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
- Jean‐Louis Mandel (1 shared paper)André Hanauer (1 shared paper)Valérie Biancalana (1 shared paper)Jean‐Philippe Julien (1 shared paper)Dominique Carles (6 shared papers)Stanislas Lyonnet (6 shared papers)Wendy P. Robinson (1 shared paper)P Balícek (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)European Journal of Pediatrics (2 papers)Human Genetics (2 papers)Nature Genetics (1 paper)Clinical Genetics (1 paper)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
F Serville
44 papers receiving 532 citations
Peers
Comparison fields: 5 of 51
- Genetics 292
- Pediatrics, Perinatology and Child Health 152
- Cellular and Molecular Neuroscience 135
- Developmental Biology 10
- Genetics 45
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 | 105 | |
| 2 | 1994 | 102 | |
| 3 | 1989 | 53 | |
| 4 | 1994 | 33 | |
| 5 | 1994 | 27 | |
| 6 | Townes-Brocks syndrome in an infant with translocation t (5;16). | 1993 | 22 |
| 7 | 1992 | 21 | |
| 8 | 1992 | 20 | |
| 9 | 1993 | 15 | |
| 10 | 1995 | 15 | |
| 11 | [Association of VACTERL and hydrocephalus: a new familial entity]. | 1984 | 14 |
| 12 | 1988 | 12 | |
| 13 | [Partial deletion of the short arm of the chromosome 9]. | 1976 | 10 |
| 14 | Idiopathic arterial calcification in a stillborn complicated by pleural hemorrhage and hydrops fetalis. | 1992 | 10 |
| 15 | [The r(14) syndrome. 3 new observations]. | 1984 | 10 |
| 16 | [Partial 7q trisomy]. | 1975 | 8 |
| 17 | Prenatal diagnosis of type III congenital cystic adenomatoid malformation of the lung. | 1986 | 6 |
| 18 | 1975 | 6 | |
| 19 | [Niemann-Pick disease in a 4-year-old child without nervous manifestations; considerable significance of pulmonary respiratory signs]. | 1965 | 5 |
| 20 | 1993 | 4 |
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 547 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 Diaphragmatic Hernia Studies (4 papers), Congenital Anomalies and Fetal Surgery (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Congenital limb and hand anomalies (3 papers) and Child Nutrition and Feeding Issues (2 papers). The work is most often cited by research in Genetics (292 citations), Pediatrics, Perinatology and Child Health (152 citations), Cellular and Molecular Neuroscience (135 citations), Developmental Biology (10 citations) and Genetics (45 citations). F Serville has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include Jean‐Louis Mandel, André Hanauer, Valérie Biancalana, Jean‐Philippe Julien, Dominique Carles, Stanislas Lyonnet, Wendy P. Robinson, P Balícek, Arnold Münnich and Memnune Yüksel‐Apak. Their work appears in journals such as Human Molecular Genetics, European Journal of Pediatrics, Human Genetics, Nature Genetics and Clinical 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.