Astrid Oudakker

2.1k total citations
20 papers, 1.1k citations indexed

About

Astrid Oudakker is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Astrid Oudakker has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Astrid Oudakker's work include Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (5 papers) and Neuroscience and Neuropharmacology Research (3 papers). Astrid Oudakker is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (5 papers) and Neuroscience and Neuropharmacology Research (3 papers). Astrid Oudakker collaborates with scholars based in Netherlands, France and United States. Astrid Oudakker's co-authors include Hans van Bokhoven, Tjitske Kleefstra, Ben C.J. Hamel, Bert B.A. de Vries, Willy M. Nillesen, Erik A. Sistermans, Han G. Brunner, Jean‐Pierre Fryns, Jan A.M. Kremer and Clotilde Lagier‐Tourenne and has published in prestigious journals such as Nature Communications, Neuron and Brain.

In The Last Decade

Astrid Oudakker

19 papers receiving 1.0k citations

Peers

Astrid Oudakker

GENET

PHEOH

Se‐Jin Yoon South Korea

Helena Sim Australia

Anne Maddalena United States

Toshiaki Hino Japan

Elisabeth Gabau Spain

Masayuki Anzai Japan

Aparna Prasad United States

Eeva-Marja Sankila Finland

Peter Teague United Kingdom

Matthew R. Avenarius United States

Se‐Jin Yoon South Korea

Astrid Oudakker

156 ×0.2

GENET

989 ×1.5

99 ×0.6

116 ×0.7

190 ×1.5

PHEOH

Citations per year, relative to Astrid Oudakker Astrid Oudakker (= 1×) peers Se‐Jin Yoon

Countries citing papers authored by Astrid Oudakker

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Oudakker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Oudakker

This figure shows the co-authorship network connecting the top 25 collaborators of Astrid Oudakker. A scholar is included among the top collaborators of Astrid Oudakker 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 Astrid Oudakker. Astrid Oudakker 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

Engelke, Udo F. H., Astrid Oudakker, Dirk J. Lefeber, et al.. (2025). Targeting AASS alleviates neurotoxicity and improves mitochondrial function in astrocyte models for pyridoxine-dependent epilepsy. Molecular Therapy — Nucleic Acids. 36(4). 102728–102728.

Lewerissa, Elly, Ellen van Beusekom, Astrid Oudakker, et al.. (2024). CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability. Brain. 148(4). 1286–1301. 5 indexed citations

Schoenmaker, Chantal, et al.. (2023). Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9. Stem Cell Research. 68. 103053–103053. 2 indexed citations

Rhijn, Jon-Ruben van, Anna Esteve‐Codina, Mandy Meijer, et al.. (2023). A human in vitro neuronal model for studying homeostatic plasticity at the network level. Stem Cell Reports. 18(11). 2222–2239. 5 indexed citations

Linda, Katrin, Elly Lewerissa, Anouk H. A. Verboven, et al.. (2021). Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders. Autophagy. 18(2). 423–442. 46 indexed citations

Frega, Monica, Martijn Selten, Britt Mossink, et al.. (2020). Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype. Cell Reports. 30(1). 173–186.e6. 37 indexed citations

Frega, Monica, Katrin Linda, Jason M. Keller, et al.. (2019). Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling. Nature Communications. 10(1). 4928–4928. 82 indexed citations

Ba, Wei, Martijn Selten, Lili Li, et al.. (2016). ARHGAP12 Functions as a Developmental Brake on Excitatory Synapse Function. Cell Reports. 14(6). 1355–1368. 22 indexed citations

Benevento, Marco, Giovanni Iacono, Martijn Selten, et al.. (2016). Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling. Neuron. 91(2). 341–355. 65 indexed citations

10.

Ansar, Muhammad, Astrid Oudakker, A. van Caam, et al.. (2013). Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. Developmental Biology. 386(2). 395–407. 55 indexed citations

11.

Brouwer, Arjan Pm de, Sander B. Nabuurs, Ingrid E.C. Verhaart, et al.. (2013). A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy. European Journal of Human Genetics. 22(4). 480–485. 29 indexed citations

12.

Mazzeu, Juliana F., Ana Cristina Victorino Krepischi, Astrid Oudakker, et al.. (2010). Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics. 77(4). 404–407. 9 indexed citations

13.

Lugtenberg, Dorien, Arjan P.M. de Brouwer, Astrid Oudakker, et al.. (2009). Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax. American Journal of Medical Genetics Part A. 149A(4). 760–766. 17 indexed citations

14.

Koscinski, Isabelle, Jan A.M. Kremer, Céline Moutou, et al.. (2007). Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia. The American Journal of Human Genetics. 81(4). 813–820. 226 indexed citations

15.

Kleefstra, Tjitske, Han G. Brunner, Jeanne Amiel, et al.. (2006). Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome. The American Journal of Human Genetics. 79(2). 370–377. 276 indexed citations

16.

Lugtenberg, Dorien, Helger G. Yntema, Astrid Oudakker, et al.. (2006). ZNF674: A New Krüppel-Associated Box–Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation. The American Journal of Human Genetics. 78(2). 265–278. 60 indexed citations

17.

Kleefstra, Tjitske, Helger G. Yntema, Willy M. Nillesen, et al.. (2003). MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics. European Journal of Human Genetics. 12(1). 24–28. 37 indexed citations

18.

Yntema, Helger G., Francis A.M. Poppelaars, Astrid Oudakker, et al.. (2002). Expanding phenotype of XNP mutations: Mild to moderate mental retardation. American Journal of Medical Genetics. 110(3). 243–247. 33 indexed citations

19.

Yntema, Helger G., Tjitske Kleefstra, Astrid Oudakker, et al.. (2002). Low frequency of MECP2 mutations in mentally retarded males. European Journal of Human Genetics. 10(8). 487–490. 43 indexed citations

20.

Tuerlings, J.H.A.M., Ron J T van Golde, Astrid Oudakker, Helger G. Yntema, & Jan A.M. Kremer. (2002). Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression. Fertility and Sterility. 77(2). 415–418. 7 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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