M. Mannens

Somatic Mosaicism for Partial Paternal Isodisomy in Wiedemann-Beckwith Syndrome: A Post-Fertilization Event

Isabelle Henry, Anne Puech, A. Riesewijk et al. · European Journal of Human Genetics · 1993 · 140 citations

Infertility, Andrology, Fertility +10

High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

J.M.N. Hoovers, M. Mannens, Rosalind M. John et al. · Genomics · 1992 · 131 citations

Functional Genomics, High-resolution Localization, Medicine +11

Genetics of Beckwith‐Wiedemann syndrome‐associated tumors: Common genetic pathways

Marja Steenman, A. Westerveld, M. Mannens · Genes Chromosomes and Cancer · 2000 · 101 citations

Beckwith-wiedemann Syndrome, Common Genetic Pathways, Several Aberrations +11

A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

Sophie Demolombe, Isabelle Baró, Yann Péréon et al. · Journal of Biological Chemistry · 1998 · 91 citations · Full text

The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts

Mariëlle Alders, Matt Hodges, Anna‐Katerina Hadjantonakis et al. · Human Molecular Genetics · 1997 · 75 citations · Full text

Extravillus Trophoblasts, Cytogenetics, Genetics +16