Sylvie Odent

1.2k total citations
15 papers, 512 citations indexed

About

Sylvie Odent is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Sylvie Odent has authored 15 papers receiving a total of 512 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Sylvie Odent's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Sylvie Odent is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Sylvie Odent collaborates with scholars based in France, Australia and Belgium. Sylvie Odent's co-authors include Laurent Pasquier, Christèle Dubourg, Claude Bendavid, Véronique David, Cathérine Henry, Laurence Faivre, Florence Coulet, Sophie Rivière, Sophie Giraud and Marie‐France Carette and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and Journal of Neurology.

In The Last Decade

Sylvie Odent

11 papers receiving 493 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-authorship network of co-authors of Sylvie Odent

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Bone mineral density in French adults with early-treated phenylketonuria 2025 ·Molecular Genetics and Metabolism ·(unknown), F. Maillot, (unknown), Alain Fouilhoux, L. Astudillo, Christian Lavigne, (unknown), Sylvie Odent, Claire Gay, Manuel Schiff, K. Mazodier, Alice Kuster, (unknown), (unknown), V. Leguy‐Seguin, Claire Douillard, Sybil Charrière	0
2	Neuropsychological profile of French adults with early-treated phenylketonuria: a multicenter study 2024 ·Journal of Neurology ·(unknown), Sybil Charrière, Claire Douillard, (unknown), Alain Fouilhoux, L. Astudillo, Christian Lavigne, (unknown), Sylvie Odent, Claire Gay, Manuel Schiff, K. Mazodier, Alice Kuster, (unknown), (unknown), V. Leguy‐Seguin, Valérie Gissot, F. Maillot	0
3	Identification and Characterization of Novel FSHR Copy Number Variations Causing Premature Ovarian Insufficiency 2024 ·American Journal of Medical Genetics Part A ·(unknown), Anne Bergougnoux, Nadège Servant, Linda Akloul, Erika Launay, (unknown), (unknown), (unknown), (unknown), (unknown), Sylvie Odent, Elena J. Tucker, Françoise Paris, Marc‐Antoine Belaud‐Rotureau, (unknown)	0
4	Expanding the TUBB3‐Related Phenotypic Landscape: Fetal Diagnosis of Novel TUBB3 Variant Linked With Phenotypic Variability Within a Single Family 2024 ·Prenatal Diagnosis ·(unknown), Chloé Quēlin, C. Rozel, Wilfrid Carré, (unknown), Sylvie Odent, (unknown)	0
5	Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age 2023 ·Journal of Clinical Medicine ·Jean Sénémaud, Marine Gaudry, Élisabeth Jouve, Arnaud Blanchard, Olivier Milleron, Yves Dulac, Laurence Olivier-Faivre, Dominique Stéphan, Sylvie Odent, Damien Lanéelle, Sophie Dupuis‐Girod, Guillaume Jondeau, (unknown)	1
6	Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia 2019 ·Cytogenetic and Genome Research ·(unknown), Elena J. Tucker, (unknown), Erika Launay, (unknown), (unknown), (unknown), Linda Akloul, Claire Bénéteau, (unknown), (unknown), Olivier Pichon, Célia Ravel, Sylvie Odent, Marc‐Antoine Belaud‐Rotureau, Sylvie Jaillard	3
7	New insights into the pathogenesis of beckwith-wiedemann and silver-russell syndromes: Contribution of small copy number variations to 11p15 imprinting defects 2011 ·Human Mutation ·Julie Demars, Sylvie Rossignol, Irène Netchine, (unknown), (unknown), Laurence Faivre, Jacques Weill, Sylvie Odent, Salah Azzi, Patrick Callier, Josette Lucas, Christèle Dubourg, Joris Andrieux, Yves Le Bouc, Assam El‐Osta, Christine Gicquel	45
8	Holoprosencephaly 2007 ·Orphanet Journal of Rare Diseases ·Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Cathérine Henry, Sylvie Odent, Véronique David	234
9	Molecular screening ofALK1/ACVRL1andENGgenes in hereditary hemorrhagic telangiectasia in France 2004 ·Human Mutation ·Gaëtan Lesca, Henri Plauchu, Florence Coulet, Sylvain Lefèbvre, Ghislaine Plessis, Sylvie Odent, Sophie Rivière, Bruno Leheup, Cyril Goizet, Marie‐France Carette, Jean-François Cordier, S. Pinson, Florent Soubrier, Alain Calender, Sophie Giraud	91
10	Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature 2002 ·European Journal of Human Genetics ·Laurence Faivre, Philippe Gosset, Valérie Cormier‐Daire, Sylvie Odent, Jeanne Amiel, Irina Giurgea, Marie‐Cécile Nassogne, Laurent Pasquier, Arnold Münnich, Serge Romana, Marguerite Prieur, Michel Vekemans, Marie‐Christine de Blois, C Turleau	58
11	Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]? 2000 ·American Journal of Medical Genetics ·Sylvain Briault, Laurent Villard, Ute C. Rogner, Johannes Coy, Sylvie Odent, Josette Lucas, E. Passage, Danping Zhu, Antony E. Shrimpton, Marcus Pembrey, Marianne Till, (unknown), (unknown), Michel Fontés, Annemarie Poustka, Claude Moraine	18
12	1q32-q41 microdeletion with reference to van der Woude syndrome and allied clefting entities 2000 ·American Journal of Medical Genetics ·Claude Houdayer, (unknown), (unknown), Marie‐Paule Vazquez, Sylvie Odent, Didier Lacombe, Yves Le Bouc, Arnold Münnich, Michel Bahuau	10
13	Mapping of a Congenital Microcoria Locus to 13q31-q32 1998 ·The American Journal of Human Genetics ·Christelle Rouillac, (unknown), Dominique Marchant, Lucien Bachner, Alexandra Kobetz, (unknown), Christophe Orssaud, (unknown), Sylvie Odent, B. Le Marec, Marc Abitbol, Jean-Louis Dufier	15
14	Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis 1998 ·Human Mutation ·Pascale Saugier-Véber, Cosette Martin, Nathalie Le Meur, Stanislas Lyonnet, Arnold Munnich, Albert David, (unknown), Delphine Héron, Philippe Jonveaux, Sylvie Odent, Sylvie Manouvrier, Anne Moncla, Nicole Morichon, Nicole Philip, Daniel Satgé, Mario Tosi, Thierry Frébourg	22
15	Opitz GBBB syndrome: Chromosomal evidence of an X‐linked form 1995 ·American Journal of Medical Genetics ·Alain Verloès, Albert David, Sylvie Odent, Annick Toutain, (unknown), Josette Lucas, B. Le Marec	15

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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