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Kristin R Muessig

6PUBLICATIONS

35CO-AUTHORS

Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markers

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Publications (6)

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|Oct 15, 2025

Patient-initiated lifestyle changes following receipt of genetic test results in a predominantly marginalized population.

Marian J Gilmore, Hannah E Frawley, Elizabeth Shuster

|Aug 30, 2023

Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.

Boya Guo, Sarah Knerr, Tia L Kauffman

|Feb 11, 2022

Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.

Kristin R Muessig, Jamilyn M Zepp, Erin Keast

|Jan 13, 2017

Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing.

Patricia Himes, Tia L Kauffman, Kristin R Muessig

|Apr 29, 2016

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.

Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker

|Apr 17, 2015

Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators.

Jennifer L Schneider, James Davis, Tia L Kauffman

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Frequent Collaborators

2 joint publications

Jessica Ezzell Hunter

2 joint publications

Benjamin S Wilfond

2 joint publications

Marian J Gilmore

2 joint publications

Michael C Leo

2 joint publications

Tia L Kauffman

2 joint publications

Jonathan S Berg

2 joint publications

Katrina A B Goddard

1 joint publications

Adam Buchanan

1 joint publications

Joanna E Bulkley

1 joint publications

Julianne O'Daniel

Frequent Collaborators

2 joint publications

Jessica Ezzell Hunter

2 joint publications

Benjamin S Wilfond

2 joint publications

Marian J Gilmore

2 joint publications

Michael C Leo

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