Dorothée Cailley

1.3k total citations
10 papers, 388 citations indexed

About

Dorothée Cailley is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dorothée Cailley has authored 10 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dorothée Cailley's work include Genomic variations and chromosomal abnormalities (5 papers), Fetal and Pediatric Neurological Disorders (2 papers) and RNA regulation and disease (2 papers). Dorothée Cailley is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Fetal and Pediatric Neurological Disorders (2 papers) and RNA regulation and disease (2 papers). Dorothée Cailley collaborates with scholars based in France, Netherlands and Belize. Dorothée Cailley's co-authors include Benoı̂t Arveiler, Caroline Rooryck, Didier Lacombe, Cyril Goizet, Julie Bouron, Françoise Auriol, F. Lorenzini, Véronique Gaston, Sanaa Eddiry and Jean‐Pierre Salles and has published in prestigious journals such as Blood, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Dorothée Cailley

10 papers receiving 365 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorothée Cailley France 8 215 166 84 73 49 10 388
Pietro Sirleto Italy 12 137 0.6× 221 1.3× 31 0.4× 33 0.5× 31 0.6× 25 399
Philip N. Mowrey United States 11 232 1.1× 162 1.0× 34 0.4× 134 1.8× 46 0.9× 22 436
Detlef Trost France 10 124 0.6× 224 1.3× 39 0.5× 48 0.7× 17 0.3× 20 346
Isabelle Gicquel France 13 236 1.1× 312 1.9× 62 0.7× 93 1.3× 9 0.2× 21 453
Josef Davidsson Sweden 11 165 0.8× 191 1.2× 123 1.5× 82 1.1× 15 0.3× 16 442
Philippe Coullin France 15 208 1.0× 268 1.6× 22 0.3× 189 2.6× 30 0.6× 28 526
Angeline Lai Singapore 10 133 0.6× 152 0.9× 26 0.3× 23 0.3× 21 0.4× 31 349
Vida Petrovic Australia 10 301 1.4× 390 2.3× 40 0.5× 64 0.9× 36 0.7× 19 600
M.H. Breuning Netherlands 8 157 0.7× 219 1.3× 34 0.4× 43 0.6× 25 0.5× 13 385
Bela Patel United States 15 146 0.7× 484 2.9× 72 0.9× 89 1.2× 21 0.4× 24 681

Countries citing papers authored by Dorothée Cailley

Since Specialization
Citations

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

Fields of papers citing papers by Dorothée Cailley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorothée Cailley

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

All Works

10 of 10 papers shown
1.
Houcinat, Nada, Brigitte Llanas, Sébastien Moutton, et al.. (2015). Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents. American Journal of Medical Genetics Part A. 167(11). 2714–2719. 21 indexed citations
2.
Bieth, Éric, Sanaa Eddiry, Véronique Gaston, et al.. (2014). Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome. European Journal of Human Genetics. 23(2). 252–255. 126 indexed citations
3.
Rooryck, Caroline, Jérôme Toutain, Dorothée Cailley, et al.. (2013). Prenatal diagnosis using array-CGH: A French experience. European Journal of Medical Genetics. 56(7). 341–345. 24 indexed citations
4.
Morice‐Picard, Fanny, Eulalie Lasseaux, Dorothée Cailley, et al.. (2013). High‐resolution array‐CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene. Pigment Cell & Melanoma Research. 27(1). 59–71. 21 indexed citations
5.
Moutton, Sébastien, Caroline Rooryck, Jérôme Toutain, et al.. (2012). Dysmorphic features in subtelomeric 20p13 deletion excluding JAG1: A recognizable microdeletion phenotype?. European Journal of Medical Genetics. 55(2). 151–155. 4 indexed citations
6.
Cailley, Dorothée, Jérôme Toutain, Julie Bouron, et al.. (2011). 1.5 Mb microdeletion in 15q24 in a patient with mild OAVS phenotype. European Journal of Medical Genetics. 55(2). 135–139. 20 indexed citations
7.
Nurden, Paquita, Najet Debili, Isabelle Coupry, et al.. (2011). Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome. Blood. 118(22). 5928–5937. 109 indexed citations
8.
Toutain, Jérôme, Martine Doco‐Fenzy, Fanny Morice‐Picard, et al.. (2011). Identification of a complex 17q rearrangement in a metanephric stromal tumor. Cancer Genetics. 204(6). 340–343. 7 indexed citations
9.
Rooryck, Caroline, Fanny Morice‐Picard, Eulalie Lasseaux, et al.. (2010). High resolution mapping of OCA2 intragenic rearrangements and identification of a founder effect associated with a deletion in Polish albino patients. Human Genetics. 129(2). 199–208. 12 indexed citations
10.
Rooryck, Caroline, Dorothée Cailley, Julie Bouron, et al.. (2010). Array‐CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum. American Journal of Medical Genetics Part A. 152A(8). 1984–1989. 44 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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