Nathalie Roëckel

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Philippe Jay, Claire Rougeulle, Annick Massacrier et al. · Nature Genetics · 1997 · 245 citations

Developmental Biology, Genetic Disorder, Medicine +8

Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex.

Danielle Pham-Dinh, Marie‐Geneviève Mattéi, J.L. Nussbaum et al. · Proceedings of the National Academy of Sciences · 1993 · 220 citations · Full text

Glycoproteomics, Immunogenetics, Developmental Biology +15

The Human Magel2 Gene and Its Mouse Homologue Are Paternally Expressed and Mapped to the Prader-Willi Region

Irène Boccaccio, Heather R. Glatt-Deeley, Françoise Watrin et al. · Human Molecular Genetics · 1999 · 184 citations

Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect

C. Mignon, Perrine Malzac, A. Moncla et al. · European Journal of Human Genetics · 1996 · 69 citations

The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene

Françoise Watrin, Elodie Le Meur, Nathalie Roëckel et al. · BMC Genetics · 2005 · 45 citations · Full text