C. Le Caignec

432 total citations
7 papers, 242 citations indexed

About

C. Le Caignec is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C. Le Caignec has authored 7 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C. Le Caignec's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (2 papers) and Spinal Fractures and Fixation Techniques (1 paper). C. Le Caignec is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (2 papers) and Spinal Fractures and Fixation Techniques (1 paper). C. Le Caignec collaborates with scholars based in France, Switzerland and Germany. C. Le Caignec's co-authors include A. David, Bertrand Isidor, Sandrine Tardieu, Madeleine Joubert, Antoine Hamel, O. Dubourg, Odile Boespflug‐Tanguy, Sébastien Jacquemont, Nataliya Di Donato and Véronique Pingault and has published in prestigious journals such as Journal of Medical Genetics, Journal of Neurology and Prenatal Diagnosis.

In The Last Decade

C. Le Caignec

7 papers receiving 221 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Le Caignec France	7	181	136	89	32	28	7	242
Anne Bazin France	8	119 0.7×	90 0.7×	74 0.8×	42 1.3×	12 0.4×	16	195
Fernando Santos Spain	9	228 1.3×	84 0.6×	193 2.2×	21 0.7×	23 0.8×	13	325
Mylène Valduga France	8	169 0.9×	90 0.7×	76 0.9×	18 0.6×	19 0.7×	17	213
Prochi F. Madon India	7	190 1.0×	163 1.2×	102 1.1×	52 1.6×	20 0.7×	25	320
Beth A. Torchia United States	7	281 1.6×	177 1.3×	139 1.6×	71 2.2×	35 1.3×	11	369
Annice Hill United States	7	212 1.2×	69 0.5×	108 1.2×	49 1.5×	16 0.6×	10	253
Alaa K. Kamel Egypt	9	180 1.0×	61 0.4×	138 1.6×	25 0.8×	21 0.8×	34	227
Olga Žilina Estonia	12	242 1.3×	92 0.7×	132 1.5×	54 1.7×	11 0.4×	23	314
M. Crocker United Kingdom	9	183 1.0×	68 0.5×	88 1.0×	52 1.6×	15 0.5×	16	245
Vera Ayres Meloni Brazil	9	233 1.3×	59 0.4×	122 1.4×	50 1.6×	17 0.6×	26	272

Countries citing papers authored by C. Le Caignec

Since Specialization

Citations

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

Fields of papers citing papers by C. Le Caignec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Le Caignec

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

All Works

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7 of 7 papers shown

1.

Donato, Nataliya Di, C. Le Caignec, Barbara Klink, et al.. (2014). Distinct phenotype of PHF6 deletions in females. European Journal of Medical Genetics. 57(2-3). 85–89. 15 indexed citations

2.

Isidor, Bertrand, Geneviève Baujat, C. Le Caignec, et al.. (2009). Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganization. American Journal of Medical Genetics Part A. 149A(8). 1734–1739. 10 indexed citations

3.

Isidor, Bertrand, Valérie Cormier‐Daire, M. Le Merrer, et al.. (2008). Autosomal dominant spondylocarpotarsal synostosis syndrome: Phenotypic homogeneity and genetic heterogeneity. American Journal of Medical Genetics Part A. 146A(12). 1593–1597. 17 indexed citations

4.

Caignec, C. Le, et al.. (2005). Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations. Journal of Medical Genetics. 42(2). 121–128. 165 indexed citations

5.

Caignec, C. Le, Christine Gicquel, Marie-Claire Gübler, et al.. (2004). Sonographic findings in Beckwith–Wiedemann syndrome related to H19 hypermethylation. Prenatal Diagnosis. 24(3). 165–168. 6 indexed citations

6.

Caignec, C. Le, et al.. (2003). Prenatal diagnosis of a small supernumerary, XIST‐negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus. Prenatal Diagnosis. 23(2). 143–145. 8 indexed citations

7.

Pingault, Véronique, Nadège Bondurand, C. Le Caignec, et al.. (2001). The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders. Journal of Neurology. 248(6). 496–499. 21 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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