Maureen Holvoet

1.1k total citations
33 papers, 607 citations indexed

About

Maureen Holvoet is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Maureen Holvoet has authored 33 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 17 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Maureen Holvoet's work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Chromosomal and Genetic Variations (8 papers). Maureen Holvoet is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Chromosomal and Genetic Variations (8 papers). Maureen Holvoet collaborates with scholars based in Belgium, United States and France. Maureen Holvoet's co-authors include Koenraad Devriendt, Joris Vermeesch, J P Fryns, Hilde Van Esch, T. Lukusa, Peter Marynen, J. P. Fryns, Jean‐Pierre Fryns, C. Schaap and G.J.C.M. van Buggenhout and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Maureen Holvoet

31 papers receiving 595 citations

Peers

Maureen Holvoet
Joanna Wiszniewska United States
Sara Loddo Italy
Anna Capalbo Italy
Aimee S. Spikes United States
Ton van Essen Netherlands
Dinah Yaeger United States
Chantal Missirian France
Ute Grasshoff Germany
Monika Cohen Germany
Rossella Caselli Italy
Joanna Wiszniewska United States
Maureen Holvoet
Citations per year, relative to Maureen Holvoet Maureen Holvoet (= 1×) peers Joanna Wiszniewska

Countries citing papers authored by Maureen Holvoet

Since Specialization
Citations

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

Fields of papers citing papers by Maureen Holvoet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maureen Holvoet

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

All Works

20 of 20 papers shown
1.
Holvoet, Maureen, et al.. (2021). Homozygous missense STRADA mutation in a patient with polyhydramnios, megalencephaly and symptomatic epilepsy syndrome. Clinical Dysmorphology. 30(3). 121–124. 5 indexed citations
2.
Roelens, Filip, et al.. (2017). SPG20 mutation in three siblings with familial hereditary spastic paraplegia. Molecular Case Studies. 3(4). a001537–a001537. 11 indexed citations
3.
Holvoet, Maureen, et al.. (2016). Bilateral renal tumors in an adult man with Smith-Magenis syndrome: The role of the FLCN gene. European Journal of Medical Genetics. 59(10). 499–501. 13 indexed citations
4.
Fieremans, Nathalie, Hilde Van Esch, Maureen Holvoet, et al.. (2016). Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern. Human Mutation. 37(8). 804–811. 65 indexed citations
5.
Isrie, Mala, Vera M. Kalscheuer, Maureen Holvoet, et al.. (2013). HUWE1 mutation explains phenotypic severity in a case of familial idiopathic intellectual disability. European Journal of Medical Genetics. 56(7). 379–382. 10 indexed citations
6.
Vandewalle, Joke, Marijke Bauters, Hilde Van Esch, et al.. (2013). The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Human Genetics. 132(10). 1177–1185. 22 indexed citations
7.
Schuurs-Hoeijmakers, Janneke, Edwin C. Oh, Lisenka E.L.M. Vissers, et al.. (2012). Recurrent De Novo Mutations in PACS1 Cause Defective Cranial-Neural-Crest Migration and Define a Recognizable Intellectual-Disability Syndrome. The American Journal of Human Genetics. 91(6). 1122–1127. 78 indexed citations
8.
Santen, Gijs W.E., Yu Sun, Antoinet C.J. Gijsbers, et al.. (2012). Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus. Journal of Medical Genetics. 49(6). 366–372. 17 indexed citations
9.
Thienpont, Bernard, Jeroen Breckpot, Maureen Holvoet, Joris Vermeesch, & Koenraad Devriendt. (2007). A microduplication of CBP in a patient with mental retardation and a congenital heart defect. American Journal of Medical Genetics Part A. 143A(18). 2160–2164. 18 indexed citations
10.
Peeters, Hilde, et al.. (2006). Partial trisomy 11q syndrome.
11.
Esch, Hilde Van, Ginevra Zanni, Maureen Holvoet, et al.. (2005). X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family. European Journal of Medical Genetics. 48(2). 145–152. 8 indexed citations
12.
Syrrou, Maria, Kathelijn Keymolen, Koenraad Devriendt, et al.. (2002). Glypican 1 gene: Good candidate for brachydactyly type E. American Journal of Medical Genetics. 108(4). 310–314. 14 indexed citations
13.
Vogels, Annick, Koenraad Devriendt, Joris Vermeesch, et al.. (2000). Cryptic translocation t(5;18) in familial mental retardation. Annales de Génétique. 43(3-4). 117–123. 9 indexed citations
14.
Thoelen, Ronald, et al.. (2000). Physical map of a 1.5 Mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint. European Journal of Human Genetics. 8(8). 561–570. 10 indexed citations
15.
Buggenhout, G.J.C.M. van, et al.. (2000). Cri du chat syndrome: Changing phenotype in older patients. American Journal of Medical Genetics. 90(3). 203–215. 46 indexed citations
16.
Lukusa, T., Koenraad Devriendt, Maureen Holvoet, & J. P. Fryns. (2000). Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: Unusual chromosome 9 variant. American Journal of Medical Genetics. 91(3). 192–197. 5 indexed citations
17.
Lukusa, T., Koenraad Devriendt, Maureen Holvoet, & JP Fryns. (1998). Severe mental retardation ‐ distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a lOq25→qter deletion. Clinical Genetics. 54(3). 224–230. 2 indexed citations
18.
Claes, Stephan, Annick Vogels, Maureen Holvoet, et al.. (1997). Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3–p22.2 (MRX49) and Xp11.3–p11.21 (MRX50). American Journal of Medical Genetics. 73(4). 474–479. 15 indexed citations
19.
Holvoet, Maureen, Bénédicte Eyskens, Peter Adriaensens, et al.. (1997). A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8. American Journal of Medical Genetics. 74(5). 515–520. 40 indexed citations
20.

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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