Barbara Bardoni

10.2k citations
100 papers · 7.7k · 3 hit papers · h-index 46

Impact in

  • Genetics top 0.1%
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Sperm and Testicular Function

Papers in

    • Genetics and Neurodevelopmental Disorders 62
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
    • RNA modifications and cancer 34
    • RNA Research and Splicing 20
    • Ubiquitin and proteasome pathways 18
    • Sexual Differentiation and Disorders 7
    • Congenital heart defects research 6

Barbara Bardoni

99 papers receiving 7.5k citations

Barbara Bardoni's Hit Papers

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita 1994 · 658 citations
6580+11+23Years since publication200400600

Peers

Barbara Bardoni
Comparison fields: 5 of 120
  • Genetics 4.9k
  • Reproductive Medicine 1.1k
  • Molecular Biology 5.3k
  • Developmental Neuroscience 181
  • Cognitive Neuroscience 676
Replace Elena Maestrini with:
Elena Maestrini Italy
Hannie Kremer Netherlands
Jacqueline Levilliers France
Claude Moraine France
Maura Pieretti United States
Aimee K. Ryan Canada
Vera M. Kalscheuer Germany
Donna M. Simmons United States
Masatsugu Ueda Japan
Laurent Journot France
Barbara Bardoni relative to Elena Maestrini Italy Elena Maestrini's profile →
Citations per field
00.5×4.3×
Elena Maestrini · 1×
Citations per year

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-authors

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

20 of 20 papers shown

Showing the 20 most-cited of 100 papers — load more, or switch the sort, to bring in the rest.

#Work
1
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
Hit paper breakdown →
1994658
2
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Hit paper breakdown →
1991637
3
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
Hit paper breakdown →
1994551
4 1995447
5 1994419
6 2001293
7 2003257
8 2006251
9 1989200
10 2008190
11 2009162
12 1997152
13 2004143
14 2005127
15 2018114
16 1999107
17 2002107
18 2007105
19 2021100
20 199196

About Barbara Bardoni

Barbara Bardoni is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Genetics, having authored 100 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (62 papers), RNA modifications and cancer (34 papers), RNA Research and Splicing (20 papers), Ubiquitin and proteasome pathways (18 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), Autism Spectrum Disorder Research (9 papers), Sexual Differentiation and Disorders (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (4.9k citations), Reproductive Medicine (1.1k citations), Molecular Biology (5.3k citations), Developmental Neuroscience (181 citations) and Cognitive Neuroscience (676 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, Proceedings of the National Academy of Sciences and Neurobiology of Disease.

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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