Daniel Satgé
Impact in
-
- Down syndrome and intellectual disability research
- Acute Lymphoblastic Leukemia research
-
- Prenatal Screening and Diagnostics
Papers in ⓘ
-
- Renal and related cancers 6
- Genetics 17
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Markus G. Seidel (1 shared paper)M O Rethoré (5 shared papers)Michel Vekemans (8 shared papers)Annie J. Sasco (7 shared papers)Motoi Nishi (6 shared papers)Jean Bénard (2 shared papers)Nicolas Sirvent (2 shared papers)Charles Stiller (2 shared papers)
- Journals
- International Journal on Disability and Human Development (3 papers)Frontiers in Immunology (2 papers)Prenatal Diagnosis (2 papers)Journal of Intellectual Disability Research (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- FranceJapanUnited Kingdom
In The Last Decade
Daniel Satgé
42 papers receiving 543 citations
Peers
Comparison fields: 5 of 70
- Public Health, Environmental and Occupational Health 201
- Pediatrics, Perinatology and Child Health 109
- Genetics 131
- Neurology 68
- Oncology 91
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 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A lack of neuroblastoma in Down syndrome: a study from 11 European countries. | 1998 | 70 |
| 2 | 2015 | 49 | |
| 3 | 2018 | 37 | |
| 4 | 2014 | 32 | |
| 5 | 2003 | 29 | |
| 6 | 2018 | 27 | |
| 7 | 2016 | 26 | |
| 8 | 2001 | 24 | |
| 9 | 2001 | 23 | |
| 10 | 2019 | 22 | |
| 11 | 1998 | 22 | |
| 12 | 2016 | 17 | |
| 13 | 2017 | 14 | |
| 14 | 2008 | 13 | |
| 15 | 2020 | 13 | |
| 16 | 1996 | 12 | |
| 17 | 1994 | 12 | |
| 18 | 1996 | 12 | |
| 19 | 1996 | 10 | |
| 20 | 2013 | 9 |
About Daniel Satgé
Daniel Satgé is a scholar working on Molecular Biology, Genetics, Public Health, Environmental and Occupational Health, Surgery and Pediatrics, Perinatology and Child Health, having authored 42 papers that have together received 557 indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (12 papers), Prenatal Screening and Diagnostics (10 papers), Neuroblastoma Research and Treatments (7 papers), Renal and related cancers (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Public Health, Environmental and Occupational Health (201 citations), Pediatrics, Perinatology and Child Health (109 citations), Genetics (131 citations), Neurology (68 citations) and Oncology (91 citations). Daniel Satgé has collaborated with scholars based in France, Japan and United Kingdom. Frequent co-authors include Markus G. Seidel, M O Rethoré, Michel Vekemans, Annie J. Sasco, Motoi Nishi, Jean Bénard, Nicolas Sirvent, Charles Stiller, Jacques Rouëssé and Herman Van den Berghe. Their work appears in journals such as International Journal on Disability and Human Development, Frontiers in Immunology, Prenatal Diagnosis, Journal of Intellectual Disability Research and European Journal of Medical 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.