Elly Lynch

1.3k total citations
26 papers, 597 citations indexed

About

Elly Lynch is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine. According to data from OpenAlex, Elly Lynch has authored 26 papers receiving a total of 597 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 7 papers in Public Health, Environmental and Occupational Health and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Elly Lynch's work include BRCA gene mutations in cancer (11 papers), Genomics and Rare Diseases (9 papers) and Ethics in Clinical Research (6 papers). Elly Lynch is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Genomics and Rare Diseases (9 papers) and Ethics in Clinical Research (6 papers). Elly Lynch collaborates with scholars based in Australia, United States and United Kingdom. Elly Lynch's co-authors include Pedro León, Jennifer L. Morrow, Mary‐Claire King, Henriette Raventós, Clara Gaff, Lara Lipton, Melissa Martyn, Finlay Macrae, Lilian Downie and Ingrid Winship and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Elly Lynch

25 papers receiving 580 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elly Lynch Australia 12 202 173 141 139 137 26 597
Ira A. Priluck United States 10 60 0.3× 201 1.2× 208 1.5× 160 1.2× 249 1.8× 12 753
Violetta Anastasiadou Cyprus 14 390 1.9× 35 0.2× 37 0.3× 31 0.2× 270 2.0× 46 718
Kandamurugu Manickam United States 15 551 2.7× 59 0.3× 14 0.1× 42 0.3× 280 2.0× 34 928
Frederick V. Schaefer United States 13 130 0.6× 31 0.2× 25 0.2× 65 0.5× 231 1.7× 29 506
Mary O’Driscoll United Kingdom 10 87 0.4× 50 0.3× 9 0.1× 47 0.3× 129 0.9× 20 390
Teresa Nutile Italy 14 128 0.6× 11 0.1× 91 0.6× 24 0.2× 159 1.2× 23 505
Karen L. David United States 12 491 2.4× 59 0.3× 16 0.1× 23 0.2× 263 1.9× 14 899
M. F. Niermeijer Netherlands 18 212 1.0× 52 0.3× 15 0.1× 23 0.2× 300 2.2× 44 902
Hannah C. Cox United States 18 340 1.7× 91 0.5× 5 0.0× 87 0.6× 218 1.6× 36 741

Countries citing papers authored by Elly Lynch

Since Specialization
Citations

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

Fields of papers citing papers by Elly Lynch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elly Lynch

This figure shows the co-authorship network connecting the top 25 collaborators of Elly Lynch. A scholar is included among the top collaborators of Elly 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 Elly Lynch. Elly 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.
Martyn, Melissa, et al.. (2024). Secondary use of genomic data: patients’ decisions at point of testing and perspectives to inform international data sharing. European Journal of Human Genetics. 32(6). 717–724. 4 indexed citations
2.
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
3.
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
4.
Martyn, Melissa, et al.. (2024). Evaluation of a two-step model of opportunistic genomic screening. European Journal of Human Genetics. 32(6). 656–664.
5.
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
6.
Downie, Lilian, Jane Halliday, Sharon Lewis, et al.. (2020). Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project. Genetics in Medicine. 22(5). 937–944. 32 indexed citations
7.
Blombery, Piers, Lucy C. Fox, Georgina L. Ryland, et al.. (2020). Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes. Haematologica. 106(1). 64–73. 11 indexed citations
8.
Martyn, Melissa, et al.. (2020). “It’s something I’ve committed to longer term”: The impact of an immersion program for physicians on adoption of genomic medicine. Patient Education and Counseling. 104(3). 480–488. 8 indexed citations
9.
Ramchand, Jay, Mathew Wallis, Ivan Macciocca, et al.. (2020). Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy. Journal of the American Heart Association. 9(2). e013346–e013346. 26 indexed citations
10.
Degeling, Koen, Melissa Martyn, Elly Lynch, et al.. (2020). Evaluating the resource implications of different service delivery models for offering additional genomic findings. Genetics in Medicine. 23(4). 606–613. 5 indexed citations
11.
Downie, Lilian, Jane Halliday, Rachel Burt, et al.. (2019). Exome sequencing in infants with congenital hearing impairment: a population-based cohort study. European Journal of Human Genetics. 28(5). 587–596. 44 indexed citations
12.
Brett, Gemma R., Ella Wilkins, Anna Jarmolowicz, et al.. (2018). Genetic Counseling in the Era of Genomics: What's all the Fuss about?. Journal of Genetic Counseling. 27(5). 1010–1021. 11 indexed citations
13.
Downie, Lilian, Jane Halliday, Rachel Burt, et al.. (2017). A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort. BMJ Paediatrics Open. 1(1). e000119–e000119. 13 indexed citations
14.
Kenen, Regina H., Audrey Ardern‐Jones, Elly Lynch, & Rosalind A. Eeles. (2011). Ownership of Uncertainty: Healthcare Professionals Counseling and Treating Women from Hereditary Breast and Ovarian Cancer Families Who Receive an Inconclusive BRCA1/2 Genetic Test Result. Genetic Testing and Molecular Biomarkers. 15(4). 243–250. 10 indexed citations
15.
Tan, Tiong Yang, et al.. (2008). Biallelic PMS2 Mutations and a Distinctive Childhood Cancer Syndrome. Journal of Pediatric Hematology/Oncology. 30(3). 254–257. 24 indexed citations
16.
Wong, CL, Peter Gibbs, Ian T. Jones, et al.. (2007). Value of database linkage: are patients at risk of familial colorectal cancer being referred for genetic counselling and testing?. Internal Medicine Journal. 38(5). 328–333. 31 indexed citations
17.
Chow, Elizabeth, Lara Lipton, Elly Lynch, et al.. (2006). Hyperplastic Polyposis Syndrome: Phenotypic Presentations and the Role of MBD4 and MYH. Gastroenterology. 131(1). 30–39. 124 indexed citations
18.
Raevaara, Tiina, Mari Korhonen, Hannes Lohi, et al.. (2005). Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of. Gastroenterology. 129(2). 537–549. 4 indexed citations
19.
Lynch, Elly, Rebecca Doherty, Clara Gaff, Finlay Macrae, & Geoffrey J. Lindeman. (2003). “Cancer in the family” and genetic testing: implications for life insurance. The Medical Journal of Australia. 179(9). 480–483. 16 indexed citations
20.
León, Pedro, Henriette Raventós, Elly Lynch, Jennifer L. Morrow, & Mary‐Claire King. (1992). The gene for an inherited form of deafness maps to chromosome 5q31.. Proceedings of the National Academy of Sciences. 89(11). 5181–5184. 148 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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