Catherine Ozilou

2.1k total citations
11 papers, 319 citations indexed

About

Catherine Ozilou is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine Ozilou has authored 11 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine Ozilou's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Catherine Ozilou is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Catherine Ozilou collaborates with scholars based in France. Catherine Ozilou's co-authors include C Turleau, Michel Vekemans, Serge Romana, Philippe Gosset, Arnold Münnich, Valérie Cormier‐Daire, O Raoul, Marie‐Christine de Blois, Laurence Colleaux and Marlène Rio and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Catherine Ozilou

11 papers receiving 295 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Catherine Ozilou France	10	273	118	72	67	29	11	319
Lindsey Campbell United States	4	268 1.0×	130 1.1×	69 1.0×	74 1.1×	28 1.0×	5	316
Erika Carter United States	10	268 1.0×	118 1.0×	82 1.1×	54 0.8×	23 0.8×	15	338
Bridgette Soileau United States	11	345 1.3×	165 1.4×	102 1.4×	71 1.1×	27 0.9×	16	408
Patricia A. Eng United States	5	243 0.9×	134 1.1×	104 1.4×	49 0.7×	12 0.4×	5	298
Antoinet C.J. Gijsbers Netherlands	12	356 1.3×	212 1.8×	94 1.3×	67 1.0×	10 0.3×	15	426
L.G. Shaffer United States	6	251 0.9×	155 1.3×	47 0.7×	56 0.8×	21 0.7×	8	297
Beth A. Torchia United States	7	281 1.0×	139 1.2×	177 2.5×	71 1.1×	16 0.6×	11	369
Fernando Santos Spain	9	228 0.8×	193 1.6×	84 1.2×	21 0.3×	13 0.4×	13	325
Patricia D. Ghidoni United States	7	257 0.9×	181 1.5×	99 1.4×	71 1.1×	21 0.7×	8	329
Julie Leana‐Cox United States	9	334 1.2×	216 1.8×	101 1.4×	139 2.1×	8 0.3×	14	412

Countries citing papers authored by Catherine Ozilou

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Ozilou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Ozilou

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

All Works

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11 of 11 papers shown

Rio, Marlène, Stéphanie Gobin, Catherine Ozilou, et al.. (2012). Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH. Clinical Genetics. 84(1). 31–36. 23 indexed citations

Golzio, Christelle, Catherine Ozilou, Sophie Thomas, et al.. (2006). Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy. Prenatal Diagnosis. 26(13). 1201–1205. 17 indexed citations

Sanlaville, Damien, Marguerite Prieur, Marie‐Christine de Blois, et al.. (2005). Functional disomy of the Xq28 chromosome region. European Journal of Human Genetics. 13(5). 579–585. 63 indexed citations

Sanlaville, Damien, Serge Romana, Jeanne Amiel, et al.. (2002). A CGH study of 27 patients with CHARGE association. Clinical Genetics. 61(2). 135–138. 21 indexed citations

Rio, Marlène, Florence Molinari, S. Heuertz, et al.. (2002). Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Journal of Medical Genetics. 39(4). 266–270. 54 indexed citations

Brisset, Sophie, Catherine Ozilou, Philippe Gosset, et al.. (2002). Molecular characterization of partial trisomy 16q24.1‐qter: Clinical report and review of the literature. American Journal of Medical Genetics. 113(4). 339–345. 39 indexed citations

Colleaux, Laurence, Marlène Rio, S. Heuertz, et al.. (2001). A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation. European Journal of Human Genetics. 9(5). 319–327. 47 indexed citations

Ozilou, Catherine, Philippe Gosset, Alain Aurias, et al.. (2001). Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype. Clinical Genetics. 60(3). 212–219. 33 indexed citations

Rio, Marlène, Catherine Ozilou, Valérie Cormier‐Daire, et al.. (2001). Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation. Human Genetics. 108(6). 511–515. 10 indexed citations

10.

Romana, Serge, Philippe Gosset, Hatem Elghezal, et al.. (2001). [Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].. PubMed. 30(1 Suppl). 75–9. 2 indexed citations

11.

Fert‐Ferrer, Sandra, Julia Tantau, Anne Lise Delezoïde, et al.. (2000). Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features. Prenatal Diagnosis. 20(6). 511–515. 10 indexed citations

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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