Gaëlle Marenne
0000-0002-4363-7170
Publication & Citation Trends
Publications
0 total
A simple demonstration of a privacy-preserving de-centralised genotype imputation workflow
Cited by 0
Semantic Scholar
Rare Variants Associated With Pediatric Cancer Treatment-Related Second Malignant Neoplasm Risk.
Cited by 0
Semantic Scholar
Benchmark of computational methods to detect digenism in sequencing data
Cited by 1
Semantic Scholar
Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual
Cited by 0
Semantic Scholar
PFMG2025–integrating genomic medicine into the national healthcare system in France
Cited by 29
Semantic Scholar
Human genetic structure in Northwest France provides new insights into West European historical demography OA
Cited by 6
Semantic Scholar
Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants OA
Cited by 9
Semantic Scholar
PSAP-genomic-regions: a method leveraging population data to prioritize coding and non-coding variants in whole genome sequencing for rare disease diagnosis OA
Cited by 2
Semantic Scholar
Research Topics
Genetic Associations and Epidemiology
(30)
Genomic variations and chromosomal abnormalities
(14)
Genomics and Rare Diseases
(12)
Pancreatic function and diabetes
(8)
Genetic Mapping and Diversity in Plants and Animals
(8)
Affiliations
University of Southern California
Université Européenne de Bretagne
Inserm
Université de Bretagne Occidentale
Délégation Paris 7