Astrid Oudakker

2.1k citations

20 papers · 1.1k indexed · h-index 14

Genetics top 5%
Molecular Biology
Cognitive Neuroscience top 10%
Reproductive Medicine top 5%
Public Health, Environmental and Occupational Health

Co-authors: 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
Topics: Genetics and Neurodevelopmental Disorders (10 papers)Epigenetics and DNA Methylation (5 papers)Neuroscience and Neuropharmacology Research (3 papers)
Cited by: Genetics Reproductive Medicine Molecular Biology
Journals: Nature Communications Neuron Brain
Partner nations: Netherlands France United States

In The Last Decade

Astrid Oudakker

19 papers receiving 1.0k citations

Peers

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

#	Work	Indexed citations
1	Targeting AASS alleviates neurotoxicity and improves mitochondrial function in astrocyte models for pyridoxine-dependent epilepsy 2025 ·Molecular Therapy — Nucleic Acids ·(unknown),Udo F. H. Engelke,(unknown),(unknown),(unknown),(unknown),(unknown),Astrid Oudakker,(unknown),Dirk J. Lefeber,Blair R. Leavitt,Clara D.M. van Karnebeek,Nael Nadif Kasri,Alejandro Garanto	0
2	CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability 2024 ·Brain ·(unknown),(unknown),(unknown),Elly Lewerissa,(unknown),(unknown),(unknown),(unknown),Ellen van Beusekom,Astrid Oudakker,Naoki Kogo,Amalia M. Dolga,Monica Frega,Dirk Schubert,(unknown),(unknown),Hans van Bokhoven	5
3	Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9 2023 ·Stem Cell Research ·(unknown),Chantal Schoenmaker,Ka Man Wu,Astrid Oudakker,Ronald Roepman,Nael Nadif Kasri	2
4	A human in vitro neuronal model for studying homeostatic plasticity at the network level 2023 ·Stem Cell Reports ·(unknown),(unknown),Jon-Ruben van Rhijn,(unknown),Anna Esteve‐Codina,Mandy Meijer,(unknown),Eline van Hugte,Astrid Oudakker,Chantal Schoenmaker,Monica Frega,Dirk Schubert,Barbara Franke,Nael Nadif Kasri	5
5	Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders 2021 ·Autophagy ·Katrin Linda,Elly Lewerissa,Anouk H. A. Verboven,Michele Gabriele,Monica Frega,Teun M. Klein Gunnewiek,Lynn Devilée,(unknown),(unknown),Astrid Oudakker,Chantal Schoenmaker,Hans van Bokhoven,Dirk Schubert,Giuseppe Testa,David A. Koolen,Bert B.A. de Vries,Nael Nadif Kasri	46
6	Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype 2020 ·Cell Reports ·Monica Frega,Martijn Selten,Britt Mossink,Jason M. Keller,Katrin Linda,(unknown),Jieqiong Qu,(unknown),Sophie Jansen,Astrid Oudakker,Tjitske Kleefstra,Hans van Bokhoven,Huiqing Zhou,Dirk Schubert,Nael Nadif Kasri	37
7	Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling 2019 ·Nature Communications ·Monica Frega,Katrin Linda,Jason M. Keller,Güvem Gümüş‐Akay,Britt Mossink,(unknown),Moritz Negwer,Teun M. Klein Gunnewiek,(unknown),(unknown),Chantal Schoenmaker,Willem M.R. van den Akker,(unknown),Astrid Oudakker,Huiqing Zhou,Tjitske Kleefstra,Dirk Schubert,Hans van Bokhoven,Nael Nadif Kasri	82
8	ARHGAP12 Functions as a Developmental Brake on Excitatory Synapse Function 2016 ·Cell Reports ·Wei Ba,Martijn Selten,(unknown),(unknown),Lili Li,Marco Benevento,Astrid Oudakker,(unknown),(unknown),Ronald Roepman,(unknown),Michael J. Courtney,Hans van Bokhoven,(unknown)	22
9	Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling 2016 ·Neuron ·Marco Benevento,Giovanni Iacono,Martijn Selten,Wei Ba,Astrid Oudakker,Monica Frega,Jason Keller,Roberta Mancini,Elly Lewerissa,Tjitske Kleefstra,Henk G. Stunnenberg,Huiqing Zhou,Hans van Bokhoven,Nael Nadif Kasri	65
10	Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice 2013 ·Developmental Biology ·(unknown),Muhammad Ansar,Astrid Oudakker,A. van Caam,(unknown),E.L. Vitters,P.M. van der Kraan,Diederik R.H. de Bruijn,Sanne Janssen,Arthur J. Kuipers,Manon M. H. Huibers,(unknown),X. Frank Walboomers,Marco Benevento,Nael Nadif Kasri,Tjitske Kleefstra,Huiqing Zhou,Catharina E.E.M. Van der Zee,Hans van Bokhoven	55
11	A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy 2013 ·European Journal of Human Genetics ·Arjan Pm de Brouwer,Sander B. Nabuurs,Ingrid E.C. Verhaart,Astrid Oudakker,Roel Hordijk,Helger G. Yntema,(unknown),Krysta Voesenek,(unknown),Ton van Essen,Wei Chen,Hao Hu,Jamel Chelly,Johan T. den Dunnen,Vera M. Kalscheuer,Annemieke Aartsma‐Rus,Ben C.J. Hamel,Hans van Bokhoven,Tjitske Kleefstra	29
12	Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome 2010 ·Clinical Genetics ·Juliana F. Mazzeu,(unknown),Ana Cristina Victorino Krepischi,Astrid Oudakker,Carla Rosenberg,Károly Szuhai,James McGill,(unknown),Hans van Bokhoven,HG Brunner	9
13	Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax 2009 ·American Journal of Medical Genetics Part A ·Dorien Lugtenberg,Arjan P.M. de Brouwer,Astrid Oudakker,Rolph Pfundt,Ben C.J. Hamel,Hans van Bokhoven,Ernie M.H.F. Bongers	17
14	Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia 2007 ·The American Journal of Human Genetics ·(unknown),Isabelle Koscinski,Jan A.M. Kremer,Céline Moutou,(unknown),Astrid Oudakker,Herman Tournaye,Nicolas Charlet‐Berguerand,Clotilde Lagier‐Tourenne,Hans van Bokhoven,Stéphane Viville	226
15	Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome 2006 ·The American Journal of Human Genetics ·Tjitske Kleefstra,Han G. Brunner,Jeanne Amiel,Astrid Oudakker,Willy M. Nillesen,Alex Magee,David Geneviève,Valérie Cormier‐Daire,Hilde Van Esch,Jean‐Pierre Fryns,Ben C.J. Hamel,Erik A. Sistermans,Bert B.A. de Vries,Hans van Bokhoven	276
16	ZNF674: A New Krüppel-Associated Box–Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation 2006 ·The American Journal of Human Genetics ·Dorien Lugtenberg,Helger G. Yntema,(unknown),Astrid Oudakker,Helen V. Firth,Lionel Willatt,Martine Raynaud,Tjitske Kleefstra,Jean‐Pierre Fryns,Hans‐Hilger Ropers,Jamel Chelly,Claude Moraine,Jozef Gécz,Jeroen van Reeuwijk,Sander B. Nabuurs,Bert B.A. de Vries,Ben C.J. Hamel,Arjan P.M. de Brouwer,Hans van Bokhoven	60
17	MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics 2003 ·European Journal of Human Genetics ·Tjitske Kleefstra,Helger G. Yntema,Willy M. Nillesen,Astrid Oudakker,Reinier A. Mullaart,(unknown),Hans van Bokhoven,(unknown),Erik A. Sistermans,Ben C.J. Hamel	37
18	Expanding phenotype of XNP mutations: Mild to moderate mental retardation 2002 ·American Journal of Medical Genetics ·Helger G. Yntema,Francis A.M. Poppelaars,(unknown),Astrid Oudakker,(unknown),Anja Jacobs,(unknown),Han G. Brunner,Ben C.J. Hamel,Hans van Bokhoven	33
19	Low frequency of MECP2 mutations in mentally retarded males 2002 ·European Journal of Human Genetics ·Helger G. Yntema,Tjitske Kleefstra,Astrid Oudakker,(unknown),Bert B.A. de Vries,Willy M. Nillesen,Erik A. Sistermans,Han G. Brunner,Ben C.J. Hamel,Hans van Bokhoven	43
20	Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression 2002 ·Fertility and Sterility ·J.H.A.M. Tuerlings,Ron J T van Golde,Astrid Oudakker,Helger G. Yntema,Jan A.M. Kremer	7

About Astrid Oudakker

Astrid Oudakker is a scholar working on Genetics, Reproductive Medicine and Molecular Biology, having authored 20 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Epigenetics and DNA Methylation (5 papers) and Neuroscience and Neuropharmacology Research (3 papers). The work is most often cited by research in Genetics (673 citations), Reproductive Medicine (176 citations) and Molecular Biology (667 citations). Astrid Oudakker has collaborated with scholars based in Netherlands, France and United States. Frequent 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. Their work appears in journals such as Nature Communications, Neuron and Brain.

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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