Daniel Satgé
Impact in
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- Down syndrome and intellectual disability research
- Palliative Care and End-of-Life Issues
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- Fetal and Pediatric Neurological Disorders
Papers in
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- Down syndrome and intellectual disability research 25
- Genetics 9
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- Michel J. J. Vekemans (15 shared papers)Motoi Nishi (6 shared papers)Paul Malet (5 shared papers)Annie Jeanne Sasco (12 shared papers)Danièle Sommelet (1 shared paper)M O Rethoré (7 shared papers)Jean Bénard (3 shared papers)Markus G. Seidel (1 shared paper)
- Journals
- International Journal on Disability and Human Development (5 papers)Ophthalmic Genetics (3 papers)Clinical Genetics (2 papers)International Journal of Cancer (2 papers)Frontiers in Immunology (2 papers)
- Partner nations
- FranceJapanUnited Kingdom
In The Last Decade
Daniel Satgé
54 papers receiving 960 citations
Peers
Comparison fields: 5 of 55
- Public Health, Environmental and Occupational Health 438
- Pediatrics, Perinatology and Child Health 99
- Cellular and Molecular Neuroscience 69
- Genetics 37
- Neurology 58
Countries citing papers authored by Daniel Satgé
This map shows the geographic impact of Daniel Satgé'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 Daniel Satgé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Satgé more than expected).
Fields of papers citing papers by Daniel Satgé
This network shows the impact of papers produced by Daniel Satgé. 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 Daniel Satgé. The network helps show where Daniel Satgé may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Satgé, 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 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 151 | |
| 2 | 2013 | 96 | |
| 3 | A lack of neuroblastoma in Down syndrome: a study from 11 European countries. | 1998 | 76 |
| 4 | 2015 | 60 | |
| 5 | 2014 | 39 | |
| 6 | 2018 | 38 | |
| 7 | 2003 | 34 | |
| 8 | 2016 | 31 | |
| 9 | 2018 | 31 | |
| 10 | 2001 | 29 | |
| 11 | 2001 | 29 | |
| 12 | 2004 | 26 | |
| 13 | 2019 | 26 | |
| 14 | 1998 | 24 | |
| 15 | 2001 | 21 | |
| 16 | 2003 | 21 | |
| 17 | 2008 | 17 | |
| 18 | 1996 | 16 | |
| 19 | 2016 | 16 | |
| 20 | 2020 | 16 |
About Daniel Satgé
Daniel Satgé is a scholar working on Public Health, Environmental and Occupational Health, Genetics, Ophthalmology, Surgery and Pediatrics, Perinatology and Child Health, having authored 56 papers that have together received 1k indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (25 papers), Genomic variations and chromosomal abnormalities (7 papers), Ocular Oncology and Treatments (4 papers), Testicular diseases and treatments (3 papers), Neuroblastoma Research and Treatments (3 papers), Prenatal Screening and Diagnostics (3 papers), Global Cancer Incidence and Screening (2 papers) and Congenital Anomalies and Fetal Surgery (2 papers). The work is most often cited by research in Public Health, Environmental and Occupational Health (438 citations), Pediatrics, Perinatology and Child Health (99 citations), Cellular and Molecular Neuroscience (69 citations), Genetics (37 citations) and Neurology (58 citations). Daniel Satgé has collaborated with scholars based in France, Japan and United Kingdom. Frequent co-authors include Michel J. J. Vekemans, Motoi Nishi, Paul Malet, Annie Jeanne Sasco, Danièle Sommelet, M O Rethoré, Jean Bénard, Markus G. Seidel, Marie‐Pierre Chenard and Nicolas Sirvent. Their work appears in journals such as International Journal on Disability and Human Development, Ophthalmic Genetics, Clinical Genetics, International Journal of Cancer and Frontiers in Immunology.
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.