G. Danglot

818 total citations
12 papers, 577 citations indexed

About

G. Danglot is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, G. Danglot has authored 12 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in G. Danglot's work include Neuroblastoma Research and Treatments (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Neurofibromatosis and Schwannoma Cases (3 papers). G. Danglot is often cited by papers focused on Neuroblastoma Research and Treatments (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Neurofibromatosis and Schwannoma Cases (3 papers). G. Danglot collaborates with scholars based in France, Spain and United States. G. Danglot's co-authors include Mounira Meddeb, Simon Cotterill, Dominique Plantaz, Maria Łastowska, A D Pearson, Holger Christiansen, Geneviève Laureys, C. Brinkschmidt, Nick Bown and Alain Bernheim and has published in prestigious journals such as New England Journal of Medicine, Biochemical and Biophysical Research Communications and Human Molecular Genetics.

In The Last Decade

G. Danglot

12 papers receiving 569 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. Danglot France 9 442 319 167 102 83 12 577
Garrett M. Brodeur United States 7 346 0.8× 284 0.9× 156 0.9× 97 1.0× 73 0.9× 8 506
Alvin Chan Netherlands 12 403 0.9× 397 1.2× 181 1.1× 101 1.0× 56 0.7× 14 634
Rose‐Marie Sjöberg Sweden 15 399 0.9× 414 1.3× 267 1.6× 141 1.4× 64 0.8× 16 629
Brodeur Gm United States 11 841 1.9× 464 1.5× 310 1.9× 152 1.5× 125 1.5× 19 939
Deepa Khazi United States 5 443 1.0× 291 0.9× 234 1.4× 127 1.2× 65 0.8× 5 530
Gisèle Danglot France 11 209 0.5× 369 1.2× 191 1.1× 264 2.6× 121 1.5× 13 710
Susanne Fransson Sweden 15 309 0.7× 359 1.1× 183 1.1× 126 1.2× 46 0.6× 38 542
Crocifissa Lo Cunsolo Italy 10 175 0.4× 227 0.7× 103 0.6× 119 1.2× 34 0.4× 17 412
Manfred Schwab Germany 8 152 0.3× 336 1.1× 142 0.9× 218 2.1× 67 0.8× 8 573
Jessica Theißen Germany 12 441 1.0× 515 1.6× 377 2.3× 153 1.5× 44 0.5× 15 754

Countries citing papers authored by G. Danglot

Since Specialization
Citations

This map shows the geographic impact of G. Danglot'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 G. Danglot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G. Danglot more than expected).

Fields of papers citing papers by G. Danglot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. Danglot. 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 G. Danglot. The network helps show where G. Danglot may publish in the future.

Co-authorship network of co-authors of G. Danglot

This figure shows the co-authorship network connecting the top 25 collaborators of G. Danglot. A scholar is included among the top collaborators of G. Danglot 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 G. Danglot. G. Danglot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Guillaud-Bataille, Marine, Olivier Brison, G. Danglot, et al.. (2009). Two populations of double minute chromosomes harbor distinct amplicons, the <i>MYC</i> locus at 8q24.2 and a 0.43-Mb region at 14q24.1, in the SW613-S human carcinoma cell line. Cytogenetic and Genome Research. 124(1). 1–11. 9 indexed citations
2.
Coullin, P., et al.. (2006). High promoter hypermethylation frequency of p14/ARF in supratentorial PNET but not in medulloblastoma. Histopathology. 48(5). 579–587. 22 indexed citations
3.
Pérot, Christine, Marine Guillaud-Bataille, G. Danglot, et al.. (2005). Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system. Histopathology. 47(6). 631–637. 27 indexed citations
4.
Bown, Nick, Simon Cotterill, Maria Łastowska, et al.. (1999). Gain of Chromosome Arm 17q and Adverse Outcome in Patients with Neuroblastoma. New England Journal of Medicine. 340(25). 1954–1961. 373 indexed citations
5.
Meddeb, Mounira, A. Valent, G. Danglot, et al.. (1996). MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14). Cytogenetic and Genome Research. 73(4). 325–330. 25 indexed citations
6.
Valent, A., et al.. (1996). Assignment of the NTRK4 (trkE) gene to chromosome 6p21. Human Genetics. 98(1). 12–15. 8 indexed citations
7.
Danglot, G., et al.. (1996). Mapping of 22 YACs on human chromosomes by fish using yeast DNA Alu-PCR products for competition.. PubMed. 39(2). 64–8. 10 indexed citations
8.
Danglot, G., et al.. (1995). Neurofibromatosis 1 (NF1) mRNAs expressed in the central nervous system are differentially spliced in the 5' part of the gene. Human Molecular Genetics. 4(5). 915–920. 72 indexed citations
9.
Diriong, Sylvie, et al.. (1995). A new hybrid cell line containing only human chromosome 15 selected through fluorescence in situ hybridization and characterized by Alu-PCR amplification of the human DNA.. PubMed. 38(1). 27–31. 1 indexed citations
10.
Danglot, G., et al.. (1994). Tissue-specific alternative splicing of neurofibromatosis 1 (NF1) mRNA. Biomedicine & Pharmacotherapy. 48(8-9). 365–372. 8 indexed citations
11.
Teinturier, Cécile, et al.. (1992). The neurofibromatosis 1 gene transcripts expressed in peripheral nerve and neurofibromas bear the additional exon located in the GAP domain. Biochemical and Biophysical Research Communications. 188(2). 851–857. 14 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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