Fiona C. Mansergh

1.5k total citations · 1 hit paper
36 papers, 1.2k citations indexed

About

Fiona C. Mansergh is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Fiona C. Mansergh has authored 36 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 8 papers in Cell Biology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Fiona C. Mansergh's work include Retinal Development and Disorders (8 papers), Pluripotent Stem Cells Research (6 papers) and Photoreceptor and optogenetics research (5 papers). Fiona C. Mansergh is often cited by papers focused on Retinal Development and Disorders (8 papers), Pluripotent Stem Cells Research (6 papers) and Photoreceptor and optogenetics research (5 papers). Fiona C. Mansergh collaborates with scholars based in Ireland, United Kingdom and Canada. Fiona C. Mansergh's co-authors include Michael A. Wride, Paul F. Kenna, G. Jane Farrar, Derrick E. Rancourt, Peter Humphries, Martin Evans, Hanan Elshelmani, Balamurali K. Ambati, Ruth Hogg and Nathan G. Lambert and has published in prestigious journals such as Bioinformatics, Gut and The American Journal of Human Genetics.

In The Last Decade

Fiona C. Mansergh

36 papers receiving 1.2k citations

Hit Papers

align trajectories sort by overperformance

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.

Risk factors and biomarkers of age-related macular degeneration

2016 261 citations Fiona C. Mansergh, Michael A. Wride et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fiona C. Mansergh Ireland	19	770	393	260	214	157	36	1.2k
Matthew J. Brooks United States	20	1.0k 1.3×	251 0.6×	325 1.3×	115 0.5×	88 0.6×	37	1.2k
Benjamin J. Frankfort United States	18	894 1.2×	398 1.0×	307 1.2×	165 0.8×	154 1.0×	44	1.3k
Felix Tonagel Germany	14	772 1.0×	347 0.9×	132 0.5×	97 0.5×	124 0.8×	33	1.0k
Alexander B. Quiambao United States	16	924 1.2×	338 0.9×	282 1.1×	117 0.5×	135 0.9×	26	1.1k
Jeffrey A. Hammer United States	14	577 0.7×	240 0.6×	241 0.9×	151 0.7×	112 0.7×	18	899
Robert B. Hufnagel United States	20	848 1.1×	307 0.8×	135 0.5×	199 0.9×	138 0.9×	97	1.3k
Samuel McLenachan Australia	20	575 0.7×	374 1.0×	216 0.8×	78 0.4×	203 1.3×	77	1.1k
Xiufeng Zhong China	20	1.4k 1.9×	428 1.1×	529 2.0×	84 0.4×	290 1.8×	59	1.9k
Manuel Simonutti France	14	509 0.7×	530 1.3×	190 0.7×	73 0.3×	211 1.3×	17	1.0k
Vanda S. Lopes United States	19	1.1k 1.4×	255 0.6×	158 0.6×	265 1.2×	60 0.4×	27	1.5k

Countries citing papers authored by Fiona C. Mansergh

Since Specialization

Citations

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

Fields of papers citing papers by Fiona C. Mansergh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fiona C. Mansergh. 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 Fiona C. Mansergh. The network helps show where Fiona C. Mansergh may publish in the future.

Co-authorship network of co-authors of Fiona C. Mansergh

This figure shows the co-authorship network connecting the top 25 collaborators of Fiona C. Mansergh. A scholar is included among the top collaborators of Fiona C. Mansergh 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 Fiona C. Mansergh. Fiona C. Mansergh 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

Mansergh, Fiona C., Matthew Carrigan, Karsten Hokamp, & G. Jane Farrar. (2015). Gene expression changes during retinal development and rod specification.. PubMed. 21. 61–87. 8 indexed citations

Farrar, G. Jane, Sophia Millington‐Ward, Naomi Chadderton, Fiona C. Mansergh, & Arpad Palfi. (2014). Gene therapies for inherited retinal disorders. Visual Neuroscience. 31(4-5). 289–307. 10 indexed citations

Mansergh, Fiona C., Naomi Chadderton, Paul F. Kenna, Oliviero L. Gobbo, & G. Jane Farrar. (2014). Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy. European Journal of Human Genetics. 22(11). 1314–1320. 20 indexed citations

Bazou, Despina, et al.. (2011). Gene Expression Analysis of Mouse Embryonic Stem Cells Following Levitation in an Ultrasound Standing Wave Trap. Ultrasound in Medicine & Biology. 37(2). 321–330. 45 indexed citations

Mansergh, Fiona C., et al.. (2009). Gene expression profiles during early differentiation of mouse embryonic stem cells. BMC Developmental Biology. 9(1). 5–5. 38 indexed citations

Mansergh, Fiona C., Susan Hunter, Miguel Jarrı́n, et al.. (2008). Developmentally regulated expression of hemoglobin subunits in avascular tissues. The International Journal of Developmental Biology. 52(7). 873–886. 23 indexed citations

Hunter, Susan, Fiona C. Mansergh, & Martin Evans. (2007). Optimization of minuscule samples for use with cDNA microarrays. Journal of Biochemical and Biophysical Methods. 70(6). 1048–1058. 10 indexed citations

Mansergh, Fiona C., Noelle C. Orton, John P. Vessey, et al.. (2005). Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina. Human Molecular Genetics. 14(20). 3035–3046. 203 indexed citations

Orton, Noelle C., Fiona C. Mansergh, John P. Vessey, et al.. (2004). Mutation of the Calcium Channel Gene Cacna1f Disrupts Calcium Signaling and Synaptic Transmission in Mouse Retina. Investigative Ophthalmology & Visual Science. 45(13). 2507–2507. 1 indexed citations

10.

Wride, Michael A., et al.. (2002). Characterization and in silico mapping of a novel murine zinc finger transcription factor. Gene. 289(1-2). 49–59. 2 indexed citations

11.

Mansergh, Fiona C., Michael A. Wride, & Derrick E. Rancourt. (2000). Neurons from stem cells: Implications for understanding nervous system development and repair. Biochemistry and Cell Biology. 78(5). 613–628. 18 indexed citations

12.

Bain, Gretchen, Fiona C. Mansergh, Michael A. Wride, et al.. (2000). ES cell neural differentiation reveals a substantial number of novel ESTs. Functional & Integrative Genomics. 1(2). 127–139. 19 indexed citations

13.

Mansergh, Fiona C., Sophia Millington‐Ward, Avril Kennan, et al.. (1999). Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene. The American Journal of Human Genetics. 64(4). 971–985. 82 indexed citations

14.

Mansergh, Fiona C., Paul F. Kenna, Carmen Ayuso, et al.. (1998). Novel mutations in the TIGR gene in early and late onset open angle glaucoma. Human Mutation. 11(3). 244–251. 62 indexed citations

15.

Mansergh, Fiona C., Paul F. Kenna, Carmen Ayuso, et al.. (1998). Novel mutations in the TIGR gene in early and late onset open angle glaucoma. Human Mutation. 11(3). 244–251. 4 indexed citations

16.

Kenna, Paul F., Fiona C. Mansergh, Sophia Millington‐Ward, et al.. (1997). Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness. British Journal of Ophthalmology. 81(3). 207–213. 4 indexed citations

17.

Humphries, Marian M., Fiona C. Mansergh, Siobhán A. Jordan, et al.. (1996). Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland. Human Mutation. 8(1). 57–63. 22 indexed citations

18.

Mansergh, Fiona C., Paul F. Kenna, Günther Rudolph, et al.. (1995). Evidence for genetic heterogeneity in Best's vitelliform macular dystrophy.. Journal of Medical Genetics. 32(11). 855–858. 7 indexed citations

19.

Mansergh, Fiona C., et al.. (1994). Three sequence polymorphisms in the PDC gene.. PubMed. 3(11). 2077–2077. 3 indexed citations

20.

Humphries, Marian M., Denise M. Sheils, G. Jane Farrar, et al.. (1993). A mutation (met→arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex. Human Mutation. 2(1). 37–42. 52 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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