Annick Vogels

4.2k total citations
63 papers, 2.1k citations indexed

About

Annick Vogels is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Annick Vogels has authored 63 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 26 papers in Molecular Biology and 12 papers in Epidemiology. Recurrent topics in Annick Vogels's work include Genetic Syndromes and Imprinting (16 papers), Congenital heart defects research (16 papers) and Genomic variations and chromosomal abnormalities (15 papers). Annick Vogels is often cited by papers focused on Genetic Syndromes and Imprinting (16 papers), Congenital heart defects research (16 papers) and Genomic variations and chromosomal abnormalities (15 papers). Annick Vogels collaborates with scholars based in Belgium, Netherlands and United States. Annick Vogels's co-authors include Koenraad Devriendt, Ann Swillen, Jean‐Pierre Fryns, Eric Legius, J P Fryns, J. P. Fryns, Griet Van Buggenhout, Joris Vermeesch, Mie‐Jef Descheemaeker and Peter Prinzie and has published in prestigious journals such as Neurology, The Lancet Neurology and The British Journal of Psychiatry.

In The Last Decade

Annick Vogels

59 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annick Vogels Belgium 25 1.3k 1.1k 351 334 281 63 2.1k
Cynthia M. Powell United States 28 1.2k 0.9× 953 0.9× 536 1.5× 182 0.5× 299 1.1× 79 2.5k
Sulagna C. Saitta United States 24 1.0k 0.8× 1.1k 1.1× 219 0.6× 244 0.7× 134 0.5× 42 1.9k
Angelo Selicorni Italy 29 1.8k 1.4× 2.5k 2.4× 553 1.6× 126 0.4× 237 0.8× 176 3.8k
J. P. Fryns Belgium 24 1.7k 1.2× 1.4k 1.3× 598 1.7× 124 0.4× 152 0.5× 124 2.7k
Bronwyn Kerr United Kingdom 32 1.3k 1.0× 1.6k 1.5× 399 1.1× 102 0.3× 436 1.6× 67 3.2k
J P Fryns Belgium 25 1.2k 0.9× 1.1k 1.0× 430 1.2× 176 0.5× 129 0.5× 90 2.2k
Brenda Finucane United States 26 1.8k 1.4× 1.2k 1.1× 163 0.5× 157 0.5× 921 3.3× 65 2.6k
Donatella Milani Italy 24 994 0.7× 1.3k 1.2× 180 0.5× 80 0.2× 183 0.7× 118 2.1k
Jorge Saraiva Portugal 20 866 0.6× 690 0.6× 277 0.8× 72 0.2× 118 0.4× 73 1.6k
Tiziano Pramparo United States 27 1.2k 0.9× 1.7k 1.6× 219 0.6× 340 1.0× 503 1.8× 50 2.7k

Countries citing papers authored by Annick Vogels

Since Specialization
Citations

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

Fields of papers citing papers by Annick Vogels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annick Vogels

This figure shows the co-authorship network connecting the top 25 collaborators of Annick Vogels. A scholar is included among the top collaborators of Annick Vogels 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 Annick Vogels. Annick Vogels 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.
Swillen, Ann, Gabriela M. Repetto, Anthony E. Lang, et al.. (2025). Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter Study. Movement Disorders Clinical Practice. 12(6). 817–822.
2.
Balkom, Ingrid D. C. van, et al.. (2023). Consensus recommendations on mental health issues in Phelan-McDermid syndrome. European Journal of Medical Genetics. 66(6). 104770–104770. 7 indexed citations
3.
Vingerhoets, Claudia, Oswald Bloemen, Erik Boot, et al.. (2019). Low prevalence of substance use in people with 22q11.2 deletion syndrome. The British Journal of Psychiatry. 215(5). 661–667. 12 indexed citations
4.
Brison, Nathalie, Kris Van Den Bogaert, Luc Dehaspe, et al.. (2016). Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies. Genetics in Medicine. 19(3). 306–313. 39 indexed citations
5.
Vogels, Annick, Griet Van Buggenhout, Ann Swillen, et al.. (2014). Presenting symptoms in adults with the 22q11 deletion syndrome. European Journal of Medical Genetics. 57(4). 157–162. 16 indexed citations
6.
Garg, Shruti, Ellen Plasschaert, Mie‐Jef Descheemaeker, et al.. (2014). Autism Spectrum Disorder Profile in Neurofibromatosis Type I. Journal of Autism and Developmental Disorders. 45(6). 1649–1657. 53 indexed citations
7.
Vaart, Thijs van der, Ellen Plasschaert, André B. Rietman, et al.. (2013). Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial. The Lancet Neurology. 12(11). 1076–1083. 89 indexed citations
8.
Hannes, Femke, Andrew J. Sharp, Heather C. Mefford, et al.. (2008). Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. Journal of Medical Genetics. 46(4). 223–232. 207 indexed citations
9.
Smedt, Bert De, Koenraad Devriendt, J. P. Fryns, et al.. (2007). Intellectual abilities in a large sample of children with Velo–Cardio–Facial Syndrome: an update. Journal of Intellectual Disability Research. 51(9). 666–670. 131 indexed citations
10.
Denayer, Ellen, Annabel Parret, Magdalena Chmara, et al.. (2007). Mutation analysis in Costello syndrome: functional and structural characterization of theHRASp.Lys117Arg mutation. Human Mutation. 29(2). 232–239. 38 indexed citations
11.
Collin, Philippe, Hans de Boer, Annick Vogels, & Leopold Curfs. (2005). Psychose bij kinderen met het Prader-Willi syndroom. Tijdschrift voor psychiatrie. 47(5). 325–328. 1 indexed citations
12.
Collin, Philippe, Harm Boer, Annick Vogels, & L.M.G. Curfs. (2005). Psychosis in children with the Prader-Willi syndrome. Journal of Applied Research in Intellectual Disabilities. 19(3). 254–254. 1 indexed citations
13.
Vogels, Annick, Marc D. Binder, Mie‐Jef Descheemaeker, et al.. (2004). Psychotic disorders in Prader–Willi syndrome. American Journal of Medical Genetics Part A. 127A(3). 238–243. 81 indexed citations
14.
Vogels, Annick, Jenneke van den Ende, Kathelijn Keymolen, et al.. (2003). Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders. European Journal of Human Genetics. 12(3). 238–240. 135 indexed citations
15.
Prinzie, Peter, Mie‐Jef Descheemaeker, Annick Vogels, et al.. (2003). Personality profiles of children and adolescents with neurofibromatosis type 1. American Journal of Medical Genetics Part A. 118A(1). 1–7. 15 indexed citations
16.
Vogels, Annick, Gert Matthijs, Koenraad Devriendt, et al.. (2002). Psychosis in Prader Willi syndrome and chromosomal 15 maternal uniparental disomy. American Journal of Medical Genetics Part A. 114(7). 824–824. 1 indexed citations
17.
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
18.
Bouras, Nick, David Clarke, Harm Boer, et al.. (1998). Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies*. Journal of Intellectual Disability Research. 42(6). 440–450. 31 indexed citations
19.
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
20.
Vogels, Annick, et al.. (1996). Trisomy 9p and triploidy: The changing phenotype with age, psychological profile and speech development. 8. 274. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Cynthia M. Powell Breakdown of academic impact, for papers by Sulagna C. Saitta Breakdown of academic impact, for papers by Angelo Selicorni Breakdown of academic impact, for papers by J. P. Fryns Breakdown of academic impact, for papers by Bronwyn Kerr Breakdown of academic impact, for papers by J P Fryns Breakdown of academic impact, for papers by Brenda Finucane Breakdown of academic impact, for papers by Donatella Milani Breakdown of academic impact, for papers by Jorge Saraiva Breakdown of academic impact, for papers by Tiziano Pramparo
Rankless by CCL
2026