Agnès Guichet

3.2k total citations
42 papers, 1.2k citations indexed

About

Agnès Guichet is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Agnès Guichet has authored 42 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 19 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Agnès Guichet's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (10 papers) and Mitochondrial Function and Pathology (6 papers). Agnès Guichet is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (10 papers) and Mitochondrial Function and Pathology (6 papers). Agnès Guichet collaborates with scholars based in France, United States and Morocco. Agnès Guichet's co-authors include Dominique Bonneau, Patrizia Amati‐Bonneau, Pascal Reynier, Guy Lenaers, Arnaud Chevrollier, Pascale Belenguer, Aurélien Olichon, Yves Malthièry, Annick Toutain and Yves Morel and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and Annals of Neurology.

In The Last Decade

Agnès Guichet

41 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Agnès Guichet France 19 777 469 204 129 127 42 1.2k
Carol Saunders United States 22 744 1.0× 635 1.4× 110 0.5× 130 1.0× 72 0.6× 59 1.3k
Maja Hempel Germany 19 511 0.7× 342 0.7× 116 0.6× 112 0.9× 58 0.5× 58 855
Alice Goldenberg France 20 678 0.9× 565 1.2× 91 0.4× 45 0.3× 100 0.8× 49 1.1k
Marion Gérard France 14 436 0.6× 386 0.8× 77 0.4× 94 0.7× 107 0.8× 29 837
Birgit Zirn Germany 19 689 0.9× 419 0.9× 167 0.8× 66 0.5× 51 0.4× 33 1.1k
Kyle Retterer United States 24 681 0.9× 906 1.9× 187 0.9× 53 0.4× 54 0.4× 37 1.4k
Kate Pope Australia 17 567 0.7× 392 0.8× 96 0.5× 63 0.5× 39 0.3× 28 867
Fabiola Quintero‐Rivera United States 16 634 0.8× 907 1.9× 357 1.8× 36 0.3× 99 0.8× 54 1.4k
Khushnooda Ramzan Saudi Arabia 18 644 0.8× 320 0.7× 73 0.4× 90 0.7× 55 0.4× 79 1.2k
Daniela del Gaudio United States 18 854 1.1× 1.0k 2.1× 388 1.9× 61 0.5× 254 2.0× 47 1.8k

Countries citing papers authored by Agnès Guichet

Since Specialization
Citations

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

Fields of papers citing papers by Agnès Guichet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Agnès Guichet

This figure shows the co-authorship network connecting the top 25 collaborators of Agnès Guichet. A scholar is included among the top collaborators of Agnès Guichet 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 Agnès Guichet. Agnès Guichet 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.
Charif, Majida, Patrizia Amati‐Bonneau, Agnès Guichet, et al.. (2025). Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation. Ocular Immunology and Inflammation. 33(5). 849–853. 1 indexed citations
2.
Tusseau, Maud, Mélanie Eyries, Nicolas Chatron, et al.. (2024). Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families. European Journal of Medical Genetics. 68. 104919–104919. 3 indexed citations
3.
Charif, Majida, Yvette C. Wong, Soojin Kim, et al.. (2021). Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy. Molecular Neurodegeneration. 16(1). 12–12. 13 indexed citations
4.
Lerat, Justine, Crystel Bonnet, François Cartault, et al.. (2018). High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. Clinical Genetics. 95(1). 177–181. 3 indexed citations
5.
Chauveau, Claire, Cédric Julien, Isabelle Duband‐Goulet, et al.. (2016). The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease. Human Molecular Genetics. 25(8). 1559–1573. 17 indexed citations
6.
Ziegler, Alban, Agnès Guichet, Magalie Barth, et al.. (2014). Extensive Mongolian spots in 4p16.3 deletion (Wolf–Hirschhorn syndrome). Clinical Dysmorphology. 23(3). 109–110. 1 indexed citations
7.
Perrin, Aurore, Nathalie Douet‐Guilbert, M.‐J. Le Bris, et al.. (2009). Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism. International Journal of Andrology. 32(3). 231–234. 18 indexed citations
8.
Meur, Nathalie Le, Muriel Holder‐Espinasse, Sylvie Jaillard, et al.. (2009). MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Journal of Medical Genetics. 47(1). 22–29. 150 indexed citations
9.
Schneider, Anouck, Brigitte Benzacken, Agnès Guichet, et al.. (2008). Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia. European Journal of Human Genetics. 16(6). 680–687. 21 indexed citations
10.
Coutant, R., Delphine Mallet, Najiba Lahlou, et al.. (2007). Heterozygous Mutation of Steroidogenic Factor-1 in 46,XY Subjects May Mimic Partial Androgen Insensitivity Syndrome. The Journal of Clinical Endocrinology & Metabolism. 92(8). 2868–2873. 63 indexed citations
11.
Loiseau, Dominique, Arnaud Chevrollier, Christophe Verny, et al.. (2007). Mitochondrial coupling defect in Charcot–Marie–Tooth type 2A disease. Annals of Neurology. 61(4). 315–323. 123 indexed citations
12.
Dubois, Séverine, et al.. (2007). Endocrine function in a 48,XXYY adult with type 2 diabetes: case report with a review of the literature. Annales d Endocrinologie. 68(5). 384–388. 3 indexed citations
13.
Nguyen, Sylvie, et al.. (2007). Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome. Epileptic Disorders. 9(3). 327–331. 9 indexed citations
14.
Amati‐Bonneau, Patrizia, Agnès Guichet, Aurélien Olichon, et al.. (2005). OPA1 R445H mutation in optic atrophy associated with sensorineural deafness. Annals of Neurology. 58(6). 958–963. 120 indexed citations
15.
DeScipio, Cheryl, Lori Schneider, Terri L. Young, et al.. (2005). Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome. American Journal of Medical Genetics Part A. 134A(1). 3–11. 54 indexed citations
16.
Guichet, Agnès, Stéphane Triau, F. Biquard, et al.. (2004). Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2. Prenatal Diagnosis. 24(10). 828–832. 20 indexed citations
17.
Coutant, R., F. Boussion, D. Loisel, et al.. (2004). Prenatal diagnosis of absence of the septum pellucidum associated with septo‐optic dysplasia. Ultrasound in Obstetrics and Gynecology. 25(1). 73–75. 35 indexed citations
18.
Guichet, Agnès, et al.. (1998). High resolution chromosome analysis andin situ hybridization on amniotic fluid for diagnosis of a cryptic translocation. Prenatal Diagnosis. 18(4). 399–403. 2 indexed citations
19.
Guichet, Agnès, et al.. (1997). Are t(X;Y) (p22;q11) translocations in females frequently associated with Madelung deformity?. Clinical Dysmorphology. 6(4). 341–345. 15 indexed citations
20.
Guichet, Agnès, et al.. (1995). Prenatal diagnosis of trisomy 8 mosaicism in cvs after abnormal ultrasound findings at 12 weeks. Prenatal Diagnosis. 15(8). 769–772. 11 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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