Kate Pope

3.2k total citations
28 papers, 867 citations indexed

About

Kate Pope is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kate Pope has authored 28 papers receiving a total of 867 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Kate Pope's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and DNA Repair Mechanisms (3 papers). Kate Pope is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and DNA Repair Mechanisms (3 papers). Kate Pope collaborates with scholars based in Australia, United States and United Kingdom. Kate Pope's co-authors include Paul J. Lockhart, Richard J. Leventer, David J. Amor, Greta Gillies, Martin B. Delatycki, Melanie Bahlo, Wirginia Maixner, A. Simon Harvey, Duncan MacGregor and Simone Mandelstam and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Kate Pope

25 papers receiving 857 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kate Pope Australia 17 567 392 147 98 96 28 867
Alexandra Afenjar France 16 521 0.9× 621 1.6× 127 0.9× 106 1.1× 113 1.2× 42 1.0k
Kyle Retterer United States 24 681 1.2× 906 2.3× 193 1.3× 72 0.7× 187 1.9× 37 1.4k
Zöe Powis United States 15 387 0.7× 562 1.4× 88 0.6× 61 0.6× 115 1.2× 34 873
Sunita Venkateswaran Canada 15 333 0.6× 261 0.7× 143 1.0× 73 0.7× 79 0.8× 33 769
Gladys Ho Australia 19 778 1.4× 855 2.2× 102 0.7× 63 0.6× 67 0.7× 43 1.4k
Nathalie Dorison France 16 293 0.5× 187 0.5× 281 1.9× 154 1.6× 163 1.7× 30 741
Emmanuelle Lemyre Canada 22 550 1.0× 879 2.2× 88 0.6× 55 0.6× 276 2.9× 52 1.3k
Alice Goldenberg France 20 678 1.2× 565 1.4× 47 0.3× 124 1.3× 91 0.9× 49 1.1k
Saad Al Shahwan Saudi Arabia 8 409 0.7× 269 0.7× 85 0.6× 243 2.5× 189 2.0× 14 900
Delphine Roussel France 15 383 0.7× 170 0.4× 100 0.7× 102 1.0× 55 0.6× 26 848

Countries citing papers authored by Kate Pope

Since Specialization
Citations

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

Fields of papers citing papers by Kate Pope

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Pope

This figure shows the co-authorship network connecting the top 25 collaborators of Kate Pope. A scholar is included among the top collaborators of Kate Pope 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 Kate Pope. Kate Pope 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
1.
Rafehi, Haloom, Liam G. Fearnley, Penny Snell, et al.. (2025). Comprehensive Characterisation of the RFC1 Repeat in an Australian Cohort. The Cerebellum. 24(4). 111–111.
2.
Coleman, Matthew, Min Wang, Penny Snell, et al.. (2024). The genetic landscape and classification of infantile epileptic spasms syndrome requiring surgery due to suspected focal brain malformations. Brain Communications. 7(1). fcaf034–fcaf034.
3.
Rafehi, Haloom, David J. Szmulewicz, Kate Pope, et al.. (2020). Rapid Diagnosis of Spinocerebellar Ataxia 36 in a Three‐Generation Family Using Short‐Read Whole‐Genome Sequencing Data. Movement Disorders. 35(9). 1675–1679. 7 indexed citations
4.
Stephenson, Sarah, Kate Pope, Greta Gillies, et al.. (2020). Genetic characterization identifies bottom-of-sulcus dysplasia as an mTORopathy. Neurology. 95(18). e2542–e2551. 30 indexed citations
5.
Stephenson, Sarah, Katherine B. Howell, Kate Pope, et al.. (2019). Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA. Annals of Clinical and Translational Neurology. 6(7). 1338–1344. 55 indexed citations
6.
Bozaoglu, Kiymet, Yujing Gao, Edouard G. Stanley, et al.. (2019). Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder. Stem Cell Research. 39. 101516–101516. 5 indexed citations
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Wan, Jijun, Janos Steffen, Michael Yourshaw, et al.. (2016). Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. Brain. 139(11). 2877–2890. 69 indexed citations
10.
Wilson, Brian T., Zornitza Stark, Sumita Danda, et al.. (2015). The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care. Genetics in Medicine. 18(5). 483–493. 108 indexed citations
11.
Scerri, Thomas, Jessica R. Riseley, Greta Gillies, et al.. (2015). Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5. Annals of Clinical and Translational Neurology. 2(5). 575–580. 77 indexed citations
12.
Scerri, Thomas, Miriam Fanjul‐Fernández, Jessica R. Riseley, et al.. (2015). Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3. Annals of Neurology. 79(1). 132–137. 102 indexed citations
13.
Leventer, Richard J., Thomas Scerri, Ashley P.L. Marsh, et al.. (2015). Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR. Neurology. 84(20). 2029–2032. 54 indexed citations
14.
Morgan, Angela, Cristina Mei, Damien Lederer, et al.. (2015). Speech and language in a genotyped cohort of individuals with Kabuki syndrome. American Journal of Medical Genetics Part A. 167(7). 1483–1492. 27 indexed citations
15.
White, Susan M., Elizabeth Fitzpatrick, Gabrielle R. Wilson, et al.. (2014). Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency. Orphanet Journal of Rare Diseases. 9(1). 43–43. 15 indexed citations
16.
Miller, Kerry A., Casey Ah-Cann, Tiong Yang Tan, et al.. (2013). Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome. PLoS Genetics. 9(8). e1003746–e1003746. 46 indexed citations
17.
Wilson, Gabrielle R., Katherine R. Smith, Kate Pope, et al.. (2013). Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. European Journal of Human Genetics. 22(6). 741–747. 30 indexed citations
18.
Pope, Kate, et al.. (2012). Job and Career Resources: Not Just for Public Libraries. Georgia Library Quarterly. 49(2).
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20.
Tan, Tiong Yang, Amanda Collins, Paul A. James, et al.. (2011). Phenotypic variability of distal 22q11.2 copy number abnormalities. American Journal of Medical Genetics Part A. 155(7). 1623–1633. 54 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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