Matilda R. Jackson

586 total citations
14 papers, 155 citations indexed

About

Matilda R. Jackson is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Matilda R. Jackson has authored 14 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in Matilda R. Jackson's work include Genetics and Neurodevelopmental Disorders (6 papers), Lysosomal Storage Disorders Research (5 papers) and Genomics and Rare Diseases (3 papers). Matilda R. Jackson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Lysosomal Storage Disorders Research (5 papers) and Genomics and Rare Diseases (3 papers). Matilda R. Jackson collaborates with scholars based in Australia, United Kingdom and Finland. Matilda R. Jackson's co-authors include Sharon Byers, Ainslie L.K. Derrick‐Roberts, Cheryl Shoubridge, Michael Field, Carmen E. Pyragius, Victoria L. Harvey, Simon C. Barry, Shervi Lie, Lachlan A. Jolly and Donald S. Anson and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Obstetrics and Gynecology and Genome biology.

In The Last Decade

Matilda R. Jackson

12 papers receiving 154 citations

Peers

Matilda R. Jackson

GENET

PHYSI

EPIDE

Leire Abalde-Atristain United States

Elżbieta Szczepanik Poland

Hormos Salimi Dafsari Germany

T Derksen Netherlands

Sonia Amabile Italy

Leanne Moynihan United Kingdom

Monia Hammer United States

Britta Haenisch Germany

Shanice Beerepoot Netherlands

L. Castelnau France

Leire Abalde-Atristain United States

Matilda R. Jackson

47 ×0.6

GENET

25 ×0.4

PHYSI

211 ×3.9

26 ×1.0

16 ×0.8

EPIDE

Citations per year, relative to Matilda R. Jackson Matilda R. Jackson (= 1×) peers Leire Abalde-Atristain

Countries citing papers authored by Matilda R. Jackson

Since Specialization

Citations

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

Fields of papers citing papers by Matilda R. Jackson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matilda R. Jackson. 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 Matilda R. Jackson. The network helps show where Matilda R. Jackson may publish in the future.

Co-authorship network of co-authors of Matilda R. Jackson

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

All Works

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14 of 14 papers shown

Jackson, Matilda R., Christopher Barnett, Hamish S. Scott, et al.. (2025). Evaluating the Clinical Utility of Genomic Sequencing After Perinatal Death. Clinical Genetics. 109(1). 109–121.

Arthurs, Anya L., Matilda R. Jackson, Hamish S. Scott, et al.. (2025). Circular RNAs accumulate in aging human placental tissue and in stillbirth, leading to DNA damage and cellular senescence. American Journal of Obstetrics and Gynecology. 234(1). 210–229.

Gayevskiy, Velimir, Ryan L. Davis, Marie Wong, et al.. (2023). Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications. Genome biology. 24(1). 118–118. 10 indexed citations

Jackson, Matilda R., et al.. (2021). Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX). Neurobiology of Disease. 153. 105329–105329. 7 indexed citations

Derrick‐Roberts, Ainslie L.K., Xenia Kaidonis, Matilda R. Jackson, et al.. (2020). Comparative analysis of brain pathology in heparan sulphate storing mucopolysaccharidoses. Molecular Genetics and Metabolism. 131(1-2). 197–205. 3 indexed citations

Shoubridge, Cheryl, Matilda R. Jackson, Bronwyn E. Grinton, et al.. (2019). Splice variant in ARX leading to loss of C‐terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathy. American Journal of Medical Genetics Part A. 179(8). 1483–1490. 7 indexed citations

Jackson, Matilda R., Claire C. Homan, Maria Arvio, et al.. (2019). Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females. Life Science Alliance. 2(4). e201900386–e201900386. 16 indexed citations

Jiang, Zhirui, Ainslie L.K. Derrick‐Roberts, Matilda R. Jackson, et al.. (2018). Delayed development of ossification centers in the tibia of prenatal and early postnatal MPS VII mice. Molecular Genetics and Metabolism. 124(2). 135–142. 13 indexed citations

Jackson, Matilda R., Shervi Lie, Lachlan A. Jolly, et al.. (2017). Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis. Translational Psychiatry. 7(5). e1110–e1110. 29 indexed citations

10.

Jackson, Matilda R., Emily J. Jaehne, Ezgi Öztürk, et al.. (2017). Extensive phenotyping of two ARX polyalanine expansion mutation mouse models that span clinical spectrum of intellectual disability and epilepsy. Neurobiology of Disease. 105. 245–256. 7 indexed citations

11.

Ewans, Lisa, Michael Field, Ying Zhu, et al.. (2017). Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy. European Journal of Human Genetics. 25(6). 763–767. 14 indexed citations

12.

Derrick‐Roberts, Ainslie L.K., et al.. (2017). Substrate Deprivation Therapy to Reduce Glycosaminoglycan Synthesis Improves Aspects of Neurological and Skeletal Pathology in MPS I Mice. SHILAP Revista de lepidopterología. 5(1). 5–5. 19 indexed citations

13.

Jackson, Matilda R., et al.. (2015). Mucopolysaccharidosis enzyme production by bone marrow and dental pulp derived human mesenchymal stem cells. Molecular Genetics and Metabolism. 114(4). 584–593. 11 indexed citations

14.

Derrick‐Roberts, Ainslie L.K., Carmen E. Pyragius, Xenia Kaidonis, et al.. (2014). Lentiviral-Mediated Gene Therapy Results in Sustained Expression of β-Glucuronidase for up to 12 Months in the Gus ^mps/mps and up to 18 Months in the Gus ^tm(L175F)Sly Mouse Models of Mucopolysaccharidosis Type VII. Human Gene Therapy. 25(9). 798–810. 19 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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