Fabien Guimiot

1.0k total citations
37 papers, 475 citations indexed

About

Fabien Guimiot is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Genetics. According to data from OpenAlex, Fabien Guimiot has authored 37 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pediatrics, Perinatology and Child Health, 11 papers in Surgery and 9 papers in Genetics. Recurrent topics in Fabien Guimiot's work include Prenatal Screening and Diagnostics (7 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Pediatric Urology and Nephrology Studies (5 papers). Fabien Guimiot is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Pediatric Urology and Nephrology Studies (5 papers). Fabien Guimiot collaborates with scholars based in France, Switzerland and Italy. Fabien Guimiot's co-authors include Anne‐Lise Delezoide, Robert P. Millar, Catherine Fallet‐Bianco, Luís Teixeira, Catherine Dodé, Jean‐Pierre Hardelin, J.-F. Oury, Suonavy Khung‐Savatovsky, Emmanuel Spaggiari and Céline Dupont and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

Fabien Guimiot

37 papers receiving 451 citations

Peers

Countries citing papers authored by Fabien Guimiot

Since Specialization

Citations

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

Fields of papers citing papers by Fabien Guimiot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabien Guimiot

This figure shows the co-authorship network connecting the top 25 collaborators of Fabien Guimiot. A scholar is included among the top collaborators of Fabien Guimiot 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 Fabien Guimiot. Fabien Guimiot 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

#	Work	Indexed citations
1	SARS‐CoV ‐2 infection as cause of in‐utero fetal death: regional multicenter cohort study 2023 ·Ultrasound in Obstetrics and Gynecology ·(unknown), M. Leruez‐Ville, Tiffany Guilleminot, (unknown), (unknown), Fabien Guimiot, (unknown), (unknown), Y. Ville, Valentine Faure‐Bardon	5
2	Tonate Virus and Fetal Abnormalities, French Guiana, 2019 2022 ·Emerging infectious diseases ·Véronique Lambert, Antoine Enfissi, Mathilde Lefebvre, Léo Pomar, (unknown), Fabien Guimiot, Gabriel Carles, Anne Lavergne, Dominique Rousset, Najeh Hcini	7
3	Feasibility of a fetal anatomy 3D atlas by computer-assisted anatomic dissection 2020 ·Journal of Gynecology Obstetrics and Human Reproduction ·Vincent Balaya, Fabien Guimiot, Matthieu Bruzzi, Salma El Batti, Alexis Guédon, (unknown), Jean‐Marc Chevallier, Richard Douard, Jean-François Uhl	3
4	EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder 2018 ·Clinical Genetics ·Jonathan Lévy, Damien Haye, Nicola Marziliano, Gavino Casu, Fabien Guimiot, Céline Dupont, N. Teissier, Brigitte Benzacken, Pierre Gressèns, Eva Pipiras, Alain Verloès, Anne‐Claude Tabet	19
5	TRAP Sequence in Monochorionic/Monoamniotic (MC/MA) Discordant Twins: Two Cases Treated with Fetoscopic Laser Surgery 2018 ·Fetal and Pediatric Pathology ·Gabriele Tonni, Gianpaolo Grisolia, (unknown), Federico Prefumo, A. Fichera, Maria Paola Bonasoni, Mathilde Lefebvre, Suonavy Khung‐Savatovsky, Fabien Guimiot, Jonathan Rosenblatt, Edward Araujo Júnior	7
6	Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in EFEMP2 2018 ·Molecular Syndromology ·(unknown), Dorien Schepers, Juliette Albuisson, Patrick Bruneval, Emmanuel Spaggiari, Gerarda van de Beek, Suonavy Khung‐Savatovsky, N. Belarbi, Yline Capri, Anne‐Lise Delezoide, Bart Loeys, Fabien Guimiot	4
7	Three-Dimensional Modelization of the Female Human Inferior Hypogastric Plexus: Implications for Nerve-Sparing Radical Hysterectomy 2018 ·Gynecologic and Obstetric Investigation ·Vincent Balaya, Fabien Guimiot, Jean-François Uhl, Charlotte Ngô, Myriam Deloménie, Hélène Bonsang‐Kitzis, (unknown), (unknown), Anne‐Sophie Bats, V. Delmas, Richard Douard, Fabrice Lécuru	5
8	Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome 2017 ·American Journal of Medical Genetics Part A ·Jonathan Lévy, Aurélie Coussement, Céline Dupont, Fabien Guimiot, Clarisse Baumann, Géraldine Viot, Sandrine Passemard, Yline Capri, Séverine Drunat, Alain Verloès, Eva Pipiras, Brigitte Benzacken, Jean‐Michel Dupont, Anne‐Claude Tabet	15
9	Mowat–Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: Advocacy for standard autopsy 2013 ·European Journal of Medical Genetics ·Emmanuel Spaggiari, Clarisse Baumann, Marianne Alison, Jean‐François Oury, N. Belarbi, Céline Dupont, Fabien Guimiot, Anne‐Lise Delezoide	13
10	Management strategy in pregnancies with elevated second-trimester maternal serum alpha-fetoprotein based on a second assay 2013 ·American Journal of Obstetrics and Gynecology ·Emmanuel Spaggiari, (unknown), Sophie Dreux, (unknown), Isabelle Czerkiewicz, Fabien Guimiot, Thomas Schmitz, Anne‐Lise Delezoide, Françoise Müller	12
11	Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene 2012 ·American Journal of Medical Genetics Part A ·Andrée Delahaye‐Duriez, Suonavy Khung‐Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean‐Luc Alessandri, Marion Gérard, Pierre Bitoun, (unknown), Stéphanie Robin, C. Huel, (unknown), Stéphane Serero, Pierre Gressèns, Jacques Élion, Alain Verloès, Brigitte Benzacken, Anne‐Lise Delezoide, Eva Pipiras	37
12	Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre–Chotzen syndrome 2012 ·European Journal of Medical Genetics ·Emmanuel Spaggiari, Azzedine Aboura, Martine Sinico, (unknown), Céline Dupont, Anne‐Lise Delezoide, Fabien Guimiot	4
13	3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome 2011 ·Clinical Genetics ·Céline Dupont, Fabien Guimiot, Laurence Perrin, Isabelle Marey, (unknown), Dominique Le Tessier, (unknown), Clarisse Baumann, Pierre Bourdoncle, (unknown), Azzedine Aboura, Brigitte Benzacken, Jean‐Michel Dupont	9
14	Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions 2010 ·Journal of Clinical Investigation ·Luís Teixeira, Fabien Guimiot, Catherine Dodé, Catherine Fallet‐Bianco, Robert P. Millar, Anne‐Lise Delezoide, Jean‐Pierre Hardelin	68
15	Abnormal muscle development of the diaphragm in a fetus with 2p14–p16 duplication 2009 ·American Journal of Medical Genetics Part A ·(unknown), Fabien Guimiot, Anne‐Claude Tabet, Suonavy Khung‐Savatovsky, (unknown), (unknown), Brigitte Benzacken, Alain Verloès, Jean‐François Oury, Anne‐Lise Delezoide, Azzedine Aboura	3
16	mRNA Expression of MDR1 and Major Metabolising Enzymes in Human Fetal Tissues 2009 ·Drug Metabolism and Pharmacokinetics ·May Fakhoury, (unknown), Fabien Guimiot, (unknown), Valery Élie, Yves Médard, Anne‐Lise Delezoide, Évelyne Jacqz-Aigrain	21
17	Very Early Twin-to-Twin Transfusion Syndrome and Discordant Activation of the Renin–Angiotensin System 2009 ·Placenta ·(unknown), Sophie Patrier, Marie-Claire Gübler, Delphine Lemercier, Fabien Guimiot, Marc Dommergues	5
18	Quantitative evaluation of collagen type VI and SOD gene expression in the nuchal skin of human fetuses with trisomy 21 2007 ·Prenatal Diagnosis ·E. Quarello, Fabien Guimiot, Jean‐Marie Moalic, (unknown), Y. Ville, Anne‐Lise Delezoide	9
19	Contribution of Diffusion-Weighted Imaging in the Evaluation of Diffuse White Matter Ischemic Lesions in Fetuses: Correlations with Fetopathologic Findings 2007 ·American Journal of Neuroradiology ·Fabien Guimiot, Cathérine Garel, (unknown), (unknown), Suonavy Khung‐Savatovsky, J.-F. Oury, G. Sebag, A. L. Delezoide	42
20	Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus 2006 ·The Journal of Clinical Endocrinology & Metabolism ·Gabor Szinnai, Ludovic Lacroix, Aurore Carré, Fabien Guimiot, Monique Talbot, Jelena Martinović, Anne‐Lise Delezoide, Michel Vekemans, Stefan Michiels, Bernard Caillou, Martin Schlumberger, Jean‐Michel Bidart, Michel Polak	49

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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