Myra I. Roche

2.3k total citations
41 papers, 890 citations indexed

About

Myra I. Roche is a scholar working on Genetics, Public Health, Environmental and Occupational Health and General Health Professions. According to data from OpenAlex, Myra I. Roche has authored 41 papers receiving a total of 890 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 15 papers in Public Health, Environmental and Occupational Health and 11 papers in General Health Professions. Recurrent topics in Myra I. Roche's work include Genomics and Rare Diseases (25 papers), BRCA gene mutations in cancer (25 papers) and Ethics in Clinical Research (12 papers). Myra I. Roche is often cited by papers focused on Genomics and Rare Diseases (25 papers), BRCA gene mutations in cancer (25 papers) and Ethics in Clinical Research (12 papers). Myra I. Roche collaborates with scholars based in United States, Qatar and Japan. Myra I. Roche's co-authors include Jonathan S. Berg, Debra Skinner, Cynthia M. Powell, Christine Rini, Donald B. Bailey, Barbara A. Bernhardt, Anya E. R. Prince, Sarah Scollon, Denise Perry and Ashley N. Tomlinson and has published in prestigious journals such as PEDIATRICS, Social Science & Medicine and The Journal of Pediatrics.

In The Last Decade

Myra I. Roche

37 papers receiving 870 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Myra I. Roche United States 18 654 252 208 116 94 41 890
Karine Sénécal Canada 17 556 0.9× 323 1.3× 262 1.3× 79 0.7× 111 1.2× 33 873
Joon‐Ho Yu United States 18 699 1.1× 349 1.4× 114 0.5× 109 0.9× 166 1.8× 38 1.1k
Catherine Wicklund United States 16 451 0.7× 202 0.8× 288 1.4× 57 0.5× 59 0.6× 41 763
Anne‐Marie Laberge Canada 15 230 0.4× 148 0.6× 215 1.0× 47 0.4× 85 0.9× 55 604
Melissa Martyn Australia 14 415 0.6× 100 0.4× 89 0.4× 43 0.4× 111 1.2× 40 647
Álvaro Mendes Portugal 14 405 0.6× 137 0.5× 116 0.6× 79 0.7× 85 0.9× 48 627
Susan Hiraki United States 14 315 0.5× 111 0.4× 61 0.3× 51 0.4× 72 0.8× 21 532
MaryAnne Aitken Australia 18 397 0.6× 120 0.5× 214 1.0× 55 0.5× 68 0.7× 35 788
Irmgard Nippert Germany 14 381 0.6× 128 0.5× 158 0.8× 44 0.4× 74 0.8× 44 592
Denise Lautenbach United States 9 363 0.6× 114 0.5× 36 0.2× 34 0.3× 60 0.6× 10 499

Countries citing papers authored by Myra I. Roche

Since Specialization
Citations

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

Fields of papers citing papers by Myra I. Roche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Myra I. Roche. 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 Myra I. Roche. The network helps show where Myra I. Roche may publish in the future.

Co-authorship network of co-authors of Myra I. Roche

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

All Works

20 of 20 papers shown
1.
2.
Moultrie, Rebecca, Ryan S. Paquin, Christine Rini, et al.. (2020). Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support. Maternal and Child Health Journal. 24(7). 856–864. 16 indexed citations
3.
Rini, Christine, Gail E. Henderson, James P. Evans, et al.. (2019). Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes. Genetics in Medicine. 22(1). 60–68. 13 indexed citations
4.
Milko, Laura V., Julianne O’Daniel, Stephanie B. Crowley, et al.. (2019). An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening. The Journal of Pediatrics. 209. 68–76. 44 indexed citations
5.
Moore, Elizabeth, et al.. (2019). Psychological adaptation to diagnostic genomic sequencing results: The role of hope fulfillment.. Health Psychology. 38(6). 527–535. 9 indexed citations
6.
Peinado, Susana, Ryan S. Paquin, Christine Rini, et al.. (2019). Values clarification and parental decision making about newborn genomic sequencing.. Health Psychology. 39(4). 335–344. 12 indexed citations
7.
Roche, Myra I., Cynthia M. Khan, Elizabeth Moore, et al.. (2018). Factors influencing NCGENES research participants- requests for non-medically actionable secondary findings. Genetics in Medicine. 21(5). 1092–1099. 10 indexed citations
8.
Skinner, Debra, Myra I. Roche, Karen E. Weck, et al.. (2018). “Possibly positive or certainly uncertain?”: participants’ responses to uncertain diagnostic results from exome sequencing. Genetics in Medicine. 20(3). 313–319. 35 indexed citations
9.
Ormond, Kelly E., Miranda L. G. Hallquist, Adam H. Buchanan, et al.. (2018). Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background. Genetics in Medicine. 21(3). 727–735. 38 indexed citations
10.
Paquin, Ryan S., Susana Peinado, Megan A. Lewis, et al.. (2018). A behavior-theoretic evaluation of values clarification on parental beliefs and intentions toward genomic sequencing for newborns. Social Science & Medicine. 271. 112037–112037. 10 indexed citations
11.
Lewis, Megan A., Ryan S. Paquin, Carol Mansfield, et al.. (2017). Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment. Genetics in Medicine. 20(2). 181–189. 26 indexed citations
12.
Rini, Christine, Cynthia M. Khan, Elizabeth Moore, et al.. (2017). The who, what, and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study. Genetics in Medicine. 20(7). 760–769. 20 indexed citations
13.
Moore, Elizabeth, Myra I. Roche, Christine Rini, et al.. (2017). Examining the Cascade of Participant Attrition in a Genomic Medicine Research Study: Barriers and Facilitators to Achieving Diversity. Public Health Genomics. 20(6). 332–342. 9 indexed citations
14.
Roche, Myra I. & Anne Greb. (2016). It’s time to ramp up genetic counseling training. Genetics in Medicine. 18(8). 768–769. 5 indexed citations
15.
Amendola, Laura M., Julianne O’Daniel, Amber Burt, et al.. (2016). Is “incidental finding” the best term?: a study of patients’ preferences. Genetics in Medicine. 19(2). 176–181. 28 indexed citations
16.
Bailey, Donald B., Anne Wheeler, Elizabeth Berry‐Kravis, et al.. (2015). Maternal Consequences of the Detection of Fragile X Carriers in Newborn Screening. PEDIATRICS. 136(2). e433–e440. 13 indexed citations
17.
Roche, Myra I. & Jonathan S. Berg. (2015). Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice. PubMed. 3(4). 166–176. 62 indexed citations
18.
Bailey, Donald B., et al.. (2012). Can a decision aid enable informed decisions in neonatal nursery recruitment for a fragile X newborn screening study?. Genetics in Medicine. 15(4). 299–306. 7 indexed citations
19.
Roche, Myra I.. (2012). Moving toward NextGenetic Counseling. Genetics in Medicine. 14(9). 777–778. 9 indexed citations
20.
Irwin, Debra E., Robert C. Millikan, R. Brian Stevens, et al.. (2004). Genomics and Public Health Practice. Journal of Public Health Management and Practice. 10(6). 539–544. 14 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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