C. Philippe

478 citations
16 papers · 342 · h-index 9

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Immune cells in cancer
    • Immune Cell Function and Interaction

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Insect and Arachnid Ecology and Behavior 2
    • Genetics and Neurodevelopmental Disorders 1
    • DNA Repair Mechanisms 1
    • Ubiquitin and proteasome pathways 1

C. Philippe

16 papers receiving 337 citations

Peers

C. Philippe
Comparison fields: 5 of 71
  • Genetics 130
  • Immunology 75
  • Biological Psychiatry 7
  • Physiology 9
  • Molecular Biology 130
Replace Yi Geng with:
Yi Geng United States
Keum-Soon Im South Korea
Prerana Wagle Germany
Tearina Chu United States
Alice Witsell United States
N S Thomas United Kingdom
Naoki Kurihara Japan
Reyad A. Elbarbary United States
Xiangyu Wang China
U Gruber‐Sedlmayr Austria
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Citations per field
00.5×
Yi Geng · 1×
Citations per year

Countries citing papers authored by C. Philippe

Since Specialization
Citations

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

Fields of papers citing papers by C. Philippe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside C. Philippe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C. Philippe Line = papers co-authored together C. Philippe links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1 1995159
2 199538
3 201633
4 199225
5 201618
6 198211
7
Incontinentia pigmenti (type 1) and X;5 translocation.
19929
8 19938
9 20078
10 19998
11
Double telomeric signals on single chromatids revealed by FISH and PRINS.
19997
12 19755
13
[Low extracellular pH has a role in the induction of NO synthase type 2 in macrophages].
19975
14 19993
15
Culture de cellules embryonnaires et d'hemocytes de blatte d'origine parthenogenetique: Maintien in vitro des formules haploides et aneuploides
19753
16 20072

About C. Philippe

C. Philippe is a scholar working on Genetics, Molecular Biology, Plant Science, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 16 papers that have together received 342 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Insect and Arachnid Ecology and Behavior (2 papers), Prenatal Screening and Diagnostics (2 papers), DNA Repair Mechanisms (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Ubiquitin and proteasome pathways (1 paper) and Insect Utilization and Effects (1 paper). The work is most often cited by research in Genetics (130 citations), Immunology (75 citations), Biological Psychiatry (7 citations), Physiology (9 citations) and Molecular Biology (130 citations). C. Philippe has collaborated with scholars based in France, Italy and Germany. Frequent co-authors include Bruno Fouqueray, Laurent Baud, J P Moulinoux, R Havouis, S Gilgenkrantz, Alain Bernheim, Catherine Léonard, J. L. Huret, M. Chery and Jacky Bonaventure. Their work appears in journals such as Clinical Genetics, Human Genetics, Chromosome Research, Experimental Cell 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.

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