Charles Coutton

6.9k total citations
74 papers, 2.5k citations indexed

About

Charles Coutton is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Charles Coutton has authored 74 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 33 papers in Molecular Biology and 32 papers in Reproductive Medicine. Recurrent topics in Charles Coutton's work include Sperm and Testicular Function (30 papers), Reproductive Biology and Fertility (29 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Charles Coutton is often cited by papers focused on Sperm and Testicular Function (30 papers), Reproductive Biology and Fertility (29 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers). Charles Coutton collaborates with scholars based in France, United States and Iran. Charles Coutton's co-authors include Pierre F. Ray, Christophe Arnoult, Guillaume Martinez, Aminata Touré, Jessica Escoffier, Zine‐Eddine Kherraf, Raoudha Zouari, Sylviane Hennebicq, Sandra Yassine and Nicolas Thierry‐Mieg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Charles Coutton

68 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charles Coutton France	27	1.4k	1.2k	1.1k	990	270	74	2.5k
Denise Escalier France	29	1.4k 1.0×	1.2k 1.0×	1.1k 1.0×	1.0k 1.0×	245 0.9×	68	2.6k
Yue‐Qiu Tan China	26	749 0.5×	810 0.7×	936 0.8×	999 1.0×	540 2.0×	139	2.2k
Guangxiu Lu China	30	1.0k 0.7×	1.2k 1.0×	848 0.8×	1.6k 1.6×	606 2.2×	229	3.2k
Carolina J. Jorgez United States	21	739 0.5×	830 0.7×	548 0.5×	1.2k 1.2×	165 0.6×	45	2.1k
Sung Keun Kang South Korea	27	820 0.6×	1.4k 1.1×	786 0.7×	1.5k 1.5×	97 0.4×	49	2.5k
Xiaoxi Sun China	28	985 0.7×	1.3k 1.0×	559 0.5×	856 0.9×	825 3.1×	121	2.4k
Fréderic Morel France	30	689 0.5×	708 0.6×	1.1k 1.0×	836 0.8×	647 2.4×	132	2.7k
Minnie Hsieh United States	16	1.0k 0.7×	1.6k 1.3×	455 0.4×	1.0k 1.0×	112 0.4×	19	2.3k
Sandrine Caburet France	23	368 0.3×	462 0.4×	686 0.6×	1.3k 1.3×	98 0.4×	39	1.9k
Saïd Assou France	35	1.2k 0.9×	1.6k 1.3×	443 0.4×	1.8k 1.8×	530 2.0×	98	3.8k

Countries citing papers authored by Charles Coutton

Since Specialization

Citations

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

Fields of papers citing papers by Charles Coutton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles Coutton

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

All Works

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20 of 20 papers shown

Kherraf, Zine‐Eddine, Anne‐Laure Barbotin, Guillaume Martinez, et al.. (2023). A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility. Clinical Genetics. 105(2). 220–225. 4 indexed citations

Sayou, Camille, Patrick Lorès, Caroline Cazin, et al.. (2023). Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans. iScience. 26(8). 107354–107354. 2 indexed citations

Friocourt, Gaëlle, Aurore Perrin, Paul A. Saunders, et al.. (2023). Bypassing Mendel’s First Law: Transmission Ratio Distortion in Mammals. International Journal of Molecular Sciences. 24(2). 1600–1600. 2 indexed citations

Mitchell, Valérie, Anne Loyens, Nathalie Rives, et al.. (2023). Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy. Reproductive BioMedicine Online. 47(5). 103328–103328. 4 indexed citations

Martinez, Guillaume, Anne‐Laure Barbotin, Caroline Cazin, et al.. (2023). New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. International Journal of Molecular Sciences. 24(3). 2559–2559. 9 indexed citations

Cazin, Caroline, Guillaume Martinez, Sélima Fourati Ben Mustapha, et al.. (2021). Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa. International Journal of Molecular Sciences. 22(4). 2187–2187. 6 indexed citations

Lorès, Patrick, Zine‐Eddine Kherraf, Amir Amiri‐Yekta, et al.. (2021). A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome. Human Genetics. 140(7). 1031–1043. 20 indexed citations

Whitfield, Marjorie, Laurence Stouvenel, Patrick Lorès, et al.. (2021). The sodium/proton exchanger SLC9C1 ( sNHE ) is essential for human sperm motility and fertility. Clinical Genetics. 99(5). 684–693. 33 indexed citations

Liu, Siyu, Jintao Zhang, Zine‐Eddine Kherraf, et al.. (2021). CFAP61 is required for sperm flagellum formation and male fertility in human and mouse. Development. 148(23). 37 indexed citations

10.

Manfrevola, Francesco, Guillaume Martinez, Charles Coutton, et al.. (2021). Ankrd31 in Sperm and Epididymal Integrity. Frontiers in Cell and Developmental Biology. 9. 741975–741975. 5 indexed citations

11.

Brouillet, Sophie, Guillaume Martinez, Charles Coutton, & S. Hamamah. (2020). Is cell-free DNA in spent embryo culture medium an alternative to embryo biopsy for preimplantation genetic testing? A systematic review. Reproductive BioMedicine Online. 40(6). 779–796. 39 indexed citations

12.

Alfaidy, Nadia, Charles Coutton, Guillaume Martinez, et al.. (2019). Prokineticin 1 is a new biomarker of human oocyte competence: expression and hormonal regulation throughout late folliculogenesis. Biology of Reproduction. 101(4). 832–841. 8 indexed citations

13.

Hashimoto, Satoru, Melanie May, Alexey Epanchintsev, et al.. (2017). MED12-related XLID disorders are dose-dependent of immediate early genes (IEGs) expression. Human Molecular Genetics. 26(11). 2062–2075. 17 indexed citations

14.

Zouari, Raoudha, Sélima Fourati Ben Mustapha, Guillaume Martinez, et al.. (2016). Patients with multiple morphological abnormalities of the sperm flagella due toDNAH1mutations have a good prognosis following intracytoplasmic sperm injection. Human Reproduction. 31(6). 1164–1172. 75 indexed citations

15.

Escoffier, Jessica, Sandra Yassine, Hoi Chang Lee, et al.. (2014). Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation. Molecular Human Reproduction. 21(2). 157–168. 71 indexed citations

16.

Karaouzène, Thomas, Michèle El Atifi, Jean‐Paul Issartel, et al.. (2013). Comparative testicular transcriptome of wild type and globozoospermic Dpy19l2knock out mice. Basic and Clinical Andrology. 23(1). 7–7. 4 indexed citations

17.

Stasia, Marie José, Cécile Martel, Véronique Satre, et al.. (2013). Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease. European Journal of Human Genetics. 21(10). 1079–1084. 14 indexed citations

18.

Coutton, Charles, Thomas Karaouzène, Damien Sanlaville, et al.. (2013). Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population. PLoS Genetics. 9(3). e1003363–e1003363. 18 indexed citations

19.

Coutton, Charles, Raoudha Zouari, Mariem Ben Khelifa, et al.. (2012). MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia. Human Reproduction. 27(8). 2549–2558. 52 indexed citations

20.

Coutton, Charles, Françoise Devillard, Gaëlle Vieville, et al.. (2012). 17p13.1 microduplication in a boy with Silver–Russell syndrome features and intellectual disability. American Journal of Medical Genetics Part A. 158A(10). 2564–2570. 25 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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