Cheryl Shoubridge

3.8k total citations
49 papers, 1.3k citations indexed

About

Cheryl Shoubridge is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cheryl Shoubridge has authored 49 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 25 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Cheryl Shoubridge's work include Genetics and Neurodevelopmental Disorders (31 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genomics and Rare Diseases (7 papers). Cheryl Shoubridge is often cited by papers focused on Genetics and Neurodevelopmental Disorders (31 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genomics and Rare Diseases (7 papers). Cheryl Shoubridge collaborates with scholars based in Australia, United States and Netherlands. Cheryl Shoubridge's co-authors include Jozef Gécz, Mark Corbett, Tod Fullston, Leanna C. Read, Victoria L. Harvey, Cory J. Xian, Vicki L. Clifton, Claire T. Roberts, Sam Buckberry and Tina Bianco‐Miotto and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neuroscience.

In The Last Decade

Cheryl Shoubridge

48 papers receiving 1.2k citations

Peers

Cheryl Shoubridge
Laura Crisponi Italy
Alix Weaver United States
Arnaud Gos Switzerland
Muhammad Mahajnah Israel
Michele Pinelli Italy
Kenji Amano Japan
Ellen C. Akeson United States
Markus Zweier Switzerland
Milen Velinov United States
Jean‐Baptiste Rivière Canada
Laura Crisponi Italy
Cheryl Shoubridge
Citations per year, relative to Cheryl Shoubridge Cheryl Shoubridge (= 1×) peers Laura Crisponi

Countries citing papers authored by Cheryl Shoubridge

Since Specialization
Citations

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

Fields of papers citing papers by Cheryl Shoubridge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl Shoubridge

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

All Works

20 of 20 papers shown
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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
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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
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Gécz, Jozef, et al.. (2016). Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in theARXhomeobox gene. Human Molecular Genetics. 25(24). ddw360–ddw360. 11 indexed citations
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Mayne, Benjamin, Tina Bianco‐Miotto, Sam Buckberry, et al.. (2016). Large Scale Gene Expression Meta-Analysis Reveals Tissue-Specific, Sex-Biased Gene Expression in Humans. Frontiers in Genetics. 7. 183–183. 79 indexed citations
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Kitamura, Kunio, et al.. (2013). Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation. Human Molecular Genetics. 23(4). 1084–1094. 19 indexed citations
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Gécz, Jozef, et al.. (2013). Challenges of “Sticky” Co-immunoprecipitation: Polyalanine Tract Protein–Protein Interactions. Methods in molecular biology. 1017. 121–133. 1 indexed citations
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Fusco, Francesca, Cheryl Shoubridge, Stefania Filosa, et al.. (2012). A Regulatory Path Associated with X-Linked Intellectual Disability and Epilepsy Links KDM5C to the Polyalanine Expansions in ARX. The American Journal of Human Genetics. 92(1). 114–125. 37 indexed citations
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Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations
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Shoubridge, Cheryl, Alison Gardner, Charles E. Schwartz, et al.. (2012). Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation?. European Journal of Human Genetics. 20(12). 1311–1314. 5 indexed citations
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Shoubridge, Cheryl & Jozef Gécz. (2012). Polyalanine Tract Disorders and Neurocognitive Phenotypes. Advances in experimental medicine and biology. 769. 185–203. 16 indexed citations
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Shoubridge, Cheryl, et al.. (2011). ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression. Human Molecular Genetics. 21(7). 1639–1647. 19 indexed citations
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Fullston, Tod, Merran Finnis, Anna Hackett, et al.. (2011). Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene. Clinical Genetics. 80(6). 510–522. 16 indexed citations
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Laumonnier, Frédéric, Cheryl Shoubridge, Catherine Antar, et al.. (2009). Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. Molecular Psychiatry. 15(7). 767–776. 89 indexed citations
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Voss, Anne K., Caitlin Collin, Cheryl Shoubridge, et al.. (2007). Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity. Gene Expression Patterns. 7(8). 858–871. 37 indexed citations
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Mangelsdorf, Marie, Merran Finnis, Gaia Colasante, et al.. (2007). Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor. Neuroscience. 146(1). 236–247. 62 indexed citations
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Xian, Cory J., Zee Upton, C. Goddard, et al.. (1996). Production of a human epidermal growth factor fusion protein and its degradation in rat gastrointestinal flushings. Journal of Molecular Endocrinology. 16(1). 89–97. 1 indexed citations
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Xian, Cory J., Cheryl Shoubridge, & Leanna C. Read. (1995). Degradation of IGF-I in the adult rat gastrointestinal tract is limited by a specific antiserum or the dietary protein casein. Journal of Endocrinology. 146(2). 215–225. 50 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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