World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
56
Citations
13066
World Ranking
3485
National Ranking
177

Overview

Barbara Bardoni is affiliated with Université Côte d'Azur in France and has contributed extensively to research in biochemistry, genetics, molecular biology, and neuroscience. Their scholarly work covers numerous facets of neurodevelopmental disorders, genetics, and molecular mechanisms underlying brain function and dysfunction.

The main fields of study where Barbara Bardoni has been active include:

  • Biochemistry, Genetics and Molecular Biology
  • Neuroscience

Their research encompasses specialized subfields such as:

  • Molecular Biology
  • Genetics
  • Cognitive Neuroscience
  • Neurology
  • Physiology

Within these areas, the primary topics of investigation are:

  • Genetics and Neurodevelopmental Disorders
  • Autism Spectrum Disorder Research
  • Phosphodiesterase function and regulation
  • RNA modifications and cancer
  • RNA Research and Splicing
  • Congenital heart defects research
  • Adenosine and Purinergic Signaling

Among the most recent published papers authored or co-authored by Barbara Bardoni are:

  • Role of phosphodiesterases in the pathophysiology of neurodevelopmental disorders, 2021, Molecular Psychiatry
  • Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice, 2021, Nature Communications
  • Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular Dysfunctions, 2021, Frontiers in Cellular Neuroscience
  • Phosphodiesterase 2A inhibition corrects the aberrant behavioral traits observed in genetic and environmental preclinical models of Autism Spectrum Disorder, 2022, Translational Psychiatry
  • Fragile X Syndrome as an interneuronopathy: a lesson for future studies and treatments, 2023, Frontiers in Neuroscience

Barbara Bardoni frequently collaborates with several researchers, including:

  • Marielle Jarjat
  • Sébastien Delhaye
  • Carole Gwizdek
  • Frédéric Brau
  • Viviana Trezza

Their work has been published repeatedly in various scientific venues, with notable frequency in:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Frontiers in Neuroscience
  • Frontiers in Molecular Biosciences
  • Neurobiology of Disease
  • Neuroscience Applied

Best Publications

  • An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

    Elena Zanaria;Françoise Muscatelli;Barbara Bardoni;Tim M. Strom

  • A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

    Brunella Franco;Silvana Guioli;Antonella Pragliola;Antonella Pragliola;Barbara Incerti

  • Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

    F Muscatelli;T M Strom;A P Walker;E Zanaria

  • A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal

    B Bardoni;E Zanaria;S Guioli;G Floridia

  • The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.

    Céline Schaeffer;Barbara Bardoni;Jean‐Louis Mandel;Bernard Ehresmann

  • 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

    Annette Schenck;Barbara Bardoni;Annamaria Moro;Claudia Bagni

  • CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

    Annette Schenck;Barbara Bardoni;Caillin Langmann;Nicholas Harden

  • Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology

    Yong Kim;Jee Young Sung;Ilaria Ceglia;Ko Woon Lee

  • Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

    A Ballabio;B Bardoni;R Carrozzo;G Andria

  • The Hsp90 chaperone controls the biogenesis of L7Ae RNPs through conserved machinery.

    Séverine Boulon;Nathalie Marmier-Gourrier;Bérengère Pradet-Balade;Laurence Wurth

  • A novel function for fragile X mental retardation protein in translational activation.

    Elias G Bechara;Marie Cecile Didiot;Mireille Melko;Mireille Melko;Laetitia Davidovic;Laetitia Davidovic

  • A Transcriptional Silencing Domain in DAX-1 Whose Mutation Causes Adrenal Hypoplasia Congenita

    Enzo Lalli;Barbara Bardoni;Emmanuel Zazopoulos;Jean-Marie Wurtz

  • Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.

    Edouard W. Khandjian;Marc-Etienne Huot;Sandra Tremblay;Laetitia Davidovic

  • Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes

    Barbara Bardoni;Jean-Louis Mandel

  • FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts

    Marie Castets;Céline Schaeffer;Elias Bechara;Annette Schenck

  • A Novel RNA-binding Nuclear Protein That Interacts With the Fragile X Mental Retardation (FMR1) Protein

    Barbara Bardoni;Annette Schenck;Jean Louis Mandel

  • The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules

    Laetitia Davidovic;Xavier H. Jaglin;Aude-Marie Lepagnol-Bestel;Sandra Tremblay

  • Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo

    Edwin J. Mientjes;Rob Willemsen;Laura L. Kirkpatrick;Ingeborg M. Nieuwenhuizen

  • The Fragile X mental retardation protein.

    Barbara Bardoni;Annette Schenck;Jean-Louis Mandel

  • A dosage sensitive locus at chromosome XP21 is involved in male to female sex reversal

    B. Bardoni;E. Zanaria;S. Guioli;G. Floridia

Frequent Co-Authors

Jean-Louis Mandel
Jean-Louis Mandel Institute of Genetics and Molecular and Cellular Biology
Orsetta Zuffardi
Orsetta Zuffardi University of Pavia
Enzo Lalli
Enzo Lalli Centre national de la recherche scientifique, CNRS
Maria Vincenza Catania
Maria Vincenza Catania National Academies of Sciences, Engineering, and Medicine
Andrea Ballabio
Andrea Ballabio Baylor College of Medicine
Pascal Barbry
Pascal Barbry Centre national de la recherche scientifique, CNRS
Bernard Mari
Bernard Mari Centre national de la recherche scientifique, CNRS
Rob Willemsen
Rob Willemsen Erasmus University Rotterdam
Jozef Gecz
Jozef Gecz University of Adelaide
Tim M. Strom
Tim M. Strom Technical University of Munich

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Exploring Genetics in the USA can lead to a range of fascinating career options in healthcare and research. Many students who study genetics also consider related fields such as nursing, where online degrees offer flexibility and affordability. For those interested in advanced practice, there are several affordable fnp programs that prepare graduates for leadership roles in nursing and patient care.

If you are searching for the cheapest way to become a nurse, online nursing programs provide cost-effective pathways to enter the profession. Registered nurses considering further qualifications can explore cheapest online bsn to dnp programs to advance their careers through specialized doctoral education.

Additionally, professionals who wish to transition from an RN to a bachelor’s degree can benefit from the rn to bsn online cost comparison to find budget-friendly programs. These related pathways expand your options in genetics, healthcare, and beyond while helping you save on tuition and related expenses.

Best Scientists Citing Barbara Bardoni

Trending Scientists

Recently Published Articles