Amanda Brandt

814 total citations
19 papers, 292 citations indexed

About

Amanda Brandt is a scholar working on Genetics, General Health Professions and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amanda Brandt has authored 19 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 3 papers in General Health Professions and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Amanda Brandt's work include BRCA gene mutations in cancer (13 papers), Ovarian cancer diagnosis and treatment (3 papers) and Genomics and Rare Diseases (2 papers). Amanda Brandt is often cited by papers focused on BRCA gene mutations in cancer (13 papers), Ovarian cancer diagnosis and treatment (3 papers) and Genomics and Rare Diseases (2 papers). Amanda Brandt collaborates with scholars based in United States and Chile. Amanda Brandt's co-authors include Karen H. Lu, Susan M. Domchek, Angela R. Bradbury, Jill E. Stopfer, Molly S. Daniels, Brian L. Egleston, Diana Harris, Shana L. Merrill, Allison Werner‐Lin and Dominique Fetzer and has published in prestigious journals such as Journal of Clinical Oncology, Obstetrics and Gynecology and Journal of Medical Internet Research.

In The Last Decade

Amanda Brandt

18 papers receiving 285 citations

Peers

Amanda Brandt

GENET

PPCH

PHEOH

ONCOL

Erica M. Bednar United States

Kimberly Childers United States

Karina L. Brierley United States

Sherry Grumet United States

Danielle Hanna Canada

Courtney D. Storm United States

Hetal S. Vig United States

Mary McCullum Canada

Anne Weidner United States

Margaret M. McGovern United States

Erica M. Bednar United States

Amanda Brandt

286 ×1.4

GENET

68 ×1.0

PPCH

54 ×0.8

PHEOH

43 ×0.8

50 ×1.0

ONCOL

Citations per year, relative to Amanda Brandt Amanda Brandt (= 1×) peers Erica M. Bednar

Countries citing papers authored by Amanda Brandt

Since Specialization

Citations

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

Fields of papers citing papers by Amanda Brandt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Brandt

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

All Works

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19 of 19 papers shown

Tang, Xiaohui, Amanda Brandt, Jianzhong Ma, et al.. (2024). Risk of anthracycline-induced cardiac dysfunction in adolescent and young adult (AYA) cancer survivors: role of genetic susceptibility loci. The Pharmacogenomics Journal. 24(4). 21–21. 1 indexed citations

Bradbury, Angela R., Brian L. Egleston, Linda Patrick‐Miller, et al.. (2020). Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients. Clinical Genetics. 97(4). 601–609. 8 indexed citations

Hamilton, Jada G., Jessica M. Long, Amanda Brandt, et al.. (2019). Patients’ Medical and Psychosocial Experiences After Detection of a CDH1 Variant With Multigene Panel Testing. JCO Precision Oncology. 3(3). 1–14. 13 indexed citations

Werner‐Lin, Allison, Shana L. Merrill, & Amanda Brandt. (2018). Talking with Children About Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents. Journal of Genetic Counseling. 27(3). 533–548. 23 indexed citations

Bradbury, Angela R., Jill B. Gaieski, Brian L. Egleston, et al.. (2018). Interest in and outcomes with web-based education for return of genetic research results for inherited susceptibility to breast cancer.. Journal of Clinical Oncology. 36(15_suppl). 1531–1531.

Bradbury, Angela R., Linda Patrick‐Miller, Brian L. Egleston, et al.. (2018). Returning Individual Genetic Research Results to Research Participants: Uptake and Outcomes Among Patients With Breast Cancer. JCO Precision Oncology. 2(2). 1–24. 19 indexed citations

Bradbury, Angela R., Linda Patrick‐Miller, Diana Harris, et al.. (2016). Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study. Journal of Medical Internet Research. 18(2). e23–e23. 75 indexed citations

Bradbury, Angela R., Linda Patrick‐Miller, Brian L. Egleston, et al.. (2015). Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing. Genetics in Medicine. 18(1). 25–33. 46 indexed citations

Bayraktar, Soley, Michelle Jackson, Angelica M. Gutierrez‐Barrera, et al.. (2015). Genotype-Phenotype Correlations by Ethnicity and Mutation Location inBRCAMutation Carriers. The Breast Journal. 21(3). 260–267. 16 indexed citations

10.

McAndrew, Nicholas P., Kara N. Maxwell, Jill E. Stopfer, et al.. (2015). Oncotype DX scores in BRCA1 and BRCA2 associated breast cancer.. Journal of Clinical Oncology. 33(15_suppl). 541–541. 2 indexed citations

11.

Yam, Clinton, Jill E. Stopfer, Amanda Brandt, et al.. (2015). Impact of prior knowledge of mutation status on tumor stage in BRCA1/2 mutation carriers with newly diagnosed breast cancer.. Journal of Clinical Oncology. 33(15_suppl). 1562–1562. 2 indexed citations

12.

Daniels, Molly S., Diana L. Urbauer, Amanda Brandt, et al.. (2014). Underestimation of Risk of a BRCA1 or BRCA2 Mutation in Women With High-Grade Serous Ovarian Cancer by BRCAPRO: A Multi-Institution Study. Journal of Clinical Oncology. 32(12). 1249–1255. 22 indexed citations

13.

Brandt, Amanda, et al.. (2012). School Bullying Hurts: Evidence of Psychological and Academic Challenges among Students with Bullying Histories.. 11(1). 2 indexed citations

14.

Brandt, Amanda, et al.. (2012). Comparison of BRCA1/2-positive and -negative women diagnosed with metachronous breast and ovarian cancers.. Journal of Clinical Oncology. 30(15_suppl). 1546–1546. 1 indexed citations

15.

Daniels, Molly S., Jennifer K. Burzawa, Amanda Brandt, Kathleen M. Schmeler, & Karen H. Lu. (2011). A clinical perspective on genetic counseling and testing during end of life care for women with recurrent progressive ovarian cancer: opportunities and challenges. Familial Cancer. 10(2). 193–197. 8 indexed citations

16.

Brandt, Amanda, Matthew L. Tschirgi, Kaylene Ready, et al.. (2010). Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes. Familial Cancer. 9(3). 479–487. 27 indexed citations

17.

Schmeler, Kathleen M., Molly S. Daniels, Amanda Brandt, & Karen H. Lu. (2009). Endometrial Cancer in an Adolescent. Obstetrics and Gynecology. 114(2). 477–479. 20 indexed citations

18.

Tacla, X, et al.. (1995). [Decrease of labor absenteeism associated with hormone replacement therapy in postmenopausal women].. PubMed. 123(8). 948–53. 3 indexed citations

19.

Tacla, X, et al.. (1994). [Knowledge and beliefs of the effect of menopause and estrogenic therapy on health. Study in women attending the Barros Luco-Trudeau Hospital].. PubMed. 59(1). 10–6. 4 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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