Marian Gilmore

发表

Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives

K. Goddard, A. Rope, S. Syngal, 2017, Familial Cancer.

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

Marian J. Gilmore, B. Bernhardt, J. Wynn, 2018, Journal of Genetic Counseling.

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

Marian J. Gilmore, K. Goddard, H. Feigelson, 2022, Hereditary cancer in clinical practice.

A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research

Sarah E Lillie, Marian J. Gilmore, Julianne M. O’Daniel, 2020, Journal of genetic counseling.

Risk‐reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system

Kathleen F. Mittendorf, Marian J. Gilmore, K. Goddard, 2022, Cancer.

The NextGen Study: patient motivation for participation in genome sequencing for carrier status

Marian J. Gilmore, K. Goddard, B. Wilfond, 2017, Molecular genetics & genomic medicine.

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews

Kathleen F. Mittendorf, K. Goddard, B. Wilfond, 2022, Hereditary cancer in clinical practice.

Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing

Marian J. Gilmore, K. Goddard, B. Wilfond, 2017, Journal of Genetic Counseling.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting

K. Goddard, A. Rope, J. Schneider, 2019, Familial Cancer.

Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.

D. Nickerson, M. Dorschner, K. Goddard, 2018, American journal of human genetics.

Generating a taxonomy for genetic conditions relevant to reproductive planning

Diane M. Korngiebel, K. Goddard, B. Wilfond, 2016, American journal of medical genetics. Part A.

Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing

K. Goddard, B. Wilfond, F. Lynch, 2018, Journal of Genetic Counseling.

“Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier Screening

K. Goddard, B. Wilfond, F. Lynch, 2015, Journal of Genetic Counseling.

Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities.

Kathleen F. Mittendorf, Marian J. Gilmore, K. Goddard, 2021, JCO precision oncology.

Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.

Kathleen F. Mittendorf, M. Dorschner, K. Goddard, 2021, Contemporary clinical trials.

ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents.

Elizabeth M Webber, Elizabeth M. Webber, Charisma L. Jenkins, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

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

D. Nickerson, M. Dorschner, K. Goddard, 2017, Genetics in Medicine.

Illustrative case studies in the return of exome and genome sequencing results

B. Bernhardt, G. Jarvik, J. Wynn, 2015, Personalized medicine.

Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study

Kathleen F. Mittendorf, Marian J. Gilmore, K. Goddard, 2020, AJOB empirical bioethics.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2018, Genetics in Medicine.

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

Kathleen F. Mittendorf, Marian J. Gilmore, K. Goddard, 2021, Familial Cancer.

Kathleen F. Mittendorf, K. Goddard, A. Rope, 2019, Hereditary Cancer in Clinical Practice.

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

Julianne M. O’Daniel, Shannon Rego, Marian Gilmore, 2021, Journal of personalized medicine.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

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

Katrina A B Goddard, Tia L Kauffman, K. Goddard, 2015, Genetics in Medicine.

Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing

K. Goddard, B. Wilfond, J. Berg, 2016, American journal of medical genetics. Part A.

Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome.

B. Wilfond, L. Karliner, M. Leo, 2023, Journal of genetic counseling.

An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.

M. Dorschner, K. Goddard, B. Wilfond, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Kathleen F. Mittendorf, Charisma L. Jenkins, Marian J. Gilmore, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.

Marian J. Gilmore, K. Goddard, B. Wilfond, 2020, Patient education and counseling.

Lessons Learned From A Study Of Genomics-Based Carrier Screening For Reproductive Decision Making.

K. Goddard, B. Wilfond, C. Richards, 2018, Health affairs.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, H. Rehm, K. Goddard, 2019, Genetics in Medicine.

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

N. Spinner, K. Goddard, L. Hindorff, 2018, Genetics in Medicine.

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Matthew S. Lebo, Victoria A. Miller, Jeffrey W. Pennington, 2016, American journal of human genetics.