Marie‐José Gregoire

The t(6;8)(q27;p11) Translocation in a Stem Cell Myeloproliferative Disorder Fuses a Novel Gene, FOP, to Fibroblast Growth Factor Receptor 1

Cornel Popovici, Bin Zhang, Marie‐José Gregoire et al. · Blood · 1999 · 198 citations

Life Sciences, Genetics, Molecular Genetics +10

The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients

Camille Leroy, Emilie Landais, Sylvain Briault et al. · European Journal of Human Genetics · 2012 · 134 citations · Full text

Life Sciences, Genetics, Psychiatry +13

Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions

Mylène Béri‐Dexheimer, Véronique Latger‐Cannard, Christophe Philippe et al. · European Journal of Human Genetics · 2008 · 94 citations

Life Sciences, Genetics, Molecular Genetics +16

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

Max Chaffanet, Cornel Popovici, Dominique Leroux et al. · Oncogene · 1998 · 61 citations

Life Sciences, Genetics, Molecular Genetics +14

Genotype–phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the ‘association des Cytogénéticiens de langue Française’

Mylène Béri‐Deixheimer, Marie‐José Gregoire, Annick Toutain et al. · European Journal of Human Genetics · 2007 · 56 citations

Life Sciences, Genetics, Molecular Genetics +17