Agnès Guichet

3.2k citations

42 papers · 1.2k · h-index 19

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

Genetics 20
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
Molecular Biology 19
- Mitochondrial Function and Pathology 6
- RNA modifications and cancer 5

Co-authors: Dominique Bonneau (17 shared papers)Patrizia Amati‐Bonneau (7 shared papers)Pascal Reynier (5 shared papers)Guy Lenaers (6 shared papers)Arnaud Chevrollier (2 shared papers)Yves Malthièry (2 shared papers)Pascale Belenguer (2 shared papers)Aurélien Olichon (2 shared papers)
Journals: Prenatal Diagnosis (6 papers)European Journal of Human Genetics (3 papers)European Journal of Medical Genetics (2 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)The Journal of Maternal-Fetal & Neonatal Medicine (2 papers)
Partner nations: France United States Morocco

In The Last Decade

Agnès Guichet

41 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside Agnès Guichet, 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 Agnès Guichet Line = papers co-authored together Agnès Guichet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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 ·Nathalie Le Meur, Muriel Holder‐Espinasse, Sylvie Jaillard, Alice Goldenberg, Sylvie Joriot, Patrizia Amati‐Bonneau, Agnès Guichet, M. Barth, Aude Charollais, Hubert Journel, Stéphane Auvin, Cécile Boucher, Jean Pierre Kerckaert, Véronique David, Sylvie Manouvrier‐Hanu, Pascale Saugier-Véber, Thierry Frébourg, Christèle Dubourg, Joris Andrieux, Dominique Bonneau	2009	150
2	Mitochondrial coupling defect in Charcot–Marie–Tooth type 2A disease Annals of Neurology ·Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, Virginie Guillet, Naïg Guéguen, Marie‐Anne Pou de Crescenzo, Marc Ferré, Marie‐Claire Malinge, Agnès Guichet, Guillaume Nicolas, Patrizia Amati‐Bonneau, Yves Malthièry, Dominique Bonneau, Pascal Reynier	2007	123
3	Effects of OPA1 mutations on mitochondrial morphology and apoptosis: Relevance to ADOA pathogenesis Journal of Cellular Physiology ·Aurélien Olichon, Thomas Landes, Laetitia Pelloquin, Laurent J. Emorine, Valérie Mils, Agnès Guichet, Cécile Delettre, Christian Hamel, Patrizia Amati‐Bonneau, Dominique Bonneau, Pascal Reynier, Guy Lenaers, Pascale Belenguer	2006	123
4	OPA1 R445H mutation in optic atrophy associated with sensorineural deafness Annals of Neurology ·Patrizia Amati‐Bonneau, Agnès Guichet, Aurélien Olichon, Arnaud Chevrollier, Frédérique Viala, Stéphanie Miot, Carmen Ayuso, Sylvie Odent, Catherine Arrouet, Christophe Verny, M. Calmels, Gilles Simard, Pascale Belenguer, Jing Wang, Jean‐Luc Puel, Christian Hamel, Yves Malthièry, Dominique Bonneau, Guy Lenaers, Pascal Reynier	2005	120
5	Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia Neurology ·Ginevra Zanni, Yoann Saillour, Majdi Nagara, Pierre Billuart, L. Castelnau, Claude Moraine, Laurence Faivre, Enrico Bertini, Alexandra Dürr, Agnès Guichet, Diana Rodriguez, V. des Portes, C. Beldjord, Jamel Chelly	2005	67
6	Heterozygous Mutation of Steroidogenic Factor-1 in 46,XY Subjects May Mimic Partial Androgen Insensitivity Syndrome The Journal of Clinical Endocrinology & Metabolism ·R. Coutant, Delphine Mallet, Najiba Lahlou, Natacha Bouhours‐Nouet, Agnès Guichet, L Coupris, Anne Croué, Yves Morel	2007	63
7	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 ·Cheryl DeScipio, Lori Schneider, Terri L. Young, Nora Wasserman, Dinah Yaeger, Fengmin Lu, Patricia G. Wheeler, Marc S. Williams, Lynn Bason, Lori Jukofsky, Ammini Menon, Ryan Geschwindt, Albert E. Chudley, Jorge Saraiva, Albert Schinzel, Agnès Guichet, William B. Dobyns, Annick Toutain, Nancy B. Spinner, Ian D. Krantz	2005	54
8	Etiology, prognosis and management of nuchal cystic hygroma: 25 new cases and literature review European Journal of Obstetrics & Gynecology and Reproductive Biology ·Ph. Descamps, O Jourdain, C. Paillet, Annick Toutain, Agnès Guichet, D. Pourcelot, F. Gold, Mercedes Castiel, G. Body	1997	53
9	New Management Strategy of Pregnancies at Risk of Congenital Adrenal Hyperplasia Using Fetal Sex Determination in Maternal Serum: French Cohort of 258 Cases (2002–2011) The Journal of Clinical Endocrinology & Metabolism ·Véronique Tardy-Guidollet, Rita Menassa, Jean‐Marc Costa, M David, Claire Bouvattier-Morel, Clarisse Baumann, Muriel Houang, F. Lorenzini, Nicole Philip, Sylvie Odent, Agnès Guichet, Yves Morel	2014	49
10	A gene for FG syndrome maps in the Xq12-q21.31 region American Journal of Medical Genetics ·Sylvain Briault, Ruth F. Hill, Antony E. Shrimpton, Danping Zhu, Marianne Till, Nathalie Ronce, Patricia Margaritte‐Jeannin, M Baraitser, Helen Middleton‐Price, Sue Malcolm, Elizabeth Thompson, Joe J. Hoo, Golder N. Wilson, Corrado Romano, Agnès Guichet, Marcus Pembrey, Michel Fontés, Annemarie Poustka, Claude Moraine	1997	38
11	Barth syndrome in a female patient Molecular Genetics and Metabolism ·Laure Cosson, Annick Toutain, Gilles Simard, Willem Kulik, Gábor Mátyás, Agnès Guichet, Hélène Blasco, Z. Maakaroun-Vermesse, Marie-Catherine Vaillant, Cédric Le Caignec, A Chantepie, F. Labarthe	2012	37
12	Prenatal diagnosis of absence of the septum pellucidum associated with septo‐optic dysplasia Ultrasound in Obstetrics and Gynecology ·Catherine Lépinard, R. Coutant, F. Boussion, D. Loisel, B. Delorme, F. Biquard, Danielle Bonneau, Agnès Guichet, P. Descamps	2004	35
13	Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion European Journal of Human Genetics ·Dominique Brémond‐Gignac, John A. Crolla, Henri Copin, Agnès Guichet, Dominique Bonneau, Laurence Taine, Didier Lacombe, Clarisse Baumann, Brigitte Benzacken, Alain Verloès	2005	32
14	Fetal intracerebral hemorrhage and cataract: think COL4A1 Journal of Perinatology ·Estelle Colin, L Sentilhes, A Sarfati, Manuèle Miné, Agnès Guichet, Claire Ploton, F. Boussion, B. Delorme, Elisabeth Tournier‐Lasserve, Dominique Bonneau	2013	23
15	Influence of ultrasonographers training on prenatal diagnosis of congenital heart diseases: a 12‐year population‐based study Prenatal Diagnosis ·Ph. Pézard, Laurent Bonnemains, F. Boussion, Loı̈c Sentilhes, P. Allory, Catherine Lépinard, Agnès Guichet, Stéphane Triau, F. Biquard, M. M. LeBlanc, Danielle Bonneau, Ph. Descamps	2008	22
16	Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia European Journal of Human Genetics ·Anouck Schneider, Brigitte Benzacken, Agnès Guichet, Alain Verloès, Dominique Bonneau, Nathalie Collot, Florence Dastot-Le-Moal, Michel Goossens, Laurence Taine, Emilie Landais, Dominique Gaillard, Martine Doco‐Fenzy	2008	21
17	Relationship of non‐visualization of the fetal gallbladder and amniotic fluid digestive enzymes analysis to outcome Prenatal Diagnosis ·Sophie Dreux, Mathias Boughanim, Catherine Lépinard, Agnès Guichet, Jean‐Marie Rival, Alix de Becdelièvre, I. Duguépéroux, Françoise Müller	2012	21
18	Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2 Prenatal Diagnosis ·Agnès Guichet, Stéphane Triau, Catherine Lépinard, Chantal Esculapavit, F. Biquard, Philippe Descamps, Férechté Encha‐Razavi, Dominique Bonneau	2004	20
19	Increased aneuploidy rates in spermatozoa of a male carrier of a trisomy 18 mosaicism International Journal of Andrology ·Aurore Perrin, Nathalie Douet‐Guilbert, M.‐J. Le Bris, Pascale May‐Panloup, Agnès Guichet, V. Amice, J. Amice, Marc De Braekeleer, Fréderic Morel	2009	18
20	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 ·Laurianne Davignon, Claire Chauveau, Cédric Julien, C. Dill, Isabelle Duband‐Goulet, Éva Cabet, Brigitte Buendia, Alain Lilienbaum, John Rendu, Marie Christine Minot, Agnès Guichet, Valérie Allamand, Nathalie Vadrot, Julien Fauré, Sylvie Odent, Leïla Lazaro, Jean Paul Leroy, Pascale Marcorelles, O. Dubourg, Ana Ferreiro	2016	17

About Agnès Guichet

Agnès Guichet is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 42 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (10 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital Anomalies and Fetal Surgery (6 papers), Mitochondrial Function and Pathology (6 papers), RNA modifications and cancer (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). The work is most often cited by research in Clinical Biochemistry (129 citations), Genetics (469 citations), Molecular Biology (777 citations), Pediatrics, Perinatology and Child Health (204 citations) and Urology (42 citations). Agnès Guichet has collaborated with scholars based in France, United States and Morocco. Frequent co-authors include Dominique Bonneau, Patrizia Amati‐Bonneau, Pascal Reynier, Guy Lenaers, Arnaud Chevrollier, Yves Malthièry, Pascale Belenguer, Aurélien Olichon, Annick Toutain and R. Coutant. Their work appears in journals such as Prenatal Diagnosis, European Journal of Human Genetics, European Journal of Medical Genetics, The Journal of Clinical Endocrinology & Metabolism and The Journal of Maternal-Fetal & Neonatal Medicine.

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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Agnès Guichet

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