Barbara Bardoni

10.1k citations

99 papers · 7.6k indexed · 3 hit papers · h-index 46

Impact in

Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Reproductive Medicine top 0.5%
- Sperm and Testicular Function
- Hypothalamic control of reproductive hormones

Papers in

Genetics 81
- Genetics and Neurodevelopmental Disorders 62
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
Molecular Biology 76
- RNA modifications and cancer 33
- RNA Research and Splicing 21
- Ubiquitin and proteasome pathways 18
- Sexual Differentiation and Disorders 7
- Congenital heart defects research 6

Co-authors: Jean‐Louis Mandel Giovanna Camerino Silvana Guioli Annette Schenck Elena Zanaria Laëtitia Davidovic M. Fraccaro Tim M. Strom
Journals: Human Molecular Genetics (8 papers)Human Genetics (7 papers)Nucleic Acids Research (6 papers)Nature (4 papers)Proceedings of the National Academy of Sciences (4 papers)
Partner nations: France Italy United States

In The Last Decade

Barbara Bardoni

97 papers receiving 7.4k citations

Hit Papers

align trajectories log scale

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita 1994 · 656 citations

Peers

Countries citing papers authored by Barbara Bardoni

Since Specialization

Citations

This map shows the geographic impact of Barbara Bardoni's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Barbara Bardoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Bardoni more than expected).

Fields of papers citing papers by Barbara Bardoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Bardoni. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Barbara Bardoni. The network helps show where Barbara Bardoni may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Barbara Bardoni, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Barbara Bardoni Line = papers co-authored together Barbara Bardoni links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	How close are we to a cAMP- and cGMP-theory-based pharmacological therapy for fragile X syndrome? Cell Reports Medicine ·Barbara Bardoni, Carole Gwizdek, Thomas Maurin	2025	0
2	Defects in AMPAR trafficking and microglia activation underlie socio-cognitive deficits associated to decreased expression of phosphodiesterase 2 a Neurobiology of Disease ·崔荣坤, Jong Gab Ho, 孙亦梁, Imke Aufderhaar, Bojana Milić, Andrei Turtoï, Mauro Giorgi, Sandra Lacas‐Gervais, Gabriele Baj, Carole Rovère, Viviana Trezza, Manuela Pellegrini, Thomas Maurin, Enzo Lalli, Barbara Bardoni	2023	5
3	Translating molecular advances in Down syndrome and Fragile X syndrome into therapies European Neuropsychopharmacology ·Victor Faúndez, Ilario De Toma, Barbara Bardoni, Maryam Sharif, Dean Nižetić, Rafael de la Torre, Roi Cohen Kadosh, Yann Hérault, Mara Dierssen, Alexey V. Smarun, (unknown), Stylianos E. Antonarakis, Maryam Sharif, Andrea Contestabile, B Bradford McKay, 貞煕崔, Alain D. Dekker, Laurence P. Prior, Alexey V. Smarun, Alexey V. Smarun, Elizabeth Fisher, Carmen Martínez‐Cué, (unknown), André Strydom	2018	10
4	The role of G-quadruplex in RNA metabolism: Involvement of FMRP and FMR2P Biochimie ·Mireille Melko, Barbara Bardoni	2010	61
5	A Novel Function for Fragile X Mental Retardation Protein in Translational Activation PLoS Biology ·Elías Bechara, Heljie Porre, Mireille Melko, Laëtitia Davidovic, Mounia Bensaid, Patrick Martin, Marie Castets, Philippe Pognonec, Édouard W. Khandjian, Hervé Moine, Barbara Bardoni	2009	160
6	The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules Human Molecular Genetics ·Laëtitia Davidovic, Xavier H. Jaglin, Aude-Marie Lepagnol-Bestel, Samuel Tremblay, Michel Simonneau, Barbara Bardoni, Edward W. Khandjian	2007	105
7	The nuclear MicroSpherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons Human Molecular Genetics ·Laëtitia Davidovic, Elías Bechara, Ming Cao, Xavier H. Jaglin, Sandra Tremblay, Attila Sı́k, Barbara Bardoni, Édouard W. Khandjian	2006	57
8	The Structure of the N-Terminal Domain of the Fragile X Mental Retardation Protein: A Platform for Protein-Protein Interaction Structure ·Andres Ramos, David Hollingworth, Salvatore Adinolfi, Marie Castets, Geoff Kelly, Thomas A. Frenkiel, Barbara Bardoni, Annalisa Pastore	2006	91
9	Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure Nucleic Acids Research ·Elías Bechara, Laëtitia Davidovic, Mireille Melko, Mounia Bensaid, Samuel Tremblay, Josiane Grosgeorge, Edward W. Khandjian, Enzo Lalli, Barbara Bardoni	2006	49
10	Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology Nature ·Yong Kim, Jee Young Sung, Ilaria Ceglia, D. De Willde, Jung‐Hyuck Ahn, Zeni Zoraia Alfonso da Silva, Bakersfield Gas Co., Seung Kwak, Jong Bae Park, Sung Ho Ryu, Annette Schenck, Barbara Bardoni, John D. Scott, Angus C. Nairn, Paul Greengard	2006	251
11	WAVE/SCAR, a multifunctional complex coordinating different aspects of neuronal connectivity Developmental Biology ·Annette Schenck, Abrar Qurashi, Pilar Carrera, Barbara Bardoni, Inshah Malik, Eyal D. Schejter, Jean‐Louis Mandel, Angela Giangrande	2004	59
12	CYFIP/Sra-1 Controls Neuronal Connectivity in Drosophila and Links the Rac1 GTPase Pathway to the Fragile X Protein Neuron ·Annette Schenck, Barbara Bardoni, India Corrin, Nicholas Harden, Jean‐Louis Mandel, Angela Giangrande	2003	255
13	Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes Current Opinion in Genetics & Development ·Barbara Bardoni, Jean‐Louis Mandel	2002	107
14	The Fragile X mental retardation protein Brain Research Bulletin ·Barbara Bardoni, Annette Schenck, Jean‐Louis Mandel	2001	66
15	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 Proceedings of the National Academy of Sciences ·Annette Schenck, Barbara Bardoni, Heather A. Dunfee, Claudia Bagni, Jean‐Louis Mandel	2001	291
16	FMR1 gene and fragile X syndrome American Journal of Medical Genetics ·Barbara Bardoni, Jean‐Louis Mandel, Gene S. Fisch	2000	53
17	A Novel RNA-binding Nuclear Protein That Interacts With the Fragile X Mental Retardation (FMR1) Protein Human Molecular Genetics ·Barbara Bardoni, Annette Schenck, Jean‐Louis Mandel	1999	107
18	[Screening of proteins interact with FMR1 by yeast two-hybrid system]. PubMed ·Qi Chen, Annie Sittler, 孝明佐々木, Barbara Bardoni, Gang Wu	1998	3
19	Xp duplications and sex reversal Philosophical Transactions of the Royal Society B Biological Sciences ·Elena Zanaria, Barbara Bardoni, Branka Dabovic, Vladimiro Calvari, M. Fraccaro, Orsetta Zuffardi, Giovanna Camerino	1995	23
20	A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms Human Genetics ·Barbara Bardoni, Silvana Guioli, Emanuela Maserati, P Maraschio, Giovanna Camerino	1988	3

About Barbara Bardoni

Barbara Bardoni is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Genetics and Neurology, having authored 99 papers that have together received 7.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (62 papers), RNA modifications and cancer (33 papers), RNA Research and Splicing (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), Ubiquitin and proteasome pathways (18 papers), Autism Spectrum Disorder Research (10 papers), Sexual Differentiation and Disorders (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (5.0k citations), Reproductive Medicine (1.2k citations), Molecular Biology (5.5k citations), Developmental Neuroscience (187 citations) and Cognitive Neuroscience (720 citations). Barbara Bardoni has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Jean‐Louis Mandel, Giovanna Camerino, Silvana Guioli, Annette Schenck, Elena Zanaria, Laëtitia Davidovic, M. Fraccaro, Tim M. Strom, Enzo Lalli and Orsetta Zuffardi. Their work appears in journals such as Human Molecular Genetics, Human Genetics, Nucleic Acids Research, Nature and Proceedings of the National Academy of Sciences.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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