Daniel Satgé

1.1k total citations
42 papers, 557 citations indexed

About

Daniel Satgé is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Daniel Satgé has authored 42 papers receiving a total of 557 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 17 papers in Genetics and 15 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Daniel Satgé's work include Down syndrome and intellectual disability research (12 papers), Prenatal Screening and Diagnostics (10 papers) and Neuroblastoma Research and Treatments (7 papers). Daniel Satgé is often cited by papers focused on Down syndrome and intellectual disability research (12 papers), Prenatal Screening and Diagnostics (10 papers) and Neuroblastoma Research and Treatments (7 papers). Daniel Satgé collaborates with scholars based in France, Japan and United Kingdom. Daniel Satgé's co-authors include Markus G. Seidel, M O Rethoré, Motoi Nishi, Annie J. Sasco, Michel Vekemans, Jean Bénard, Nicolas Sirvent, Charles Stiller, Jacques Rouëssé and Marie-Pierre Chenard and has published in prestigious journals such as Frontiers in Immunology, Australasian Journal of Paramedicine and Seminars in Cancer Biology.

In The Last Decade

Daniel Satgé

42 papers receiving 543 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Daniel Satgé France 14 201 141 131 109 96 42 557
A Cohen Italy 14 214 1.1× 82 0.6× 85 0.6× 209 1.9× 53 0.6× 20 632
Hisaya Nakadate Japan 21 259 1.3× 341 2.4× 112 0.9× 269 2.5× 95 1.0× 65 919
Nicholas D. Yeager United States 13 184 0.9× 87 0.6× 92 0.7× 212 1.9× 64 0.7× 51 587
Pascale Blouin France 9 88 0.4× 122 0.9× 49 0.4× 100 0.9× 38 0.4× 23 394
Yasmin Gosiengfiao United States 12 241 1.2× 179 1.3× 58 0.4× 101 0.9× 101 1.1× 30 600
I M Franklin United Kingdom 17 171 0.9× 127 0.9× 86 0.7× 57 0.5× 36 0.4× 28 742
Andrea Jarisch Germany 18 177 0.9× 107 0.8× 83 0.6× 137 1.3× 63 0.7× 62 776
Claudette Hajaj Gonzalez Brazil 15 148 0.7× 193 1.4× 196 1.5× 207 1.9× 172 1.8× 33 712
Janet Horsman United Kingdom 14 95 0.5× 109 0.8× 65 0.5× 79 0.7× 74 0.8× 33 746
Luciano Dalla Pozza Australia 13 177 0.9× 133 0.9× 43 0.3× 102 0.9× 30 0.3× 24 425

Countries citing papers authored by Daniel Satgé

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Daniel Satgé

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Satgé. A scholar is included among the top collaborators of Daniel Satgé based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniel Satgé. Daniel Satgé is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rethoré, M O, Jacques Rouëssé, & Daniel Satgé. (2019). Cancer screening in adults with down syndrome, a proposal. European Journal of Medical Genetics. 63(4). 103783–103783. 22 indexed citations
2.
Satgé, Daniel & Markus G. Seidel. (2018). The Pattern of Malignancies in Down Syndrome and Its Potential Context With the Immune System. Frontiers in Immunology. 9. 3058–3058. 37 indexed citations
3.
Satgé, Daniel, Motoi Nishi, Nicolas Sirvent, & Michel Vekemans. (2016). A tumor profile in Edwards syndrome (trisomy 18). American Journal of Medical Genetics Part C Seminars in Medical Genetics. 172(3). 296–306. 26 indexed citations
4.
Satgé, Daniel, et al.. (2012). Adolescent Girl with Down Syndrome and Lumbar Cutaneous Melanoma. Pediatric Dermatology. 31(1). 108–109. 5 indexed citations
5.
Willis, Diane, Daniel Satgé, & Sheena G. Sullivan. (2011). Breast cancer surveillance. ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam). 1 indexed citations
6.
Satgé, Daniel, Annie J. Sasco, Steven M. Day, & Stéphane Culine. (2009). A Lower Risk of Dying from Urological Cancer in Down Syndrome: Clue for Cancer Protecting Genes on Chromosome 21. Urologia Internationalis. 82(3). 296–300. 8 indexed citations
7.
Satgé, Daniel, Louis H. Honoré, A J Sasco, et al.. (2006). An ovarian dysgerminoma in Down syndrome. Hypothesis about the association. International Journal of Gynecological Cancer. 16(S1). 375–379. 8 indexed citations
8.
Satgé, Daniel, et al.. (2004). A Third Case of Cardiac Neoplasm in a Fetus with Beckwith-Wiedemann Syndrome: Epicardial Angiofibroma. Fetal Diagnosis and Therapy. 20(1). 44–47. 7 indexed citations
9.
Satgé, Daniel, Sam W. Moore, Charles Stiller, et al.. (2003). Abnormal constitutional karyotypes in patients with neuroblastoma: a report of four new cases and review of 47 others in the literature. Cancer Genetics and Cytogenetics. 147(2). 89–98. 29 indexed citations
10.
Satgé, Daniel, Piotr Gembara, Annie J. Sasco, et al.. (2001). An infant with Down syndrome and retinoblastoma A possible non-fortuitous association. Ophthalmic Genetics. 22(2). 117–123. 4 indexed citations
11.
Satgé, Daniel, Annie J. Sasco, H Pujol, & M O Rethoré. (2001). Les cancers mammaires des femmes trisomiques 21. Bulletin de l Académie Nationale de Médecine. 185(7). 1239–1254. 24 indexed citations
12.
Satgé, Daniel, et al.. (2001). An umbilical cord teratoma in a 17‐week‐old fetus. Prenatal Diagnosis. 21(4). 284–288. 23 indexed citations
13.
Satgé, Daniel, et al.. (2001). A fetus with pseudo Fryns syndrome and t(18;22) translocation.. PubMed. 12(2). 169–71. 2 indexed citations
14.
Satgé, Daniel, et al.. (1999). [Fatal mesenteric ischemic accident caused by mesenteric inflammatory veno-occlusive disease].. PubMed. 19(6). 525–8. 4 indexed citations
15.
Satgé, Daniel, Annie J. Sasco, Niels Carlsen, et al.. (1998). A lack of neuroblastoma in Down syndrome: a study from 11 European countries.. Data Archiving and Networked Services (DANS). 58(3). 448–52. 70 indexed citations
16.
Saugier-Véber, Pascale, Cosette Martin, Nathalie Le Meur, et al.. (1998). Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis. Human Mutation. 12(4). 259–266. 22 indexed citations
17.
Satgé, Daniel, A. Le Tourneau, Sophie Lefort, et al.. (1996). A Case Report of Down Syndrome and Centroblastic Lymphoma. Pathology - Research and Practice. 192(12). 1266–1269. 12 indexed citations
18.
Satgé, Daniel & Herman Van den Berghe. (1996). Aspects of the neoplasms observed in patients with constitutional autosomal trisomy. Cancer Genetics and Cytogenetics. 87(1). 63–70. 12 indexed citations
19.
Satgé, Daniel. (1996). A decreased incidence of neuroblastomas in Down's syndrome and overproduction of S-100 b protein. Medical Hypotheses. 46(4). 393–399. 10 indexed citations
20.
Satgé, Daniel, et al.. (1994). Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesis. Prenatal Diagnosis. 14(4). 303–306. 12 indexed citations

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.

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