Valérie Jacquemin
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Microtubule and mitosis dynamics, Prenatal Screening and Diagnostics, Cancer Genomics and Diagnostics
Most-Cited Works
- → Dynamic Cancer Cell Heterogeneity: Diagnostic and Therapeutic Implications(2022)71 cited
- → Population-based, first-tier genomic newborn screening in the maternity ward(2025)31 cited
- → Digenic inheritance of human primary microcephaly delineates centrosomal and non‐centrosomal pathways(2019)24 cited
- → TrkA mediates effect of novel KIDINS220 mutation in human brain ventriculomegaly(2020)20 cited
- → Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy(2021)17 cited
- → Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population(2019)17 cited
- → Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance(2023)10 cited
- → An exome-wide study of renal operational tolerance(2023)3 cited
- → Population-Based, First-Tier Genomic Newborn Screening in a Single Maternity Ward in Belgium: Results of Babydetect Project(2024)2 cited
- → Analytical Validation of a Genomic Newborn Screening Workflow(2025)1 cited