C. Mignon

546 total citations
14 papers, 434 citations indexed

About

C. Mignon is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, C. Mignon has authored 14 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 2 papers in Oncology. Recurrent topics in C. Mignon's work include Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). C. Mignon is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Epigenetics and DNA Methylation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). C. Mignon collaborates with scholars based in France, United States and Gabon. C. Mignon's co-authors include Marie‐Geneviève Mattéi, Nathalie Roëckel, D. Depétris, Michel Fontés, Carlos Cardoso, Laurence Colleaux, Gilles Hetet, A. Moncla, Christine M. Distèche and Laurence Lacroix and has published in prestigious journals such as Genomics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

C. Mignon

14 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Mignon France	11	327	176	74	65	46	14	434
Jan‐Gowth Chang Taiwan	14	258 0.8×	106 0.6×	25 0.3×	62 1.0×	22 0.5×	23	503
Jaime Garcia‐Heras United States	14	208 0.6×	244 1.4×	93 1.3×	25 0.4×	79 1.7×	25	440
Hirofumi Ohashi Japan	11	198 0.6×	125 0.7×	73 1.0×	28 0.4×	16 0.3×	12	321
Sophie Monnot France	13	403 1.2×	206 1.2×	98 1.3×	18 0.3×	8 0.2×	27	585
Marie‐Louise Bondeson Sweden	10	202 0.6×	108 0.6×	39 0.5×	60 0.9×	17 0.4×	13	305
George J. Kargul United States	6	331 1.0×	100 0.6×	24 0.3×	38 0.6×	9 0.2×	7	448
Michele Traversa Italy	11	183 0.6×	232 1.3×	45 0.6×	23 0.4×	20 0.4×	16	393
Caterina Barbieri Italy	9	228 0.7×	79 0.4×	24 0.3×	28 0.4×	11 0.2×	18	392
Anju Paudyal United Kingdom	10	325 1.0×	112 0.6×	37 0.5×	12 0.2×	10 0.2×	14	456
Jamie L Morris United States	4	383 1.2×	298 1.7×	46 0.6×	37 0.6×	28 0.6×	5	828

Countries citing papers authored by C. Mignon

Since Specialization

Citations

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

Fields of papers citing papers by C. Mignon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Mignon

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

All Works

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14 of 14 papers shown

Cardoso, Carlos, et al.. (2000). The human EZH2 gene: genomic organisation and revised mapping in 7q35 within the critical region for malignant myeloid disorders. European Journal of Human Genetics. 8(3). 174–180. 81 indexed citations

Metzler‐Guillemain, Catherine, Yves Usson, C. Mignon, et al.. (2000). Organization of the X and Y chromosomes in human, chimpanzee and mouse pachytene nuclei using molecular cytogenetics and three-dimensional confocal analyses. Chromosome Research. 8(7). 571–584. 14 indexed citations

Metzler‐Guillemain, Catherine, C. Mignon, D. Depétris, Marie-Roberte Guichaoua, & Marie‐Geneviève Mattéi. (1999). Bivalent 15 Regularly Associates With the Sex Vesicle in Normal Male Meiosis. Chromosome Research. 7(5). 369–378. 27 indexed citations

Mignon, C., B Delobel, A. Moncla, et al.. (1998). Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.. Journal of Medical Genetics. 35(11). 932–938. 10 indexed citations

Watrin, Françoise, Nathalie Roëckel, Laurence Lacroix, et al.. (1998). The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.. PubMed. 5(5). 324–32. 34 indexed citations

Raimond, Jacques, Drazen B. Zimonjic, C. Mignon, et al.. (1997). Mapping of the galectin-3 gene (LGALS3) to human Chromosome 14 at region 14q21-22. Mammalian Genome. 8(9). 706–707. 54 indexed citations

Watrin, Françoise, Nathalie Roëckel, Laurence Lacroix, et al.. (1997). The Mouse Necdin Gene Is Expressed from the Paternal Allele Only and Lies in the 7C Region of the Mouse Chromosome 7, a Region of Conserved Synteny to the Human Prader-Willi Syndrome Region. European Journal of Human Genetics. 5(5). 324–332. 29 indexed citations

Mignon, C., Fabienne Parente, Patrick Collignon, et al.. (1997). Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.. Journal of Medical Genetics. 34(3). 217–222. 7 indexed citations

Mignon, C., et al.. (1996). Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11→q12 and mouse chromosome 14D1-E1 by in situ hybridization. Cytogenetic and Genome Research. 72(2-3). 185–186. 25 indexed citations

10.

Mignon, C., Perrine Malzac, A. Moncla, et al.. (1996). Clinical Heterogeneity in 16 Patientswith inv dup 15 Chromosome:Cytogenetic and Molecular Studies,Search for an Imprinting Effect. European Journal of Human Genetics. 4(2). 88–100. 54 indexed citations

11.

Mignon, C., et al.. (1996). Mapping of the MR60/ERGIC-53 gene to human Chromosome 18q21.3–18q22 by in situ hybridization. Mammalian Genome. 7(10). 791–792. 5 indexed citations

12.

Mignon, C., A Okada, Marie‐Geneviève Mattéi, & Paul Basset. (1995). Assignment of the Human Membrane-Type Matrix Metalloproteinase (MMP14) Gene to 14q11-q12 by in Situ Hybridization. Genomics. 28(2). 360–361. 14 indexed citations

13.

Sobieszczuk, Peter, et al.. (1995). Locations of the ets Subfamily Membersnet, elk1,andsap1(ELK3, ELK1, and ELK4) on Three Homologous Regions of the Mouse and Human Genomes. Genomics. 29(3). 769–772. 20 indexed citations

14.

Voilley, Nicolas, Frédéric Bassilana, C. Mignon, et al.. (1995). Cloning, Chromosomal Localization, and Physical Linkage of the β and γ Subunits (SCNN1B and SCNN1G) of the Human Epithelial Amiloride-Sensitive Sodium Channel. Genomics. 28(3). 560–565. 60 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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