Giulia Barcia
Impact in
- Psychiatry and Mental health top 2%
- Epilepsy research and treatment
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
-
- Mitochondrial Function and Pathology 16
- RNA modifications and cancer 6
- Ion channel regulation and function 4
- Genetics 18
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 10
- Co-authors
- Rima Nabbout (22 shared papers)Olivier Dulac (5 shared papers)Isabelle Desguerre (20 shared papers)Nathalie Boddaert (24 shared papers)Arnold Münnich (26 shared papers)Nicole Chémaly (12 shared papers)Laurence Colleaux (6 shared papers)Leonard K. Kaczmarek (4 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)Journal of Medical Genetics (3 papers)European Journal of Human Genetics (3 papers)Orphanet Journal of Rare Diseases (3 papers)Epilepsia Open (3 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Giulia Barcia
56 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 83
- Psychiatry and Mental health 498
- Clinical Biochemistry 115
- Genetics 422
- Cellular and Molecular Neuroscience 271
- Molecular Biology 556
Countries citing papers authored by Giulia Barcia
This map shows the geographic impact of Giulia Barcia'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 Giulia Barcia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giulia Barcia more than expected).
Fields of papers citing papers by Giulia Barcia
This network shows the impact of papers produced by Giulia Barcia. 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 Giulia Barcia. The network helps show where Giulia Barcia may publish in the future.
Co-authors
The 25 scholars most cited alongside Giulia Barcia, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 364 | |
| 2 | 2013 | 156 | |
| 3 | 2010 | 99 | |
| 4 | 2014 | 90 | |
| 5 | 2018 | 48 | |
| 6 | 2011 | 45 | |
| 7 | 2016 | 44 | |
| 8 | 2013 | 42 | |
| 9 | 2014 | 38 | |
| 10 | 2016 | 32 | |
| 11 | 2020 | 29 | |
| 12 | 2016 | 27 | |
| 13 | 2019 | 26 | |
| 14 | 2019 | 22 | |
| 15 | 2021 | 20 | |
| 16 | 2021 | 20 | |
| 17 | 2020 | 17 | |
| 18 | 2018 | 15 | |
| 19 | 2019 | 15 | |
| 20 | 2018 | 14 |
About Giulia Barcia
Giulia Barcia is a scholar working on Molecular Biology, Genetics, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 57 papers that have together received 1.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (16 papers), Genetics and Neurodevelopmental Disorders (12 papers), Epilepsy research and treatment (11 papers), Genomics and Rare Diseases (10 papers), RNA modifications and cancer (6 papers), Metabolism and Genetic Disorders (5 papers), Autism Spectrum Disorder Research (4 papers) and Ion channel regulation and function (4 papers). The work is most often cited by research in Psychiatry and Mental health (498 citations), Clinical Biochemistry (115 citations), Genetics (422 citations), Cellular and Molecular Neuroscience (271 citations) and Molecular Biology (556 citations). Giulia Barcia has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Rima Nabbout, Olivier Dulac, Isabelle Desguerre, Nathalie Boddaert, Arnold Münnich, Nicole Chémaly, Laurence Colleaux, Leonard K. Kaczmarek, Jack Kronengold and Anna Kamińska. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Orphanet Journal of Rare Diseases and Epilepsia Open.
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.