N. Philip

5.0k total citations
82 papers, 1.9k citations indexed

About

N. Philip is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N. Philip has authored 82 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 33 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N. Philip's work include Genomic variations and chromosomal abnormalities (13 papers), Congenital heart defects research (11 papers) and Prenatal Screening and Diagnostics (11 papers). N. Philip is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Congenital heart defects research (11 papers) and Prenatal Screening and Diagnostics (11 papers). N. Philip collaborates with scholars based in France, Belgium and Netherlands. N. Philip's co-authors include J. F. Mattéi, Marie‐Geneviève Mattéi, E. Passage, Jean‐Louis Mandel, Jean‐Paul Moisan, Sabine Sigaudy, Ségolène Aymé, D. Gambarelli, A. Moncla and Myriam Dubuc and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Epidemiology & Community Health and British Journal of Dermatology.

In The Last Decade

N. Philip

75 papers receiving 1.9k 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. Philip France 24 829 796 371 331 278 82 1.9k
Agnes Bankier Australia 27 990 1.2× 767 1.0× 389 1.0× 357 1.1× 286 1.0× 80 2.0k
Clarisse Baumann France 26 853 1.0× 969 1.2× 495 1.3× 252 0.8× 330 1.2× 73 2.1k
Rika Kosaki Japan 25 846 1.0× 1.3k 1.6× 297 0.8× 255 0.8× 236 0.8× 113 2.3k
Ahmad S. Teebi Canada 31 1.3k 1.6× 1.3k 1.6× 522 1.4× 323 1.0× 226 0.8× 111 3.2k
J P Fryns Belgium 25 1.2k 1.5× 1.1k 1.4× 304 0.8× 430 1.3× 259 0.9× 90 2.2k
Carol L. Clericuzio United States 29 872 1.1× 834 1.0× 393 1.1× 377 1.1× 112 0.4× 58 1.9k
Kenneth N. Rosenbaum United States 26 1.0k 1.2× 627 0.8× 344 0.9× 244 0.7× 183 0.7× 59 2.2k
P. Nagesh Rao United States 26 625 0.8× 842 1.1× 249 0.7× 272 0.8× 124 0.4× 77 2.2k
Mahin Golabi United States 26 1.2k 1.4× 1.3k 1.6× 470 1.3× 386 1.2× 146 0.5× 59 2.4k
Sabine Sigaudy France 21 535 0.6× 629 0.8× 205 0.6× 220 0.7× 215 0.8× 70 1.3k

Countries citing papers authored by N. Philip

Since Specialization
Citations

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

Fields of papers citing papers by N. Philip

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Philip

This figure shows the co-authorship network connecting the top 25 collaborators of N. Philip. A scholar is included among the top collaborators of N. Philip 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. Philip. N. Philip 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.
Lesieur, Emmanuelle, A. Dabadie, Marina Colombani, et al.. (2016). Prenatal diagnosis of bowel malposition using T2-weighted fetal MRI sequences. Diagnostic and Interventional Imaging. 97(9). 857–861. 5 indexed citations
2.
Dabadie, A., B. Bourlière‐Najean, N. Philip, et al.. (2014). Contribution of the foetal uro-MRI in the prenatal diagnosis of uronephropathies. Diagnostic and Interventional Imaging. 95(6). 573–578. 12 indexed citations
3.
Gorincour, G., Katia Chaumoître, B. Bourlière‐Najean, et al.. (2014). Fetal skeletal computed tomography: When? How? Why?. Diagnostic and Interventional Imaging. 95(11). 1045–1053. 15 indexed citations
4.
Bretelle, Florence, et al.. (2010). Mise en place du dépistage combiné de la trisomie 21 au sein des centres pluridisciplinaires de diagnostic prénatal marseillais. Gynécologie Obstétrique & Fertilité. 38(12). 786–788. 3 indexed citations
5.
Philip, N., E. Quarello, G. Gorincour, & Sabine Sigaudy. (2010). Approche de la dysmorphologie fœtale in utero. Gynécologie Obstétrique & Fertilité. 38(11). 677–685. 5 indexed citations
6.
Philip, N. & Rachel Reynaud. (2008). Hypocalcémie et microdélétion 22q11.2. Archives de Pédiatrie. 15(5). 648–649. 1 indexed citations
7.
Gorincour, G., B. Bourlière‐Najean, Béatrice Bonello, et al.. (2007). Feasibility of fetal cardiac magnetic resonance imaging: preliminary experience. Ultrasound in Obstetrics and Gynecology. 29(1). 105–108. 51 indexed citations
8.
Philip, N., Laurence Colleaux, Sabine Sigaudy, et al.. (2005). Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation. American Journal of Medical Genetics Part A. 134A(1). 39–44. 4 indexed citations
9.
Lévy, Nicolas, Claire Navarro, Irène Boccaccio, et al.. (2003). Functional exploration of A type lamins and associated proteins in patients affected with Hutchinson-Gilford progeria syndrome caused by G608G mutation in LMNA. The American Journal of Human Genetics. 73(5). 554. 1 indexed citations
10.
Bourlière‐Najean, B., M. Panuel, Marie‐Dominique Piercecchi‐Marti, et al.. (2003). Value of fetal skeletal radiographs in the diagnosis of fetal death. European Radiology. 13(5). 1046–1049. 10 indexed citations
11.
Granel, B., N. Philip, J. Serratrice, et al.. (2003). <i>CIAS1</i> Mutation in a Patient with Overlap between Muckle-Wells and Chronic Infantile Neurological Cutaneous and Articular Syndromes. Dermatology. 206(3). 257–259. 31 indexed citations
12.
Richard, Martín, Jean‐Jacques Grob, N. Philip, et al.. (1998). Physiopathogenic Investigations in a Case of Familial Stiff-Skin Syndrome. Dermatology. 197(2). 127–131. 17 indexed citations
13.
Lévy, A., Gérard Michel, Martine LeMerrer, & N. Philip. (1997). Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: A new component manifestation of deletion 22q11?. American Journal of Medical Genetics. 69(4). 356–359. 35 indexed citations
14.
Levy‐Mozziconacci, Annie, et al.. (1996). La microdélétion du chromosome 22q11 chez l'enfant: à propos d'une série de 49 patients. Archives de Pédiatrie. 3(8). 761–768. 11 indexed citations
15.
Philip, N., A. Moncla, Sabine Sigaudy, et al.. (1995). Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndrome. Clinical Dysmorphology. 4(4). 347–351. 29 indexed citations
16.
Schrander‐Stumpel, C. T. R. M., Peter Meinecke, Golder N. Wilson, et al.. (1994). The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients. European Journal of Pediatrics. 153(6). 438–445. 88 indexed citations
17.
Muscatelli, Françoise, N. Philip, A. Moncla, et al.. (1992). Physical mapping of an Xq-proximal interstitial duplication in a male. Human Genetics. 88(6). 691–694. 11 indexed citations
18.
Genitori, Lorenzo, D. Lang, N. Philip, et al.. (1992). Cranioectodermal dysplasia with sagittal craniosynostosis (Sensenbrenner's syndrome): Case report and review of the literature. British Journal of Neurosurgery. 6(6). 601–606. 2 indexed citations
19.
Voelckel, Marie‐Antoinette, N. Philip, I. Oberlé, et al.. (1989). Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation. Human Genetics. 81(4). 353–357. 25 indexed citations
20.
Voelckel, Marie‐Antoinette, Marie‐Geneviève Mattéi, Catherine Nguyen, et al.. (1988). Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation. Human Genetics. 80(4). 375–378. 15 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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