Tiffani A. DeMarco

2.2k total citations
56 papers, 1.8k citations indexed

About

Tiffani A. DeMarco is a scholar working on Genetics, Sociology and Political Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Tiffani A. DeMarco has authored 56 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 30 papers in Sociology and Political Science and 26 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Tiffani A. DeMarco's work include BRCA gene mutations in cancer (53 papers), Family Support in Illness (29 papers) and Childhood Cancer Survivors' Quality of Life (16 papers). Tiffani A. DeMarco is often cited by papers focused on BRCA gene mutations in cancer (53 papers), Family Support in Illness (29 papers) and Childhood Cancer Survivors' Quality of Life (16 papers). Tiffani A. DeMarco collaborates with scholars based in United States, Iceland and Canada. Tiffani A. DeMarco's co-authors include Beth N. Peshkin, Marc D. Schwartz, Claudine Isaacs, Kenneth P. Tercyak, Heiðdís Valdimarsdóttir, Caryn Lerman, Clinton Finch, Chanita Hughes Halbert, Karen Brown and Judy E. Garber and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and PEDIATRICS.

In The Last Decade

Tiffani A. DeMarco

55 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tiffani A. DeMarco United States	26	1.5k	502	478	306	303	56	1.8k
Chanita Hughes United States	18	1.5k 1.0×	439 0.9×	482 1.0×	368 1.2×	356 1.2×	20	1.7k
Mary‐Anne Young Australia	23	1.0k 0.7×	307 0.6×	189 0.4×	545 1.8×	235 0.8×	78	1.7k
Judith Benkendorf United States	16	1.1k 0.8×	740 1.5×	163 0.3×	158 0.5×	405 1.3×	31	1.8k
Jada G. Hamilton United States	20	630 0.4×	246 0.5×	189 0.4×	213 0.7×	371 1.2×	74	1.3k
Colleen Burke Sands United States	13	877 0.6×	343 0.7×	506 1.1×	562 1.8×	144 0.5×	18	1.4k
Sue Gessler United Kingdom	20	651 0.4×	221 0.4×	128 0.3×	409 1.3×	254 0.8×	34	1.3k
Rachel Nusbaum United States	17	785 0.5×	239 0.5×	124 0.3×	176 0.6×	170 0.6×	28	1.0k
Stephanie A. Cohen United States	17	735 0.5×	238 0.5×	98 0.2×	206 0.7×	183 0.6×	42	1.1k
Agnes Masny United States	12	625 0.4×	188 0.4×	237 0.5×	250 0.8×	129 0.4×	17	930
Heather Zierhut United States	20	635 0.4×	306 0.6×	113 0.2×	174 0.6×	269 0.9×	74	1.4k

Countries citing papers authored by Tiffani A. DeMarco

Since Specialization

Citations

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

Fields of papers citing papers by Tiffani A. DeMarco

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tiffani A. DeMarco. 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 Tiffani A. DeMarco. The network helps show where Tiffani A. DeMarco may publish in the future.

Co-authorship network of co-authors of Tiffani A. DeMarco

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

1.

Cannon, Timothy Lewis, et al.. (2019). Patient attendance at molecular tumor board: A new means of shared decision making?. Journal of Clinical Oncology. 37(15_suppl). e18001–e18001. 1 indexed citations

2.

Peshkin, Beth N., Heiðdís Valdimarsdóttir, Rachel Nusbaum, et al.. (2017). Randomized Noninferiority Trial of Telephone vs In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer: A 12-Month Follow-Up. JNCI Cancer Spectrum. 1(1). pkx002–pkx002. 15 indexed citations

3.

Hamilton, Jada G., Darren Mays, Tiffani A. DeMarco, & Kenneth P. Tercyak. (2016). Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk. Familial Cancer. 15(4). 513–522. 6 indexed citations

4.

Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations

5.

DeMarco, Tiffani A., Darren Mays, Beth N. Peshkin, et al.. (2011). Parenting Through Genetic Uncertainty: Themes in the Disclosure of Breast Cancer Risk Information to Children. Genetic Testing and Molecular Biomarkers. 16(5). 376–382. 31 indexed citations

6.

Schwartz, Marc D., Heiðdís Valdimarsdóttir, Tiffani A. DeMarco, et al.. (2009). Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: Impact on measures of decision making and satisfaction.. Health Psychology. 28(1). 11–19. 90 indexed citations

7.

DeMarco, Tiffani A., Rachel Nusbaum, Beth N. Peshkin, et al.. (2009). Prevalence and correlates of mothers and fathers attending pretest cancer genetic counseling together. Patient Education and Counseling. 78(1). 29–33. 7 indexed citations

8.

Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 0(0). 2685938514–2685938514. 1 indexed citations

9.

Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 12(1). 37–52. 41 indexed citations

10.

Peshkin, Beth N., Tiffani A. DeMarco, J. E. Garber, et al.. (2008). Brief Assessment of Parents' Attitudes Toward Testing Minor Children for Hereditary Breast/Ovarian Cancer Genes: Development and Validation of the Pediatric BRCA1/2 Testing Attitudes Scale (P-TAS). Journal of Pediatric Psychology. 34(6). 627–638. 28 indexed citations

11.

DeMarco, Tiffani A., Beth N. Peshkin, Heiðdís Valdimarsdóttir, et al.. (2008). Role of Parenting Relationship Quality in Communicating about Maternal BRCA1/2 Genetic Test Results with Children. Journal of Genetic Counseling. 17(3). 283–287. 15 indexed citations

12.

Zhang, Bifeng, James D. Fackenthal, Qun Niu, et al.. (2008). Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry. Familial Cancer. 8(1). 15–22. 20 indexed citations

13.

DeMarco, Tiffani A., Karen L. Smith, Rachel Nusbaum, et al.. (2007). Practical Aspects of Delivering Hereditary Cancer Risk Counseling. Seminars in Oncology. 34(5). 369–378. 23 indexed citations

14.

Tercyak, Kenneth P., Beth N. Peshkin, Tiffani A. DeMarco, et al.. (2007). Information Needs of Mothers Regarding Communicating BRCA1/2 Cancer Genetic Test Results to Their Children. Genetic Testing. 11(3). 249–255. 40 indexed citations

15.

Schwartz, Marc D., Caryn Lerman, Beth N. Peshkin, et al.. (2005). Utilization of BRCA1/BRCA2 Mutation Testing in Newly Diagnosed Breast Cancer Patients. Cancer Epidemiology Biomarkers & Prevention. 14(4). 1003–1007. 69 indexed citations

16.

Schwartz, Marc D., Caryn Lerman, Beth N. Peshkin, et al.. (2004). Impact of BRCA1/BRCA2 Counseling and Testing on Newly Diagnosed Breast Cancer Patients. Journal of Clinical Oncology. 22(10). 1823–1829. 206 indexed citations

17.

Tercyak, Kenneth P., et al.. (2004). Women's satisfaction with genetic counseling for hereditary breast‐ovarian cancer: Psychological aspects. American Journal of Medical Genetics Part A. 131A(1). 36–41. 28 indexed citations

18.

Halbert, Chanita Hughes, Lari Wenzel, Caryn Lerman, et al.. (2004). Predictors of Participation in Psychosocial Telephone Counseling following Genetic Testing for BRCA1 and BRCA2 Mutations. Cancer Epidemiology Biomarkers & Prevention. 13(5). 875–881. 20 indexed citations

19.

Schwartz, Marc D., Elizabeth Kaufman, Beth N. Peshkin, et al.. (2003). Bilateral Prophylactic Oophorectomy and Ovarian Cancer Screening Following BRCA1/BRCA2 Mutation Testing. Journal of Clinical Oncology. 21(21). 4034–4041. 106 indexed citations

20.

Peshkin, Beth N., et al.. (2001). BRCA1/2 Testing: Complex Themes in Result Interpretation. Journal of Clinical Oncology. 19(9). 2555–2565. 38 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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