Odile Boute

4.9k citations

88 papers · 3.7k · h-index 30

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cleft Lip and Palate Research
- Connective tissue disorders research
Developmental Biology top 5%

Papers in

Genetics 55
- Genomic variations and chromosomal abnormalities 19
- Genomics and Rare Diseases 16
- Genetics and Neurodevelopmental Disorders 14
- Connective tissue disorders research 8
- Cleft Lip and Palate Research 6
Pediatrics, Perinatology and Child Health 16
- Prenatal Screening and Diagnostics 9
- Fetal and Pediatric Neurological Disorders 6

Co-authors: Sylvie Manouvrier (12 shared papers)Emmanuel Jacquemin (1 shared paper)Michelle Hadchouel (1 shared paper)Danièle Cresteil (1 shared paper)Nicole Revençu (3 shared papers)Didier Lacombe (2 shared papers)Raphaël Helaers (1 shared paper)Bernard Devauchelle (1 shared paper)
Journals: Clinical Genetics (11 papers)European Journal of Human Genetics (9 papers)Genetics in Medicine (7 papers)European Journal of Medical Genetics (7 papers)The American Journal of Human Genetics (4 papers)
Partner nations: France United States Netherlands

In The Last Decade

Odile Boute

86 papers receiving 3.5k citations

Peers

Countries citing papers authored by Odile Boute

Since Specialization

Citations

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

Fields of papers citing papers by Odile Boute

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Odile Boute, 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 Odile Boute Line = papers co-authored together Odile Boute 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 88 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 Nature ·Robin G. Walters, Sébastien Jacquemont, Armand Valsesia, Adam J. de Smith, Danielle Martinet, Johanna C. Andersson‐Assarsson, Mario Falchi, Fei Chen	2010	420
2	Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Nature ·Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G. Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen	2011	372
3	Heterozygous non-sense mutation of the MDR3 gene in familial intrahepatic cholestasis of pregnancy The Lancet ·Emmanuel Jacquemin, Danièle Cresteil, Sylvie Manouvrier, Odile Boute, Michelle Hadchouel	1999	303
4	Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients Human Mutation ·Gijs W.E. Santen, Emmelien Aten, Anneke T. Vulto‐van Silfhout, Caroline Pottinger, Bregje W.M. van Bon, Ivonne J.H.M. van Minderhout, Ronelle Snowdowne, Christian A.C. van der Lans	2013	177
5	Stickler syndrome caused by COL2A1 mutations: genotype–phenotype correlation in a series of 100 patients European Journal of Human Genetics ·Kristien Hoornaert, Inge Vereecke, Chantal Dewinter, Thomas Rosenberg, Frits A. Beemer, Jules G. Leroy, Laila Bendix, Erik Björck	2010	114
6	Delineation of 15q13.3 microdeletions Clinical Genetics ·Alice Masurel‐Paulet, Joris Andrieux, Patrick Callier, J.M. Cuisset, Cédric Le Caignec, Muriel Holder, Christel Thauvin‐Robinet, Bérénice Doray	2010	111
7	Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases European Journal of Medical Genetics ·Caroline Schluth‐Bolard, Bruno Delobel, Damien Sanlaville, Odile Boute, Jean‐Marie Cuisset, Sylvie Sukno, Audrey Labalme, Bénédicte Duban‐Bedu	2009	109
8	Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome Genetics in Medicine ·Renata Lúcia Leite Ferreira de Lima, Sarah A. Hoper, Michella Ghassibe‐Sabbagh, Margaret E. Cooper, Nicholas K. Rorick, Shinji Kondo, Lori Katz, Mary L. Marazita	2009	107
9	Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing Genetics in Medicine ·Paul Kuentz, Judith St‐Onge, Yannis Duffourd, Jean‐Benoît Courcet, Virginie Carmignac, Thibaud Jouan, Arthur Sorlin, Claire Abasq‐Thomas	2017	93
10	Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures The American Journal of Human Genetics ·Jeanne Amiel, Yolanda Espinosa‐Parrilla, Julie Steffann, Philippe Gosset, Anna Pelet, Marguerite Prieur, Odile Boute, Agnès Choiset	2001	92
11	15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients European Journal of Medical Genetics ·Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent‐Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder‐Espinasse, Bruno Delobel	2015	88
12	BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects European Journal of Human Genetics ·Emma N. Hilton, Jennifer J. Johnston, Sandra Whalen, Nobuhiko Okamoto, Yoshikazu Hatsukawa, Juntaro NISHIO, Hiroshi Kohara, Yoshiko Hirano	2009	84
13	New insights into genotype–phenotype correlation for GLI3 mutations European Journal of Human Genetics ·Florence Démurger, Amale Ichkou, Soumaya Mougou-Zerelli, Martine Le Merrer, Géraldine Goudefroye, Anne‐Lise Delezoide, Chloé Quēlin, Sylvie Manouvrier	2014	84
14	Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes Journal of Medical Genetics ·M. H. Basha, Bénédicte Demeer, Nicole Revençu, Raphaël Helaers, Stéphanie Theys, Sami Bou Saba, Odile Boute, Bernard Devauchelle	2018	78
15	Phenotypic Spectrum of Simpson– G olabi– B ehmel Syndrome in a Series of 42 Cases With a Mutation in GPC 3 and Review of the Literature American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Edouard Cottereau, Isabelle Mortemousque, Marie‐Pierre Moizard, Lydie Bürglen, Didier Lacombe, Brigitte Gilbert‐Dussardier, Sabine Sigaudy, Odile Boute	2013	78
16	Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature Human Mutation ·Bert Louis Callewaert, Bart Loeys, Anna Ficcadenti, Sascha Vermeer, Magnus Landgren, Hester Y. Kroes, Yuval Yaron, Michael Pope	2008	76
17	Frontometaphyseal dysplasia: Mutations in FLNA and phenotypic diversity American Journal of Medical Genetics Part A ·Stephen P. Robertson, Zandra A. Jenkins, Timothy Morgan, Lesley C. Adès, Salim F. Aftimos, Odile Boute, Torunn Fiskerstrand, Sixto García‐Miñaúr	2006	67
18	Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases Clinical Genetics ·Sarah Baer, Alexandra Afenjar, Thomas Smol, Amélie Piton, Bénédicte Gérard, Yves Alembik, Thierry Bienvenu, Guilaine Boursier	2018	65
19	Interstitial 22q13 deletions not involving SHANK3 gene: A new contiguous gene syndrome American Journal of Medical Genetics Part A ·Vittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Mafalda Mucciolo, Annabella Marozza, Chiara F. Di Marco, Antonio Massarelli, Valentina Canocchi	2014	63
20	Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization Human Mutation ·Frédéric Brioude, Irène Netchine, Françoise Praz, Marilyne Le Jule, Claire Calmel, Didier Lacombe, Patrick Edery, Martin Catala	2015	59

About Odile Boute

Odile Boute is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Developmental Biology, having authored 88 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genomics and Rare Diseases (16 papers), Genetics and Neurodevelopmental Disorders (14 papers), Prenatal Screening and Diagnostics (9 papers), Connective tissue disorders research (8 papers), Fetal and Pediatric Neurological Disorders (6 papers), Congenital heart defects research (6 papers) and Cleft Lip and Palate Research (6 papers). The work is most often cited by research in Genetics (2.1k citations), Developmental Biology (50 citations), Pediatrics, Perinatology and Child Health (389 citations), Molecular Biology (1.4k citations) and Genetics (190 citations). Odile Boute has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Sylvie Manouvrier, Emmanuel Jacquemin, Michelle Hadchouel, Danièle Cresteil, Nicole Revençu, Didier Lacombe, Raphaël Helaers, Bernard Devauchelle, Miikka Vikkula and Nicole Philip. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Genetics in Medicine, European Journal of Medical Genetics and The American Journal of 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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