Amanda Willis

661 total citations
17 papers, 384 citations indexed

About

Amanda Willis is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Amanda Willis has authored 17 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Amanda Willis's work include BRCA gene mutations in cancer (9 papers), Genomics and Rare Diseases (5 papers) and Oral microbiology and periodontitis research (3 papers). Amanda Willis is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Genomics and Rare Diseases (5 papers) and Oral microbiology and periodontitis research (3 papers). Amanda Willis collaborates with scholars based in Australia, United States and United Kingdom. Amanda Willis's co-authors include J. R. Hayes, W. A. Coulter, P. M. Bell, Bettina Meiser, P J Lamey, Tatiane Yanes, Mary‐Anne Young, Mandy L. Ballinger, P.‐J. Lamey and Kathy Tucker and has published in prestigious journals such as Diabetic Medicine, The American Journal of the Medical Sciences and Genetics in Medicine.

In The Last Decade

Amanda Willis

16 papers receiving 367 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda Willis Australia 9 147 132 96 93 46 17 384
Edward J M Monk United Kingdom 8 87 0.6× 59 0.4× 10 0.1× 60 0.6× 16 0.3× 17 341
Anna Di Lonardo Italy 12 32 0.2× 37 0.3× 25 0.3× 225 2.4× 52 1.1× 37 436
Mehmet Harman Türkiye 13 58 0.4× 26 0.2× 39 0.4× 135 1.5× 197 4.3× 41 411
Edgardo Chouela Argentina 13 185 1.3× 10 0.1× 15 0.2× 133 1.4× 26 0.6× 38 599
Luanda Mara da Silva Oliveira Brazil 13 86 0.6× 10 0.1× 17 0.2× 62 0.7× 72 1.6× 31 501
Anna Cäcilia Ingham Denmark 12 70 0.5× 13 0.1× 6 0.1× 51 0.5× 51 1.1× 24 424
Clare Marriott United Kingdom 9 80 0.5× 54 0.4× 4 0.0× 65 0.7× 12 0.3× 11 698
Mayla Sgrulletti Italy 5 78 0.5× 52 0.4× 4 0.0× 75 0.8× 18 0.4× 18 253
Matthew Rosenthal United States 6 50 0.3× 8 0.1× 114 1.2× 59 0.6× 17 0.4× 11 247

Countries citing papers authored by Amanda Willis

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Willis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Willis

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Willis. A scholar is included among the top collaborators of Amanda Willis 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 Amanda Willis. Amanda Willis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Willis, Amanda, et al.. (2024). Pediatric atopic dermatitis and attention-deficit hyperactivity disorder. The American Journal of the Medical Sciences. 367. S391–S392. 1 indexed citations
2.
Young, Mary‐Anne, et al.. (2024). Systematic review of the uptake and outcomes from returning secondary findings to adult participants in research genomic testing. Journal of Genetic Counseling. 33(6). 1145–1158. 2 indexed citations
3.
Morrow, April, Alison L. Young, Kathy Tucker, et al.. (2023). “Out of the blue”: A qualitative study exploring the experiences of women and next of kin receiving unexpected results from BRA‐STRAP research gene panel testing. Journal of Genetic Counseling. 33(5). 973–984.
4.
Yanes, Tatiane, Mary‐Anne Young, Amanda Willis, et al.. (2023). Development and evaluation of a novel educational program for providers on the use of polygenic risk scores. Genetics in Medicine. 25(8). 100876–100876. 4 indexed citations
5.
Willis, Amanda, et al.. (2021). Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology. Journal of Community Genetics. 12(4). 653–662. 6 indexed citations
6.
Willis, Amanda, et al.. (2021). My Research Results: a program to facilitate return of clinically actionable genomic research findings. European Journal of Human Genetics. 30(3). 363–366. 7 indexed citations
7.
Willis, Amanda, Sian K. Smith, Bettina Meiser, et al.. (2021). Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: ‘Another piece of the pie’. Journal of Genetic Counseling. 30(3). 849–860. 13 indexed citations
8.
Askar, Medhat, Amanda Willis, Shalini Pereira, et al.. (2019). An Ultrasensitive Next Generation Sequencing Method for the Detection of Minimal Residual Disease and the Assessment of Chimerism Following Hematopoietic Cell Transplantation. Biology of Blood and Marrow Transplantation. 25(3). S325–S325. 1 indexed citations
10.
Willis, Amanda, Sian K. Smith, Bettina Meiser, et al.. (2018). Development and Pilot Testing of a Decision Aid for Genomic Research Participants Notified of Clinically Actionable Research Findings for Cancer Risk. Journal of Genetic Counseling. 27(5). 1055–1066. 5 indexed citations
11.
Yanes, Tatiane, Amanda Willis, Bettina Meiser, Kathy Tucker, & Megan Best. (2018). Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review. European Journal of Human Genetics. 27(1). 28–35. 56 indexed citations
12.
Sousa, Mariana S., Michelle Peate, Craig Lewis, et al.. (2018). Exploring knowledge, attitudes and experience of genitourinary symptoms in women with early breast cancer on adjuvant endocrine therapy. European Journal of Cancer Care. 27(2). e12820–e12820. 8 indexed citations
13.
Willis, Amanda, Sian K. Smith, Bettina Meiser, et al.. (2016). Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review. Clinical Genetics. 92(2). 121–133. 49 indexed citations
14.
Willis, Amanda, et al.. (2001). The influence of antifungal drugs on virulence properties of Candida albicans in patients with diabetes mellitus. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 91(3). 317–321. 32 indexed citations
15.
Willis, Amanda, W. A. Coulter, Derek J. Sullivan, et al.. (2000). Isolation of C. dubliniensis from insulin‐using diabetes mellitus patients. Journal of Oral Pathology and Medicine. 29(2). 86–90. 62 indexed citations
16.
Willis, Amanda, W. A. Coulter, J. R. Hayes, P. M. Bell, & P.‐J. Lamey. (2000). Factors affecting the adhesion of Candida albicans to epithelial cells of insulin-using diabetes mellitus patients. Journal of Medical Microbiology. 49(3). 291–293. 15 indexed citations
17.
Willis, Amanda, et al.. (1999). Oral candidal carriage and infection in insulin‐treated diabetic patients. Diabetic Medicine. 16(8). 675–679. 87 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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