Wendy R. Uhlmann

3.1k total citations
89 papers, 2.1k citations indexed

About

Wendy R. Uhlmann is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Wendy R. Uhlmann has authored 89 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Genetics, 19 papers in Public Health, Environmental and Occupational Health and 17 papers in Molecular Biology. Recurrent topics in Wendy R. Uhlmann's work include BRCA gene mutations in cancer (42 papers), Genomics and Rare Diseases (18 papers) and Ethics in Clinical Research (11 papers). Wendy R. Uhlmann is often cited by papers focused on BRCA gene mutations in cancer (42 papers), Genomics and Rare Diseases (18 papers) and Ethics in Clinical Research (11 papers). Wendy R. Uhlmann collaborates with scholars based in United States, Canada and Poland. Wendy R. Uhlmann's co-authors include J. Scott Roberts, Beverly M. Yashar, Jane L. Schuette, Robert C. Green, Mack T. Ruffin, Michele C. Gornick, Deanna Alexis Carere, Alan E. Guttmacher, Jean Jenkins and Kurt D. Christensen and has published in prestigious journals such as JAMA, SHILAP Revista de lepidopterología and Annals of Internal Medicine.

In The Last Decade

Wendy R. Uhlmann

81 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wendy R. Uhlmann United States	23	1.2k	523	443	232	221	89	2.1k
Danya F. Vears Australia	25	944 0.8×	489 0.9×	592 1.3×	237 1.0×	201 0.9×	110	2.3k
Kristine Barlow‐Stewart Australia	24	1.1k 0.9×	369 0.7×	545 1.2×	167 0.7×	220 1.0×	116	1.9k
Benjamin E. Berkman United States	19	598 0.5×	439 0.8×	363 0.8×	152 0.7×	134 0.6×	64	1.4k
Kimberly A. Quaid United States	25	628 0.5×	318 0.6×	219 0.5×	326 1.4×	144 0.7×	54	1.8k
Kyle B. Brothers United States	25	808 0.7×	660 1.3×	339 0.8×	202 0.9×	263 1.2×	85	1.8k
Suzanne C. O’Neill United States	24	722 0.6×	286 0.5×	242 0.5×	191 0.8×	302 1.4×	98	2.1k
Janet K. Williams United States	34	1.4k 1.2×	539 1.0×	486 1.1×	734 3.2×	323 1.5×	159	3.6k
Yvonne Bombard Canada	30	1.2k 1.0×	631 1.2×	505 1.1×	452 1.9×	725 3.3×	98	3.1k
Sylvia A. Metcalfe Australia	33	1.4k 1.1×	442 0.8×	716 1.6×	669 2.9×	165 0.7×	113	3.0k
Holly L. Peay United States	27	403 0.3×	349 0.7×	222 0.5×	423 1.8×	291 1.3×	122	1.8k

Countries citing papers authored by Wendy R. Uhlmann

Since Specialization

Citations

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

Fields of papers citing papers by Wendy R. Uhlmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy R. Uhlmann. 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 Wendy R. Uhlmann. The network helps show where Wendy R. Uhlmann may publish in the future.

Co-authorship network of co-authors of Wendy R. Uhlmann

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy R. Uhlmann. A scholar is included among the top collaborators of Wendy R. Uhlmann 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 Wendy R. Uhlmann. Wendy R. Uhlmann 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

Srinivasan, Sharan R., et al.. (2025). Practice Recommendations for Genetic Testing of Ataxias. Annals of Clinical and Translational Neurology. 12(12). 2398–2409. 1 indexed citations

Jenny, Kim, Kristiana Salmon, Ashley Crook, et al.. (2025). The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders. Neurology. 105(3). e213814–e213814.

Ames, Elizabeth G., Shane C. Quinonez, Anthony Scott, et al.. (2025). Genetics Evaluation Outcomes From an Academic Multidisciplinary Atypical Diabetes Program. Journal of the Endocrine Society. 9(8). bvaf091–bvaf091.

Uhlmann, Wendy R., et al.. (2024). The Genetic Information Nondiscrimination Act and workplace genetic testing: Knowledge and perceptions of employed adults in the United States. Journal of Genetic Counseling. 34(2). e1945–e1945. 5 indexed citations

Rodriguez, Sophia, María Cabán, Wendy R. Uhlmann, et al.. (2024). Designing and implementing the IDEAL Study: A randomized clinical trial of APOE genotype disclosure for late‐onset Alzheimer's disease in an urban Latino population. Alzheimer s & Dementia Translational Research & Clinical Interventions. 10(4). e70016–e70016. 1 indexed citations

Pal, Subhamoy, Wendy R. Uhlmann, Kunal Sanghavi, et al.. (2024). Health care utilization and behavior changes after workplace genetic testing at a large US health care system. Genetics in Medicine. 26(8). 101160–101160. 4 indexed citations

Griggs, Jennifer J., Ken Resnicow, Kelley M. Kidwell, et al.. (2023). The Michigan Genetic Hereditary Testing (MiGHT) study’s innovative approaches to promote uptake of clinical genetic testing among cancer patients: a study protocol for a 3-arm randomized controlled trial. Trials. 24(1). 105–105. 4 indexed citations

Chambers, Chelsea, et al.. (2023). Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders. Neurology Clinical Practice. 13(5). e200201–e200201. 7 indexed citations

Goldman, Jill, Wendy R. Uhlmann, Ali Naini, Robert Klitzman, & Karen Marder. (2023). Genetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines. Movement Disorders. 38(12). 2151–2154. 3 indexed citations

10.

Cook, Lola, Wendy R. Uhlmann, Karen Marder, et al.. (2022). Tools for communicating risk for Parkinson’s disease. npj Parkinson s Disease. 8(1). 164–164. 3 indexed citations

11.

Uhlmann, Wendy R., et al.. (2021). Genetic counseling, virtual visits, and equity in the era of COVID‐19 and beyond. Journal of Genetic Counseling. 30(4). 1038–1045. 17 indexed citations

12.

Ormond, Kelly E., Miranda L. G. Hallquist, Adam H. Buchanan, et al.. (2021). Defining the Critical Components of Informed Consent for Genetic Testing. Journal of Personalized Medicine. 11(12). 1304–1304. 18 indexed citations

13.

Uhlmann, Wendy R., et al.. (2020). 40 years and beyond for the National Society of Genetic Counselors: Reflections on genetic counseling practice. Journal of Genetic Counseling. 29(6). 888–893. 5 indexed citations

14.

Ryan, Kerry A., Raymond De Vries, Wendy R. Uhlmann, J. Scott Roberts, & Michele C. Gornick. (2017). Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice. Journal of Genetic Counseling. 26(6). 1197–1212. 17 indexed citations

15.

Murray, Brittney, Beverly M. Yashar, Wendy R. Uhlmann, Daniel J. Clauw, & Elizabeth M. Petty. (2013). Ehlers–Danlos syndrome, hypermobility type: A characterization of the patients' lived experience. American Journal of Medical Genetics Part A. 161(12). 2981–2988. 68 indexed citations

16.

Chen, Clara, et al.. (2011). Willingness to Pay for Genetic Testing for Alzheimer's Disease: A Measure of Personal Utility. Genetic Testing and Molecular Biomarkers. 15(12). 871–875. 48 indexed citations

17.

Christensen, Kurt D., J. Scott Roberts, Wendy R. Uhlmann, & Robert C. Green. (2011). Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk. Genetics in Medicine. 13(5). 409–414. 35 indexed citations

18.

Uhlmann, Wendy R.. (2010). The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease. The American Journal of Human Genetics. 86(6). 830–831. 2 indexed citations

19.

Uhlmann, Wendy R., Jane L. Schuette, & Beverly M. Yashar. (1998). A guide to genetic counseling. Wiley-Blackwell eBooks. 235 indexed citations

20.

Johnson, Mark P., et al.. (1991). Postmortem chorionic villus sampling: Correlation of cytogenetic and ultrasound findings. American Journal of Medical Genetics. 39(3). 314–316. 20 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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