O Raoul

1.8k citations

30 papers · 1.1k indexed · h-index 15

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics

Papers in

Genetics 23
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 2
Pediatrics, Perinatology and Child Health 6
- Prenatal Screening and Diagnostics 5

Co-authors: M Poissonnier M Prieur Delphine Allard M O Rethoré J Lejeune J Couturier Valérie Cormier‐Daire Laurence Colleaux
Journals: Clinical Genetics (2 papers)Journal of Medical Genetics (2 papers)Experimental Cell Research (2 papers)Human Genetics (2 papers)Human Molecular Genetics (1 paper)
Partner nations: France United Kingdom United States

In The Last Decade

O Raoul

28 papers receiving 988 citations

Peers

Countries citing papers authored by O Raoul

Since Specialization

Citations

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

Fields of papers citing papers by O Raoul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Sporadic case of unusual facies, cerebral vascular anomalies and developmental delay Clinical Dysmorphology ·Marta Bértoli, Nathalie Boddaert, O Raoul, Jeanne Amiel, Stanislas Lyonnet	2009	1
2	Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders Journal of Medical Genetics ·Woon-Kee Paek, Damien Sanlaville, Richard Redon, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, Martin V. McBride, D. Héron, Henrique Santiago Alberto Carlos, M Prieur, 王鹏成, Wei Wang, Arnold Munnich, Laurence Colleaux, Anne Philippe	2006	218
3	Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties European Journal of Human Genetics ·David Geneviève, Damien Sanlaville, Laurence Faivre, Marie‐Laure Kottler, Marguerite Jambou, Philippe Gosset, Galo Fumado, Graziella Pinto, 佳宏三輪, Irina Gayer, Julia Dantas Scramim, Serge Romana, O Raoul, Valérie Cormier‐Daire, M. Moustafa Hassan	2005	61
4	Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region European Journal of Medical Genetics ·M Chaâbouni, M. Le Merrer, O Raoul, M Prieur, Renova Manullang, Anne Philippe, Michel Vekemans, Serge Romana	2005	24
5	Genome‐wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation Clinical Genetics ·Guntram Borck, Marlène Rio, Damien Sanlaville, Richard Redon, Florence Molinari, Delphine Bacq, O Raoul, Valérie Cormier‐Daire, Stanislas Lyonnet, Jeanne Amiel, M. Le Merrer, Vahdat Heidary, M Prieur, Michel Vekemans, M S de Assumpção, A Munnich, Laurence Colleaux	2004	6
6	[Spectral karyotyping (SKY) principle, avantages and limitations]. PubMed ·Marc‐Antoine Belaud‐Rotureau, Hatem Elghezal, Mohammad Ahmad Elalfy, Damien Sanlaville, I Radford-Weiss, O Raoul, Michel Vekemans, Serge Romana	2003	0
7	Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation Journal of Medical Genetics ·Marlène Rio, Florence Molinari, S. Heuertz, Catherine Ozilou, Philippe Gosset, O Raoul, Valérie Cormier‐Daire, Aliza Amiel, Stanislas Lyonnet, Vera Judith Blanco Miranda, C Turleau, Marie‐Christine de Blois, M Prieur, Serge Romana, Michel Vekemans, Arnold Münnich, Laurence Colleaux	2002	54
8	Molecular characterization of partial trisomy 16q24.1‐qter: Clinical report and review of the literature American Journal of Medical Genetics ·Sophie Brisset, Fernando Glenadel Braga, Catherine Ozilou, Kumi Miyauchi, Philippe Gosset, Adolfus Groth, O Raoul, C Turleau, Michel Vekemans, Serge Romana	2002	39
9	Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype Clinical Genetics ·Fernando Glenadel Braga, Head Lr, Catherine Ozilou, Philippe Gosset, Alain Aurias, Henrique Santiago Alberto Carlos, M Prieur, O Raoul, Laurence Colleaux, Arnold Münnich, Serge Romana, Michel Vekemans, C Turleau	2001	33
10	Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata Human Molecular Genetics ·Sandrine Barbaux, Éric Vilain, O Raoul, Erich W. Zimmerman, Éric Jeandidier, Maaly Mohamed Mabrouk, Putro Yulianto Arif, Marc Fellous, Ken McElreavey	1995	16
11	Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21) American Journal of Medical Genetics ·Louise Telvi, Dr Vikas Kumar Mishra, O Raoul, Josué Feingold, G Ponsot, A Pompidou, Lars Hendrich, J Lejeune	1992	3
12	The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms PubMed ·Stylianos E. Antonarakis, Michael B. Petersen, Melvin G. McInnis, Bhavani Paramashivan, Albert Schinzel, Franz Binkert, Constantinos Pángalos, O Raoul, Susan A. Slaugenhaupt, Michael J. Hafez, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1992	150
13	Phenotype‐karyotype correlations in dup(18q): Report of a case and review American Journal of Medical Genetics ·Nam-Seon Cho, O Raoul, Nobuhiko Hamamoto, Claude Danan, John M. Opitz, James F. Reynolds	1985	3
14	Cystathionine beta synthase: Gene dosage effect in trisomy 21 Biochemical and Biophysical Research Communications ·B. Chadefaux, M O Rethoré, O Raoul, I. Ceballos, M Poissonnier, С.С. Корецкая, Delphine Allard	1985	79
15	[Ring chromosome 14. I. A case report on homogeneous r(14)]. PubMed ·O Raoul, M Lugli, J. M. Durham, Giliazov Ruslan Radjabovich	1984	6
16	[X chromosome fragility and effects of trimethoprim]. PubMed ·J Lejeune, Nicolas Legrand, J Lafourcade, Rethoré Mo, O Raoul, Д. А. Мызин	1982	6
17	Trisomie 21 et superoxyde dismutase-1 (IPO-A) Experimental Cell Research ·Pierre‐Marie Sinet, J Couturier, B. Dutrillaux, M Poissonnier, O Raoul, M O Rethoré, Delphine Allard, J Lejeune, H Jérôme	1976	146
18	[Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)]. PubMed ·O Raoul, Rethoré Mo, Lochana Patar, Ursula Schiefthaler, J Lejeune	1975	22
19	[Mosaicism 45, X-47, XY,+21]. PubMed ·M Prieur, B. Dutrillaux, S. Carpentier, Шипилова Елена Владимировна, O Raoul, Rethoré Mo, J Lejeune	1972	5
20	[Congenital glaucoma associated with chromosome abnormality]. PubMed ·Yongjie Zhang, Hee-Jin Jo, O Raoul, Jun Hyung Roh, R. Mallet, J Lejeune	1972	1

About O Raoul

O Raoul is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pharmacy, Plant Science and Clinical Biochemistry, having authored 30 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (7 papers), Chromosomal and Genetic Variations (6 papers), Prenatal Screening and Diagnostics (5 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (2 papers), Epigenetics and DNA Methylation (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Genetics (715 citations), Pediatrics, Perinatology and Child Health (286 citations), Cognitive Neuroscience (156 citations), Molecular Biology (474 citations) and Rheumatology (97 citations). O Raoul has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include M Poissonnier, M Prieur, Delphine Allard, M O Rethoré, J Lejeune, J Couturier, Valérie Cormier‐Daire, Laurence Colleaux, Damien Sanlaville and Serge Romana. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Experimental Cell Research, Human Genetics and Human Molecular Genetics.

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