Danielle Hanna

551 total citations
9 papers, 435 citations indexed

About

Danielle Hanna is a scholar working on Genetics, Sociology and Political Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Danielle Hanna has authored 9 papers receiving a total of 435 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Sociology and Political Science and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Danielle Hanna's work include BRCA gene mutations in cancer (7 papers), Family Support in Illness (4 papers) and Childhood Cancer Survivors' Quality of Life (2 papers). Danielle Hanna is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Family Support in Illness (4 papers) and Childhood Cancer Survivors' Quality of Life (2 papers). Danielle Hanna collaborates with scholars based in Canada and United States. Danielle Hanna's co-authors include Steven A. Narod, Kelly Metcalfe, Carrie Snyder, Alexander Liede, David Main, Marc D. Schwartz, Kenneth P. Tercyak, Chanita Hughes, Caryn Lerman and Claudine Isaacs and has published in prestigious journals such as American Journal of Epidemiology, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Danielle Hanna

9 papers receiving 419 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle Hanna Canada 7 374 119 87 79 79 9 435
Kara J. Milliron United States 12 405 1.1× 94 0.8× 101 1.2× 82 1.0× 82 1.0× 29 546
Shelley R. McCormick United States 9 361 1.0× 70 0.6× 125 1.4× 91 1.2× 99 1.3× 16 518
Therese R. Giambarresi United States 9 346 0.9× 112 0.9× 109 1.3× 51 0.6× 67 0.8× 9 493
Lori d’Agincourt-Canning Canada 8 307 0.8× 112 0.9× 117 1.3× 41 0.5× 101 1.3× 15 441
Sherry Grumet United States 6 322 0.9× 56 0.5× 84 1.0× 49 0.6× 81 1.0× 13 428
Ruth Bingler United States 7 251 0.7× 82 0.7× 74 0.9× 44 0.6× 95 1.2× 7 449
Monica Marvin United States 13 335 0.9× 84 0.7× 114 1.3× 106 1.3× 69 0.9× 27 594
Christine Lasset France 12 436 1.2× 116 1.0× 107 1.2× 76 1.0× 97 1.2× 29 572
Y Aurran France 12 269 0.7× 74 0.6× 195 2.2× 84 1.1× 65 0.8× 17 495
Lesley Andrews Australia 15 326 0.9× 95 0.8× 68 0.8× 81 1.0× 83 1.1× 45 562

Countries citing papers authored by Danielle Hanna

Since Specialization
Citations

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

Fields of papers citing papers by Danielle Hanna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle Hanna

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

All Works

9 of 9 papers shown
1.
Wynn, Julia, Elana Levinson, Melissa White, et al.. (2022). Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk. The Journal of Pediatrics. 251. 113–119.e7. 2 indexed citations
2.
Knight, Julia A., Rebecca D. Kehm, Lisa A. Schwartz, et al.. (2020). Prepubertal Internalizing Symptoms and Timing of Puberty Onset in Girls. American Journal of Epidemiology. 190(3). 431–438. 15 indexed citations
3.
Lilge, Lothar, Mary Beth Terry, Dushanthi Pinnaduwage, et al.. (2017). Non-invasive optical spectroscopic monitoring of breast development during puberty. Breast Cancer Research. 19(1). 12–12. 8 indexed citations
4.
Glendon, Gord, Caren J. Frost, Irene L. Andrulis, et al.. (2009). A qualitative study evaluating parental attitudes towards the creation of a female youth cohort (LEGACY) in the Breast Cancer Family Registry. Psycho-Oncology. 19(1). 93–101. 4 indexed citations
5.
Metcalfe, Kelly, et al.. (2005). The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation. Familial Cancer. 4(2). 97–103. 67 indexed citations
6.
Metcalfe, Kelly, Alexander Liede, Martina Trinkaus, Danielle Hanna, & SA Narod. (2002). Evaluation of the needs of spouses of female carriers of mutations in BRCA1 and BRCA2. Clinical Genetics. 62(6). 464–469. 28 indexed citations
7.
Phelan, Catherine M., Elaine Kwan, Elaine Jack, et al.. (2002). A low frequency of non-founder BRCA1 mutations in Ashkenazi Jewish breast-ovarian cancer families. Human Mutation. 20(5). 352–357. 56 indexed citations
8.
Hughes, Chanita, Caryn Lerman, Marc D. Schwartz, et al.. (2001). All in the family: Evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results. American Journal of Medical Genetics. 107(2). 143–150. 169 indexed citations
9.
Liede, Alexander, Kelly Metcalfe, Danielle Hanna, et al.. (2000). Evaluation of the Needs of Male Carriers of Mutations in BRCA1 or BRCA2 Who Have Undergone Genetic Counseling. The American Journal of Human Genetics. 67(6). 1494–1504. 86 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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