Erynn S. Gordon

1.8k total citations
39 papers, 1.0k citations indexed

About

Erynn S. Gordon is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Erynn S. Gordon has authored 39 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Erynn S. Gordon's work include BRCA gene mutations in cancer (21 papers), Genomics and Rare Diseases (8 papers) and Nutrition, Genetics, and Disease (7 papers). Erynn S. Gordon is often cited by papers focused on BRCA gene mutations in cancer (21 papers), Genomics and Rare Diseases (8 papers) and Nutrition, Genetics, and Disease (7 papers). Erynn S. Gordon collaborates with scholars based in United States, United Kingdom and Canada. Erynn S. Gordon's co-authors include Michael F. Christman, Barbara A. Bernhardt, Eric P. Hoffman, Tara Schmidlen, Sarah E. Gollust, Georgia Griffin, Reed E. Pyeritz, Neda Gharani, Norman P. Gerry and Margaret Keller and has published in prestigious journals such as Neurology, The Journal of Physiology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Erynn S. Gordon

39 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erynn S. Gordon United States 19 510 352 193 147 104 39 1.0k
Carl‐Joachim Partsch Germany 29 637 1.2× 1.1k 3.1× 193 1.0× 130 0.9× 38 0.4× 81 2.4k
Jennifer Friedman United States 20 526 1.0× 444 1.3× 142 0.7× 423 2.9× 13 0.1× 57 1.6k
Neda Gharani United States 22 648 1.3× 436 1.2× 778 4.0× 49 0.3× 76 0.7× 32 1.9k
David Margulies United States 15 407 0.8× 370 1.1× 87 0.5× 68 0.5× 13 0.1× 31 1.2k
Raymond K. Walters United States 9 1.1k 2.1× 359 1.0× 66 0.3× 31 0.2× 16 0.2× 18 1.6k
Michele C. Gornick United States 17 442 0.9× 184 0.5× 181 0.9× 170 1.2× 14 0.1× 30 1.3k
James F. Hyde United States 21 88 0.2× 228 0.6× 102 0.5× 274 1.9× 30 0.3× 50 1.1k
Michael D. Powers United States 14 168 0.3× 706 2.0× 25 0.1× 192 1.3× 83 0.8× 41 1.7k
Kimberly A. Quaid United States 25 628 1.2× 326 0.9× 318 1.6× 363 2.5× 24 0.2× 54 1.8k
Jill O. Robinson United States 20 752 1.5× 119 0.3× 412 2.1× 38 0.3× 26 0.3× 70 1.2k

Countries citing papers authored by Erynn S. Gordon

Since Specialization
Citations

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

Fields of papers citing papers by Erynn S. Gordon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erynn S. Gordon. 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 Erynn S. Gordon. The network helps show where Erynn S. Gordon may publish in the future.

Co-authorship network of co-authors of Erynn S. Gordon

This figure shows the co-authorship network connecting the top 25 collaborators of Erynn S. Gordon. A scholar is included among the top collaborators of Erynn S. Gordon 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 Erynn S. Gordon. Erynn S. Gordon 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.
Kusic, Dara, Stefan Zajic, Neda Gharani, et al.. (2023). Genome-wide Association Study of Caffeine Consumption Using Coriell Personalized Medicine Collaborative Data. 5(1). 1 indexed citations
2.
Schmidlen, Tara, Amy C. Sturm, Shelly R. Hovick, et al.. (2018). Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing. Journal of Genetic Counseling. 27(5). 1111–1129. 22 indexed citations
3.
Gordon, Erynn S., et al.. (2018). The future is now: Technology's impact on the practice of genetic counseling. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(1). 15–23. 32 indexed citations
4.
Sweet, Kevin, Amy C. Sturm, Tara Schmidlen, et al.. (2017). Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports. Journal of Genetic Counseling. 26(5). 980–998. 17 indexed citations
5.
Sweet, Kevin, Shelly R. Hovick, Amy C. Sturm, et al.. (2016). Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study. Journal of Genetic Counseling. 26(4). 738–751. 16 indexed citations
6.
Kay, Chris, Jennifer A. Collins, Zosia Miedzybrodzka, et al.. (2016). Huntington disease reduced penetrance alleles occur at high frequency in the general population. Neurology. 87(3). 282–288. 61 indexed citations
7.
Shahabi, Payman, Laura Scheinfeldt, D.E. Lynch, et al.. (2016). An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance. Thrombosis and Haemostasis. 116(8). 337–348. 14 indexed citations
8.
Scheinfeldt, Laura, Tara Schmidlen, Neda Gharani, et al.. (2016). Coronary artery disease genetic risk awareness motivates heart health behaviors in the Coriell Personalized Medicine Collaborative. Expert Review of Precision Medicine and Drug Development. 1(4). 407–413. 8 indexed citations
9.
Scheinfeldt, Laura, Neda Gharani, Rachel Kasper, et al.. (2015). Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(8). 697–705. 28 indexed citations
10.
Scheinfeldt, Laura, Rachel Kasper, Ruixue Zhaoyang, et al.. (2015). Common Genetic Risk for Melanoma Encourages Preventive Behavior Change. Journal of Personalized Medicine. 5(1). 36–49. 24 indexed citations
11.
12.
Gharani, Neda, Margaret Keller, Catharine B. Stack, et al.. (2013). The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system. Genome Medicine. 5(10). 93–93. 33 indexed citations
13.
Sparks, Susan, Susana Quijano‐Roy, Amy Harper, et al.. (2012). Congenital Muscular Dystrophy Overview. 38 indexed citations
14.
Stack, Catharine B., Neda Gharani, Erynn S. Gordon, et al.. (2011). Genetic risk estimation in the Coriell Personalized Medicine Collaborative. Genetics in Medicine. 13(2). 131–139. 35 indexed citations
15.
Scharner, Juergen, Charlotte A. Brown, Matthew Bower, et al.. (2010). Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations. Human Mutation. 32(2). 152–167. 55 indexed citations
16.
Gordon, Erynn S.. (2009). GENOMICS IN PA PRACTICE. JAAPA. 22(9). 61–63. 1 indexed citations
17.
Kesari, Akanchha, et al.. (2008). Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule. Human Mutation. 29(5). 728–737. 69 indexed citations
18.
Gordon, Erynn S., et al.. (2005). The genetics of muscle atrophy and growth: The impact and implications of polymorphisms in animals and humans. The International Journal of Biochemistry & Cell Biology. 37(10). 2064–2074. 12 indexed citations
19.
Gordon, Erynn S., Heather Gordish‐Dressman, Joseph M. Devaney, et al.. (2005). Nondisease genetic testing: reporting of muscle SNPs shows effects on self-concept and health orientation scales. European Journal of Human Genetics. 13(9). 1047–1054. 9 indexed citations
20.
Gordon, Erynn S. & Eric P. Hoffman. (2001). The ABCʼs of limb-girdle muscular dystrophy: α-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more. Current Opinion in Neurology. 14(5). 567–573. 16 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

Breakdown of academic impact, for papers by Carl‐Joachim Partsch Breakdown of academic impact, for papers by Jennifer Friedman Breakdown of academic impact, for papers by Neda Gharani Breakdown of academic impact, for papers by David Margulies Breakdown of academic impact, for papers by Raymond K. Walters Breakdown of academic impact, for papers by Michele C. Gornick Breakdown of academic impact, for papers by James F. Hyde Breakdown of academic impact, for papers by Michael D. Powers Breakdown of academic impact, for papers by Kimberly A. Quaid Breakdown of academic impact, for papers by Jill O. Robinson
Rankless by CCL
2026