Concepedia

M Prieur

MP

Statistics

Publications

43

Citations

4.2K

H-Index

27

Active since

1972

Affiliations

Hôpital Necker-Enfants Malades(Current)

Institut Curie

Centre National de la Recherche Scientifique

Inserm

Institut Necker Enfants Malades

M Prieur is an author at Hôpital Necker-Enfants Malades specializing in genetics, life sciences, and human genetics.

Publications per year

1972–2007

43

Publications

43

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A K Ryan, Judith A. Goodship, David I. Wilson et al. · Journal of Medical Genetics · 1997 · 1.2K citations · Full text

, , +16

Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes

Julie Aubert, Luce Dauphinot, Isabelle Rivals et al. · The American Journal of Human Genetics · 2007 · 342 citations · Full text

, , +12

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

M-L Jacquemont, Damien Sanlaville, Richard Redon et al. · Journal of Medical Genetics · 2006 · 304 citations · Full text

, , +17

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome

Marc Jeanpierre, C Turleau, Alain Aurias et al. · Human Molecular Genetics · 1993 · 287 citations

, , +17

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

Zohra Rahmani, Jean‐Louis Blouin, N. Créau-Goldberg et al. · Proceedings of the National Academy of Sciences · 1989 · 260 citations · Full text

, , +15

1–5 of 43