Amy Nisselle

2.3k total citations · 1 hit paper
49 papers, 1.3k citations indexed

About

Amy Nisselle is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Hematology. According to data from OpenAlex, Amy Nisselle has authored 49 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 14 papers in Public Health, Environmental and Occupational Health and 8 papers in Hematology. Recurrent topics in Amy Nisselle's work include BRCA gene mutations in cancer (26 papers), Genomics and Rare Diseases (16 papers) and Iron Metabolism and Disorders (8 papers). Amy Nisselle is often cited by papers focused on BRCA gene mutations in cancer (26 papers), Genomics and Rare Diseases (16 papers) and Iron Metabolism and Disorders (8 papers). Amy Nisselle collaborates with scholars based in Australia, United States and Canada. Amy Nisselle's co-authors include Clara Gaff, Belinda McClaren, Sylvia A. Metcalfe, Katrina J. Allen, Martin B. Delatycki, Christine E. McLaren, John K. Olynyk, John L. Hopper, Dorota M. Gertig and Gregory J. Anderson and has published in prestigious journals such as Science, New England Journal of Medicine and The Lancet.

In The Last Decade

Amy Nisselle

47 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.

Iron-Overload–Related Disease inHFEHereditary Hemochromatosis

2008 494 citations Katrina J. Allen, Lyle C. Gurrin et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amy Nisselle Australia	16	551	479	447	377	229	49	1.3k
Elizabeth J. Thomson United States	11	799 1.5×	265 0.6×	661 1.5×	512 1.4×	103 0.4×	24	1.3k
Ghazi Omar Tadmouri Türkiye	14	258 0.5×	229 0.5×	336 0.8×	39 0.1×	116 0.5×	31	957
Lisa Feuchtbaum United States	22	157 0.3×	195 0.4×	246 0.6×	27 0.1×	94 0.4×	39	1.2k
A. R. Al-Swailem Saudi Arabia	13	204 0.4×	126 0.3×	268 0.6×	28 0.1×	55 0.2×	32	728
Kristin Anderson United States	13	83 0.2×	319 0.7×	83 0.2×	24 0.1×	131 0.6×	17	1.3k
Roya Dolatkhah Iran	15	141 0.3×	56 0.1×	110 0.2×	29 0.1×	61 0.3×	80	864
Emily Riehm Meier United States	19	701 1.3×	80 0.2×	827 1.9×	12 0.0×	53 0.2×	76	1.2k
Amy E. Schmidt United States	21	489 0.9×	58 0.1×	222 0.5×	38 0.1×	27 0.1×	68	1.2k
Christine Patch United Kingdom	24	63 0.1×	1.1k 2.2×	55 0.1×	30 0.1×	293 1.3×	80	1.6k
Ellen Butensky United States	12	343 0.6×	15 0.0×	368 0.8×	81 0.2×	40 0.2×	18	783

Countries citing papers authored by Amy Nisselle

Since Specialization

Citations

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

Fields of papers citing papers by Amy Nisselle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Nisselle

This figure shows the co-authorship network connecting the top 25 collaborators of Amy Nisselle. A scholar is included among the top collaborators of Amy Nisselle 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 Amy Nisselle. Amy Nisselle 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

Mackley, Michael P., Pankaj B. Agrawal, Sara Ali, et al.. (2025). Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation. European Journal of Human Genetics. 33(11). 1402–1413. 1 indexed citations

Macintosh, Rebecca, Joanna Sweeting, Jodie Ingles, et al.. (2024). A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101865–101865.

Nisselle, Amy, et al.. (2024). Ensuring best practice in genomics education: A theory- and empirically informed evaluation framework. The American Journal of Human Genetics. 111(8). 1497–1507. 3 indexed citations

Dragojlovic, Nick, et al.. (2023). Workforce Implications of Increased Referrals to Hereditary Cancer Services in Canada: A Scenario-Based Analysis. Current Oncology. 30(8). 7241–7251. 5 indexed citations

Nisselle, Amy, Bronwyn Terrill, Belinda McClaren, et al.. (2023). Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation. npj Genomic Medicine. 8(1). 13–13. 12 indexed citations

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

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

Nisselle, Amy, et al.. (2021). Measuring physician practice, preparedness and preferences for genomic medicine: a national survey. BMJ Open. 11(7). e044408–e044408. 29 indexed citations

Hickerton, Chriselle, Amy Nisselle, Belinda McClaren, et al.. (2021). General practitioners’ views on genomics, practice and education: A qualitative interview study. Australian Journal of General Practice. 50(10). 747–752. 13 indexed citations

10.

McClaren, Belinda, et al.. (2020). Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education. Frontiers in Genetics. 11. 59–59. 23 indexed citations

11.

Dragojlovic, Nick, Ursula Ellis, Patricia Birch, et al.. (2020). The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review. Genetics in Medicine. 22(9). 1437–1449. 83 indexed citations

12.

Ellis, Ursula, Patricia Birch, Shelin Adam, et al.. (2020). Correction: The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review. Genetics in Medicine. 22(9). 1570–1570. 2 indexed citations

13.

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

14.

Hopkins, Liza, Amy Nisselle, Tsharni Zazryn, & Julie Green. (2013). Hospitalised adolescents: A framework for assessing educational risk. Youth studies Australia. 32(1). 37. 8 indexed citations

15.

Nisselle, Amy, Jane Halliday, Sylvia A. Metcalfe, et al.. (2012). Why Do People Choose Not to Have Screening for Hemochromatosis?. Genetic Testing and Molecular Biomarkers. 17(1). 21–24. 1 indexed citations

16.

Allen, Katrina J., Lyle C. Gurrin, Clare C. Constantine, et al.. (2008). Iron-Overload–Related Disease inHFEHereditary Hemochromatosis. New England Journal of Medicine. 358(3). 221–230. 494 indexed citations breakdown →

17.

Nisselle, Amy, et al.. (2008). Consumer contribution to the delivery of genetic health services. American Journal of Medical Genetics Part A. 146A(17). 2266–2274. 6 indexed citations

18.

Allen, Katrina J., Lyle C. Gurrin, Nicholas J. Osborne, et al.. (2007). Healthiron: a longitudinal population study defining the burden of disease in HFE-associated hereditary hemochromatosis. Queensland's institutional digital repository (The University of Queensland). 2 indexed citations

19.

Osborne, Nicholas J., Lyle C. Gurrin, Katrina J. Allen, et al.. (2007). Homozygosity for the C282Y mutation in the HFE gene is associated with increased risk of colorectailand breast cancer in Australian population. Queensland's institutional digital repository (The University of Queensland). 2 indexed citations

20.

Nisselle, Amy, et al.. (2006). Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosis. Clinical Genetics. 69(2). 163–170. 10 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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