Cheryl Shoubridge

3.8k citations

49 papers · 1.3k indexed · h-index 20

Genetics top 2%
Molecular Biology top 10%
Cellular and Molecular Neuroscience top 10%
Cognitive Neuroscience top 10%
Cell Biology

Co-authors: Jozef Gécz Mark Corbett Tod Fullston Leanna C. Read Victoria L. Harvey Cory J. Xian Vicki L. Clifton Claire T. Roberts
Topics: Genetics and Neurodevelopmental Disorders (31 papers)Genomic variations and chromosomal abnormalities (15 papers)Genomics and Rare Diseases (7 papers)
Cited by: Genetics Molecular Biology Developmental Neuroscience
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Neuroscience
Partner nations: Australia United States Netherlands

In The Last Decade

Cheryl Shoubridge

48 papers receiving 1.2k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Health Navigator intervention to address the unmet social needs of populations living with cancer attending outpatient treatment at a major metropolitan hospital in Australia: protocol for a mixed-methods feasibility trial 2024 ·BMJ Open ·(unknown),Annabel L. Smith,Sean Martin,Mark Boyd,Christopher Hocking,Cheryl Shoubridge	1
2	Early 17β-estradiol treatment reduces seizures but not abnormal behaviour in mice with expanded polyalanine tracts in the Aristaless related homeobox gene (ARX) 2021 ·Neurobiology of Disease ·(unknown),(unknown),(unknown),(unknown),Matilda R. Jackson,Jeffrey L. Noebels,Cheryl Shoubridge	7
3	Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis 2017 ·Translational Psychiatry ·(unknown),Matilda R. Jackson,Shervi Lie,Lachlan A. Jolly,Michael Field,Simon C. Barry,Victoria L. Harvey,Cheryl Shoubridge	29
4	Extensive phenotyping of two ARX polyalanine expansion mutation mouse models that span clinical spectrum of intellectual disability and epilepsy 2017 ·Neurobiology of Disease ·Matilda R. Jackson,(unknown),(unknown),Emily J. Jaehne,Ezgi Öztürk,Bernhard T. Baune,Terence J. O’Brien,Nigel C. Jones,Cheryl Shoubridge	7
5	Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in theARXhomeobox gene 2016 ·Human Molecular Genetics ·(unknown),(unknown),Jozef Gécz,Gaëlle Friocourt,Cheryl Shoubridge	11
6	Large Scale Gene Expression Meta-Analysis Reveals Tissue-Specific, Sex-Biased Gene Expression in Humans 2016 ·Frontiers in Genetics ·Benjamin Mayne,Tina Bianco‐Miotto,Sam Buckberry,James Breen,Vicki L. Clifton,Cheryl Shoubridge,Claire T. Roberts	79
7	Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation 2013 ·Human Molecular Genetics ·(unknown),(unknown),Kunio Kitamura,Jozef Gécz,Cheryl Shoubridge	19
8	Challenges of “Sticky” Co-immunoprecipitation: Polyalanine Tract Protein–Protein Interactions 2013 ·Methods in molecular biology ·(unknown),(unknown),Jozef Gécz,Cheryl Shoubridge	1
9	A Regulatory Path Associated with X-Linked Intellectual Disability and Epilepsy Links KDM5C to the Polyalanine Expansions in ARX 2012 ·The American Journal of Human Genetics ·(unknown),Francesca Fusco,(unknown),Cheryl Shoubridge,(unknown),Stefania Filosa,Mariateresa Paciolla,Monica Courtney,Patrick Collombat,Maria Brigida Lioi,Jozef Gécz,Matilde Valeria Ursini,Maria Giuseppina Miano	37
10	A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability 2012 ·The American Journal of Human Genetics ·Lingli Huang,Lachlan A. Jolly,Saffron A.G. Willis‐Owen,Alison Gardner,Raman Kumar,Evelyn Douglas,Cheryl Shoubridge,Dagmar Wieczorek,Andreas Tzschach,Monika Cohen,Anna Hackett,Michael Field,Guy Froyen,Hao Hu,Stefan A. Haas,Hans‐Hilger Ropers,Vera M. Kalscheuer,Mark Corbett,Jozef Gécz	73
11	Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation? 2012 ·European Journal of Human Genetics ·Cheryl Shoubridge,Alison Gardner,Charles E. Schwartz,Anna Hackett,Michael Field,Jozef Gécz	5
12	Polyalanine Tract Disorders and Neurocognitive Phenotypes 2012 ·Advances in experimental medicine and biology ·Cheryl Shoubridge,Jozef Gécz	16
13	ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression 2011 ·Human Molecular Genetics ·Cheryl Shoubridge,(unknown),(unknown),Jozef Gécz	19
14	Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene 2011 ·Clinical Genetics ·Tod Fullston,Merran Finnis,Anna Hackett,Bree Hodgson,L A Brueton,Gareth Baynam,Andrew Norman,Orit Reish,Cheryl Shoubridge,Jozef Gécz	16
15	Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism 2009 ·Molecular Psychiatry ·Frédéric Laumonnier,Cheryl Shoubridge,Catherine Antar,Lam Son Nguyen,Hilde Van Esch,Tjitske Kleefstra,Sylvain Briault,J. P. Fryns,B Hamel,Jamel Chelly,Hans‐Hilger Ropers,Nathalie Ronce,(unknown),Claude Moraine,Jozef Gécz,Martine Raynaud	89
16	Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity 2007 ·Gene Expression Patterns ·Anne K. Voss,(unknown),Caitlin Collin,Cheryl Shoubridge,Mark Corbett,Jozef Gécz,Tim Thomas	37
17	Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor 2007 ·Neuroscience ·(unknown),(unknown),Marie Mangelsdorf,Merran Finnis,Gaia Colasante,Cheryl Shoubridge,Stefano Stifani,Jozef Gécz,Vania Broccoli	62
18	Systemically but Not Orogastrically Delivered Insulin-Like Growth Factor (IGF)-I and Long [Arg3]IGF-I Stimulates Intestinal Disaccharidase Activity in Two Age Groups of Suckling Rats 1998 ·Pediatric Research ·(unknown),(unknown),Cheryl Shoubridge,David Tivey,(unknown),Leanna C. Read	12
19	Production of a human epidermal growth factor fusion protein and its degradation in rat gastrointestinal flushings 1996 ·Journal of Molecular Endocrinology ·Cory J. Xian,Zee Upton,C. Goddard,Cheryl Shoubridge,Kerrie A. McNeil,John C. Wallace,Leanna C. Read,Geoffrey L. Francis	1
20	Degradation of IGF-I in the adult rat gastrointestinal tract is limited by a specific antiserum or the dietary protein casein 1995 ·Journal of Endocrinology ·Cory J. Xian,Cheryl Shoubridge,Leanna C. Read	50

About Cheryl Shoubridge

Cheryl Shoubridge is a scholar working on Genetics, Molecular Biology and Developmental Neuroscience, having authored 49 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (31 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (748 citations), Molecular Biology (726 citations) and Developmental Neuroscience (37 citations). Cheryl Shoubridge has collaborated with scholars based in Australia, United States and Netherlands. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neuroscience.

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.

Explore authors with similar magnitude of impact