Gaelle Marenne

Brest, France

Last Updated: 09/26/2026

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Found 34 publications

A simple demonstration of a privacy-preserving de-centralised genotype imputation workflow.

A simple demonstration of a privacy-preserving de-centralised genotype imputation workflow.

Journal: PloS one

Published: December 03, 2025

Rare Variants Associated With Pediatric Cancer Treatment-Related Second Malignant Neoplasm Risk.

Rare Variants Associated With Pediatric Cancer Treatment-Related Second Malignant Neoplasm Risk.

Journal: JCO precision oncology

Published: September 17, 2025

SURFBAT: a surrogate family based association test building on large imputation reference panels.

SURFBAT: a surrogate family based association test building on large imputation reference panels.

Journal: G3 (Bethesda, Md.)

Published: September 06, 2024

Benchmark of computational methods to detect digenism in sequencing data.

Benchmark of computational methods to detect digenism in sequencing data.

Journal: European journal of human genetics : EJHG

Published: August 22, 2024

Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual.

Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual.

Journal: Human heredity

Published: August 01, 2024

PSAP-Genomic-Regions: A Method Leveraging Population Data to Prioritize Coding and Non-Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis.

PSAP-Genomic-Regions: A Method Leveraging Population Data to Prioritize Coding and Non-Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis.

Journal: Genetic epidemiology

Published: June 05, 2024

Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants.

Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants.

Journal: Human genomics

Published: November 09, 2023

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization.

Journal: Wellcome open research

Published: October 02, 2023

Human genetic structure in Northwest France provides new insights into West European historical demography.

Human genetic structure in Northwest France provides new insights into West European historical demography.

Journal: Nature communications

Published: June 21, 2023

Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes.

Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes.

Journal: Genetic epidemiology

Published: February 02, 2023

Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.

Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.

Journal: PLoS genetics

Published: November 04, 2021

RAVAQ: An integrative pipeline from quality control to region-based rare variant association analysis.

RAVAQ: An integrative pipeline from quality control to region-based rare variant association analysis.

Journal: Genetic epidemiology

Published: October 13, 2021

Showing 1-12 of 34

Last Updated: 09/26/2026