Anne Destrèe

3.0k total citations
13 papers, 458 citations indexed

About

Anne Destrèe is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Anne Destrèe has authored 13 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Anne Destrèe's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Connective tissue disorders research (2 papers). Anne Destrèe is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Connective tissue disorders research (2 papers). Anne Destrèe collaborates with scholars based in Belgium, United States and France. Anne Destrèe's co-authors include C. Charlton Mabry, Mark Veugelers, Jean-François Lefaivre, Cynthia C. Morton, Craig T. Basson, Michael Bressan, Alan Zunamon, Deborah A. McDermott, Stanislawa Weremowicz and Bernard Grisart and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Scientific Reports.

In The Last Decade

Anne Destrèe

13 papers receiving 428 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Destrèe Belgium 11 253 219 68 68 52 13 458
Andrea M. Oza United States 8 271 1.1× 294 1.3× 34 0.5× 43 0.6× 24 0.5× 13 593
Helen Fryssira Greece 16 278 1.1× 312 1.4× 33 0.5× 25 0.4× 55 1.1× 39 600
Pietro Palumbo Italy 15 325 1.3× 314 1.4× 31 0.5× 33 0.5× 67 1.3× 64 620
Elisa Tassano Italy 15 272 1.1× 310 1.4× 47 0.7× 17 0.3× 85 1.6× 54 596
Lanying Song United States 16 205 0.8× 557 2.5× 44 0.6× 52 0.8× 90 1.7× 22 749
Sı̇bel Aylı̇n Uğur İşerı̇ Türkiye 13 218 0.9× 283 1.3× 74 1.1× 19 0.3× 40 0.8× 39 690
Sandra Mercier France 13 331 1.3× 486 2.2× 104 1.5× 45 0.7× 60 1.2× 41 662
Ayse Bilge Ozel United States 14 131 0.5× 245 1.1× 111 1.6× 33 0.5× 28 0.5× 26 635
Heather J. Stalker United States 12 277 1.1× 272 1.2× 46 0.7× 16 0.2× 78 1.5× 26 503
Katherine Holman Australia 15 522 2.1× 529 2.4× 28 0.4× 76 1.1× 58 1.1× 31 911

Countries citing papers authored by Anne Destrèe

Since Specialization
Citations

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

Fields of papers citing papers by Anne Destrèe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Destrèe

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

All Works

13 of 13 papers shown
1.
Destrèe, Anne, Marie Deprez, Hazim Kadhim, et al.. (2022). ASC1 complex related conditions: Two novel paediatric patients with TRIP4 pathogenic variants and review of literature. European Journal of Medical Genetics. 65(4). 104469–104469. 1 indexed citations
2.
Johannesen, Katrine M., Anne Destrèe, Filippo Manti, et al.. (2021). Adult phenotype of KCNQ2 encephalopathy. Journal of Medical Genetics. 59(6). 528–535. 19 indexed citations
3.
Arno, Gavin, Julie De Zaeytijd, Hannah Verdin, et al.. (2020). The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56. Scientific Reports. 10(1). 1289–1289. 21 indexed citations
4.
Syx, Delfien, Florence Petit, Nathalie Goemans, et al.. (2019). Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers–Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix. Genetics in Medicine. 22(1). 112–123. 38 indexed citations
5.
Lambert, Sophie, Isabelle Maystadt, Pascal Vrielynck, et al.. (2016). Expanding phenotype of p.Ala140Val mutation in MECP2 in a 4 generation family with X-linked intellectual disability and spasticity. European Journal of Medical Genetics. 59(10). 522–525. 13 indexed citations
6.
Allou, Lila, Laëtitia Lambert, Daniel Amsallem, et al.. (2012). 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements. European Journal of Human Genetics. 20(12). 1216–1223. 50 indexed citations
7.
Goff, Carine Le, Clémentine Mahaut, Avinash Abhyankar, et al.. (2011). Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome. Nature Genetics. 44(1). 85–88. 117 indexed citations
8.
Moortgat, Stéphanie, Christine Verellen‐Dumoulin, Isabelle Maystadt, et al.. (2010). Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1–q25.32: Genotype–phenotype correlations of chromosome 3q25 deletion syndrome. European Journal of Medical Genetics. 54(2). 177–180. 4 indexed citations
9.
10.
Grisart, Bernard, Lionel Willatt, Anne Destrèe, et al.. (2009). 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction. Journal of Medical Genetics. 46(8). 524–530. 41 indexed citations
11.
Grisart, Bernard, Katrina Rack, Pascale Hilbert, et al.. (2008). NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?. European Journal of Human Genetics. 16(3). 305–311. 22 indexed citations
12.
Destrèe, Anne, et al.. (2005). Prenatal diagnosis of trisomy 6 mosaicism. Prenatal Diagnosis. 25(5). 354–357. 22 indexed citations
13.
Veugelers, Mark, Michael Bressan, Deborah A. McDermott, et al.. (2004). Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant. New England Journal of Medicine. 351(5). 460–469. 94 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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