Robert Saura
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Developmental Biology top 5%
Papers in
-
- Prenatal Screening and Diagnostics 20
- Fetal and Pediatric Neurological Disorders 4
- Genetics 14
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 3
- Co-authors
- J. Horovitz (23 shared papers)Laurence Taine (19 shared papers)Didier Lacombe (16 shared papers)Robert Farinotti (1 shared paper)F Forestier (1 shared paper)Sophie Gil (1 shared paper)Jérôme Toutain (9 shared papers)B. Maugey‐Laulom (7 shared papers)
- Journals
- Prenatal Diagnosis (6 papers)Fetal Diagnosis and Therapy (3 papers)European Journal of Medical Genetics (3 papers)European Journal of Obstetrics & Gynecology and Reproductive Biology (2 papers)PLoS ONE (2 papers)
- Partner nations
- FranceBelizeNetherlands
In The Last Decade
Robert Saura
48 papers receiving 826 citations
Peers
Comparison fields: 5 of 71
- Pediatrics, Perinatology and Child Health 446
- Developmental Biology 56
- Obstetrics and Gynecology 101
- Genetics 319
- Cancer Research 53
Countries citing papers authored by Robert Saura
This map shows the geographic impact of Robert Saura'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 Robert Saura with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Saura more than expected).
Fields of papers citing papers by Robert Saura
This network shows the impact of papers produced by Robert Saura. 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 Robert Saura. The network helps show where Robert Saura may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Saura, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 124 | |
| 2 | 1992 | 72 | |
| 3 | 2004 | 69 | |
| 4 | 1995 | 63 | |
| 5 | 2003 | 61 | |
| 6 | 2018 | 45 | |
| 7 | 2013 | 41 | |
| 8 | 1998 | 41 | |
| 9 | 2006 | 38 | |
| 10 | 2010 | 33 | |
| 11 | 2001 | 32 | |
| 12 | 1993 | 27 | |
| 13 | 2003 | 26 | |
| 14 | Trisomy 22 with thyroid isthmus agenesis and absent gall bladder. | 2004 | 26 |
| 15 | 2013 | 24 | |
| 16 | 2005 | 23 | |
| 17 | Townes-Brocks syndrome in an infant with translocation t (5;16). | 1993 | 23 |
| 18 | 2010 | 21 | |
| 19 | 2010 | 20 | |
| 20 | 2003 | 20 |
About Robert Saura
Robert Saura is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Molecular Biology and Pathology and Forensic Medicine, having authored 50 papers that have together received 1.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (20 papers), Genomic variations and chromosomal abnormalities (10 papers), Congenital Anomalies and Fetal Surgery (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Pregnancy and preeclampsia studies (3 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (3 papers), Genetic Syndromes and Imprinting (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (446 citations), Developmental Biology (56 citations), Obstetrics and Gynecology (101 citations), Genetics (319 citations) and Cancer Research (53 citations). Robert Saura has collaborated with scholars based in France, Belize and Netherlands. Frequent co-authors include J. Horovitz, Laurence Taine, Didier Lacombe, Robert Farinotti, F Forestier, Sophie Gil, Jérôme Toutain, B. Maugey‐Laulom, Denis Roux and Dominique Carles. Their work appears in journals such as Prenatal Diagnosis, Fetal Diagnosis and Therapy, European Journal of Medical Genetics, European Journal of Obstetrics & Gynecology and Reproductive Biology and PLoS ONE.
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.