Ryan Bernhisel

808 total citations
23 papers, 462 citations indexed

About

Ryan Bernhisel is a scholar working on Genetics, Oncology and Cancer Research. According to data from OpenAlex, Ryan Bernhisel has authored 23 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Oncology and 10 papers in Cancer Research. Recurrent topics in Ryan Bernhisel's work include BRCA gene mutations in cancer (13 papers), Cancer Genomics and Diagnostics (7 papers) and Genetic factors in colorectal cancer (6 papers). Ryan Bernhisel is often cited by papers focused on BRCA gene mutations in cancer (13 papers), Cancer Genomics and Diagnostics (7 papers) and Genetic factors in colorectal cancer (6 papers). Ryan Bernhisel collaborates with scholars based in United States, Germany and Austria. Ryan Bernhisel's co-authors include Eric T. Rosenthal, Johnathan M. Lancaster, Krystal Brown, Susan Manley, Allison W. Kurian, Elisha Hughes, John Kidd, Michael J. Hall, Nanda A. Singh and Hannah C. Cox and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and Cancer.

In The Last Decade

Ryan Bernhisel

22 papers receiving 459 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ryan Bernhisel United States	12	260	184	162	142	137	23	462
Abigail Thomas United States	6	420 1.6×	280 1.5×	230 1.4×	286 2.0×	162 1.2×	8	688
Susan Manley United States	11	436 1.7×	223 1.2×	115 0.7×	170 1.2×	151 1.1×	15	581
Zoe Kemp United Kingdom	12	316 1.2×	148 0.8×	258 1.6×	225 1.6×	179 1.3×	27	580
Kun Y. Lee United States	8	212 0.8×	290 1.6×	342 2.1×	200 1.4×	127 0.9×	11	557
Rohan Gnanaolivu United States	6	165 0.6×	247 1.3×	302 1.9×	155 1.1×	108 0.8×	9	467
Marit Muri Holmen Norway	10	123 0.5×	187 1.0×	141 0.9×	91 0.6×	114 0.8×	19	491
Amal Yussuf United States	11	178 0.7×	125 0.7×	95 0.6×	92 0.6×	90 0.7×	29	322
Joellen Schildkraut United States	6	270 1.0×	144 0.8×	153 0.9×	126 0.9×	121 0.9×	12	464
Helen Byers United Kingdom	14	429 1.6×	144 0.8×	217 1.3×	183 1.3×	71 0.5×	30	651
Gemma Llort Spain	14	435 1.7×	161 0.9×	149 0.9×	314 2.2×	144 1.1×	32	638

Countries citing papers authored by Ryan Bernhisel

Since Specialization

Citations

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

Fields of papers citing papers by Ryan Bernhisel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryan Bernhisel

This figure shows the co-authorship network connecting the top 25 collaborators of Ryan Bernhisel. A scholar is included among the top collaborators of Ryan Bernhisel 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 Bernhisel. Ryan Bernhisel 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

Kurian, Allison W., Elisha Hughes, Ryan Bernhisel, et al.. (2025). Breast Cancer Risk Modification in Women with Pathogenic Variants in BRCA1 , BRCA2 , ATM , CHEK2 , and PALB2. Cancer Research Communications. 5(5). 783–791.

Daly, Mary B., Eric T. Rosenthal, Shelly Cummings, et al.. (2023). The association between age at breast cancer diagnosis and prevalence of pathogenic variants. Breast Cancer Research and Treatment. 199(3). 617–626. 5 indexed citations

Hall, Michael J., Ryan Bernhisel, Elisha Hughes, et al.. (2021). Germline Pathogenic Variants in the Ataxia Telangiectasia Mutated ( ATM ) Gene are Associated with High and Moderate Risks for Multiple Cancers. Cancer Prevention Research. 14(4). 433–440. 102 indexed citations

Weitzel, Jeffrey N., John Kidd, Ryan Bernhisel, et al.. (2021). Multigene assessment of genetic risk for women for two or more breast cancers. Breast Cancer Research and Treatment. 188(3). 759–768. 5 indexed citations

Cummings, Shelly, Jennifer Saam, Ryan Bernhisel, et al.. (2021). Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing. Journal of Ovarian Research. 14(1). 61–61. 11 indexed citations

Kurian, Allison W., Elisha Hughes, Timothy Simmons, et al.. (2021). Performance of the IBIS/Tyrer‐Cuzick model of breast cancer risk by race and ethnicity in the Women's Health Initiative. Cancer. 127(20). 3742–3750. 27 indexed citations

Constantinidou, Anastasia, Yiola Marcou, Ryan Bernhisel, et al.. (2021). Clinical validation of EndoPredict in premenopausal women with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) primary breast cancer.. Journal of Clinical Oncology. 39(15_suppl). 537–537. 1 indexed citations

Rainville, Irene, Eric T. Rosenthal, Ryan Bernhisel, et al.. (2020). High risk of breast cancer in women with biallelic pathogenic variants in CHEK2. Breast Cancer Research and Treatment. 180(2). 503–509. 31 indexed citations

Calip, Gregory S., John Kidd, Ryan Bernhisel, et al.. (2020). Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counseling. Breast Cancer Research and Treatment. 185(1). 195–204. 9 indexed citations

10.

Kurian, Allison W., Elisha Hughes, Ryan Bernhisel, et al.. (2020). Performance of the IBIS/Tyrer-Cuzick (TC) Model by race/ethnicity in the Women’s Health Initiative.. Journal of Clinical Oncology. 38(15_suppl). 1503–1503. 2 indexed citations

11.

Stoll, Jessica, et al.. (2020). No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing. JCO Precision Oncology. 4(4). 51–60. 18 indexed citations

12.

Telli, Melinda L., Charles C. Chu, Sunil Badve, et al.. (2019). Association of Tumor-Infiltrating Lymphocytes with Homologous Recombination Deficiency and BRCA1/2 Status in Patients with Early Triple-Negative Breast Cancer: A Pooled Analysis. Clinical Cancer Research. 26(11). 2704–2710. 23 indexed citations

13.

Mancini‐DiNardo, Debora, Thaddeus Judkins, John Kidd, et al.. (2019). Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing. BMC Medical Genomics. 12(1). 138–138. 16 indexed citations

14.

Slavin, Thomas P., Bradford Coffee, Ryan Bernhisel, et al.. (2019). Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testing. Cancer Genetics. 235-236. 31–38. 24 indexed citations

15.

Filipits, Martin, Peter Dubsky, Margaretha Rudas, et al.. (2019). Prediction of Distant Recurrence Using EndoPredict Among Women with ER+, HER2− Node-Positive and Node-Negative Breast Cancer Treated with Endocrine Therapy Only. Clinical Cancer Research. 25(13). 3865–3872. 54 indexed citations

16.

Coffee, Bradford, Hannah C. Cox, Ryan Bernhisel, et al.. (2019). A substantial proportion of apparently heterozygousTP53pathogenic variants detected with a next‐generation sequencing hereditary pan‐cancer panel are acquired somatically. Human Mutation. 41(1). 203–211. 19 indexed citations

17.

Teerlink, Craig C., Ryan Bernhisel, Lisa Cannon‐Albright, & Michael D. Rollins. (2018). A genealogical assessment of familial clustering of anorectal malformations. Journal of Human Genetics. 63(10). 1029–1034. 7 indexed citations

18.

DeFrancesco, Mark S., et al.. (2018). Hereditary Cancer Risk Assessment and Genetic Testing in the Community-Practice Setting. Obstetrics and Gynecology. 132(5). 1121–1129. 19 indexed citations

19.

Teerlink, Craig C., Ryan Bernhisel, Lisa Cannon‐Albright, & Michael D. Rollins. (2017). A population-based description of familial clustering of Hirschsprung disease. Journal of Pediatric Surgery. 53(7). 1355–1359. 4 indexed citations

20.

Rosenthal, Eric T., Ryan Bernhisel, Krystal Brown, John Kidd, & Susan Manley. (2017). Clinical testing with a panel of 25 genes associated with increased cancer risk results in a significant increase in clinically significant findings across a broad range of cancer histories. Cancer Genetics. 218-219. 58–68. 58 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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