Stéphane Serero
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
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- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- 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
- N'Guyen Van Cong (4 shared papers)Jean Frézal (4 shared papers)Odile Cohen‐Haguenauer (4 shared papers)M.-F. de Tand (2 shared papers)Jean‐Yves Picard (1 shared paper)Nathalie Josso (1 shared paper)Daniel Guerrier (1 shared paper)Marie‐Geneviève Mattéi (1 shared paper)
In The Last Decade
Stéphane Serero
14 papers receiving 238 citations
Peers
Comparison fields: 5 of 42
- Pediatrics, Perinatology and Child Health 100
- Genetics 130
- Reproductive Medicine 34
- Urology 8
- Molecular Biology 89
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 | 66 | |
| 2 | 2011 | 43 | |
| 3 | 1994 | 39 | |
| 4 | 2012 | 38 | |
| 5 | 1988 | 15 | |
| 6 | 2005 | 15 | |
| 7 | Regional mapping of the human renin gene to 1q32 by in situ hybridization. | 1989 | 13 |
| 8 | 2008 | 12 | |
| 9 | 2005 | 7 | |
| 10 | 1988 | 6 | |
| 11 | 2022 | 6 | |
| 12 | 2007 | 3 | |
| 13 | 2009 | 1 | |
| 14 | 2022 | 1 | |
| 15 | 2017 | 0 |
About Stéphane Serero
Stéphane Serero is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Pathology and Forensic Medicine, Obstetrics and Gynecology and Reproductive Medicine, having authored 15 papers that have together received 265 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), Pancreatic function and diabetes (1 paper), Pregnancy and preeclampsia studies (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (100 citations), Genetics (130 citations), Reproductive Medicine (34 citations), Urology (8 citations) and Molecular Biology (89 citations). Stéphane Serero has collaborated with scholars based in France, Réunion and Canada. Frequent co-authors include N'Guyen Van Cong, Jean Frézal, Odile Cohen‐Haguenauer, M.-F. de Tand, Jean‐Yves Picard, Nathalie Josso, Daniel Guerrier, Marie‐Geneviève Mattéi, M. C. Hors‐Cayla and Gérard Tachdjian. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Fetal Diagnosis and Therapy, 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.