Mona Grimmel

582 total citations
11 papers, 93 citations indexed

About

Mona Grimmel is a scholar working on Rheumatology, Cell Biology and Genetics. According to data from OpenAlex, Mona Grimmel has authored 11 papers receiving a total of 93 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Rheumatology, 3 papers in Cell Biology and 3 papers in Genetics. Recurrent topics in Mona Grimmel's work include Genetics and Neurodevelopmental Disorders (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Autophagy in Disease and Therapy (2 papers). Mona Grimmel is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Glycogen Storage Diseases and Myoclonus (2 papers) and Autophagy in Disease and Therapy (2 papers). Mona Grimmel collaborates with scholars based in Germany, United States and Chile. Mona Grimmel's co-authors include Tassula Proikas‐Cezanne, Tobias B. Haack, Marc Sturm, Stefanie Beck‐Wödl, Dagmar Wieczorek, Zsuzsanna Takács, Katja Lohmann, Andreas Dufke, Karin Schäferhoff and Rebecca Herzog and has published in prestigious journals such as Brain, Cells and Human Genetics.

In The Last Decade

Mona Grimmel

11 papers receiving 92 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mona Grimmel Germany	5	38	26	19	15	12	11	93
Ilya Kanivets Russia	7	91 2.4×	61 2.3×	15 0.8×	10 0.7×	12 1.0×	39	162
Charu Kaiwar United States	6	56 1.5×	61 2.3×	8 0.4×	8 0.5×	10 0.8×	10	103
Christel Thauvin France	6	81 2.1×	37 1.4×	9 0.5×	8 0.5×	40 3.3×	11	146
Yan Ren China	6	68 1.8×	19 0.7×	17 0.9×	5 0.3×	15 1.3×	17	134
Tatiana Krylova Russia	7	78 2.1×	12 0.5×	10 0.5×	27 1.8×	6 0.5×	26	125
Muhsin Elmas Türkiye	6	47 1.2×	32 1.2×	6 0.3×	4 0.3×	11 0.9×	25	89
Khalid Hundallah Saudi Arabia	7	88 2.3×	48 1.8×	17 0.9×	4 0.3×	15 1.3×	21	165
İbrahim Öncel Türkiye	7	87 2.3×	18 0.7×	18 0.9×	10 0.7×	20 1.7×	23	153
Bronwyn Ridge Australia	12	67 1.8×	26 1.0×	24 1.3×	3 0.2×	17 1.4×	25	352
Lucia Laugwitz Germany	7	47 1.2×	12 0.5×	17 0.9×	6 0.4×	12 1.0×	15	97

Countries citing papers authored by Mona Grimmel

Since Specialization

Citations

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

Fields of papers citing papers by Mona Grimmel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mona Grimmel

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

All Works

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11 of 11 papers shown

Laugwitz, Lucia, Rebecca Buchert, Mona Grimmel, et al.. (2024). Elevated cholesterol is a common phenotype for dominant and recessive ATAD3-associated disorders. Brain. 148(4). e24–e28. 1 indexed citations

Thiels, Charlotte, Thomas Lücke, Tobias Rothoeft, et al.. (2023). ACOX1 Gain-of-Function Variant in Two German Pediatric Patients, in One Case Mimicking Autoimmune Inflammatory Disease. Neuropediatrics. 55(2). 140–145. 4 indexed citations

Grimmel, Mona, Darius Ebrahimi‐Fakhari, Angelika Rieß, et al.. (2022). Expansion of the phenotypic and molecular spectrum of CWF19L1 ‐related disorder. Clinical Genetics. 103(5). 566–573. 2 indexed citations

Bernhard, Wolfgang, et al.. (2021). Resolution of severe hepatosteatosis in a cystic fibrosis patient with multifactorial choline deficiency: A case report. Nutrition. 89. 111348–111348. 2 indexed citations

Grünert, Sarah C., Luciana Hannibal, Anke Schumann, et al.. (2021). Identification and Characterization of a Novel Splice Site Mutation Associated with Glycogen Storage Disease Type VI in Two Unrelated Turkish Families. Diagnostics. 11(3). 500–500. 2 indexed citations

Herzog, Rebecca, Yorck Hellenbroich, Norbert Brüggemann, et al.. (2021). Zonisamide‐responsive myoclonus in SEMA6B‐associated progressive myoclonic epilepsy. Annals of Clinical and Translational Neurology. 8(7). 1524–1527. 11 indexed citations

Laugwitz, Lucia, Rebecca Buchert, Samuel Groeschel, et al.. (2020). Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?. European Journal of Medical Genetics. 63(7). 103938–103938. 5 indexed citations

Park, Joohyun, Karin Schäferhoff, Luigi Janiri, et al.. (2019). Novel HIVEP2 Variants in Patients with Intellectual Disability. Molecular Syndromology. 10(4). 195–201. 7 indexed citations

Takács, Zsuzsanna, et al.. (2019). ATG-18 and EPG-6 are Both Required for Autophagy but Differentially Contribute to Lifespan Control in Caenorhabditis elegans. Cells. 8(3). 236–236. 3 indexed citations

10.

Kuechler, Alma, Mona Grimmel, Jessica Becker, et al.. (2018). De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. Human Genetics. 137(5). 401–411. 16 indexed citations

11.

Grimmel, Mona, et al.. (2015). WIPI-Mediated Autophagy and Longevity. Cells. 4(2). 202–217. 40 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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