Susanne E. Boonen

2.6k total citations
20 papers, 768 citations indexed

About

Susanne E. Boonen is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Susanne E. Boonen has authored 20 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Susanne E. Boonen's work include Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (5 papers). Susanne E. Boonen is often cited by papers focused on Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (6 papers) and Prenatal Screening and Diagnostics (5 papers). Susanne E. Boonen collaborates with scholars based in Denmark, United Kingdom and Germany. Susanne E. Boonen's co-authors include Johanne M D Hahnemann, Deborah Mackay, I. Karen Temple, David Robinson, Helen White, Helen V. Firth, Sian Ellard, Judith A. Goodship, Jonathan L A Callaway and Andrew T. Hattersley and has published in prestigious journals such as Nature Genetics, Neurology and Scientific Reports.

In The Last Decade

Susanne E. Boonen

17 papers receiving 753 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susanne E. Boonen Denmark 11 594 576 310 122 52 20 768
Alice S. Brooks Netherlands 14 304 0.5× 325 0.6× 121 0.4× 97 0.8× 34 0.7× 29 595
Christopher C. Glenn United States 11 815 1.4× 907 1.6× 454 1.5× 43 0.4× 13 0.3× 14 1.1k
R. Dwain Blackston United States 11 232 0.4× 279 0.5× 303 1.0× 62 0.5× 166 3.2× 16 741
Elaine Whidden United States 7 285 0.5× 375 0.7× 118 0.4× 40 0.3× 20 0.4× 7 566
Steven D. Klein United States 15 221 0.4× 145 0.3× 32 0.1× 239 2.0× 22 0.4× 31 677
Rosario Berardi Italy 14 146 0.2× 189 0.3× 108 0.3× 49 0.4× 21 0.4× 29 422
Ameeta Mehta United Kingdom 10 270 0.5× 270 0.5× 73 0.2× 90 0.7× 461 8.9× 11 682
Konstantinos Douroudis United Kingdom 15 245 0.4× 171 0.3× 28 0.1× 70 0.6× 49 0.9× 27 567
Luigina Spaccini Italy 13 208 0.4× 159 0.3× 104 0.3× 57 0.5× 7 0.1× 47 455
P Driscoll United States 8 196 0.3× 140 0.2× 153 0.5× 206 1.7× 368 7.1× 10 685

Countries citing papers authored by Susanne E. Boonen

Since Specialization
Citations

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

Fields of papers citing papers by Susanne E. Boonen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susanne E. Boonen. 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 Susanne E. Boonen. The network helps show where Susanne E. Boonen may publish in the future.

Co-authorship network of co-authors of Susanne E. Boonen

This figure shows the co-authorship network connecting the top 25 collaborators of Susanne E. Boonen. A scholar is included among the top collaborators of Susanne E. Boonen 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 Susanne E. Boonen. Susanne E. Boonen 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.
Turnpenny, Peter D., Ute Moog, Edward S. Tobias, et al.. (2025). The European Certificate in Medical Genetics and Genomics (ECMGG). European Journal of Human Genetics. 33(9). 1113–1120.
2.
Frederiksen, Jane Hübertz, Ulf Birkedal, Lene Juel Rasmussen, et al.. (2024). Reclassification of Two MLH1 Variants of Uncertain Significance Utilizing Clinical and Functional Data. Molecular Genetics & Genomic Medicine. 12(11). e70026–e70026.
3.
Lildballe, Dorte L., Anja Lisbeth Frederiksen, Bitten Schönewolf‐Greulich, et al.. (2023). National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark. European Journal of Medical Genetics. 66(12). 104872–104872.
4.
Hao, Qin, Martin J. Larsen, Anne‐Vibeke Lænkholm, et al.. (2023). Validation of the BOADICEA model for predicting the likelihood of carrying pathogenic variants in eight breast and ovarian cancer susceptibility genes. Scientific Reports. 13(1). 8536–8536. 2 indexed citations
5.
Thomassen, Mads, et al.. (2022). Germline pathogenic variants associated with ovarian cancer: A historical overview. Gynecologic Oncology Reports. 44. 101105–101105. 1 indexed citations
6.
Fernández‐Guerra, Paula, Susanne E. Boonen, Julie Courraud, et al.. (2021). Bioenergetic and Proteomic Profiling of Immune Cells in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients: An Exploratory Study. Biomolecules. 11(7). 961–961. 19 indexed citations
7.
Brinth, Louise, Kim Varming, Susanne E. Boonen, et al.. (2019). Myalgisk encefalomyelitis eller kronisk træthedssyndrom. University of Southern Denmark Research Portal (University of Southern Denmark). 181(21). 2025–2027. 1 indexed citations
8.
Brinth, Louise, Henrik Nielsen, Kim Varming, et al.. (2019). [Myalgic encephalomyelitis or chronic fatigue syndrome].. PubMed. 181(24). 4 indexed citations
9.
Gilling, Mette, Esben Budtz–Jørgensen, Susanne E. Boonen, et al.. (2017). The Danish HD Registry—a nationwide family registry of HD families in Denmark. Clinical Genetics. 92(3). 338–341. 7 indexed citations
10.
Bak, Mads, Susanne E. Boonen, Christina Dahl, et al.. (2016). Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57. BMC Medical Genetics. 17(1). 29–29. 26 indexed citations
11.
Boonen, Susanne E., Andrea Freschi, Rikke Christensen, et al.. (2016). Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes. Clinical Epigenetics. 8(1). 69–69. 6 indexed citations
12.
Gilling, Mette, Hanne B. Rasmussen, Kirstine Calløe, et al.. (2013). Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders. Frontiers in Genetics. 4. 54–54. 40 indexed citations
13.
Boonen, Susanne E., Johanne M D Hahnemann, Deborah Mackay, et al.. (2011). No evidence for pathogenic variants or maternal effect of ZFP57 as the cause of Beckwith–Wiedemann Syndrome. European Journal of Human Genetics. 20(1). 119–121. 14 indexed citations
14.
Grønskov, Karen, Rebecca Poole, Johanne M D Hahnemann, et al.. (2011). Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver–Russell syndrome and growth retardation. Journal of Medical Genetics. 48(5). 308–311. 31 indexed citations
15.
Goris, An, Robin Lemmens, Michael A. van Es, et al.. (2010). Tau levels do not influence human ALS or motor neuron degeneration in the SOD1 G93A mouse. Neurology. 74(21). 1687–1693. 14 indexed citations
16.
Boonen, Susanne E., Sven Pörksen, Deborah Mackay, et al.. (2008). Clinical characterisation of the multiple maternal hypomethylation syndrome in siblings. European Journal of Human Genetics. 16(4). 453–461. 39 indexed citations
17.
Mackay, Deborah, Jonathan L A Callaway, Helen White, et al.. (2008). Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57. Nature Genetics. 40(8). 949–951. 374 indexed citations
18.
Mackay, Deborah, Susanne E. Boonen, Jill Clayton‐Smith, et al.. (2006). A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus. Human Genetics. 120(2). 262–269. 117 indexed citations
19.
Mackay, Deborah, Johanne M D Hahnemann, Susanne E. Boonen, et al.. (2006). Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus. Human Genetics. 119(1-2). 179–184. 47 indexed citations
20.
Boonen, Susanne E., David A. Stahl, Sven Kreiborg, et al.. (2004). Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome. American Journal of Medical Genetics Part A. 132A(3). 324–328. 26 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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