Susen Schaake

1.4k total citations
22 papers, 407 citations indexed

About

Susen Schaake is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Susen Schaake has authored 22 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Susen Schaake's work include Neurological disorders and treatments (7 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Genetic Neurodegenerative Diseases (5 papers). Susen Schaake is often cited by papers focused on Neurological disorders and treatments (7 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Genetic Neurodegenerative Diseases (5 papers). Susen Schaake collaborates with scholars based in Germany, Canada and United States. Susen Schaake's co-authors include Christine Klein, Katja Lohmann, Connie Marras, Joanne Trinh, Meike Kasten, Harutyun Madoev, Inke R. König, Sonja Petkovic, Anne Grünewald and Ana Westenberger and has published in prestigious journals such as Brain, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Susen Schaake

21 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susen Schaake Germany 11 234 137 115 68 67 22 407
Harutyun Madoev Germany 5 172 0.7× 91 0.7× 65 0.6× 50 0.7× 46 0.7× 9 277
Lucía Schottlaender United Kingdom 10 175 0.7× 118 0.9× 129 1.1× 90 1.3× 29 0.4× 15 437
Edoardo Monfrini Italy 13 196 0.8× 88 0.6× 141 1.2× 50 0.7× 58 0.9× 46 393
Anna Sułek Poland 13 95 0.4× 238 1.7× 156 1.4× 101 1.5× 68 1.0× 53 397
Eleni Zamba‐Papanicolaou Cyprus 14 160 0.7× 230 1.7× 290 2.5× 77 1.1× 38 0.6× 45 597
Luan Cen China 10 126 0.5× 85 0.6× 156 1.4× 95 1.4× 21 0.3× 16 368
Monica Gagliardi Italy 9 70 0.3× 46 0.3× 99 0.9× 33 0.5× 81 1.2× 33 257
Simone Olgiati Netherlands 13 374 1.6× 198 1.4× 182 1.6× 188 2.8× 87 1.3× 15 680
Chengyuan Song China 11 156 0.7× 105 0.8× 193 1.7× 72 1.1× 53 0.8× 24 427
Yoshitaka Tashiro Japan 13 115 0.5× 71 0.5× 260 2.3× 60 0.9× 36 0.5× 20 505

Countries citing papers authored by Susen Schaake

Since Specialization
Citations

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

Fields of papers citing papers by Susen Schaake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susen Schaake

This figure shows the co-authorship network connecting the top 25 collaborators of Susen Schaake. A scholar is included among the top collaborators of Susen Schaake 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 Susen Schaake. Susen Schaake 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.
Rossi, Malco, Susen Schaake, Tatiana Usnich, et al.. (2025). Classification and Genotype–Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review. Movement Disorders. 40(4). 605–618. 4 indexed citations
2.
Thomsen, Mirja, Max Borsche, Susen Schaake, et al.. (2025). FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?. Brain. 148(11). 4072–4083.
3.
Wallings, Rebecca L., Karen N. McFarland, Susen Schaake, et al.. (2024). The R1441C-Lrrk2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner in mice. Science Translational Medicine. 16(772). eadl1535–eadl1535. 6 indexed citations
4.
Schaake, Susen, Björn‐Hergen Laabs, Roland Dominic G. Jamora, et al.. (2024). Stability of Mosaic Divergent Repeat Interruptions in X‐Linked Dystonia‐Parkinsonism. Movement Disorders. 39(7). 1145–1153. 2 indexed citations
5.
Trinh, Joanne, Susen Schaake, Sally A. Cowley, et al.. (2024). Optical genome mapping of structural variants in Parkinson’s disease-related induced pluripotent stem cells. BMC Genomics. 25(1). 980–980. 1 indexed citations
6.
Kluge, Annika, Max Borsche, Susen Schaake, et al.. (2024). α‐Synuclein Pathology in PRKN‐Linked Parkinson's Disease: New Insights from a Blood‐Based Seed Amplification Assay. Annals of Neurology. 95(6). 1173–1177. 15 indexed citations
7.
Borsche, Max, H. Baumann, Sinem Tunç, et al.. (2023). POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the Literature. The Cerebellum. 23(2). 479–488. 4 indexed citations
8.
Schaake, Susen, et al.. (2023). GBA1 in Parkinson’s disease: variant detection and pathogenicity scoring matters. BMC Genomics. 24(1). 322–322. 6 indexed citations
9.
Trinh, Joanne, Susen Schaake, Björn‐Hergen Laabs, et al.. (2022). Mosaic divergent repeat interruptions in XDP influence repeat stability and disease onset. Brain. 146(3). 1075–1082. 15 indexed citations
10.
Schaake, Susen, et al.. (2022). Benchmarking Low-Frequency Variant Calling With Long-Read Data on Mitochondrial DNA. Frontiers in Genetics. 13. 887644–887644. 8 indexed citations
11.
Graspeuntner, Simon, et al.. (2022). Improving analysis of the vaginal microbiota of women undergoing assisted reproduction using nanopore sequencing. Journal of Assisted Reproduction and Genetics. 39(11). 2659–2667. 5 indexed citations
12.
Schaake, Susen, Inken Wohlers, Jelena Pozojevic, et al.. (2022). Elucidating Hexanucleotide Repeat Number and Methylation within the X-Linked Dystonia-Parkinsonism (XDP)-Related SVA Retrotransposon in TAF1 with Nanopore Sequencing. Genes. 13(1). 126–126. 13 indexed citations
13.
Wasner, Kobi, Christine Klein, Susen Schaake, et al.. (2021). Nanopore Single-Molecule Sequencing for Mitochondrial DNA Methylation Analysis: Investigating Parkin-Associated Parkinsonism as a Proof of Concept. Frontiers in Aging Neuroscience. 13. 713084–713084. 18 indexed citations
14.
Lange, Lara M., Johanna Junker, Sebastian Loens, et al.. (2021). Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review. Movement Disorders. 36(5). 1086–1103. 69 indexed citations
15.
Laabs, Björn‐Hergen, Susen Schaake, Raphaela Ardicoglu, et al.. (2021). Brain Regional Differences in Hexanucleotide Repeat Length in X-Linked Dystonia-Parkinsonism Using Nanopore Sequencing. Neurology Genetics. 7(4). e608–e608. 17 indexed citations
16.
Schaake, Susen, Karen Grütz, Inke R. König, et al.. (2020). DNA Methylation as a Potential Molecular Mechanism in X‐linked Dystonia‐Parkinsonism. Movement Disorders. 35(12). 2220–2229. 6 indexed citations
17.
Simon, David K., Cai Wu, Barbara C. Tilley, et al.. (2017). Caffeine, creatine, GRIN2A and Parkinson's disease progression. Journal of the Neurological Sciences. 375. 355–359. 26 indexed citations
18.
Reiz, Benedikt, et al.. (2017). Dystonia-causing mutations in the transcription factor THAP1 disrupt HCFC1 cofactor recruitment and alter gene expression. Human Molecular Genetics. 26(15). 2975–2983. 12 indexed citations
19.
Vulinović, Franca, Susen Schaake, Aloysius Domingo, et al.. (2017). Screening study of TUBB4A in isolated dystonia. Parkinsonism & Related Disorders. 41. 118–120. 4 indexed citations
20.
Nibbeling, Esther, Susen Schaake, Marina A.J. Tijssen, et al.. (2015). Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia. Journal of Neurology. 262(5). 1340–1343. 15 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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