Fiona Lynch

655 total citations
36 papers, 323 citations indexed

About

Fiona Lynch is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Fiona Lynch has authored 36 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 7 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Fiona Lynch's work include Genomics and Rare Diseases (20 papers), BRCA gene mutations in cancer (13 papers) and Prenatal Screening and Diagnostics (8 papers). Fiona Lynch is often cited by papers focused on Genomics and Rare Diseases (20 papers), BRCA gene mutations in cancer (13 papers) and Prenatal Screening and Diagnostics (8 papers). Fiona Lynch collaborates with scholars based in Australia, United Kingdom and Singapore. Fiona Lynch's co-authors include Amy Nisselle, Clara Gaff, Zornitza Stark, Belinda McClaren, Alan Landay, Geza Paukovics, Anthony Jaworowski, Suzanne M. Crowe, Christopher Gyngell and Maëlenn Gouillou and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PEDIATRICS.

In The Last Decade

Fiona Lynch

32 papers receiving 318 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fiona Lynch Australia 9 138 70 70 65 51 36 323
Janet Lioy United States 10 48 0.3× 36 0.5× 19 0.3× 64 1.0× 23 0.5× 26 279
Rozanne C. M. Adams South Africa 7 23 0.2× 40 0.6× 21 0.3× 42 0.6× 18 0.4× 9 365
Nishanth Dev India 11 25 0.2× 12 0.2× 32 0.5× 21 0.3× 26 0.5× 30 292
Herbert E Cushing United States 8 43 0.3× 9 0.1× 55 0.8× 34 0.5× 39 0.8× 19 241
PeterM. Dunn United Kingdom 6 63 0.5× 90 1.3× 10 0.1× 48 0.7× 32 0.6× 11 395
Lorraine Marshall Australia 11 137 1.0× 24 0.3× 6 0.1× 49 0.8× 29 0.6× 26 359
Yalçın Büyük Türkiye 11 13 0.1× 27 0.4× 167 2.4× 9 0.1× 61 1.2× 46 414
Maya Gopalakrishnan India 9 118 0.9× 7 0.1× 6 0.1× 82 1.3× 25 0.5× 43 326
Romano Arcieri Italy 13 14 0.1× 21 0.3× 33 0.5× 48 0.7× 8 0.2× 32 405
Michael A. Dempsey United States 3 17 0.1× 20 0.3× 124 1.8× 74 1.1× 12 0.2× 3 330

Countries citing papers authored by Fiona Lynch

Since Specialization
Citations

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

Fields of papers citing papers by Fiona Lynch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiona Lynch

This figure shows the co-authorship network connecting the top 25 collaborators of Fiona Lynch. A scholar is included among the top collaborators of Fiona Lynch 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 Lynch. Fiona Lynch 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.
Brown, Jeremy, Darius Armstrong‐James, Jonathan Ayling-Smith, et al.. (2025). British Thoracic Society Clinical Statement onAspergillus-related chronic lung disease. Thorax. 80(Suppl 1). 3–21. 1 indexed citations
2.
Lynch, Fiona, et al.. (2025). Collaborative coding in inductive content analysis: Why, when, and how to do it. Journal of Genetic Counseling. 34(3). e70030–e70030.
3.
4.
Lynch, Fiona, et al.. (2024). Analysis of public perceptions on the use of artificial intelligence in genomic medicine. Human Genomics. 18(1). 128–128.
5.
Lynch, Fiona, Stephanie Best, Clara Gaff, et al.. (2024). Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation. International Journal of Neonatal Screening. 10(1). 6–6. 17 indexed citations
6.
Best, Stephanie, C. Richards, Michael C. Quinn, et al.. (2024). Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European Journal of Human Genetics. 32(11). 1428–1435. 2 indexed citations
7.
Patel, Chirag, John Christodoulou, Belinda McClaren, et al.. (2024). A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability. Genetics in Medicine. 26(10). 101224–101224. 3 indexed citations
8.
Boggs, Kirsten, Fiona Lynch, Michelle C. Ward, et al.. (2024). Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101878–101878. 2 indexed citations
9.
Gyngell, Christopher, Fiona Lynch, Tsutomu Sawai, & Julian Savulescu. (2024). Stem cell-derived embryo models: moral advance or moral obfuscation?. Journal of Medical Ethics. 51(6). 361–364. 4 indexed citations
10.
Lynch, Fiona, Stephanie Best, Ilias Goranitis, et al.. (2023). Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations. European Journal of Human Genetics. 32(3). 295–301. 3 indexed citations
11.
Lynch, Fiona, Zornitza Stark, Dominic Wilkinson, et al.. (2023). Intensive Care Clinicians’ Perspectives on Ethical Challenges Raised by Rapid Genomic Testing in Critically Ill Infants. Children. 10(6). 970–970. 1 indexed citations
12.
Vears, Danya F., Fiona Lynch, Amy Nisselle, Samantha Ayres, & Zornitza Stark. (2023). Rapid genomic testing in critically ill patients with genetic conditions: position statement by the Human Genetics Society of Australasia. European Journal of Human Genetics. 32(2). 150–154. 6 indexed citations
13.
Lewis, Sarah J., et al.. (2023). Australian parental perceptions of genomic newborn screening for non-communicable diseases. Frontiers in Genetics. 14. 1209762–1209762. 2 indexed citations
14.
Lee, Ling, Fiona Lynch, Melissa Martyn, et al.. (2023). Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol. BMJ Open. 13(6). e072999–e072999. 7 indexed citations
15.
Brett, Gemma R., Elizabeth E. Palmer, Kirsten Boggs, et al.. (2022). Co-design, implementation, and evaluation of plain language genomic test reports. npj Genomic Medicine. 7(1). 61–61. 6 indexed citations
16.
Lynch, Fiona, Sharon Lewis, Ivan Macciocca, & Jeffrey M. Craig. (2021). Public knowledge and opinion of epigenetics and epigenetic concepts. Journal of Developmental Origins of Health and Disease. 13(4). 431–440. 7 indexed citations
17.
Stark, Zornitza, Amy Nisselle, Belinda McClaren, et al.. (2019). Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care. European Journal of Human Genetics. 27(10). 1493–1501. 37 indexed citations
18.
Martin, Geneviève, Maëlenn Gouillou, Anna C. Hearps, et al.. (2013). Age-Associated Changes in Monocyte and Innate Immune Activation Markers Occur More Rapidly in HIV Infected Women. PLoS ONE. 8(1). e55279–e55279. 95 indexed citations
19.
Lynch, Fiona. (2009). Arterial blood gas analysis: implications for nursing. Paediatric Care. 21(1). 41–44. 11 indexed citations
20.
Lynch, Fiona, et al.. (2008). NASAL PRESSURE ULCERS: A NATIONAL SURVEY OF CURRENT PRACTICE AND OCCURRENCE IN PAEDIATRIC AND NEONATAL. Archives of Disease in Childhood. 93. 3 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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