Georgina E. Hollway

2.9k total citations
28 papers, 1.5k citations indexed

About

Georgina E. Hollway is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Georgina E. Hollway has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Georgina E. Hollway's work include Developmental Biology and Gene Regulation (7 papers), Genomics and Rare Diseases (6 papers) and Congenital heart defects research (6 papers). Georgina E. Hollway is often cited by papers focused on Developmental Biology and Gene Regulation (7 papers), Genomics and Rare Diseases (6 papers) and Congenital heart defects research (6 papers). Georgina E. Hollway collaborates with scholars based in Australia, United Kingdom and United States. Georgina E. Hollway's co-authors include Peter D. Currie, Nicholas J. Cole, Robert J. Bryson‐Richardson, Thomas E. Hall, Silke Berger, Eric Haan, Jozef Gécz, Philippe Gautier, Andrew J. Donnelly and Helen J. Eyre and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Georgina E. Hollway

28 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Georgina E. Hollway Australia	19	1.0k	502	347	145	133	28	1.5k
Kris Vleminckx Belgium	24	1.4k 1.4×	291 0.6×	252 0.7×	235 1.6×	98 0.7×	58	1.8k
Hajime Ogino Japan	25	1.6k 1.6×	460 0.9×	235 0.7×	83 0.6×	132 1.0×	59	1.9k
Sara Powell United States	15	993 1.0×	356 0.7×	149 0.4×	165 1.1×	77 0.6×	18	1.2k
Claudia Gerri United Kingdom	12	1.5k 1.5×	384 0.8×	561 1.6×	93 0.6×	189 1.4×	16	2.1k
Mary Elizabeth Pownall United Kingdom	21	2.1k 2.0×	441 0.9×	450 1.3×	65 0.4×	109 0.8×	46	2.4k
Ruth M. Arkell Australia	27	2.2k 2.1×	773 1.5×	354 1.0×	136 0.9×	115 0.9×	57	2.7k
Anne Harrington United States	13	1.1k 1.1×	289 0.6×	236 0.7×	102 0.7×	112 0.8×	20	1.5k
Daniel J. Hampshire United Kingdom	15	1.5k 1.5×	1.0k 2.1×	818 2.4×	199 1.4×	91 0.7×	23	2.3k
Mayada Tassabehji United Kingdom	15	1.2k 1.2×	621 1.2×	600 1.7×	71 0.5×	117 0.9×	17	2.2k

Countries citing papers authored by Georgina E. Hollway

Since Specialization

Citations

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

Fields of papers citing papers by Georgina E. Hollway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Georgina E. Hollway. 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 Georgina E. Hollway. The network helps show where Georgina E. Hollway may publish in the future.

Co-authorship network of co-authors of Georgina E. Hollway

This figure shows the co-authorship network connecting the top 25 collaborators of Georgina E. Hollway. A scholar is included among the top collaborators of Georgina E. Hollway 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 Georgina E. Hollway. Georgina E. Hollway 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

Dale, Russell C., Shekeeb S. Mohammad, Velda X. Han, et al.. (2025). Pathogenic variants in chromatin‐related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disorders. Developmental Medicine & Child Neurology. 67(8). 1095–1102. 1 indexed citations

Yanes, Tatiane, et al.. (2023). Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity. European Journal of Human Genetics. 31(10). 1125–1132. 9 indexed citations

Gordon, Louisa G., et al.. (2022). Early cost–utility analysis of genetically guided therapy for patients with drug‐resistant epilepsy. Epilepsia. 63(12). 3111–3121. 1 indexed citations

Mallawaarachchi, Amali, Ben Lundie, Yvonne Hort, et al.. (2021). Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics. 29(5). 760–770. 30 indexed citations

Rodriguez‐Acevedo, Astrid J., Louisa G. Gordon, Nicola Waddell, Georgina E. Hollway, & Lata Vadlamudi. (2021). Developing a Gene Panel for Pharmacoresistant Epilepsy: A Review of Epilepsy Pharmacogenetics. Pharmacogenomics. 22(4). 225–234. 9 indexed citations

Nones, Kátia, Felicity Newell, Olga Kondrashova, et al.. (2019). Detection of actionable variants in various cancer types reveals value of whole-genome sequencing over in-silico whole-exome and hotspot panel sequencing. Annals of Oncology. 30. vii33–vii33. 1 indexed citations

Pajic, Marina, Danielle Froio, Sheridan Daly, et al.. (2017). miR-139-5p Modulates Radiotherapy Resistance in Breast Cancer by Repressing Multiple Gene Networks of DNA Repair and ROS Defense. Cancer Research. 78(2). 501–515. 110 indexed citations

Nguyen, Phong D., Georgina E. Hollway, C. Sonntag, et al.. (2014). Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1. Nature. 512(7514). 314–318. 108 indexed citations

Johnson, Jacque-Lynne, Thomas E. Hall, Jennifer M. Dyson, et al.. (2012). Scube activity is necessary for Hedgehog signal transduction in vivo. Developmental Biology. 368(2). 193–202. 51 indexed citations

10.

Hall, Thomas E., Robert J. Bryson‐Richardson, Silke Berger, et al.. (2007). The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy. Proceedings of the National Academy of Sciences. 104(17). 7092–7097. 145 indexed citations

11.

Hollway, Georgina E., Robert J. Bryson‐Richardson, Silke Berger, et al.. (2007). Whole-Somite Rotation Generates Muscle Progenitor Cell Compartments in the Developing Zebrafish Embryo. Developmental Cell. 12(2). 207–219. 147 indexed citations

12.

Hollway, Georgina E., John Maule, Philippe Gautier, et al.. (2006). Scube2 mediates Hedgehog signalling in the zebrafish embryo. Developmental Biology. 294(1). 104–118. 88 indexed citations

13.

Hollway, Georgina E. & Peter D. Currie. (2005). Vertebrate myotome development. Birth Defects Research Part C Embryo Today Reviews. 75(3). 172–179. 39 indexed citations

14.

Daggett, David F., Robert J. Bryson‐Richardson, Christine Neyt, et al.. (2003). Cadherin-Mediated Differential Cell Adhesion Controls Slow Muscle Cell Migration in the Developing Zebrafish Myotome. Developmental Cell. 5(6). 865–876. 83 indexed citations

15.

Hollway, Georgina E. & Peter D. Currie. (2003). Myotome meanderings. EMBO Reports. 4(9). 855–860. 33 indexed citations

16.

Gécz, Jozef, Shaun Barnett, Jianjun Liu, et al.. (1999). Characterization of the Human Glutamate Receptor Subunit 3 Gene (GRIA3), a Candidate for Bipolar Disorder and Nonspecific X-Linked Mental Retardation. Genomics. 62(3). 356–368. 73 indexed citations

17.

Hollway, Georgina E. & John C. Mulley. (1998). Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders. Clinical Genetics. 54(2). 152–154. 3 indexed citations

18.

Tavner, Fiona, Georgina E. Hollway, Mark Fegan, et al.. (1997). A novel method for development of species and strain-specific DNA probes and PCR primers for identifying Burkholderia solanacearum (formerly Pseudomonas solanacearum). Queensland's institutional digital repository (The University of Queensland). 5(1). 19–30. 129 indexed citations

19.

Hollway, Georgina E., Hilary A. Phillips, Lesley C. Adès, Eric Haan, & John C. Mulley. (1995). Localization of craniosynostosis Adelaide type to 4p16. Human Molecular Genetics. 4(4). 681–683. 39 indexed citations

20.

Edwards, Matthew, Richard J. Roberts, M. W. Partington, et al.. (1994). Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1. American Journal of Medical Genetics. 53(1). 65–71. 18 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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