Mundt E - Search Results

1

Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.

Mersch J, Brown N, Pirzadeh-Miller S, Mundt E, Cox HC, Brown K, Aston M, Esterling L, Manley S, Ross T. Mersch J, et al. Among authors: mundt e. JAMA. 2018 Sep 25;320(12):1266-1274. doi: 10.1001/jama.2018.13152. JAMA. 2018. PMID: 30264118 Free PMC article.

2

Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes.

Kerr ID, Cox HC, Moyes K, Evans B, Burdett BC, van Kan A, McElroy H, Vail PJ, Brown KL, Sumampong DB, Monteferrante NJ, Hardman KL, Theisen A, Mundt E, Wenstrup RJ, Eggington JM. Kerr ID, et al. Among authors: mundt e. J Community Genet. 2017 Apr;8(2):87-95. doi: 10.1007/s12687-016-0289-x. Epub 2017 Jan 3. J Community Genet. 2017. PMID: 28050887 Free PMC article.

3

Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory.

Gradishar W, Johnson K, Brown K, Mundt E, Manley S. Gradishar W, et al. Among authors: mundt e. Oncologist. 2017 Jul;22(7):797-803. doi: 10.1634/theoncologist.2016-0431. Epub 2017 Apr 13. Oncologist. 2017. PMID: 28408614 Free PMC article.

4

In Reply.

Gradishar W, Brown K, Mundt E, Manley S. Gradishar W, et al. Among authors: mundt e. Oncologist. 2017 Dec;22(12):1540. doi: 10.1634/theoncologist.2017-0320. Epub 2017 Aug 29. Oncologist. 2017. PMID: 28851761 Free PMC article.

5

Complexities of Variant Classification in Clinical Hereditary Cancer Genetic Testing.

Mundt E, Nix P, Brown K, Bowles KR, Manley S. Mundt E, et al. J Clin Oncol. 2017 Dec 1;35(34):3796-3799. doi: 10.1200/JCO.2017.74.5182. Epub 2017 Oct 5. J Clin Oncol. 2017. PMID: 28981386 No abstract available.

6

High risk of breast cancer in women with biallelic pathogenic variants in CHEK2.

Rainville I, Hatcher S, Rosenthal E, Larson K, Bernhisel R, Meek S, Gorringe H, Mundt E, Manley S. Rainville I, et al. Among authors: mundt e. Breast Cancer Res Treat. 2020 Apr;180(2):503-509. doi: 10.1007/s10549-020-05543-3. Epub 2020 Jan 28. Breast Cancer Res Treat. 2020. PMID: 31993860 Free PMC article.

7

Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis.

Nix P, Mundt E, Coffee B, Goossen E, Warf BM, Brown K, Bowles K, Roa B. Nix P, et al. Among authors: mundt e. Fam Cancer. 2022 Jan;21(1):7-19. doi: 10.1007/s10689-020-00224-y. Epub 2021 Jan 20. Fam Cancer. 2022. PMID: 33469799 Free PMC article.

8

Functional RNA Studies Are a Useful Tool in Variant Classification but Must Be Used With Caution: A Case Study of One BRCA2 Variant.

Nix P, Mundt E, Manley S, Coffee B, Roa B. Nix P, et al. Among authors: mundt e. JCO Precis Oncol. 2020 Nov;4:730-735. doi: 10.1200/PO.20.00118. JCO Precis Oncol. 2020. PMID: 35050751 No abstract available.

9

Reply to R. Karam et al.

Nix P, Mundt E, Manley S, Coffee B, Roa B. Nix P, et al. Among authors: mundt e. JCO Precis Oncol. 2020 Nov;4:1224-1225. doi: 10.1200/PO.20.00347. JCO Precis Oncol. 2020. PMID: 35050779 No abstract available.

10

Discordance between germline genetic findings and abnormal tumor immunohistochemistry staining of mismatch repair proteins in individuals with suspected Lynch syndrome.

Pan S, Cox H, Willmott J, Mundt E, Gorringe H, Landon M, Bowles KR, Coffee B, Roa BB, Mancini-DiNardo D. Pan S, et al. Among authors: mundt e. Front Oncol. 2023 Jan 30;13:1069467. doi: 10.3389/fonc.2023.1069467. eCollection 2023. Front Oncol. 2023. PMID: 36793599 Free PMC article.

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