Caroline Rooryck

6.3k total citations · 1 hit paper
75 papers, 1.9k citations indexed

About

Caroline Rooryck is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Caroline Rooryck has authored 75 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 32 papers in Genetics and 14 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Caroline Rooryck's work include Genomic variations and chromosomal abnormalities (15 papers), RNA regulation and disease (10 papers) and Prenatal Screening and Diagnostics (9 papers). Caroline Rooryck is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), RNA regulation and disease (10 papers) and Prenatal Screening and Diagnostics (9 papers). Caroline Rooryck collaborates with scholars based in France, Germany and Martinique. Caroline Rooryck's co-authors include Benoı̂t Arveiler, Didier Lacombe, Jérôme Toutain, Dorothée Cailley, Perrine Pennamen, Aurélien Trimouille, Eulalie Lasseaux, Cyril Goizet, Veronique Guyonnet‐Dupérat and Fanny Morice‐Picard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Caroline Rooryck

72 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations

2019 310 citations Jérôme Toutain, Perrine Pennamen et al. profile →

Peers

Caroline Rooryck

GENET

CCM

SURGE

Shalini N. Jhangiani United States

Anthonie J. van Essen Netherlands

Éliane Chouery Lebanon

Aslıhan Tolun Türkiye

Antoaneta Mincheva Germany

S Malcolm United Kingdom

Simon D. Bamforth United Kingdom

Valentina Guida Italy

Giorgio Bernardi France

Rika Kosaki Japan

Shalini N. Jhangiani United States

Caroline Rooryck

1.1k ×1.0

801 ×1.2

GENET

71 ×0.3

CCM

142 ×0.6

142 ×0.9

SURGE

Citations per year, relative to Caroline Rooryck Caroline Rooryck (= 1×) peers Shalini N. Jhangiani

Countries citing papers authored by Caroline Rooryck

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Rooryck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Rooryck

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

All Works

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20 of 20 papers shown

Fergelot, Patricia, Caroline Rooryck, Dominique P. Germain, et al.. (2024). Prevalence of Fabry disease in patients with chronic pain: Lessons from the DOUFAB and DOUFABIS studies. European Journal of Pain. 29(1). e4708–e4708.

Vadrot, Nathalie, Flavie Ader, Maryline Moulin, et al.. (2023). Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies. Cells. 12(2). 337–337. 4 indexed citations

Ader, Flavie, Caroline Rooryck, Fanny Pelluard, et al.. (2023). Morphological and genetic causes of fetal cardiomyopathies. Clinical Genetics. 104(1). 63–72. 2 indexed citations

Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Rachel Stapleton, et al.. (2021). A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum. Human Genetics. 140(6). 933–944. 16 indexed citations

Trimouille, Aurélien, Angèle Tingaud‐Sequeira, Didier Lacombe, et al.. (2020). Description of a family with X‐linked oculo‐auriculo‐vertebral spectrum associated with polyalanine tract expansion in ZIC3 . Clinical Genetics. 98(4). 384–389. 12 indexed citations

Ader, Flavie, Pascal de Groote, Patricia Réant, et al.. (2019). FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations. Clinical Genetics. 96(4). 317–329. 57 indexed citations

Benoîst, David, François Roubertie, Marion Constantin, et al.. (2018). Arrhythmogenic Remodeling of the Left Ventricle in a Porcine Model of Repaired Tetralogy of Fallot. Circulation Arrhythmia and Electrophysiology. 11(10). e006059–e006059. 11 indexed citations

Lasseaux, Eulalie, Christian Hamel, Sabine Defoort‐Dhellemmes, et al.. (2018). Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene. British Journal of Ophthalmology. 103(9). 1239–1247. 26 indexed citations

Tingaud‐Sequeira, Angèle, Maria Isabel Melaragno, Ana Beatriz Alvarez Pérez, et al.. (2017). A novel de novo mutation in MYT1, the unique OAVS gene identified so far. European Journal of Human Genetics. 25(9). 1083–1086. 33 indexed citations

10.

Marguet, Florent, Caroline Rooryck, Marie‐Laure Vuillaume, et al.. (2017). Early fetal presentation of Koolen-de Vries: Case report with literature review. European Journal of Medical Genetics. 60(11). 605–609. 1 indexed citations

11.

Benoîst, David, François Roubertie, Sabine Charron, et al.. (2016). Proarrhythmic remodelling of the right ventricle in a porcine model of repaired tetralogy of Fallot. Heart. 103(5). 347–354. 16 indexed citations

12.

Réant, Patricia, Amélie Reynaud, Xavier Pillois, et al.. (2014). Comparison of Resting and Exercise Echocardiographic Parameters as Indicators of Outcomes in Hypertrophic Cardiomyopathy. Journal of the American Society of Echocardiography. 28(2). 194–203. 38 indexed citations

13.

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

14.

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

15.

Fergelot, Patricia, Isabelle Coupry, Caroline Rooryck, et al.. (2012). Atypical male and female presentations of FLNA-related periventricular nodular heterotopia. European Journal of Medical Genetics. 55(5). 313–318. 18 indexed citations

16.

Faguer, Stanislas, Nicolas Chassaing, Isabel Bandı́n, et al.. (2011). A 17q12 chromosomal duplication associated with renal disease and esophageal atresia. European Journal of Medical Genetics. 54(4). e437–e440. 27 indexed citations

17.

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

18.

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

19.

Rooryck, Caroline, et al.. (2009). Genetic basis of oculocutaneous albinism. Expert Review of Dermatology. 4(6). 611–622. 14 indexed citations

20.

Morice‐Picard, Fanny, Sandrine Marlin, Caroline Rooryck, et al.. (2009). Hallerman–Streiff-like syndrome presenting with laterality and cardiac defects. Clinical Dysmorphology. 18(2). 116–119. 5 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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