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Author Details

Kathleen F Mittendorf
Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center
2011
36
13
PMIDPaper TitleJournal TitlePublished Year
37860921Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.J Am Med Inform Assoc2024
36383166Utilization of electronic health record data to evaluate the association of urban environment with systemic lupus erythematosus symptoms.Rheumatology (Oxford)2023
37667436Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.J Genet Couns2023
37644850Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.Cancer Med2023
37126135Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project.J Community Genet2023
37012912Accelerated curation of checkpoint inhibitor-induced colitis cases from electronic health records.JAMIA Open2023
37470892Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.Breast Cancer Res Treat2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
34302314Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.J Genet Couns2022
35679147Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.Cancer2022
35707062Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.HGG Adv2022
35833928Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.Genet Med2022
35689290Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.Hered Cancer Clin Pract2022
35933674Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts.Perm J2022
33754278Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>â¿¢) for lynch syndrome risk assessment in a diverse population.Fam Cancer2022
35227608Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER Consortium.Genet Med2022
35123916Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432].Contemp Clin Trials2022
32981477Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.AJOB Empir Bioeth2021
34554823My Cancer Genome: Coevolution of Precision Oncology and a Molecular Oncology Knowledgebase.JCO Clin Cancer Inform2021
34778694Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities.JCO Precis Oncol2021
34448595Creating accessible Spanish language materials for Clinical Sequencing Evidence-Generating Research consortium genomic projects: challenges and lessons learned.Per Med2021
33984519Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.Contemp Clin Trials2021
32483629The My Cancer Genome clinical trial data model and trial curation workflow.J Am Med Inform Assoc2020
32575981Bicelles Rich in both Sphingolipids and Cholesterol and Their Use in Studies of Membrane Proteins.J Am Chem Soc2020
31028355Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders.Genet Med2019
31890059Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.Hered Cancer Clin Pract2019
30311382Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.Hum Mutat2018
30131438Primary Ovarian Insufficiency and Adolescent Vaccination.Pediatrics2018
27673321While the revolution will not be crystallized, biochemistry reigns supreme.Protein Sci2017
28695207Peripheral myelin protein 22 alters membrane architecture.Sci Adv2017
26102530Conformational Stability and Pathogenic Misfolding of the Integral Membrane Protein PMP22.J Am Chem Soc2015
24564538Impact of bilayer lipid composition on the structure and topology of the transmembrane amyloid precursor C99 protein.J Am Chem Soc2014
25243937The homology model of PMP22 suggests mutations resulting in peripheral neuropathy disrupt transmembrane helix packing.Biochemistry2014
23639031Reversible folding of human peripheral myelin protein 22, a tetraspan membrane protein.Biochemistry2013
22708632Tailoring of membrane proteins by alternative splicing of pre-mRNA.Biochemistry2012
21848311Tolerance to changes in membrane lipid composition as a selected trait of membrane proteins.Biochemistry2011
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Collaborators

Katrina A B Goddard
Center for Health Research, Kaiser Permanente Northwest
Co-authored papers 15
Tia L Kauffman
Kaiser Permanente Center for Health Research
Co-authored papers 12
Benjamin S Wilfond
University of Washington School of Medicine.
Co-authored papers 11
Heather Spencer Feigelson
Co-authored papers 8
Stephanie A Kraft
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Co-authored papers 7
Jessica Ezzell Hunter
Kaiser Permanente Center for Health Research
Co-authored papers 7
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 7
David L Veenstra
University of Washington
Co-authored papers 5
Kathryn M Porter
Seattle Children's Hospital
Co-authored papers 4
Laura M Amendola
Illumina Inc.
Co-authored papers 4
Priyanka Murali
University of Washington
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Christine M Micheel
Vanderbilt Ingram Cancer Center, Vanderbilt University Medical Center
Co-authored papers 3
Marc S Williams
University of Washington Medical Center
Co-authored papers 3
Michele L LeNoue-Newton
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Lucia A Hindorff
National Human Genome Research Institute, National Institutes of Health
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Stephanie M Fullerton
University of Washington School of Medicine
Co-authored papers 2
Anne Slavotinek
Cincinnati Children's Hospital Medical Center
Co-authored papers 2
David R Crosslin
University of Washington Medical Center
Co-authored papers 2
Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 2
Sandra Soo-Jin Lee
Division of Ethics, Department of Medical Humanities and Ethics, Columbia University
Co-authored papers 2
Nita A Limdi
Heersink School of Medicine, University of Alabama at Birmingham
Co-authored papers 2
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 2
Emily Beth Devine
University of Washington
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Leah C Kottyan
Cincinnati Children's Hospital Medical Center
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Barbara B Biesecker
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Release 1.2