Maren T. Scheuner

4.7k total citations
71 papers, 2.6k citations indexed

About

Maren T. Scheuner is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine. According to data from OpenAlex, Maren T. Scheuner has authored 71 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 21 papers in Public Health, Environmental and Occupational Health and 13 papers in Pathology and Forensic Medicine. Recurrent topics in Maren T. Scheuner's work include BRCA gene mutations in cancer (34 papers), Ethics in Clinical Research (18 papers) and Genomics and Rare Diseases (17 papers). Maren T. Scheuner is often cited by papers focused on BRCA gene mutations in cancer (34 papers), Ethics in Clinical Research (18 papers) and Genomics and Rare Diseases (17 papers). Maren T. Scheuner collaborates with scholars based in United States, Germany and Australia. Maren T. Scheuner's co-authors include Paula W. Yoon, Muin J. Khoury, Paul G Shekelle, Marta Gwinn, Jerome I. Rotter, Leslie J. Raffel, Roger S. Blumenthal, Muin J. Khoury, Andrew N. Freedman and Timothy S. McNeel and has published in prestigious journals such as JAMA, Circulation and SHILAP Revista de lepidopterología.

In The Last Decade

Maren T. Scheuner

69 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maren T. Scheuner United States	27	1.5k	516	371	346	271	71	2.6k
Laure El ghormli United States	23	585 0.4×	481 0.9×	251 0.7×	268 0.8×	155 0.6×	58	2.7k
Ingrid Oakley‐Girvan United States	27	632 0.4×	471 0.9×	105 0.3×	927 2.7×	205 0.8×	68	2.7k
Rami Nassir United States	21	650 0.4×	289 0.6×	248 0.7×	454 1.3×	134 0.5×	73	1.9k
Angela R. Bradbury United States	28	1.4k 0.9×	431 0.8×	259 0.7×	638 1.8×	411 1.5×	121	2.8k
Jeannette T. Bensen United States	32	661 0.4×	486 0.9×	240 0.6×	1.4k 4.0×	242 0.9×	162	3.9k
Karen Ruth United States	33	329 0.2×	442 0.9×	372 1.0×	1.2k 3.6×	255 0.9×	129	3.3k
DeAnn Lazovich United States	31	296 0.2×	684 1.3×	182 0.5×	1.2k 3.4×	345 1.3×	88	3.4k
Amy C. Sturm United States	25	825 0.6×	276 0.5×	919 2.5×	69 0.2×	123 0.5×	103	2.5k
Johnny S. H. Kwan Hong Kong	17	506 0.3×	207 0.4×	339 0.9×	146 0.4×	85 0.3×	30	1.7k
Penny C. Sharp United States	19	822 0.6×	311 0.6×	152 0.4×	395 1.1×	222 0.8×	34	2.0k

Countries citing papers authored by Maren T. Scheuner

Since Specialization

Citations

This map shows the geographic impact of Maren T. Scheuner'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 Maren T. Scheuner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maren T. Scheuner more than expected).

Fields of papers citing papers by Maren T. Scheuner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maren T. Scheuner. 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 Maren T. Scheuner. The network helps show where Maren T. Scheuner may publish in the future.

Co-authorship network of co-authors of Maren T. Scheuner

This figure shows the co-authorship network connecting the top 25 collaborators of Maren T. Scheuner. A scholar is included among the top collaborators of Maren T. Scheuner 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 Maren T. Scheuner. Maren T. Scheuner 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

Kwon, Daniel H., Maren T. Scheuner, Evan J. Walker, et al.. (2025). Veterans' Decision Making for Prostate Cancer Germline Testing After Informed Consent With Their Oncologist: A Mixed-Methods Study. JCO Oncology Practice. 22(3). 502–515.

Kwon, Daniel H., Maren T. Scheuner, Evan J. Walker, et al.. (2024). Germline testing for veterans with advanced prostate cancer: concerns about service-connected benefits. JNCI Cancer Spectrum. 8(5). 1 indexed citations

Lynch, Julie A., J M Petersen, Lori Hoffman-Hōgg, et al.. (2023). On-Site Nurse-Led Cancer Genetics Program Increases Cancer Genetic Testing Completion in Black Veterans. JCO Oncology Practice. 19(8). 637–644. 6 indexed citations

Voils, Corrine I., Cynthia J. Coffman, R. Ryanne Wu, et al.. (2022). A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer. Journal of General Internal Medicine. 38(6). 1375–1383. 4 indexed citations

Rehm, Heidi L., et al.. (2021). Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance. Genetics in Medicine. 23(10). 1977–1983. 5 indexed citations

Lin, Grace A., Julia R. Trosman, Michael P. Douglas, et al.. (2021). Influence of payer coverage and out‐of‐pocket costs on ordering of NGS panel tests for hereditary cancer in diverse settings. Journal of Genetic Counseling. 31(1). 130–139. 21 indexed citations

Scheuner, Maren T., et al.. (2021). Laboratory business models and practices: implications for availability and access to germline genetic testing. Genetics in Medicine. 23(9). 1681–1688. 4 indexed citations

Bean, Lora Jh, Maren T. Scheuner, Michael F. Murray, et al.. (2021). DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(6). 979–988. 18 indexed citations

Hull, Leland E., Jason L. Vassy, Annjanette Stone, et al.. (2020). Identifying End Users' Preferences about Structuring Pharmacogenetic Test Orders in an Electronic Health Record System. Journal of Molecular Diagnostics. 22(10). 1264–1271. 3 indexed citations

10.

Mohapatra, Shyam S., Surinder K. Batra, Michael Bouvet, et al.. (2018). Precision Medicine for CRC Patients in the Veteran Population: State-of-the-Art, Challenges and Research Directions. Digestive Diseases and Sciences. 63(5). 1123–1138. 9 indexed citations

11.

Chanfreau‐Coffinier, Catherine, Marcia M. Russell, Elizabeth M. Yano, et al.. (2018). A logic model for precision medicine implementation informed by stakeholder views and implementation science. Genetics in Medicine. 21(5). 1139–1154. 24 indexed citations

12.

Vassy, Jason L., Annjanette Stone, John T. Callaghan, et al.. (2018). Pharmacogenetic testing in the Veterans Health Administration (VHA): policy recommendations from the VHA Clinical Pharmacogenetics Subcommittee. Genetics in Medicine. 21(2). 382–390. 10 indexed citations

13.

Scheuner, Maren T., Alison Brown, Lee H. Hilborne, et al.. (2016). Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists. Genetics in Medicine. 19(1). 112–120. 6 indexed citations

14.

Oishi, Sabine, et al.. (2015). Assessing multilevel determinants of adoption and implementation of genomic medicine: an organizational mixed-methods approach. Genetics in Medicine. 17(11). 919–926. 8 indexed citations

15.

Scheuner, Maren T., Judith Benkendorf, Bruce Bowdish, et al.. (2014). Reporting genomic secondary findings: ACMG members weigh in. Genetics in Medicine. 17(1). 27–35. 39 indexed citations

16.

Brown, Alison, et al.. (2013). Factors influencing organizational adoption and implementation of clinical genetic services. Genetics in Medicine. 16(3). 238–245. 61 indexed citations

17.

Scheuner, Maren T., et al.. (2012). A Report Template for Molecular Genetic Tests Designed to Improve Communication Between the Clinician and Laboratory. Genetic Testing and Molecular Biomarkers. 16(7). 761–769. 26 indexed citations

18.

Setodji, Claude Messan, Maren T. Scheuner, James S. Pankow, et al.. (2012). A graphical method for assessing risk factor threshold values using the generalized additive model: the multi-ethnic study of atherosclerosis. Health Services and Outcomes Research Methodology. 12(1). 62–79. 21 indexed citations

19.

Scheuner, Maren T., Timothy S. McNeel, & Andrew N. Freedman. (2010). Population prevalence of familial cancer and common hereditary cancer syndromes. The 2005 California Health Interview Survey. Genetics in Medicine. 12(11). 726–735. 64 indexed citations

20.

Scheuner, Maren T., William C. Whitworth, Henraya McGruder, Paula W. Yoon, & Muin J. Khoury. (2006). Expanding the definition of a positive family history for early-onset coronary heart disease. Genetics in Medicine. 8(8). 491–501. 51 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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