Gemma Poke

1.4k total citations
24 papers, 406 citations indexed

About

Gemma Poke is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Gemma Poke has authored 24 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Genetics. Recurrent topics in Gemma Poke's work include Neurogenetic and Muscular Disorders Research (5 papers), Genetic Neurodegenerative Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gemma Poke is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), Genetic Neurodegenerative Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gemma Poke collaborates with scholars based in New Zealand, Australia and United Kingdom. Gemma Poke's co-authors include John Caird, D. Gareth Evans, James O’Sullivan, Sanjeev S. Bhaskar, William G. Newman, David Fitzpatrick, Diana Eccles, Kristen D. Hadfield, Saba Sharif and Daniel du Plessis and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Gemma Poke

24 papers receiving 403 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gemma Poke New Zealand 10 206 110 102 96 61 24 406
Cecilie F. Rustad Norway 11 210 1.0× 111 1.0× 170 1.7× 116 1.2× 72 1.2× 18 491
Paweł Daszkiewicz Poland 12 107 0.5× 66 0.6× 87 0.9× 41 0.4× 158 2.6× 44 464
Hyung-Jin Shin South Korea 14 64 0.3× 116 1.1× 178 1.7× 56 0.6× 148 2.4× 22 521
Judith M.A. Verhagen Netherlands 11 184 0.9× 84 0.8× 36 0.4× 161 1.7× 19 0.3× 35 464
Teresa Giugliano Italy 12 189 0.9× 37 0.3× 110 1.1× 94 1.0× 51 0.8× 21 339
Marylène Rousseau Canada 8 106 0.5× 58 0.5× 111 1.1× 125 1.3× 11 0.2× 9 345
Susanne Gerit Kircher Austria 12 81 0.4× 115 1.0× 19 0.2× 73 0.8× 22 0.4× 48 420
You-Nam Chung South Korea 11 70 0.3× 61 0.6× 144 1.4× 20 0.2× 76 1.2× 26 401
Nesrin Karabul Germany 15 101 0.5× 130 1.2× 46 0.5× 30 0.3× 41 0.7× 24 580
Tetsuya Oishi Japan 10 105 0.5× 51 0.5× 37 0.4× 40 0.4× 77 1.3× 33 420

Countries citing papers authored by Gemma Poke

Since Specialization
Citations

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

Fields of papers citing papers by Gemma Poke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gemma Poke

This figure shows the co-authorship network connecting the top 25 collaborators of Gemma Poke. A scholar is included among the top collaborators of Gemma Poke 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 Gemma Poke. Gemma Poke 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.
Loddo, Sara, Gemma Poke, Valérie Malan, et al.. (2024). Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions. American Journal of Medical Genetics Part A. 194(7). e63580–e63580. 1 indexed citations
2.
Xu, Zhao, Lynette G. Sadleir, Himanshu Goel, et al.. (2024). Genotype and phenotype correlation of PHACTR1-related neurological disorders. Journal of Medical Genetics. 61(6). 536–542. 1 indexed citations
3.
Wilson, Callum, Howard Potter, Andrea L. Vincent, et al.. (2023). Mitochondrial disease in New Zealand: a nationwide prevalence study. Internal Medicine Journal. 54(3). 388–397. 2 indexed citations
4.
Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations
5.
Theadom, Alice, Miriam Rodrigues, Annemarei Ranta, et al.. (2021). Impact and predictors of quality of life in adults diagnosed with a genetic muscle disorder: a nationwide population-based study. Quality of Life Research. 31(6). 1657–1666. 4 indexed citations
6.
Poke, Gemma, et al.. (2021). Epidemiological, clinical, pathological and genetic characteristics of epidermolysis bullosa in New Zealand. Australasian Journal of Dermatology. 63(1). 62–67. 6 indexed citations
7.
Poke, Gemma, et al.. (2020). Perry syndrome: a case of atypical parkinsonism with confirmed DCTN1 mutation.. PubMed. 133(1513). 116–118. 2 indexed citations
8.
Theadom, Alice, Miriam Rodrigues, Gemma Poke, et al.. (2019). A Nationwide, Population-Based Prevalence Study of Genetic Muscle Disorders. Neuroepidemiology. 52(3-4). 128–135. 26 indexed citations
9.
Ngo, Kathie J., Gemma Poke, Katherine Neas, & Brent L. Fogel. (2019). Spinocerebellar Ataxia type 29 in a family of Māori descent. SHILAP Revista de lepidopterología. 6(1). 14–14. 4 indexed citations
10.
Malerba, Natascia, Patrizia Benzoni, Gabriella Maria Squeo, et al.. (2019). Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line. Stem Cell Research. 40. 101547–101547. 2 indexed citations
11.
Kamien, Benjamin, Anne Ronan, Gemma Poke, et al.. (2018). A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing. Molecular Syndromology. 9(2). 70–82. 32 indexed citations
12.
Mossman, Stuart, et al.. (2018). A Novel CACNA1A Nonsense Variant [c.4054C>T (p.Arg1352⁎)] Causing Episodic Ataxia Type 2. SHILAP Revista de lepidopterología. 2018. 1–3. 1 indexed citations
13.
Wong, William, et al.. (2016). Phenotypic variability of Dent disease in a large New Zealand kindred. Pediatric Nephrology. 32(2). 365–369. 12 indexed citations
14.
Ravenscroft, Gianina, Nataliya Di Donato, Gabriele Hahn, et al.. (2016). Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria. Neuromuscular Disorders. 26(11). 744–748. 39 indexed citations
15.
Ravenscroft, Gianina, Nataliya Di Donato, Mark R. Davis, et al.. (2016). Recurrent de novo BICD2 mutation associated with severe arthrogryposis and polymicrogyria: Expanding the phenotype. Neuromuscular Disorders. 26. S106–S107. 1 indexed citations
16.
Theadom, Alice, Richard Roxburgh, Gina O’Grady, et al.. (2016). Prevalence of genetic muscle disorders (MD-Prev): A national, population-based study. Neuromuscular Disorders. 26. S206–S206. 1 indexed citations
17.
Smith, Miriam J., Sanjeev S. Bhaskar, Kristen D. Hadfield, et al.. (2014). Involvement of the SWI/SNF Complex in Familial Meningiomatosis. Cancer Genetics. 207(9). 445–445. 1 indexed citations
18.
Smith, Miriam J., James O’Sullivan, Sanjeev S. Bhaskar, et al.. (2013). Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas. Nature Genetics. 45(3). 295–298. 168 indexed citations
19.
Poke, Gemma, et al.. (2012). Segmental Maternal UPD6 with Prenatal Growth Restriction. Molecular Syndromology. 3(6). 270–273. 11 indexed citations
20.
Huang, Lingli, Gemma Poke, Jozef Gécz, & Kate Gibson. (2012). A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disability. American Journal of Medical Genetics Part A. 158A(10). 2511–2518. 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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