N Philippe

2.3k total citations
33 papers, 1.5k citations indexed

About

N Philippe is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, N Philippe has authored 33 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Hematology, 10 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in N Philippe's work include Acute Myeloid Leukemia Research (15 papers), Eosinophilic Disorders and Syndromes (5 papers) and Chronic Myeloid Leukemia Treatments (5 papers). N Philippe is often cited by papers focused on Acute Myeloid Leukemia Research (15 papers), Eosinophilic Disorders and Syndromes (5 papers) and Chronic Myeloid Leukemia Treatments (5 papers). N Philippe collaborates with scholars based in France, United States and Portugal. N Philippe's co-authors include Claude Preudhomme, Pierre Fenaux, Catherine Roche‐Lestienne, Jean-Luc Laı̈, Bruno Quesnel, Valérie Soenen, Nathalie Grardel, Thierry Façon, Nicolas Boissel and Hervé Dombret and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and Blood.

In The Last Decade

N Philippe

31 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N Philippe France 13 1.1k 626 545 231 226 33 1.5k
Isabelle Tigaud France 22 1.0k 1.0× 494 0.8× 732 1.3× 121 0.5× 316 1.4× 65 1.6k
George F. Barker United States 6 924 0.9× 470 0.8× 713 1.3× 376 1.6× 204 0.9× 7 1.6k
JL Laï France 11 1.2k 1.1× 1.1k 1.7× 543 1.0× 356 1.5× 147 0.7× 18 1.5k
G Grosveld Netherlands 8 1.1k 1.1× 761 1.2× 441 0.8× 293 1.3× 289 1.3× 13 1.5k
Hadrian Szpurka United States 17 1.4k 1.3× 972 1.6× 939 1.7× 206 0.9× 128 0.6× 35 2.0k
Sandrine Hayette France 22 1.1k 1.0× 579 0.9× 672 1.2× 261 1.1× 490 2.2× 75 1.8k
Nathalie Grardel France 15 848 0.8× 591 0.9× 322 0.6× 250 1.1× 281 1.2× 40 1.3k
Luisa Anelli Italy 23 693 0.6× 436 0.7× 563 1.0× 101 0.4× 237 1.0× 87 1.3k
B Heinze Germany 17 1.1k 1.0× 616 1.0× 301 0.6× 318 1.4× 426 1.9× 37 1.4k
Antonella Zagaria Italy 23 637 0.6× 403 0.6× 504 0.9× 98 0.4× 223 1.0× 80 1.2k

Countries citing papers authored by N Philippe

Since Specialization
Citations

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

Fields of papers citing papers by N Philippe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N Philippe

This figure shows the co-authorship network connecting the top 25 collaborators of N Philippe. A scholar is included among the top collaborators of N Philippe 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 N Philippe. N Philippe 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.
Cornet, Édouard, Christophe Roumier, Pascale Lepelley, et al.. (2012). Involvement of a common progenitor cell in core binding factor acute myeloid leukaemia associated with mastocytosis. Leukemia Research. 36(11). 1330–1333. 6 indexed citations
2.
Ghoumid, Jamal, Joris Andrieux, Bernard Sablonnière, et al.. (2011). Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus. European Journal of Human Genetics. 19(11). 1198–1201. 6 indexed citations
3.
Nibourel, Olivier, Olivier Kosmider, Meyling Cheok, et al.. (2009). Association of TET2 Alterations with NPM1 Mutations and Prognostic Value in De Novo Acute Myeloid Leukemia (AML).. Blood. 114(22). 163–163. 6 indexed citations
4.
Renneville, Aline, Nicolas Boissel, Valéria Biggio, et al.. (2009). Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia. Cancer. 115(16). 3719–3727. 56 indexed citations
5.
Preudhomme, Claude, Aline Renneville, Violaine Bourdon, et al.. (2009). High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder. Blood. 113(22). 5583–5587. 118 indexed citations
6.
Idziorek, Thierry, Sélim Corm, Dominique Hétuin, et al.. (2008). BCR-ABL mutants spread resistance to non-mutated cells through a paracrine mechanism. Leukemia. 22(4). 791–799. 33 indexed citations
7.
8.
Boissel, Nicolas, Harmony Leroy, Benoît Brethon, et al.. (2006). Incidence and prognostic impact of c-Kit, FLT3, and Ras gene mutations in core binding factor acute myeloid leukemia (CBF-AML). Leukemia. 20(6). 965–970. 256 indexed citations
9.
10.
Kaspers, Gertjan J.L., Michel Zimmermann, G. Fleischhack, et al.. (2005). Relapsed Acute Myeloid Leukemia in Children and Adolescents: Interim Results of the International Randomised Phase III Study “Relapsed AML 2001/01”.. Blood. 106(11). 897–897. 4 indexed citations
11.
Boissel, Nicolas, Stéphane de Botton, Thierry Leblanc, et al.. (2004). Incidence and Prognosis of RTKs and RAS Mutations in CBF AML. A Retrospective Study of French Adult ALFA and Pediatric LAME Trials.. Blood. 104(11). 2022–2022. 4 indexed citations
12.
Cavé, Hélène, N Philippe, Nathalie Grardel, et al.. (2004). Ras Pathway Activation in Childhood B-Lineage Acute Lymphoblastic Leukemia: Ras, Ptpn11, and Flt3 Mutations.. Blood. 104(11). 166–166. 2 indexed citations
13.
Lutz, P, G Souillet, Y Bertrand, et al.. (1996). Juvenile myelomonocytic leukemia: analyses of treatment results in the EORTC Children's Leukemia Cooperative Group (CLCG).. PubMed. 18(6). 1111–6. 31 indexed citations
14.
Quesnel, Bruno, Pierre Fenaux, N Philippe, et al.. (1995). Analysis of p16 gene deletion and point mutation in breast carcinoma. British Journal of Cancer. 72(2). 351–353. 27 indexed citations
15.
Quesnel, Bruno, Claude Preudhomme, N Philippe, et al.. (1995). p16 gene homozygous deletions in acute lymphoblastic leukemia. Blood. 85(3). 657–663. 117 indexed citations
16.
Bouvier, R, et al.. (1993). Jaundice associated with concomitant use of norethandrolone and cyclosporine.. PubMed. 56(2). 470–1. 1 indexed citations
17.
Saeland, Sem, V Duvert, Isabelle Durand, et al.. (1992). Interleukin 4 inhibits in vitro proliferation of leukemic and normal human B cell precursors.. Journal of Clinical Investigation. 90(5). 1697–1706. 28 indexed citations
18.
Capdeville, Renaud, et al.. (1990). [Granulocytic sarcoma (chloroma): rare extramedullary tumors associated with acute non-lymphoblastic leukemia].. PubMed. 45(4). 245–50. 2 indexed citations
19.
Freyçon, F, et al.. (1986). [Seriousness of severe acquired aplastic anemia in children. Apropos of 32 cases].. PubMed. 43(10). 757–63. 1 indexed citations
20.
Philippe, N, et al.. (1979). [A 45 X/46 X dic (Yq) puberal male without genital ambiguity. Critical study of the peculiarities of his phenotype].. PubMed. 36(2). 162–72. 2 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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