Stéphane Serero
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
-
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 9
- Fetal and Pediatric Neurological Disorders 2
- Genetics 7
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 1
- Co-authors
- J Frézal (4 shared papers)Odile Cohen‐Haguenauer (4 shared papers)N. Van Cong (4 shared papers)M.-F. de Tand (2 shared papers)Nathalie Josso (1 shared paper)Jean‐Yves Picard (1 shared paper)M. C. Hors‐Cayla (1 shared paper)Marie‐Geneviève Mattéi (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Fetal Diagnosis and Therapy (2 papers)Human Genetics (2 papers)Frontiers in Genetics (1 paper)Genes (1 paper)
- Partner nations
- FranceUnited StatesRéunion
In The Last Decade
Stéphane Serero
13 papers receiving 220 citations
Peers
Comparison fields: 5 of 40
- Pediatrics, Perinatology and Child Health 96
- Genetics 115
- Reproductive Medicine 33
- Urology 7
- Public Health, Environmental and Occupational Health 31
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 | 2008 | 59 | |
| 2 | 2011 | 40 | |
| 3 | 1994 | 37 | |
| 4 | 2012 | 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 | 2022 | 0 | |
| 15 | 2017 | 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 241 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Fetal and Pediatric Neurological Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Tumors and Oncological Cases (2 papers), Genetic Syndromes and Imprinting (1 paper), Ovarian function and disorders (1 paper) and Fungal and yeast genetics research (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (96 citations), Genetics (115 citations), Reproductive Medicine (33 citations), Urology (7 citations) and Public Health, Environmental and Occupational Health (31 citations). Stéphane Serero has collaborated with scholars based in France, United States and Réunion. Frequent co-authors include J Frézal, Odile Cohen‐Haguenauer, N. Van Cong, M.-F. de Tand, Nathalie Josso, Jean‐Yves Picard, M. C. Hors‐Cayla, Marie‐Geneviève Mattéi, Daniel Guerrier and Philippe Blot. Their work appears in journals such as Prenatal Diagnosis, Fetal Diagnosis and Therapy, Human Genetics, Frontiers in Genetics and Genes.
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.