F Serville
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
-
- Prenatal Screening and Diagnostics
Papers in
-
- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 4
- Co-authors
- Valérie Biancalana (1 shared paper)Jean‐Louis Mandel (1 shared paper)Jean‐Philippe Julien (1 shared paper)André Hanauer (1 shared paper)Stanislas Lyonnet (6 shared papers)Dominique Carles (6 shared papers)Arnold Münnich (5 shared papers)Giovanni Neri (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)European Journal of Pediatrics (2 papers)Human Genetics (2 papers)Journal of Medical Genetics (1 paper)Nature Genetics (1 paper)
- Partner nations
- FranceSwitzerlandGermany
In The Last Decade
F Serville
45 papers receiving 563 citations
Peers
Comparison fields: 5 of 50
- Genetics 290
- Pediatrics, Perinatology and Child Health 147
- Cellular and Molecular Neuroscience 143
- Genetics 45
- Molecular Biology 259
Countries citing papers authored by F Serville
This map shows the geographic impact of F Serville'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 F Serville with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Serville more than expected).
Fields of papers citing papers by F Serville
This network shows the impact of papers produced by F Serville. 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 F Serville. The network helps show where F Serville may publish in the future.
Co-authors
The 25 scholars most cited alongside F Serville, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 110 | |
| 2 | 1994 | 109 | |
| 3 | 1989 | 57 | |
| 4 | 1994 | 38 | |
| 5 | 1994 | 27 | |
| 6 | 1992 | 25 | |
| 7 | 1992 | 23 | |
| 8 | Townes-Brocks syndrome in an infant with translocation t (5;16). | 1993 | 23 |
| 9 | 1995 | 17 | |
| 10 | 1988 | 15 | |
| 11 | 1993 | 15 | |
| 12 | [Association of VACTERL and hydrocephalus: a new familial entity]. | 1984 | 15 |
| 13 | Idiopathic arterial calcification in a stillborn complicated by pleural hemorrhage and hydrops fetalis. | 1992 | 11 |
| 14 | [Partial deletion of the short arm of the chromosome 9]. | 1976 | 10 |
| 15 | [The r(14) syndrome. 3 new observations]. | 1984 | 10 |
| 16 | 1975 | 8 | |
| 17 | [Partial 7q trisomy]. | 1975 | 8 |
| 18 | 1993 | 7 | |
| 19 | Prenatal diagnosis of type III congenital cystic adenomatoid malformation of the lung. | 1986 | 7 |
| 20 | [Niemann-Pick disease in a 4-year-old child without nervous manifestations; considerable significance of pulmonary respiratory signs]. | 1965 | 6 |
About F Serville
F Serville is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics, Surgery and Physiology, having authored 45 papers that have together received 591 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers), Fetal and Pediatric Neurological Disorders (4 papers), Congenital Anomalies and Fetal Surgery (4 papers), Congenital Diaphragmatic Hernia Studies (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Congenital limb and hand anomalies (3 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Genetics (290 citations), Pediatrics, Perinatology and Child Health (147 citations), Cellular and Molecular Neuroscience (143 citations), Genetics (45 citations) and Molecular Biology (259 citations). F Serville has collaborated with scholars based in France, Switzerland and Germany. Frequent co-authors include Valérie Biancalana, Jean‐Louis Mandel, Jean‐Philippe Julien, André Hanauer, Stanislas Lyonnet, Dominique Carles, Arnold Münnich, Giovanni Neri, Memnune Yüksel‐Apak and Wendy P. Robinson. Their work appears in journals such as Human Molecular Genetics, European Journal of Pediatrics, Human Genetics, Journal of Medical Genetics and Nature Genetics.
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.