Isabelle Marey

1.2k total citations
15 papers, 139 citations indexed

About

Isabelle Marey is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Molecular Biology. According to data from OpenAlex, Isabelle Marey has authored 15 papers receiving a total of 139 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Public Health, Environmental and Occupational Health, 6 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Isabelle Marey's work include Down syndrome and intellectual disability research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Isabelle Marey is often cited by papers focused on Down syndrome and intellectual disability research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Isabelle Marey collaborates with scholars based in France, United Kingdom and Italy. Isabelle Marey's co-authors include Aimé Ravel, Cécile Cieuta‐Walti, Clotilde Mircher, M O Rethoré, Anne‐Sophie Rebillat, Franck Sturtz, Laurence Perrin, Samantha Stora, M David and Cybel Mehawej and has published in prestigious journals such as Clinical Genetics, Neuromuscular Disorders and Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

In The Last Decade

Isabelle Marey

14 papers receiving 137 citations

Peers

Isabelle Marey

PHEOH

GENET

PPCH

Ryan Kammeyer United States

Kitiwan Rojnueangnit Thailand

Charles‐Joris Roux France

Julien Hébert United States

Anna Karin Lind Sweden

Tufan Çankaya Türkiye

Anna Stittrich Germany

Ken Porche United States

M Kaur United Kingdom

Tristan McCaughey Australia

Ryan Kammeyer United States

Isabelle Marey

40 ×0.7

22 ×0.5

PHEOH

30 ×1.0

GENET

9 ×0.5

11 ×0.8

PPCH

Citations per year, relative to Isabelle Marey Isabelle Marey (= 1×) peers Ryan Kammeyer

Countries citing papers authored by Isabelle Marey

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Marey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Marey

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

All Works

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15 of 15 papers shown

Fauroux, Brigitte, Silvia Sacco, Vincent Couloigner, et al.. (2024). Early detection and treatment of obstructive sleep apnoea in infants with Down syndrome: a prospective, non-randomised, controlled, interventional study. The Lancet Regional Health - Europe. 45. 101035–101035. 8 indexed citations

Sacco, Silvia, Isabelle Marey, Nathalie Dorison, et al.. (2021). Psychomotor development in infants and young children with Down syndrome—A prospective, repeated measure, post‐hoc analysis. American Journal of Medical Genetics Part A. 188(3). 818–827.

Marey, Isabelle, Véronique Fressart, Caroline Rambaud, et al.. (2020). Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy. Open Medicine. 15(1). 435–446. 12 indexed citations

Viaux‐Savelon, Sylvie, Nicolas Bodeau, Y. Ville, et al.. (2020). Le dépistage anténatal sur puces ADN (ACPA) lors des anomalies mineures de l’échographie fœtale affecte les représentations et l’état émotionnel maternel : une étude exploratoire. Devenir. Vol. 32(2). 105–117. 2 indexed citations

Cieuta‐Walti, Cécile, et al.. (2019). P.078 Clinical trials in children with Down Syndrome: now and future. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 46(s1). S35–S35. 1 indexed citations

Mehawej, Cybel, Alexander Hoischen, Roula Farah, et al.. (2017). Homozygous mutation in ELMO2 may cause Ramon syndrome. Clinical Genetics. 93(3). 703–706. 15 indexed citations

Cieuta‐Walti, Cécile, Clotilde Mircher, Anne‐Sophie Rebillat, et al.. (2017). Acute regression in young people with Down Syndrome. European Journal of Paediatric Neurology. 21. e23–e23. 2 indexed citations

Mircher, Clotilde, Cécile Cieuta‐Walti, Isabelle Marey, et al.. (2017). Anthropometric charts and congenital anomalies in newborns with Down syndrome. American Journal of Medical Genetics Part A. 173(8). 2166–2175. 8 indexed citations

Mircher, Clotilde, Cécile Cieuta‐Walti, Isabelle Marey, et al.. (2017). Acute Regression in Young People with Down Syndrome. Brain Sciences. 7(6). 57–57. 42 indexed citations

10.

Xavier, Jean, et al.. (2016). Bipolar Disorder Type 1 in a 17-Year-Old Girl with Wolfram Syndrome. Journal of Child and Adolescent Psychopharmacology. 26(8). 750–755. 7 indexed citations

11.

Brioude, Frédéric, Isabelle Marey, S. Gaillard, et al.. (2016). Hypercortisolism due to a Pituitary Adenoma Associated with Beckwith-Wiedemann Syndrome. Hormone Research in Paediatrics. 86(3). 206–211. 10 indexed citations

12.

Rambaud, Jérôme, Isabelle Marey, Céline Dupont, et al.. (2012). Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication. American Journal of Medical Genetics Part A. 158A(9). 2277–2282. 2 indexed citations

13.

Dupont, Céline, Fabien Guimiot, Laurence Perrin, et al.. (2011). 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome. Clinical Genetics. 82(2). 187–192. 9 indexed citations

14.

Osimani, Sara, Isabelle Husson, Sandrine Passemard, et al.. (2010). Craniosynostosis: A rare complication of pycnodysostosis. European Journal of Medical Genetics. 53(2). 89–92. 20 indexed citations

15.

Cossée, Mireille, Marc Bartoli, Valérie Allamand, et al.. (2010). P1.15 DNA micro-arrays for revisiting molecular pathology in neuromuscular disorders. Neuromuscular Disorders. 20(9-10). 604–604. 1 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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