Robert Saura
Impact in
-
- Prenatal Screening and Diagnostics
- Reproductive Medicine top 2%
- Hypothalamic control of reproductive hormones
Papers in
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- Prenatal Screening and Diagnostics 38
- Fetal and Pediatric Neurological Disorders 2
- Genetics 21
- Genomic variations and chromosomal abnormalities 15
- Craniofacial Disorders and Treatments 2
- Co-authors
- J. Horovitz (41 shared papers)Laurence Taine (28 shared papers)Didier Lacombe (17 shared papers)Denis Roux (13 shared papers)Sophie Gil (1 shared paper)François Forestier (1 shared paper)Robert Farinotti (1 shared paper)Brigitte Maugey‐Laulom (8 shared papers)
- Journals
- Prenatal Diagnosis (16 papers)The Lancet (4 papers)Fetal Diagnosis and Therapy (3 papers)European Journal of Medical Genetics (3 papers)BJOG An International Journal of Obstetrics & Gynaecology (2 papers)
- Partner nations
- FranceUnited StatesNetherlands
In The Last Decade
Robert Saura
68 papers receiving 1.7k citations
Robert Saura's Hit Papers
Peers
Comparison fields: 5 of 70
- Pediatrics, Perinatology and Child Health 555
- Reproductive Medicine 399
- Developmental Biology 70
- Genetics 491
- Obstetrics and Gynecology 88
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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome Hit paper breakdown → | 2003 | 675 |
| 2 | 2004 | 125 | |
| 3 | 1992 | 80 | |
| 4 | 2004 | 72 | |
| 5 | 2008 | 72 | |
| 6 | 1995 | 63 | |
| 7 | 2003 | 63 | |
| 8 | 2018 | 54 | |
| 9 | 1998 | 43 | |
| 10 | 2010 | 42 | |
| 11 | 2013 | 41 | |
| 12 | 2006 | 38 | |
| 13 | Townes-Brocks syndrome in an infant with translocation t (5;16). | 1993 | 36 |
| 14 | 2001 | 34 | |
| 15 | 2013 | 28 | |
| 16 | 1993 | 27 | |
| 17 | Trisomy 22 with thyroid isthmus agenesis and absent gall bladder. | 2004 | 26 |
| 18 | 2005 | 26 | |
| 19 | 2003 | 25 | |
| 20 | 2010 | 24 |
About Robert Saura
Robert Saura is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Developmental Biology, Obstetrics and Gynecology and Pathology and Forensic Medicine, having authored 73 papers that have together received 2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (38 papers), Genomic variations and chromosomal abnormalities (15 papers), Congenital limb and hand anomalies (5 papers), Genetic factors in colorectal cancer (4 papers), Pregnancy and preeclampsia studies (4 papers), Fetal and Pediatric Neurological Disorders (2 papers), Craniofacial Disorders and Treatments (2 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (555 citations), Reproductive Medicine (399 citations), Developmental Biology (70 citations), Genetics (491 citations) and Obstetrics and Gynecology (88 citations). Robert Saura has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include J. Horovitz, Laurence Taine, Didier Lacombe, Denis Roux, Sophie Gil, François Forestier, Robert Farinotti, Brigitte Maugey‐Laulom, Dominique Carles and Frédéric Guyon. Their work appears in journals such as Prenatal Diagnosis, The Lancet, Fetal Diagnosis and Therapy, European Journal of Medical Genetics and BJOG An International Journal of Obstetrics & Gynaecology.
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.