Barbara Bardoni
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut de Pharmacologie Moléculaire et Cellulaire(FR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, RNA modifications and cancer, RNA Research and Splicing, Ubiquitin and proteasome pathways, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Most-Cited Works
- → An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita(1994)858 cited
- → A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules(1991)851 cited
- → Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism(1994)768 cited
- → A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal(1994)587 cited
- → A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P(2001)360 cited
- → CYFIP/Sra-1 Controls Neuronal Connectivity in Drosophila and Links the Rac1 GTPase Pathway to the Fragile X Protein(2003)313 cited