medical genetics

Published: July 05, 2022

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Journal: American journal of human genetics

Published: June 15, 2021

The PI3K/mTOR Pathway Is Targeted by Rare Germline Variants in Patients with Both Melanoma and Renal Cell Carcinoma.

The PI3K/mTOR Pathway Is Targeted by Rare Germline Variants in Patients with Both Melanoma and Renal Cell Carcinoma.

Journal: Cancers

Published: March 10, 2021

Genomic Instability Signature of Palindromic Non-Coding Somatic Mutations in Bladder Cancer.

Genomic Instability Signature of Palindromic Non-Coding Somatic Mutations in Bladder Cancer.

Journal: Cancers

Published: September 24, 2020

Comparison of Pathogenicity Prediction Tools on Somatic Variants.

Comparison of Pathogenicity Prediction Tools on Somatic Variants.

Journal: The Journal of molecular diagnostics : JMD

Published: April 14, 2020

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Last Updated: 09/26/2026