C Piussan
- Molecular Biology
- Genetics
- Cardiology and Cardiovascular Medicine
- Cellular and Molecular Neuroscience
- Physiology
- Co-authors
- Junko OshimaGeorge M. MartinJun NakuraT. MikiGerard D. SchellenbergEllen M. WijsmanYing‐Hui FuJohn Mulligan
- Topics
- DNA Repair Mechanisms (5 papers)Nuclear Structure and Function (4 papers)Mitochondrial Function and Pathology (2 papers)
- Cited by
- AgingEndocrinologyMolecular Biology
- Partner nations
- FranceUnited StatesFinland
In The Last Decade
C Piussan
31 papers receiving 547 citations
Peers
Comparison fields: 5 of 76
- Molecular Biology 371
- Genetics 122
- Cardiology and Cardiovascular Medicine 63
- Cellular and Molecular Neuroscience 60
- Physiology 60
Countries citing papers authored by C Piussan
This map shows the geographic impact of C Piussan'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 C Piussan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Piussan more than expected).
Fields of papers citing papers by C Piussan
This network shows the impact of papers produced by C Piussan. 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 C Piussan. The network helps show where C Piussan may publish in the future.
Co-authorship network of co-authors of C Piussan
This figure shows the co-authorship network connecting the top 25 collaborators of C Piussan. A scholar is included among the top collaborators of C Piussan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C Piussan. C Piussan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 0 | |
| 3 | 3 | |
| 4 | 57 | |
| 5 | Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group. | 118 |
| 6 | [Neurologic complications in a case of Werner syndrome]. | 3 |
| 7 | Cirrhosis could be associated with severe mutations of the cystic fibrosis gene | 1 |
| 8 | 43 | |
| 9 | 4 | |
| 10 | [Apert's syndrome with polymetatarsia]. | 1 |
| 11 | 21 | |
| 12 | [Role of ultrasound in studying the first urinary infection in children]. | 1 |
| 13 | [Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations]. | 4 |
| 14 | [Presence of interferon in cerebrospinal fluid in nontumoral opsomyoclonic ataxia]. | 1 |
| 15 | [Meningitis due to Salmonella. Apropos of 3 cases]. | 0 |
| 16 | [Wiedemann and Beckwith syndrome: a new familial case]. | 3 |
| 17 | [A new case of vaginal endodermal sinus tumor in an infant]. | 1 |
| 18 | [Course and treatment of 205 cases of bacterial meningitis]. | 1 |
| 19 | [Radiological study of a case of osteodysplasia (author's transl)]. | 1 |
| 20 | [Aldosterone secretion rate and plasma renin activity in a case of pseudo-hypoaldosteronism]. | 2 |
About C Piussan
C Piussan is a scholar working on Developmental Biology, Genetics and Parasitology, having authored 34 papers that have together received 563 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (5 papers), Nuclear Structure and Function (4 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Aging (35 citations), Endocrinology (52 citations) and Molecular Biology (371 citations). C Piussan has collaborated with scholars based in France, United States and Finland. Frequent co-authors include Junko Oshima, George M. Martin, Jun Nakura, T. Miki, Gerard D. Schellenberg, Ellen M. Wijsman, Ying‐Hui Fu, John Mulligan, P. Lapie and Alexis Elbaz. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Human Mutation.
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.