Concepedia

Author

Erin Mundt

Myriad Genetics

Also Known As

E MUNDT, Erin A Mundt, Erin Mundt, Lindor, Noralane M.

23

Publications

631

Citations

11

H-Index

17

Concepts

All Affiliations

Myriad GeneticsMayo Clinic in Arizona
EM

About

Erin Mundt is an author at Myriad Genetics specializing in pathology, medicine, and molecular oncology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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Pathology

2

2

65

3

Public Health

1

1

13

4

Cancer Genetics

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1

52

5

Clinical Genetics

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52

Erin Mundt

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9

Publications

492

Citations

9

H-Index

YearCitations

Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing

Jacqueline Mersch, Nichole Brown, Sara Pirzadeh‐Miller,

JAMA

2018

259

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

Christophe Rosty, Michael D. Walsh, Noralane M. Lindor,

Familial Cancer

2014

52

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

Irene Rainville, Shanell Hatcher, Eric T. Rosenthal,

Breast Cancer Research and Treatment

2020

50

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

William J. Gradishar, KariAnne Johnson, Krystal Brown,

The Oncologist

2017

41

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

Iain D. Kerr, Hannah C. Cox, Kelsey Moyes,

Journal of Community Genetics

2017

28

Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants

Erin Mundt, Brent Mabey, Irene Rainville,

Cancer Genetics

2023

23

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Tuya Pal, Erin Mundt, Marcy E. Richardson,

npj Precision Oncology

2024

15

Complexities of Variant Classification in Clinical Hereditary Cancer Genetic Testing

Erin Mundt, Paola Nix, Krystal Brown,

Journal of Clinical Oncology

2017

13

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

Paola Nix, Erin Mundt, Bradford Coffee,

Familial Cancer

2021

11

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