Gabrielle Wheway

3.6k total citations · 1 hit paper
38 papers, 1.4k citations indexed

About

Gabrielle Wheway is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gabrielle Wheway has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 25 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gabrielle Wheway's work include Genetic and Kidney Cyst Diseases (22 papers), Renal and related cancers (15 papers) and Genetic Syndromes and Imprinting (8 papers). Gabrielle Wheway is often cited by papers focused on Genetic and Kidney Cyst Diseases (22 papers), Renal and related cancers (15 papers) and Genetic Syndromes and Imprinting (8 papers). Gabrielle Wheway collaborates with scholars based in United Kingdom, Egypt and United States. Gabrielle Wheway's co-authors include Liliya Nazlamova, John T. Hancock, Colin A. Johnson, Katarzyna Szymańska, David Parry, Hannah M. Mitchison, Carmel Toomes, Subaashini Natarajan, Matthew Adams and Chris F. Inglehearn and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Cell Science.

In The Last Decade

Gabrielle Wheway

36 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Signaling through the Primary Cilium

2018 340 citations Gabrielle Wheway, Liliya Nazlamova et al. Frontiers in Cell and Developmental Biology profile →

Peers

Gabrielle Wheway

GENET

PPCH

SURGE

Dorien Lugtenberg Netherlands

Jennifer L. Silhavy United States

Abdulrahman Alswaid Saudi Arabia

Norann A. Zaghloul United States

E. Ferda Perçin Türkiye

Pierre Bitoun France

Steffen Lenzner Germany

Boglárka Banizs United States

Rolf W. Stottmann United States

Shuling Fan United States

Dorien Lugtenberg Netherlands

Gabrielle Wheway

1.0k ×1.0

920 ×1.0

GENET

121 ×0.5

97 ×0.7

PPCH

72 ×0.8

SURGE

Citations per year, relative to Gabrielle Wheway Gabrielle Wheway (= 1×) peers Dorien Lugtenberg

Countries citing papers authored by Gabrielle Wheway

Since Specialization

Citations

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

Fields of papers citing papers by Gabrielle Wheway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabrielle Wheway

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

All Works

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20 of 20 papers shown

Wheway, Gabrielle, Htoo A. Wai, Woolf T. Walker, et al.. (2024). Uplift of genetic diagnosis of rare respiratory disease using airway epithelium transcriptome analysis. Human Molecular Genetics. 34(2). 148–160.

Basu, Basudha, Katarzyna Szymańska, Gabrielle Wheway, et al.. (2023). Racgap1 knockdown results in cells with multiple cilia due to cytokinesis failure. Annals of Human Genetics. 88(1). 45–57. 4 indexed citations

Ellard, Sian, Karen Stals, Emma L. Baple, et al.. (2022). Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome. The American Journal of Human Genetics. 109(7). 1217–1241. 22 indexed citations

Jackson, Claire, Janice Coles, Amanda Harris, et al.. (2022). Temporal Whole-Transcriptomic Analysis of Characterized In Vitro and Ex Vivo Primary Nasal Epithelia. Frontiers in Cell and Developmental Biology. 10. 907511–907511. 4 indexed citations

Lord, Jenny, Rebekah Penrice-Randal, Andrés F. Vallejo, et al.. (2022). Evaluating the Immune Response in Treatment-Naive Hospitalised Patients With Influenza and COVID-19. Frontiers in Immunology. 13. 853265–853265. 5 indexed citations

Wheway, Gabrielle, et al.. (2022). Pathogenic KDM5B variants in the context of developmental disorders. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1865(5). 194848–194848. 6 indexed citations

Nazlamova, Liliya, et al.. (2022). Microtubule modification defects underlie cilium degeneration in cell models of retinitis pigmentosa associated with pre-mRNA splicing factor mutations. Frontiers in Genetics. 13. 1009430–1009430. 6 indexed citations

Penrice-Randal, Rebekah, Xiaofeng Dong, Aaron Gardner, et al.. (2022). Blood gene expression predicts intensive care unit admission in hospitalised patients with COVID-19. Frontiers in Immunology. 13. 988685–988685. 5 indexed citations

Wheway, Gabrielle, N. Simon Thomas, Mary Carroll, et al.. (2021). Whole genome sequencing in the diagnosis of primary ciliary dyskinesia. BMC Medical Genomics. 14(1). 234–234. 20 indexed citations

10.

Cheung, Man‐Kim, Tim J. Craig, Gabrielle Wheway, et al.. (2020). WT1 activates transcription of the splice factor kinase SRPK1 gene in PC3 and K562 cancer cells in the absence of corepressor BASP1. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1863(12). 194642–194642. 15 indexed citations

11.

Wheway, Gabrielle, Andrew G. L. Douglas, Diana Baralle, & Elsa G. Guillot. (2020). Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy. Experimental Eye Research. 192. 107950–107950. 42 indexed citations

12.

Abdelhamed, Zakia A., Mohammed E. El‐Asrag, Subaashini Natarajan, et al.. (2019). The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5. Scientific Reports. 9(1). 5446–5446. 13 indexed citations

13.

Wheway, Gabrielle, Liliya Nazlamova, Dann Turner, & Stephen Cross. (2019). 661W Photoreceptor Cell Line as a Cell Model for Studying Retinal Ciliopathies. Frontiers in Genetics. 10. 308–308. 41 indexed citations

14.

Wheway, Gabrielle, Liliya Nazlamova, & John T. Hancock. (2018). Signaling through the Primary Cilium. Frontiers in Cell and Developmental Biology. 6. 8–8. 340 indexed citations breakdown →

15.

Blom, Ashley, et al.. (2018). Development and biological evaluation of fluorophosphonate-modified hydroxyapatite for orthopaedic applications. Journal of Materials Science Materials in Medicine. 29(8). 122–122. 9 indexed citations

16.

Hartill, Verity, Katarzyna Szymańska, Saghira Malik Sharif, Gabrielle Wheway, & Colin A. Johnson. (2017). Meckel–Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances. Frontiers in Pediatrics. 5. 244–244. 99 indexed citations

17.

Abdelhamed, Zakia A., Subaashini Natarajan, Gabrielle Wheway, et al.. (2015). The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway. Disease Models & Mechanisms. 8(6). 527–541. 38 indexed citations

18.

Wheway, Gabrielle, David Parry, & Colin A. Johnson. (2013). The role of primary cilia in the development and disease of the retina. Organogenesis. 10(1). 69–85. 101 indexed citations

19.

Wheway, Gabrielle, Katarzyna Szymańska, Matthew Adams, et al.. (2012). Human Homolog of Drosophila Ariadne (HHARI) is a marker of cellular proliferation associated with nuclear bodies. Experimental Cell Research. 319(3). 161–172. 23 indexed citations

20.

Adams, Matthew, Roslyn Simms, Zakia Abdelhamed, et al.. (2011). A meckelin–filamin A interaction mediates ciliogenesis. Human Molecular Genetics. 21(6). 1272–1286. 85 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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