Tatiane Yanes

968 total citations
43 papers, 565 citations indexed

About

Tatiane Yanes is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Oncology. According to data from OpenAlex, Tatiane Yanes has authored 43 papers receiving a total of 565 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 10 papers in Oncology. Recurrent topics in Tatiane Yanes's work include BRCA gene mutations in cancer (29 papers), Genetic Associations and Epidemiology (11 papers) and Genomics and Rare Diseases (10 papers). Tatiane Yanes is often cited by papers focused on BRCA gene mutations in cancer (29 papers), Genetic Associations and Epidemiology (11 papers) and Genomics and Rare Diseases (10 papers). Tatiane Yanes collaborates with scholars based in Australia, United States and United Kingdom. Tatiane Yanes's co-authors include Bettina Meiser, Mary‐Anne Young, Paul A. James, Aideen McInerney‐Leo, Amanda Willis, Shelly Cummings, Barbara B. Biesecker, Matthew H. Law, Kristine Barlow‐Stewart and Rajneesh Kaur and has published in prestigious journals such as PLoS ONE, JNCI Journal of the National Cancer Institute and Human Molecular Genetics.

In The Last Decade

Tatiane Yanes

40 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tatiane Yanes Australia 14 326 121 84 76 52 43 565
Sherry Grumet United States 6 322 1.0× 75 0.6× 81 1.0× 84 1.1× 49 0.9× 13 428
Belinda Rahman Australia 13 434 1.3× 158 1.3× 128 1.5× 115 1.5× 101 1.9× 27 633
Kara J. Milliron United States 12 405 1.2× 140 1.2× 82 1.0× 101 1.3× 82 1.6× 29 546
Margaret Gleeson Australia 18 390 1.2× 123 1.0× 97 1.2× 118 1.6× 95 1.8× 55 804
Karen Powell United States 15 374 1.1× 109 0.9× 150 1.8× 64 0.8× 48 0.9× 22 565
Lesley Andrews Australia 15 326 1.0× 152 1.3× 83 1.0× 68 0.9× 81 1.6× 45 562
Shelley R. McCormick United States 9 361 1.1× 125 1.0× 99 1.2× 125 1.6× 91 1.8× 16 518
Sue Friedman United States 14 453 1.4× 120 1.0× 134 1.6× 169 2.2× 73 1.4× 29 616
Amelia K. Smit Australia 13 212 0.7× 129 1.1× 84 1.0× 39 0.5× 45 0.9× 47 421
Suzanne M. O’Neill United States 15 344 1.1× 146 1.2× 170 2.0× 83 1.1× 28 0.5× 23 650

Countries citing papers authored by Tatiane Yanes

Since Specialization
Citations

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

Fields of papers citing papers by Tatiane Yanes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tatiane Yanes

This figure shows the co-authorship network connecting the top 25 collaborators of Tatiane Yanes. A scholar is included among the top collaborators of Tatiane Yanes 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 Tatiane Yanes. Tatiane Yanes 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.
McGahan, Eugene, Tatiane Yanes, Jennifer Berkman, et al.. (2025). Utility of Germline, Somatic and ctDNA Testing in Adults With Cancer. Cancer Medicine. 14(15). e71080–e71080.
2.
Yanes, Tatiane, et al.. (2024). Genetic counsellors: facilitating the integration of genomics into health care. The Medical Journal of Australia. 222(3). 114–117. 3 indexed citations
3.
Steinberg, Julia, et al.. (2024). Mainstreaming Cancer Genomic Testing: A Scoping Review of the Acceptability, Efficacy, and Impact. Clinical Genetics. 107(2). 123–135. 1 indexed citations
4.
Clark, Amy, et al.. (2024). Exploring the journey to genomic testing and genetic services: A qualitative study of parental perspectives of children with rare conditions. Journal of Genetic Counseling. 34(3). e1996–e1996. 1 indexed citations
5.
Yanes, Tatiane, et al.. (2024). Narrative therapy and family therapy in genetic counseling: A scoping review. Journal of Genetic Counseling. 34(2). e1938–e1938. 4 indexed citations
6.
Yanes, Tatiane, Jane Tiller, Margaret Otlowski, et al.. (2024). Future implications of polygenic risk scores for life insurance underwriting. npj Genomic Medicine. 9(1). 25–25. 8 indexed citations
7.
Yanes, Tatiane, Vaishnavi Nathan, Rhonda Faragher, et al.. (2023). Australasian genetic counselors' attitudes toward disability and prenatal testing: Findings from a cross‐sectional survey. Journal of Genetic Counseling. 33(4). 822–833. 2 indexed citations
8.
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
9.
Yanes, Tatiane, et al.. (2023). Evaluation and pilot testing of a multidisciplinary model of care to mainstream genomic testing for paediatric inborn errors of immunity. European Journal of Human Genetics. 31(10). 1125–1132. 9 indexed citations
10.
Primiero, Clare, et al.. (2022). Protocol to evaluate a pilot program to upskill clinicians in providing genetic testing for familial melanoma. PLoS ONE. 17(12). e0275926–e0275926. 4 indexed citations
11.
Primiero, Clare, Tatiane Yanes, Anna Finnane, H. Peter Soyer, & Aideen McInerney‐Leo. (2021). A Systematic Review on the Impact of Genetic Testing for Familial Melanoma II: Psychosocial Outcomes and Attitudes. Dermatology. 237(5). 816–826. 6 indexed citations
12.
Smit, Amelia K., David Espinoza, Mary‐Anne Young, et al.. (2021). Knowledge, views and expectations for cancer polygenic risk testing in clinical practice: A cross‐sectional survey of health professionals. Clinical Genetics. 100(4). 430–439. 24 indexed citations
13.
Primiero, Clare, Tatiane Yanes, Anna Finnane, H. Peter Soyer, & Aideen McInerney‐Leo. (2021). A Systematic Review on the Impact of Genetic Testing for Familial Melanoma I: Primary and Secondary Preventative Behaviours. Dermatology. 237(5). 806–815. 6 indexed citations
14.
Yanes, Tatiane, Bettina Meiser, Rajneesh Kaur, et al.. (2021). Breast cancer polygenic risk scores: a 12-month prospective study of patient reported outcomes and risk management behavior. Genetics in Medicine. 23(12). 2316–2323. 15 indexed citations
15.
Yanes, Tatiane, Rajneesh Kaur, Bettina Meiser, et al.. (2020). Women’s responses and understanding of polygenic breast cancer risk information. Familial Cancer. 19(4). 297–306. 15 indexed citations
16.
Yanes, Tatiane, Bettina Meiser, Rajneesh Kaur, et al.. (2020). Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder. Journal of Affective Disorders. 265. 342–350. 16 indexed citations
17.
Yanes, Tatiane, Bettina Meiser, Rajneesh Kaur, et al.. (2019). Uptake of polygenic risk information among women at increased risk of breast cancer. Clinical Genetics. 97(3). 492–501. 19 indexed citations
18.
Yanes, Tatiane, Bettina Meiser, Rajneesh Kaur, et al.. (2018). Polygenic breast cancer risk: A prospective study of uptake and outcomes among high-risk women. Twin Research and Human Genetics. 1 indexed citations
19.
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
20.
Jamal, Leila, Julie C. Sapp, Katie L. Lewis, et al.. (2013). Research participants’ attitudes towards the confidentiality of genomic sequence information. European Journal of Human Genetics. 22(8). 964–968. 37 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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