Sylvie Odent

14.0k citations

152 papers · 3.8k indexed · h-index 36

Impact in

Developmental Biology top 2%
Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Cleft Lip and Palate Research

Papers in

Developmental Biology 8
Genetics 84
- Genomic variations and chromosomal abnormalities 33
- Genetic Syndromes and Imprinting 12
- Genetics and Neurodevelopmental Disorders 11

Co-authors: Christèle Dubourg Véronique David Laurent Pasquier Claude Bendavid Martine Blayau Dominique Bonneau B. Le Marec Sandra Mercier
Journals: European Journal of Medical Genetics (13 papers)Human Mutation (10 papers)Journal of Medical Genetics (6 papers)Prenatal Diagnosis (6 papers)Human Genetics (6 papers)
Partner nations: France United States Italy

In The Last Decade

Sylvie Odent

144 papers receiving 3.8k citations

Peers

Countries citing papers authored by Sylvie Odent

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Odent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Pathogenic variants affecting the TB5 domain of the fibrillin-1 protein: not only in geleophysic/acromicric dysplasias but also in Marfan syndrome Journal of Medical Genetics ·Pauline Arnaud, Zakaria Mougin, Geneviève Baujat, Valérie Drouin‐Garraud, Salima El Chehadeh, Laurent Gouya, Sylvie Odent, Guillaume Jondeau, Cathérine Boileau, Nadine Hanna, Carine Le Goff	2024	0
2	Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility Acta Obstetricia Et Gynecologica Scandinavica ·Auriane Cospain, Ludivine Dion, Maud Bidet, Krystel Nyangoh Timoh, Chloé Quēlin, Isis Carton, Alinoë Lavillaureix, Karine Morcel, Paul Rollier, Laurent Pasquier, Bénédicte Nouyou, Sylvie Odent, Daniel Guerrier, Erika Launay, Marc‐Antoine Belaud Rotureau, Mélanie Fradin, Sylvie Jaillard, Vincent Lavoué	2024	0
3	Gene Editing Corrects In Vitro a G > A GLB1 Transition from a GM1 Gangliosidosis Patient The CRISPR Journal ·Delphine Leclerc, Louise Goujon, Sylvie Jaillard, Bénédicte Nouyou, Laurence Cluzeau, Léna Damaj, Christèle Dubourg, Amandine Etcheverry, Thierry Levade, Roseline Froissart, Stéphane Dréano, X. Guillory, Leif A. Eriksson, Erika Launay, F. Mouriaux, Marc‐Antoine Belaud‐Rotureau, Sylvie Odent, David Gilot	2023	2
4	PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect European Journal of Medical Genetics ·Silvestre Cuinat, Chloé Quēlin, Laurent Pasquier, Philippe Loget, Dominique Aussel, Sylvie Odent, Annie Laquerrière, Maïa Proisy, Sylvie Mazoyer, Marion Delous, Patrick Edery, Nicolas Chatron, Gaëtan Lesca, Audrey Putoux	2023	0
5	Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization Biological Psychiatry ·Vittoria Mariano, Alexandros K. Kanellopoulos, Claudia Ricci, Daniele Di Marino, Sarah C. Borrie, Sebastián Dupraz, Frank Bradke, Tilmann Achsel, Eric Legius, Sylvie Odent, Pierre Billuart, Thierry Bienvenu, Claudia Bagni	2023	7
6	Skraban‐Deardorff syndrome: Six new cases of WDR 26 ‐related disease and expansion of the clinical phenotype Clinical Genetics ·Auriane Cospain, Élise Schaefer, Marie Faoucher, Christèle Dubourg, Wilfrid Carré, Varoona Bizaoui, Jessica Assoumani, Lionel Van Maldergem, Amélie Piton, Bénédicte Gérard, Frédéric Tran Mau‐Them, Ange‐Line Bruel, Laurence Faivre, Florence Démurger, Laurent Pasquier, Sylvie Odent, Mélanie Fradin, Alinoë Lavillaureix	2021	4
7	Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility Maturitas ·Sylvie Jaillard, Rajini Sreenivasan, Marion Beaumont, Gorjana Robevska, Christèle Dubourg, Ingrid Knarston, Linda Akloul, Jocelyn van den Bergen, Sylvie Odent, Brittany Croft, G Jouve, Sonia Grover, Solène Duros, Céline Pimentel, Marc‐Antoine Belaud‐Rotureau, Katie Ayers, Célia Ravel, Elena J. Tucker, Andrew Sinclair	2019	26
8	Primal health research in the age of epigenetic clocks Medical Hypotheses ·Sylvie Odent, Michel Odent	2019	3
9	Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis American Journal of Medical Genetics Part A ·Chloé Quēlin, Philippe Loget, Lucile Boutaud, Nadia Elkhartoufi, J Milon, Sylvie Odent, Mélanie Fradin, Florence Démurger, Laurent Pasquier, Sophie Thomas, Tania Attié‐Bitach	2018	11
10	A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis Acta Neuropathologica Communications ·Myriam Vézain, Matthieu Lecuyer, Marina Rubio, Valérie Dupé, Leslie Ratié, Véronique David, Laurent Pasquier, Sylvie Odent, Sophie Coutant, Isabelle Tournier, Laetitia Trestard, Homa Adle‐Biassette, Denis Vivien, Thierry Frébourg, Bruno J. Gonzalez, Annie Laquerrière, Pascale Saugier-Véber	2018	16
11	Ultrasound Presentation of a Disseminated Fetal and Neonatal Rhabdoid Tumor Case Reports in Obstetrics and Gynecology ·Yolaine Joueidi, Aline Rousselin, C. Rozel, Philippe Loget, Dominique Ranchère Vince, Sylvie Odent, Franck Bourdeaut, Vincent Lavoué, Maëla Le Lous	2018	1
12	FG syndrome: The FGS2 locus revisited American Journal of Medical Genetics Part A ·Olivier Perche, Béatrice Laudier, Arnaud Menuet, Sylvie Odent, Frédéric Laumonnier, Sylvain Briault	2012	3
13	Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus European Journal of Human Genetics ·Jamal Ghoumid, Joris Andrieux, Bernard Sablonnière, Sylvie Odent, N Philippe, Xavier Zanlonghi, Pascale Saugier-Véber, Thomas Bardyn, Sylvie Manouvrier‐Hanu, Muriel Holder‐Espinasse	2011	6
14	Diagnosis of fetal urinary tract malformations: prenatal management and postnatal outcome Prenatal Diagnosis ·A. Ryckewaert‐D'Halluin, G. Le Bouar, Sylvie Odent, J Milon, Dominique D’Hervé, Josette Lucas, Florence Rouget, Philippe Loget, P. Poulain, E. Le Gall, Sophie Taque	2011	6
15	Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci Human Mutation ·Claude Bendavid, Lucie Rochard, ChristÃ ̈le Dubourg, Jonathan Séguin, Isabelle Gicquel, Laurent Pasquier, Jaqueline Vigneron, Annie LaquerriÃ ̈re, Pascale Marcorelles, Corinne Jeanne‐Pasquier, Caroline Rouleau, Sylvie Jaillard, Jean Mosser, Sylvie Odent, Véronique David	2009	35
16	Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis Neuromuscular Disorders ·Kathrin Huehne, Christiane Zweier, K Raab, Sylvie Odent, Martine Bonnaure‐Mallet, Jean-louis Sixou, P. Landrieu, Cyril Goizet, J Sarlangue, Matthias Baumann, Thomas Eggermann, Anita Rauch, Sinje Ruppert, Georg M. Stettner, Bernd Rautenstrauß	2008	29
17	Functional Characterization of Sonic Hedgehog Mutations Associated with Holoprosencephaly Journal of Biological Chemistry ·Élisabeth Traiffort, Christèle Dubourg, Hélène Faure, Didier Rognan, Sylvie Odent, Marie‐Renée Durou, Véronique David, Martial Ruat	2004	60
18	X‐linked Opitz syndrome: Novel mutations in the MID1 gene and redefinition of the clinical spectrum American Journal of Medical Genetics Part A ·Francesca De Falco, Silvia Cainarca, Grazia Andolfi, Rosa Ferrentino, Caterina Berti, Germán Rodríguez Criado, Olaf Rittinger, N R Dennis, Sylvie Odent, Amit Rastogi, Jan Liebelt, David Chitayat, Robin Winter, Harindar Jawanda, Andrea Ballabio, Brunella Franco, Germana Meroni	2003	72
19	Chromosome 20 en anneau et épilepsie : diversité des crises étudiées en vidéo-EEG. Un mécanisme sous-cortical d’épileptogenèse est-il au premier plan ? A. Biraben, Sylvie Odent, J. Lucas, K. Michez, Fanny Lemée, Carole Henry, Catherine Le Berre, Nathalie De Grissac, Augustin Bernard, Jean‐Marie Scarabin	2001	2
20	Ring chromosome 20 and epilepsy: diversity of seizures presented by the patients as studied in video-EEG study. Is a subcortical dysfunctionning mainly involved in the epileptogenesis? Arnaud Biraben, Sylvie Odent, John C Lucas, K. Michez, F. Lemée, C. E. Henry, Catherine Le Berre, Nathalie De Grissac, A. Bernard, Jean‐Marie Scarabin	2001	1

About Sylvie Odent

Sylvie Odent is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Clinical Biochemistry, having authored 152 papers that have together received 3.8k indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (34 papers), Genomic variations and chromosomal abnormalities (33 papers), Prenatal Screening and Diagnostics (18 papers), Congenital heart defects research (14 papers), Genetic Syndromes and Imprinting (12 papers), Epigenetics and DNA Methylation (12 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Fetal and Pediatric Neurological Disorders (10 papers). The work is most often cited by research in Developmental Biology (151 citations), Genetics (1.5k citations), Molecular Biology (2.7k citations), Genetics (350 citations) and Pediatrics, Perinatology and Child Health (562 citations). Sylvie Odent has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Christèle Dubourg, Véronique David, Laurent Pasquier, Claude Bendavid, Martine Blayau, Dominique Bonneau, B. Le Marec, Sandra Mercier, Hélène Dollfus and Philippe Loget. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Journal of Medical Genetics, Prenatal Diagnosis and Human Genetics.

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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