Erik Boot

3.8k total citations
78 papers, 1.5k citations indexed

About

Erik Boot is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Erik Boot has authored 78 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 36 papers in Epidemiology and 27 papers in Genetics. Recurrent topics in Erik Boot's work include Congenital heart defects research (50 papers), Congenital Heart Disease Studies (34 papers) and Coronary Artery Anomalies (24 papers). Erik Boot is often cited by papers focused on Congenital heart defects research (50 papers), Congenital Heart Disease Studies (34 papers) and Coronary Artery Anomalies (24 papers). Erik Boot collaborates with scholars based in Netherlands, Canada and United States. Erik Boot's co-authors include Anne S. Bassett, Thérèse van Amelsvoort, Nancy J. Butcher, Jan Booij, Eva W.C. Chow, Janneke Zinkstok, Thérèse A. van Amelsvoort, Lieuwe de Haan, Don Linszen and Wai Lun Alan Fung and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Erik Boot

73 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erik Boot Netherlands 22 881 455 432 316 255 78 1.5k
Tamar Green United States 20 632 0.7× 382 0.8× 223 0.5× 226 0.7× 286 1.1× 51 1.2k
Lisa J. Strug Canada 26 523 0.6× 606 1.3× 100 0.2× 663 2.1× 310 1.2× 81 2.2k
George Apostol United States 17 441 0.5× 507 1.1× 71 0.2× 280 0.9× 447 1.8× 23 1.3k
Maude L. Blundell United States 19 474 0.5× 359 0.8× 109 0.3× 130 0.4× 292 1.1× 21 1.3k
Danielle M. Andrade Canada 30 769 0.9× 717 1.6× 275 0.6× 182 0.6× 414 1.6× 111 2.5k
Karen Walton–Bowen United States 17 289 0.3× 552 1.2× 324 0.8× 532 1.7× 541 2.1× 24 1.9k
Joke Beuten United States 25 979 1.1× 625 1.4× 122 0.3× 184 0.6× 88 0.3× 39 1.8k
Janneke Zinkstok Netherlands 20 353 0.4× 368 0.8× 153 0.4× 86 0.3× 555 2.2× 57 1.2k
Sandra Leistner‐Segal Brazil 22 276 0.3× 190 0.4× 378 0.9× 64 0.2× 99 0.4× 88 1.6k
Astrid M. Vicente Portugal 20 497 0.6× 664 1.5× 113 0.3× 37 0.1× 631 2.5× 72 1.7k

Countries citing papers authored by Erik Boot

Since Specialization
Citations

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

Fields of papers citing papers by Erik Boot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erik Boot

This figure shows the co-authorship network connecting the top 25 collaborators of Erik Boot. A scholar is included among the top collaborators of Erik Boot 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 Erik Boot. Erik Boot 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.
Grippe, Talyta, Tracy Heung, Robert Chen, et al.. (2025). Dissecting the Phenotypic Spectrum and Complexity of Movement Disorders in 22q11.2 Deletion Syndrome. European Journal of Neurology. 32(6). e70256–e70256.
2.
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.
3.
Goldmuntz, Elizabeth, Anne S. Bassett, Erik Boot, et al.. (2024). Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation. Prenatal Diagnosis. 44(6-7). 804–814. 2 indexed citations
4.
Rossum, Elisabeth F. C. van, Mieke M. van Haelst, Claudia Vingerhoets, et al.. (2024). Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion. International Journal of Obesity. 49(4). 642–648.
5.
Brands, Marion M., Lotte Haverman, Caroline B. Terwee, et al.. (2024). Navigating the outcome maze: a scoping review of outcomes and instruments in clinical trials in genetic neurodevelopmental disorders and intellectual disability. PubMed. 5. 931155481–931155481. 5 indexed citations
6.
Blagowidow, Natalie, Beata Nowakowska, Erica Schindewolf, et al.. (2023). Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14(1). 160–160. 15 indexed citations
7.
Shirzadi, Zahra, Henk Mutsaerts, Erik Boot, et al.. (2022). Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The World Journal of Biological Psychiatry. 24(3). 260–265.
8.
Amelsvoort, Thérèse van, et al.. (2022). Post-traumatic stress in adults with 22q11.2 deletion syndrome. BJPsych Open. 8(4). e126–e126. 1 indexed citations
9.
Eeghen, Agnies M. van, Tom J. de Koning, Mark L. Kuijf, et al.. (2022). Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review. Movement Disorders Clinical Practice. 10(1). 17–31. 6 indexed citations
10.
Bauer, Noël J.C., Tos T. J. M. Berendschot, Levinus A. Bok, et al.. (2021). Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study. American Journal of Medical Genetics Part A. 188(2). 569–578. 3 indexed citations
11.
Boot, Erik, et al.. (2021). Possible underreporting of pathogenic variants in RAI1 causing Smith–Magenis syndrome. American Journal of Medical Genetics Part A. 185(10). 3167–3169. 9 indexed citations
12.
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
13.
Eeghen, Agnies M. van, et al.. (2019). Somatische comorbiditeit bij kinderen en volwassenen met een verstandelijke beperking en een psychiatrische aandoening. Tijdschrift voor psychiatrie. 6(11). 773–778. 1 indexed citations
14.
Malecki, Sarah, Elemi Breetvelt, Maria Corral, et al.. (2019). A genetic model for multimorbidity in young adults. Genetics in Medicine. 22(1). 132–141. 29 indexed citations
15.
Butcher, Nancy J., Connie Marras, Margarita Pondal, et al.. (2017). Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease. Brain. 140(5). 1371–1383. 34 indexed citations
16.
Boot, Erik, Nancy J. Butcher, Samantha Cooper, et al.. (2016). Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine. 19(2). 204–208. 55 indexed citations
17.
Evers, L. J. M., Leopold Curfs, Jaap Bakker, et al.. (2014). Serotonergic, noradrenergic and dopaminergic markers are related to cognitive function in adults with 22q11 deletion syndrome. The International Journal of Neuropsychopharmacology. 17(8). 1159–1165. 15 indexed citations
18.
Beveren, Nico J.M. van, Lianne C. Krab, Sigrid Swagemakers, et al.. (2012). Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome. PLoS ONE. 7(4). 5 indexed citations
19.
Beveren, Nico J.M. van, Lianne C. Krab, Sigrid Swagemakers, et al.. (2012). Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome. PLoS ONE. 7(3). e33473–e33473. 26 indexed citations
20.
Boot, Erik, Jan Booij, Janneke Zinkstok, et al.. (2011). COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome. Synapse. 65(9). 967–970. 16 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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