Ilse Wallaard

406 total citations
9 papers, 249 citations indexed

About

Ilse Wallaard is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Ilse Wallaard has authored 9 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Physiology. Recurrent topics in Ilse Wallaard's work include Genetics and Neurodevelopmental Disorders (6 papers), Genetic Syndromes and Imprinting (5 papers) and Epigenetics and DNA Methylation (4 papers). Ilse Wallaard is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genetic Syndromes and Imprinting (5 papers) and Epigenetics and DNA Methylation (4 papers). Ilse Wallaard collaborates with scholars based in Netherlands, United States and Switzerland. Ilse Wallaard's co-authors include Ype Elgersma, Geeske M. van Woerden, Diana C. Rotaru, Monica Sonzogni, Martina Proietti Onori, Edwin Mientjes, Kamille Dumong Erichsen, Thomas Kremer, Marius C. Hoener and Meghan T. Miller and has published in prestigious journals such as Journal of Neuroscience, Translational Psychiatry and European Journal of Human Genetics.

In The Last Decade

Ilse Wallaard

9 papers receiving 247 citations

Peers

Ilse Wallaard

GENET

MB

CMN

CN

PHYSI

Caroline F. Bruinsma Netherlands

Sonia Amabile Italy

Madelyn A. Gillentine United States

Emilie Landais France

Jin Szatkiewicz United States

Elizabeth S. Barrie United States

Ryan A. Szeto United States

Holger Trucks Germany

Paula Jorge Portugal

Aline Dubos France

Caroline F. Bruinsma Netherlands

Ilse Wallaard

225 ×1.3

GENET

223 ×1.4

MB

30 ×0.9

CMN

45 ×1.4

CN

47 ×1.6

PHYSI

Citations per year, relative to Ilse Wallaard Ilse Wallaard (= 1×) peers Caroline F. Bruinsma

Countries citing papers authored by Ilse Wallaard

Since Specialization

Citations

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

Fields of papers citing papers by Ilse Wallaard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilse Wallaard

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

All Works

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9 of 9 papers shown

1.

Saqib, Muhammad Arif Nadeem, Edwin Mientjes, Anushree Acharya, et al.. (2023). A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome. European Journal of Human Genetics. 31(12). 1447–1454. 3 indexed citations

2.

Rotaru, Diana C., et al.. (2023). UBE3A expression during early postnatal brain development is required for proper dorsomedial striatal maturation. JCI Insight. 8(4). 9 indexed citations

3.

Wang, Li, et al.. (2022). Multidimensional analysis of behavior predicts genotype with high accuracy in a mouse model of Angelman syndrome. Translational Psychiatry. 12(1). 426–426. 6 indexed citations

4.

Wallaard, Ilse, et al.. (2022). Adult Camk2a gene reinstatement restores the learning and plasticity deficits of Camk2a knockout mice. iScience. 25(11). 105303–105303. 6 indexed citations

5.

Mientjes, Edwin, Ilse Wallaard, Kamille Dumong Erichsen, et al.. (2021). Antisense oligonucleotide treatment rescues UBE3A expression and multiple phenotypes of an Angelman syndrome mouse model. JCI Insight. 6(15). 49 indexed citations

6.

Wallaard, Ilse, et al.. (2021). Identifying the temporal electrophysiological and molecular changes that contribute to TSC-associated epileptogenesis. JCI Insight. 6(23). 13 indexed citations

7.

Onori, Martina Proietti, et al.. (2019). Effects of antiepileptic drugs in a new TSC/mTOR‐dependent epilepsy mouse model. Annals of Clinical and Translational Neurology. 6(7). 1273–1291. 34 indexed citations

8.

Rotaru, Diana C., Geeske M. van Woerden, Ilse Wallaard, & Ype Elgersma. (2018). Adult Ube3a Gene Reinstatement Restores the Electrophysiological Deficits of Prefrontal Cortex Layer 5 Neurons in a Mouse Model of Angelman Syndrome. Journal of Neuroscience. 38(37). 8011–8030. 55 indexed citations

9.

Sonzogni, Monica, et al.. (2018). A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants. Molecular Autism. 9(1). 47–47. 74 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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