Erin Mundt

638 total citations
14 papers, 415 citations indexed

About

Erin Mundt is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Erin Mundt has authored 14 papers receiving a total of 415 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pathology and Forensic Medicine and 4 papers in Molecular Biology. Recurrent topics in Erin Mundt's work include Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (6 papers) and Genetic factors in colorectal cancer (6 papers). Erin Mundt is often cited by papers focused on Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (6 papers) and Genetic factors in colorectal cancer (6 papers). Erin Mundt collaborates with scholars based in United States, Germany and Australia. Erin Mundt's co-authors include Susan Manley, Krystal Brown, Hannah C. Cox, Sara Pirzadeh‐Miller, Theodora S. Ross, Jacqueline Mersch, Lisa E. Esterling, Michael D. Bates, Joshua D. Schiffman and James I. Geller and has published in prestigious journals such as JAMA, Journal of Clinical Oncology and The Oncologist.

In The Last Decade

Erin Mundt

14 papers receiving 407 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erin Mundt United States 9 249 125 113 105 67 14 415
Nicolette M. Chun United States 9 262 1.1× 119 1.0× 142 1.3× 87 0.8× 58 0.9× 24 382
Amal Yussuf United States 11 178 0.7× 125 1.0× 92 0.8× 90 0.9× 95 1.4× 29 322
Jacqueline Mersch United States 3 333 1.3× 148 1.2× 185 1.6× 123 1.2× 173 2.6× 9 544
Érika Maria Monteiro Santos Brazil 14 174 0.7× 172 1.4× 140 1.2× 240 2.3× 200 3.0× 33 506
Ryan J. Schmidt United States 8 121 0.5× 65 0.5× 119 1.1× 52 0.5× 28 0.4× 37 321
Catarina Santos Portugal 15 192 0.8× 153 1.2× 234 2.1× 128 1.2× 146 2.2× 40 510
Sock Hoai Chan Singapore 10 110 0.4× 87 0.7× 108 1.0× 73 0.7× 76 1.1× 25 271
J Lorenzo Bermejo Germany 9 108 0.4× 60 0.5× 95 0.8× 83 0.8× 105 1.6× 13 302
Kristiina Aittomäki Finland 7 162 0.7× 84 0.7× 171 1.5× 117 1.1× 136 2.0× 8 471
Ashley Woodson United States 9 113 0.5× 116 0.9× 90 0.8× 23 0.2× 76 1.1× 18 242

Countries citing papers authored by Erin Mundt

Since Specialization
Citations

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

Fields of papers citing papers by Erin Mundt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erin Mundt

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

All Works

14 of 14 papers shown
1.
Pal, Tuya, Erin Mundt, Marcy E. Richardson, et al.. (2024). Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing. npj Precision Oncology. 8(1). 247–247. 3 indexed citations
2.
Pan, Shujuan, Hannah C. Cox, Erin Mundt, et al.. (2023). Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome. Frontiers in Oncology. 13. 1069467–1069467. 5 indexed citations
3.
Mundt, Erin, Irene Rainville, Charité Ricker, et al.. (2023). Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants. Cancer Genetics. 278-279. 84–90. 12 indexed citations
4.
5.
Mundt, Erin, et al.. (2020). Functional RNA Studies Are a Useful Tool in Variant Classification but Must Be Used With Caution: A Case Study of One BRCA2 Variant. JCO Precision Oncology. 4(4). 730–735. 3 indexed citations
6.
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
7.
Mersch, Jacqueline, Sara Pirzadeh‐Miller, Erin Mundt, et al.. (2018). Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing. JAMA. 320(12). 1266–1266. 175 indexed citations
8.
Mundt, Erin, et al.. (2017). Complexities of Variant Classification in Clinical Hereditary Cancer Genetic Testing. Journal of Clinical Oncology. 35(34). 3796–3799. 10 indexed citations
9.
Pan, Shujuan, Hannah C. Cox, Krystal Brown, et al.. (2017). Pan-cancer panel testing in individuals with abnormal immunohistochemistry (IHC) staining of the mismatch-repair (MMR) genes.. Journal of Clinical Oncology. 35(15_suppl). e13014–e13014. 1 indexed citations
10.
Kerr, Iain D., Hannah C. Cox, Kelsey Moyes, et al.. (2017). Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes. Journal of Community Genetics. 8(2). 87–95. 22 indexed citations
11.
Gradishar, William J., et al.. (2017). Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory. The Oncologist. 22(7). 797–803. 29 indexed citations
12.
Rosty, Christophe, Michael D. Walsh, Noralane M. Lindor, et al.. (2014). High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry. Familial Cancer. 13(4). 573–582. 39 indexed citations
13.
Schiffman, Joshua D., et al.. (2013). Update on pediatric cancer predisposition syndromes. Pediatric Blood & Cancer. 60(8). 1247–1252. 45 indexed citations
14.
Mundt, Erin & Michael D. Bates. (2010). Genetics of Hirschsprung disease and anorectal malformations. Seminars in Pediatric Surgery. 19(2). 107–117. 33 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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2026