James P. Evans

11.9k total citations · 2 hit papers
126 papers, 6.0k citations indexed

About

James P. Evans is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, James P. Evans has authored 126 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Genetics, 24 papers in Public Health, Environmental and Occupational Health and 22 papers in Molecular Biology. Recurrent topics in James P. Evans's work include BRCA gene mutations in cancer (45 papers), Genomics and Rare Diseases (34 papers) and Ethics in Clinical Research (16 papers). James P. Evans is often cited by papers focused on BRCA gene mutations in cancer (45 papers), Genomics and Rare Diseases (34 papers) and Ethics in Clinical Research (16 papers). James P. Evans collaborates with scholars based in United States, United Kingdom and Canada. James P. Evans's co-authors include Jonathan S. Berg, Michael S. Watson, F. J. Gould, Christa Lese Martin, Cécile Skrzynia, Wylie Burke, Ralph E. Steuer, Jon W. Tolle, Muin J. Khoury and Kent D. McKelvey and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

James P. Evans

122 papers receiving 5.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

2016 1.0k citations Sarah S. Kalia, Sherri J. Bale et al. Genetics in Medicine profile →
ClinGen — The Clinical Genome Resource

2015 776 citations Jonathan S. Berg, James P. Evans et al. profile →

Peers

James P. Evans

GENET

PHEOH

PFM

Daniel F. Heitjan United States

Shelley B. Bull Canada

Alan E. Guttmacher United States

Sharon L. R. Kardia United States

Wendy S. Rubinstein United States

Michael S. Watson United States

Carl Johan Sundberg Sweden

Fred H. Menko Netherlands

Borut Peterlin Slovenia

Peter N. Robinson Germany

Daniel F. Heitjan United States

James P. Evans

1.3k ×0.4

GENET

2.6k ×2.1

391 ×0.4

PHEOH

975 ×1.1

1.0k ×1.5

PFM

Citations per year, relative to James P. Evans James P. Evans (= 1×) peers Daniel F. Heitjan

Countries citing papers authored by James P. Evans

Since Specialization

Citations

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

Fields of papers citing papers by James P. Evans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James P. Evans. 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 James P. Evans. The network helps show where James P. Evans may publish in the future.

Co-authorship network of co-authors of James P. Evans

This figure shows the co-authorship network connecting the top 25 collaborators of James P. Evans. A scholar is included among the top collaborators of James P. Evans 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 James P. Evans. James P. Evans 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

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

Burke, Wylie, Ellen Wright Clayton, Susan M. Wolf, et al.. (2019). Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines. Genetics in Medicine. 21(11). 2431–2438. 14 indexed citations

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

Butterfield, Rita M., James P. Evans, Christine Rini, et al.. (2018). Returning negative results to individuals in a genomic screening program: lessons learned. Genetics in Medicine. 21(2). 409–416. 35 indexed citations

May, Thomas & James P. Evans. (2018). Addressing perceived economic obstacles to genetic testing as a way to mitigate disparities in family health history for adoptees. Health Economics Policy and Law. 15(2). 277–287. 5 indexed citations

Prince, Anya E. R., Gail E. Henderson, James P. Evans, et al.. (2017). Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review. Pharmacogenomics and Personalized Medicine. Volume10. 49–60. 11 indexed citations

Lin, Feng‐Chang, et al.. (2016). Plagiarism in submitted manuscripts: incidence, characteristics and optimization of screening—case study in a major specialty medical journal. PubMed. 1(1). 13–13. 42 indexed citations

Kalia, Sarah S., Sherri J. Bale, Wendy K. Chung, et al.. (2016). Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genetics in Medicine. 19(2). 249–255. 1023 indexed citations breakdown →

Adams, Michael C. C., James P. Evans, Gail E. Henderson, & Jonathan S. Berg. (2015). The promise and peril of genomic screening in the general population. Genetics in Medicine. 18(6). 593–599. 39 indexed citations

10.

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

11.

Foreman, Ann Katherine M., Kristy Lee, & James P. Evans. (2013). The NCGENES Project: Exploring the New World of Genome Sequencing. North Carolina Medical Journal. 74(6). 500–504. 14 indexed citations

12.

Evans, James P.. (2012). The policy-driven health plan: a road map for value-based reimbursement.. PubMed Central. 1 indexed citations

13.

Funkhouser, William K., Ira M. Lubin, Federico A. Monzon, et al.. (2012). Relevance, Pathogenesis, and Testing Algorithm for Mismatch Repair–Defective Colorectal Carcinomas. Journal of Molecular Diagnostics. 14(2). 91–103. 145 indexed citations

14.

Evans, James P. & Jonathan S. Berg. (2011). Next-Generation DNA Sequencing, Regulation, and the Limits of Paternalism. JAMA. 306(21). 2376–7. 25 indexed citations

15.

Evans, James P.. (2011). Looking ahead, looking behind. Genetics in Medicine. 13(3). 177–178. 4 indexed citations

16.

Berg, Jonathan S., James P. Evans, Margaret W. Leigh, et al.. (2011). Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing. Genetics in Medicine. 13(3). 218–229. 41 indexed citations

17.

Burke, Wylie & James P. Evans. (2010). Teaching with single nucleotide polymorphisms: Learning the right lessons. Genetics in Medicine. 13(1). 17–18. 3 indexed citations

18.

Booker, Jessica K., et al.. (2009). Validation of Clinical Testing for Warfarin Sensitivity. Journal of Molecular Diagnostics. 11(3). 216–225. 38 indexed citations

19.

Evans, James P. & Robert C. Green. (2009). Direct to consumer genetic testing: Avoiding a culture war. Genetics in Medicine. 11(8). 568–569. 52 indexed citations

20.

Neklason, Deborah W., Richard A. Kerber, Hoda Anton‐Culver, et al.. (2008). Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis. Cancer Research. 68(21). 8993–8997. 27 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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