Sharon F. Terry

15.7k total citations · 1 hit paper
175 papers, 4.5k citations indexed

About

Sharon F. Terry is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Cell Biology. According to data from OpenAlex, Sharon F. Terry has authored 175 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 95 papers in Genetics, 55 papers in Public Health, Environmental and Occupational Health and 33 papers in Cell Biology. Recurrent topics in Sharon F. Terry's work include Dermatological and Skeletal Disorders (47 papers), Ethics in Clinical Research (45 papers) and Skin and Cellular Biology Research (33 papers). Sharon F. Terry is often cited by papers focused on Dermatological and Skeletal Disorders (47 papers), Ethics in Clinical Research (45 papers) and Skin and Cellular Biology Research (33 papers). Sharon F. Terry collaborates with scholars based in United States, United Kingdom and Italy. Sharon F. Terry's co-authors include Lionel Bercovitch, Jouni Uitto, Patrick F. Terry, I. Pasquali‐Ronchetti, Charles D. Boyd, Olivier Le Saux, F M Pope, Daniela Quaglino, Arthur A. Bergen and Anne De Paepe and has published in prestigious journals such as Nature, Science and JAMA.

In The Last Decade

Sharon F. Terry

166 papers receiving 4.4k citations

Hit Papers

Adopt a moratorium on heritable genome editing 2019 2026 2021 2023 2019 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sharon F. Terry United States 34 2.6k 1.2k 1.1k 935 566 175 4.5k
Laura‐Maria Peltonen Finland 36 973 0.4× 1.6k 1.3× 619 0.5× 375 0.4× 257 0.5× 185 4.6k
Mary Porteous United Kingdom 40 1.5k 0.6× 2.0k 1.7× 264 0.2× 709 0.8× 256 0.5× 101 7.4k
Alan E. Guttmacher United States 28 1.8k 0.7× 2.0k 1.7× 109 0.1× 569 0.6× 216 0.4× 56 8.0k
Domenica Taruscio Italy 36 1.1k 0.4× 1.1k 0.9× 137 0.1× 392 0.4× 207 0.4× 194 3.8k
Michael S. Watson United States 41 5.2k 2.0× 2.4k 2.0× 138 0.1× 995 1.1× 817 1.4× 115 9.7k
Neil A. Holtzman United States 41 1.7k 0.6× 873 0.7× 132 0.1× 871 0.9× 191 0.3× 159 5.3k
Saundra S. Buys United States 36 1.8k 0.7× 1.5k 1.2× 120 0.1× 579 0.6× 237 0.4× 137 6.1k
Peter Clayton United Kingdom 50 1.9k 0.7× 2.6k 2.2× 151 0.1× 645 0.7× 171 0.3× 305 9.5k
Ségolène Aymé France 38 1.9k 0.7× 1.2k 1.0× 90 0.1× 683 0.7× 433 0.8× 161 4.7k

Countries citing papers authored by Sharon F. Terry

Since Specialization
Citations

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

Fields of papers citing papers by Sharon F. Terry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharon F. Terry. 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 Sharon F. Terry. The network helps show where Sharon F. Terry may publish in the future.

Co-authorship network of co-authors of Sharon F. Terry

This figure shows the co-authorship network connecting the top 25 collaborators of Sharon F. Terry. A scholar is included among the top collaborators of Sharon F. Terry 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 Sharon F. Terry. Sharon F. Terry 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.
Szeri, Flóra, Nastassia Navasiolava, Ambrus Kaposi, et al.. (2022). The pathogenic c.1171A>G (p.Arg391Gly) and c.2359G>A (p.Val787Ile) ABCC6 variants display incomplete penetrance causing pseudoxanthoma elasticum in a subset of individuals. Human Mutation. 43(12). 1872–1881. 3 indexed citations
2.
Terry, Sharon F., et al.. (2022). Building iHope Genetic Health. Genetic Testing and Molecular Biomarkers. 26(3). 105–106.
3.
Terry, Sharon F.. (2021). Whole Genome Screening for Sick Newborns: Equity Now. Genetic Testing and Molecular Biomarkers. 25(10). 625–626. 2 indexed citations
4.
Lander, Eric S., Françoise Βaylis, Feng Zhang, et al.. (2019). Adopt a moratorium on heritable genome editing. Nature. 567(7747). 165–168. 251 indexed citations breakdown →
5.
Moitra, Karobi, et al.. (2017). ABCC6 and Pseudoxanthoma Elasticum: The Face of a Rare Disease from Genetics to Advocacy. International Journal of Molecular Sciences. 18(7). 1488–1488. 19 indexed citations
6.
Edwards, K. A., et al.. (2016). Realizing Our Potential in Biobanking: Disease Advocacy Organizations Enliven Translational Research. Biopreservation and Biobanking. 14(4). 314–318. 3 indexed citations
7.
Terry, Sharon F.. (2015). Participating in Next Generation Sequencing. Genetic Testing and Molecular Biomarkers. 19(4). 174–174. 1 indexed citations
8.
Terry, Sharon F.. (2014). Sharing Your Thoughts About Sharing Clinical Trial Data. Genetic Testing and Molecular Biomarkers. 18(4). 221–222. 1 indexed citations
9.
Terry, Sharon F.. (2013). Disease advocacy organizations catalyze translational research. Frontiers in Genetics. 4. 101–101. 12 indexed citations
10.
Terry, Sharon F., et al.. (2013). The Haystack Is Made of Needles. Genetic Testing and Molecular Biomarkers. 17(3). 175–177. 20 indexed citations
11.
Terry, Sharon F. & Natasha Bonhomme. (2013). Nothing About Us Without Us: Guidelines for Genetic Testing. Genetic Testing and Molecular Biomarkers. 17(5). 357–358. 5 indexed citations
12.
Terry, Sharon F., et al.. (2013). The Need to Build Trust: A Perspective on Disparities in Genetic Testing. Genetic Testing and Molecular Biomarkers. 17(9). 647–648. 33 indexed citations
13.
Horn, Elizabeth J. & Sharon F. Terry. (2012). Precision Medicine: Generating Real-World Evidence for Companion Diagnostics. Genetic Testing and Molecular Biomarkers. 16(2). 75–76. 2 indexed citations
14.
Bercovitch, Lionel, Ludovic Martin, Timothy Hefferon, et al.. (2011). Acquired pseudoxanthoma elasticum presenting after liver transplantation. Journal of the American Academy of Dermatology. 64(5). 873–878. 14 indexed citations
15.
Field, Amanda, et al.. (2011). “Insufficient Evidence” Isn't Sufficient Anymore. Genetic Testing and Molecular Biomarkers. 15(3). 115–116. 1 indexed citations
16.
Ramsay, Michèle, Zané Lombard, Robyn Labrum, et al.. (2009). Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals. Journal of Dermatological Science. 54(3). 198–204. 8 indexed citations
17.
Shi, Yanggu, Sharon F. Terry, Patrick F. Terry, Lionel Bercovitch, & Gary F. Gerard. (2007). Development of a Rapid, Reliable Genetic Test for Pseudoxanthoma Elasticum. Journal of Molecular Diagnostics. 9(1). 105–112. 16 indexed citations
18.
Vanakker, Olivier, Ludovic Martin, Dealba Gheduzzi, et al.. (2006). Pseudoxanthoma Elasticum-Like Phenotype with Cutis Laxa and Multiple Coagulation Factor Deficiency Represents a Separate Genetic Entity. Journal of Investigative Dermatology. 127(3). 581–587. 139 indexed citations
19.
Terry, Sharon F., et al.. (2005). Testicular Microlithiasis in Association with Pseudoxanthoma Elasticum. Radiology. 237(2). 550–554. 18 indexed citations
20.
Saux, Olivier Le, Zsolt Urbán, Cordula Tschuch, et al.. (2000). Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum. Nature Genetics. 25(2). 223–227. 420 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026