Stéphane Serero
Impact in
- Reproductive Medicine top 10%
- Ovarian function and disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 11
- Fetal and Pediatric Neurological Disorders 3
- Genetics 8
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- J Frézal (4 shared papers)N. Van Cong (4 shared papers)Odile Cohen‐Haguenauer (4 shared papers)Daniel Guerrier (1 shared paper)M.-F. de Tand (2 shared papers)Marie‐Geneviève Mattéi (1 shared paper)Nathalie Josso (1 shared paper)Jean‐Yves Picard (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Fetal Diagnosis and Therapy (2 papers)Human Genetics (2 papers)Frontiers in Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- FranceUnited StatesRéunion
In The Last Decade
Stéphane Serero
13 papers receiving 300 citations
Peers
Comparison fields: 5 of 46
- Reproductive Medicine 62
- Genetics 188
- Pediatrics, Perinatology and Child Health 110
- Urology 24
- Rheumatology 35
Countries citing papers authored by Stéphane Serero
This map shows the geographic impact of Stéphane Serero'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 Stéphane Serero with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphane Serero more than expected).
Fields of papers citing papers by Stéphane Serero
This network shows the impact of papers produced by Stéphane Serero. 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 Stéphane Serero. The network helps show where Stéphane Serero may publish in the future.
Co-authors
The 25 scholars most cited alongside Stéphane Serero, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 146 | |
| 2 | 2011 | 40 | |
| 3 | 2012 | 37 | |
| 4 | 1994 | 37 | |
| 5 | 2005 | 15 | |
| 6 | 1988 | 13 | |
| 7 | Regional mapping of the human renin gene to 1q32 by in situ hybridization. | 1989 | 11 |
| 8 | 2008 | 9 | |
| 9 | 1988 | 6 | |
| 10 | 2005 | 5 | |
| 11 | 2022 | 5 | |
| 12 | 2007 | 3 | |
| 13 | 2009 | 1 | |
| 14 | 2017 | 0 | |
| 15 | 2022 | 0 |
About Stéphane Serero
Stéphane Serero is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Pathology and Forensic Medicine and Plant Science, having authored 15 papers that have together received 328 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Fetal and Pediatric Neurological Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Tumors and Oncological Cases (3 papers), Pancreatic function and diabetes (1 paper), MicroRNA in disease regulation (1 paper) and Ovarian function and disorders (1 paper). The work is most often cited by research in Reproductive Medicine (62 citations), Genetics (188 citations), Pediatrics, Perinatology and Child Health (110 citations), Urology (24 citations) and Rheumatology (35 citations). Stéphane Serero has collaborated with scholars based in France, United States and Réunion. Frequent co-authors include J Frézal, N. Van Cong, Odile Cohen‐Haguenauer, Daniel Guerrier, M.-F. de Tand, Marie‐Geneviève Mattéi, Nathalie Josso, Jean‐Yves Picard, M. C. Hors‐Cayla and Philippe Blot. Their work appears in journals such as Prenatal Diagnosis, Fetal Diagnosis and Therapy, Human Genetics, Frontiers in Genetics and Cytogenetic and Genome Research.
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.