Ryan Noss

549 total citations
17 papers, 339 citations indexed

About

Ryan Noss is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ryan Noss has authored 17 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ryan Noss's work include BRCA gene mutations in cancer (11 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ryan Noss is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ryan Noss collaborates with scholars based in United States and Germany. Ryan Noss's co-authors include Robert Pilarski, James L. Fisher, Julie Stephens, T. Prior, Holly J. Pederson, Charis Eng, Samantha Greenberg, Stephanie A. Cohen, Stephen R. Grobmyer and Anne L. Matthews and has published in prestigious journals such as Journal of the American College of Surgeons, Annals of Surgical Oncology and Journal of Medical Genetics.

In The Last Decade

Ryan Noss

16 papers receiving 333 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryan Noss United States 10 182 88 60 48 48 17 339
Rebecca Doherty United Kingdom 8 182 1.0× 83 0.9× 71 1.2× 72 1.5× 27 0.6× 28 345
Eliza Courtney Singapore 11 185 1.0× 81 0.9× 57 0.9× 60 1.3× 44 0.9× 27 319
Christine Stanislaw United States 9 232 1.3× 60 0.7× 29 0.5× 53 1.1× 53 1.1× 16 345
Ingrid Slade United Kingdom 9 238 1.3× 132 1.5× 106 1.8× 72 1.5× 51 1.1× 10 431
Victor Evangelista de Faria Ferraz Brazil 11 192 1.1× 97 1.1× 47 0.8× 49 1.0× 35 0.7× 34 377
Wendy Kohlmann United States 10 185 1.0× 58 0.7× 112 1.9× 52 1.1× 54 1.1× 23 338
Karina L. Brierley United States 8 305 1.7× 94 1.1× 49 0.8× 70 1.5× 85 1.8× 10 416
Hannah Wand United States 13 195 1.1× 107 1.2× 19 0.3× 44 0.9× 38 0.8× 23 484
Sari Lieberman Israel 9 207 1.1× 74 0.8× 33 0.6× 57 1.2× 33 0.7× 19 276
Kristen J. Vogel United States 13 231 1.3× 100 1.1× 125 2.1× 100 2.1× 37 0.8× 19 430

Countries citing papers authored by Ryan Noss

Since Specialization
Citations

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

Fields of papers citing papers by Ryan Noss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan Noss. 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 Ryan Noss. The network helps show where Ryan Noss may publish in the future.

Co-authorship network of co-authors of Ryan Noss

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

All Works

17 of 17 papers shown
1.
Hogan, Elizabeth, et al.. (2023). An analysis of the impact of annual cancer genetic testing guideline updates on a past patient population. Journal of Genetic Counseling. 33(5). 1082–1088.
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Linfield, Debra T., et al.. (2022). Primary care physician referral practices regarding BRCA1/2 genetic counseling in a major health system. Breast Cancer Research and Treatment. 195(2). 153–160. 10 indexed citations
5.
Noss, Ryan, et al.. (2022). Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all. Health and Technology. 12(4). 839–844. 2 indexed citations
6.
Pederson, Holly J. & Ryan Noss. (2020). Updates in hereditary breast cancer genetic testing and practical high risk breast management in gene carriers. Seminars in Oncology. 47(4). 182–186. 8 indexed citations
7.
Kewan, Tariq, Ryan Noss, Lucy A. Godley, Heesun J. Rogers, & Hetty E. Carraway. (2020). Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome. Journal of Investigative Medicine High Impact Case Reports. 8. 2737404093–2737404093. 6 indexed citations
8.
Greenberg, Samantha, et al.. (2020). Genetic Counseling Service Delivery Models in the United States: Assessment of changes in use from 2010 to 2017. Journal of Genetic Counseling. 29(6). 1126–1141. 45 indexed citations
9.
Noss, Ryan, et al.. (2019). The current state of genetic counseling assistants in the United States. Journal of Genetic Counseling. 28(5). 962–973. 25 indexed citations
10.
Pederson, Holly J., et al.. (2018). Impact of an embedded genetic counselor on breast cancer treatment. Breast Cancer Research and Treatment. 169(1). 43–46. 34 indexed citations
11.
Pederson, Holly J., et al.. (2018). Impact of Multigene Panel Testing on Surgical Decision Making in Breast Cancer Patients. Journal of the American College of Surgeons. 226(4). 560–565. 19 indexed citations
12.
Shealy, Amy, Allison Schreiber, Ryan Noss, et al.. (2017). Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care. Clinical and Translational Science. 11(1). 71–76. 10 indexed citations
13.
Heald, Brandie, Lisa Rybicki, Jessica Marquard, et al.. (2016). Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices. npj Genomic Medicine. 1(1). 16010–16010. 28 indexed citations
14.
Noss, Ryan, Rachel Mills, & Nancy P. Callanan. (2014). The Incorporation of Predictive Genomic Testing into Genetic Counseling Programs. Journal of Genetic Counseling. 23(4). 671–678. 3 indexed citations
15.
Pilarski, Robert, Julie Stephens, Ryan Noss, James L. Fisher, & T. Prior. (2011). Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features. Journal of Medical Genetics. 48(8). 505–512. 99 indexed citations
16.
Abdel‐Rahman, Mohamed H., Robert Pilarski, James B. Massengill, et al.. (2011). Melanoma candidate genes CDKN2A/p16/INK4A, p14ARF, and CDK4 sequencing in patients with uveal melanoma with relative high-risk for hereditary cancer predisposition. Melanoma Research. 21(3). 175–179. 16 indexed citations
17.
Noss, Ryan, et al.. (2003). Design and Development of the 2002 Penn State University Parallel Hybrid Electric Explorer, the Wattmuncher. SAE technical papers on CD-ROM/SAE technical paper series. 1. 4 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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