Ilona Krey

1.9k total citations
21 papers, 203 citations indexed

About

Ilona Krey is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Ilona Krey has authored 21 papers receiving a total of 203 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 8 papers in Psychiatry and Mental health and 6 papers in Molecular Biology. Recurrent topics in Ilona Krey's work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Epilepsy research and treatment (8 papers). Ilona Krey is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers) and Epilepsy research and treatment (8 papers). Ilona Krey collaborates with scholars based in Germany, Denmark and United States. Ilona Krey's co-authors include Johannes R. Lemke, Hongjie Yuan, Tim A. Benke, Stephen F. Traynelis, Kristen Park, Chad R. Camp, Amy J. Ramsey, Rui Song, Konrad Platzer and Julia Hentschel and has published in prestigious journals such as Neurology, Human Molecular Genetics and Epilepsia.

In The Last Decade

Ilona Krey

19 papers receiving 200 citations

Peers

Ilona Krey

GENET

PMH

CMN

PPCH

Susanne Ruf Germany

Estelle Fédirko France

McKenna Kelly United States

Roberta Solazzi Italy

Kirill Shkura United Kingdom

Raffaella Minardi Italy

Matthew Zemel United States

Bing-Mei Li China

Kameryn M. Butler United States

Anne Hempelmann Germany

Susanne Ruf Germany

Ilona Krey

112 ×1.0

GENET

83 ×1.0

PMH

103 ×1.3

74 ×1.4

CMN

30 ×1.1

PPCH

Citations per year, relative to Ilona Krey Ilona Krey (= 1×) peers Susanne Ruf

Countries citing papers authored by Ilona Krey

Since Specialization

Citations

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

Fields of papers citing papers by Ilona Krey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilona Krey

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

All Works

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20 of 20 papers shown

Krey, Ilona, Irene Zarra‐Ferro, & Matias Wagner. (2025). Antisense oligonucleotide therapies for monogenic disorders. Medizinische Genetik. 37(3). 179–187. 1 indexed citations

Krey, Ilona, Konrad Platzer, Andrea Ciolfi, et al.. (2025). Diagnosis of Angelman Syndrome, With 66 Years of Delay, Using Hypothesis‐Free DNA Methylation Profiling. Clinical Genetics. 108(3). 369–370. 1 indexed citations

Krey, Ilona, Janina Gburek‐Augustat, Johannes R. Lemke, et al.. (2024). Precision Medicine in Angelman Syndrome. Neuropediatrics. 56(2). 69–82. 2 indexed citations

Holst, Bjørn, Charlotte Brasch‐Andersen, Rikke S. Møller, et al.. (2024). Generation of two patient specific GABRD variants and their isogenic controls for modeling epilepsy. Stem Cell Research. 76. 103372–103372. 1 indexed citations

Montanucci, Ludovica, Tobias Brünger, Nisha Bhattarai, et al.. (2024). Ligand distances as key predictors of pathogenicity and function in NMDA receptors. Human Molecular Genetics. 34(2). 128–139. 2 indexed citations

Krey, Ilona, et al.. (2024). Spectrum of NMDA Receptor Variants in Neurodevelopmental Disorders and Epilepsy. Methods in molecular biology. 1–11. 2 indexed citations

Brandt, Christian, Christian G. Bien, Ilona Krey, et al.. (2024). Rare and complex epilepsies—Challenges in diagnostics and treatment. English Version. 37(S3). 170–176.

Boßelmann, Christian M., Ingo Borggräfe, Walid Fazeli, et al.. (2023). Genetische Diagnostik der Epilepsien: Empfehlung der Kommission Epilepsie und Genetik der Deutschen Gesellschaft für Epileptologie (DGfE). 36(3). 224–237. 7 indexed citations

Camp, Chad R., Ilona Krey, Tue G. Banke, et al.. (2023). Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons. Communications Biology. 6(1). 952–952. 15 indexed citations

10.

Krey, Ilona, et al.. (2022). Klimawandel und Kindergesundheit – Ein Aufruf zum Handeln. Monatsschrift Kinderheilkunde. 171(1). 63–71.

11.

Krey, Ilona, et al.. (2022). Genetic testing in adults with developmental and epileptic encephalopathy – what do we know?. Medizinische Genetik. 34(3). 207–213. 3 indexed citations

12.

Krey, Ilona, Konrad Platzer, & Johannes R. Lemke. (2022). Monogenetic epilepsies and how to approach them in 2022. Medizinische Genetik. 34(3). 201–205. 1 indexed citations

13.

Zacher, Pia, Tobias Bartolomaeus, Diana Le Duc, et al.. (2021). The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals. Genetics in Medicine. 23(8). 1492–1497. 31 indexed citations

14.

Benke, Tim A., Kristen Park, Ilona Krey, et al.. (2021). Clinical and therapeutic significance of genetic variation in the GRIN gene family encoding NMDARs. Neuropharmacology. 199. 108805–108805. 43 indexed citations

15.

Krey, Ilona, Rami Abou Jamra, Tobias Bartolomaeus, et al.. (2021). Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain. European Journal of Human Genetics. 30(1). 101–110. 2 indexed citations

16.

Meyer, Robert, et al.. (2021). Career satisfaction of German human genetics residents. Medizinische Genetik. 33(4). 343–351. 1 indexed citations

17.

Krey, Ilona, Rikke S. Møller, Sarah Weckhuysen, et al.. (2021). The Angelman Syndrome Online Registry – A multilingual approach to support global research. European Journal of Medical Genetics. 64(12). 104349–104349. 2 indexed citations

18.

Krey, Ilona, Julia Hentschel, Steffen Syrbe, et al.. (2019). Genotype-phenotype correlation on 45 individuals with West syndrome. European Journal of Paediatric Neurology. 25. 134–138. 20 indexed citations

19.

Wengert, Eric R., Jacy L. Wagnon, Katrine M. Johannesen, et al.. (2019). Biallelic inherited SCN8A variants, a rare cause of SCN8A‐related developmental and epileptic encephalopathy. Epilepsia. 60(11). 2277–2285. 11 indexed citations

20.

Hayer, Stefanie N., Ilona Krey, Christian Barro, et al.. (2018). NfL is a biomarker for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. Neurology. 91(16). 755–757. 13 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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