Deborah Maiese

550 total citations
17 papers, 309 citations indexed

About

Deborah Maiese is a scholar working on Public Health, Environmental and Occupational Health, Genetics and General Health Professions. According to data from OpenAlex, Deborah Maiese has authored 17 papers receiving a total of 309 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Public Health, Environmental and Occupational Health, 5 papers in Genetics and 4 papers in General Health Professions. Recurrent topics in Deborah Maiese's work include BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Ethics in Clinical Research (3 papers). Deborah Maiese is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Ethics in Clinical Research (3 papers). Deborah Maiese collaborates with scholars based in United States, United Kingdom and Canada. Deborah Maiese's co-authors include Michael S. Watson, David B. Flannery, Miriam G. Blitzer, Joann Bodurtha, Maximilian Muenke, Mathew J. Edick, Matthew R.G. Taylor, Hans C. Andersson, Brittany D. Jenkins and Catherine G. Fischer and has published in prestigious journals such as SHILAP Revista de lepidopterología, JNCI Journal of the National Cancer Institute and American Journal of Obstetrics and Gynecology.

In The Last Decade

Deborah Maiese

16 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah Maiese United States 6 161 89 59 39 33 17 309
Rachel Horton United Kingdom 10 186 1.2× 104 1.2× 57 1.0× 90 2.3× 26 0.8× 31 440
Meghan E. Carey United States 9 200 1.2× 84 0.9× 80 1.4× 20 0.5× 33 1.0× 24 401
Kendall L. Umstead United States 7 197 1.2× 77 0.9× 73 1.2× 24 0.6× 36 1.1× 11 314
Anna Chan United States 9 184 1.1× 51 0.6× 55 0.9× 25 0.6× 35 1.1× 17 400
Kate Dunlop Australia 13 229 1.4× 91 1.0× 42 0.7× 23 0.6× 33 1.0× 34 369
Sabrina A. Suckiel United States 13 323 2.0× 142 1.6× 48 0.8× 92 2.4× 43 1.3× 23 467
Penny Kyler United States 8 243 1.5× 130 1.5× 141 2.4× 53 1.4× 86 2.6× 9 455
Tabitha Hendershot United States 10 75 0.5× 48 0.5× 30 0.5× 47 1.2× 42 1.3× 30 404
Elizabeth Gettig United States 14 260 1.6× 97 1.1× 144 2.4× 61 1.6× 83 2.5× 28 546
Ellen Otten Netherlands 7 182 1.1× 86 1.0× 45 0.8× 33 0.8× 34 1.0× 7 311

Countries citing papers authored by Deborah Maiese

Since Specialization
Citations

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

Fields of papers citing papers by Deborah Maiese

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah Maiese

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah Maiese. A scholar is included among the top collaborators of Deborah Maiese 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 Deborah Maiese. Deborah Maiese 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.
Maiese, Deborah, Miriam G. Blitzer, Vivian Pan, et al.. (2025). The 2023 medical genetics workforce in the United States. Genetics in Medicine. 27(10). 101461–101461.
2.
Marshall, Vanessa, Keith C. Norris, Myles Cockburn, et al.. (2024). The PhenX Toolkit: Recommended Measurement Protocols for Social Determinants of Health Research. Current Protocols. 4(3). e977–e977. 2 indexed citations
3.
Maiese, Deborah, et al.. (2024). P499: US genetics professional workforce in 2023. SHILAP Revista de lepidopterología. 2. 101398–101398. 1 indexed citations
4.
Nekhlyudov, Larissa, Keith M. Bellizzi, Bellinda L. King‐Kallimanis, et al.. (2023). The PhenX Toolkit: standard measurement resources for cancer outcomes and survivorship research. JNCI Journal of the National Cancer Institute. 115(4). 473–476. 1 indexed citations
5.
Bierut, Laura J., Tabitha Hendershot, Neal L. Benowitz, et al.. (2023). Smoking cessation, harm reduction, and biomarkers protocols in the PhenX Toolkit: Tools for standardized data collection. SHILAP Revista de lepidopterología. 7. 100081–100081. 1 indexed citations
6.
Maiese, Deborah, et al.. (2023). The 2019 medical genetics workforce: A focus on laboratory geneticists. Genetics in Medicine. 25(6). 100834–100834. 4 indexed citations
7.
Ropelewski, Alexander J., Megan A. Rizzo, Jason R. Swedlow, et al.. (2022). Standard metadata for 3D microscopy. Scientific Data. 9(1). 449–449. 8 indexed citations
8.
Chung, Wendy K., Kyle B. Brothers, Angela R. Bradbury, et al.. (2021). Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection. Genetics in Medicine. 23(9). 1783–1788. 2 indexed citations
9.
Jenkins, Brittany D., Catherine G. Fischer, Deborah Maiese, et al.. (2021). The 2019 US medical genetics workforce: a focus on clinical genetics. Genetics in Medicine. 23(8). 1458–1464. 96 indexed citations
10.
Lichstein, Jesse C., et al.. (2021). Children with genetic conditions in the United States: Prevalence estimates from the 2016-2017 National Survey of Children’s Health. Genetics in Medicine. 24(1). 170–178. 2 indexed citations
11.
Morton, Cynthia C., Mary L. Marazita, Beate Peter, et al.. (2021). Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit. Annals of Human Genetics. 86(1). 45–51. 2 indexed citations
12.
Maiese, Deborah, et al.. (2019). Current conditions in medical genetics practice. Genetics in Medicine. 21(8). 1874–1877. 104 indexed citations
13.
Phillips, M., Joann Bodurtha, Rodolfo Valdéz, et al.. (2017). PhenX measures for phenotyping rare genetic conditions. Genetics in Medicine. 19(7). 834–837. 2 indexed citations
14.
Malinowski, Ann Kinga, Cande V. Ananth, Patrick M. Catalano, et al.. (2017). Research standardization tools: pregnancy measures in the PhenX Toolkit. American Journal of Obstetrics and Gynecology. 217(3). 249–262. 3 indexed citations
15.
Homan, Sharon M., et al.. (2015). Healthcare Coordination and Transition for Individuals with Genetic Conditions. Maternal and Child Health Journal. 19(10). 2215–2222. 8 indexed citations
16.
Conway, Kevin P., Genevieve C. Vullo, Ashley Kennedy, et al.. (2014). Data compatibility in the addiction sciences: An examination of measure commonality. Drug and Alcohol Dependence. 141. 153–158. 27 indexed citations
17.
Maiese, Deborah. (2002). Healthy people 2010—leading health indicators for women. Women s Health Issues. 12(4). 155–164. 46 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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