D. Cragun

发表

Psychosocial and Skill-based Differences between Dental and Dental Hygiene Students Regarding Secondary Prevention of Eating Disorders

H. Severson, K. Isringhausen, R. DeBate, 2014 .

IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results

J. Whisenant, T. Pal, J. Beckstead, 2021, BMC cancer.

Complexities of genetic screening and testing in hereditary colorectal cancer

T. Pal, D. Cragun, Joy Kechik, 2018, Seminars in Colon and Rectal Surgery.

A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer.

S. Vadaparampil, Jongphil Kim, T. Pal, 2013, Genetic testing and molecular biomarkers.

Exploring racial and ethnic minority individuals’ journey to becoming genetic counselors: Mapping paths to diversifying the genetic counseling profession

D. Cragun, Tatiana E Alvarado-Wing, J. Marshall, 2021, Journal of genetic counseling.

Genetic counselor training for the next generation: Where do we go from here?

R. Grubs, D. Cragun, D. Riconda, 2018, American journal of medical genetics. Part C, Seminars in medical genetics.

A Web-Based Tool to Automate Portions of Pretest Genetic Counseling for Inherited Cancer.

T. Pal, G. Wiesner, D. Cragun, 2020, Journal of the National Comprehensive Cancer Network : JNCCN.

Genetic Counselors’ Religiosity & Spirituality: Are Genetic Counselors Different from the General Population?

Ryan T. Cragun, M. Myers, D. Cragun, 2009, Journal of Genetic Counseling.

Disparities in BRCA counseling across providers in a diverse population of young breast cancer survivors

X. Shu, S. Vadaparampil, T. Pal, 2020, Genetics in Medicine.

Implementing universal cancer screening programs can help sustain genomic medicine programs.

A. Rahm, H. Hampel, D. Cragun, 2019, Personalized medicine.

Iron Hack - A symposium/hackathon focused on porphyrias, Friedreich’s ataxia, and other rare iron-related diseases

Linh M Duong, S. Fatumo, Chengqi Wang, 2019, F1000Research.

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling

A. Trepanier, L. Madlensky, Barbara Lerner, 2017, Journal of Genetic Counseling.

The Inherited Cancer Registry (ICARE) Initiative: An Academic-Community Partnership for Patients and Providers

T. Pal, G. Wiesner, D. Cragun, 2018, Oncology Issues.

Differences in BRCA counseling and testing practices based on ordering provider type

T. Sellers, A. Monteiro, S. Vadaparampil, 2014, Genetics in Medicine.

A high frequency of BRCA mutations in young black women with breast cancer residing in Florida

A. Monteiro, S. Vadaparampil, S. Narod, 2015, Cancer.

Family communication of genetic test results among women with inherited breast cancer genes

T. Pal, D. Cragun, A. Tezak, 2020, Journal of genetic counseling.

Cancer risk management among female BRCA1/2, PALB2, CHEK2, and ATM carriers

T. Pal, D. Cragun, A. Tezak, 2020, Breast Cancer Research and Treatment.

Racial disparities in BRCA testing and cancer risk management across a population‐based sample of young breast cancer survivors

S. Vadaparampil, D. Bonner, Jongphil Kim, 2017, Cancer.

Hereditary Cancer: Example of a Public Health Approach to Ensure Population Health Benefits of Genetic Medicine

T. Pal, D. Cragun, Courtney Lewis, 2016, Healthcare.

Universal Tumor Screening for Lynch Syndrome

H. Hampel, D. Cragun, R. Pearlman, 2018 .

Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens

T. Sellers, D. Coppola, Ji‐Hyun Lee, 2017, Familial Cancer.

Association between IHC and MSI testing to identify mismatch repair-deficient patients with ovarian cancer.

T. Sellers, D. Coppola, S. Nicosia, 2014, Genetic testing and molecular biomarkers.

Colorectal cancer survivors' interest in genetic testing for hereditary cancer: implications for universal tumor screening.

D. Shibata, S. Vadaparampil, T. Pal, 2012, Genetic testing and molecular biomarkers.

The big reveal: Family disclosure patterns of BRCA genetic test results among young Black women with invasive breast cancer

S. Vadaparampil, C. Knott, Jongphil Kim, 2020, Journal of genetic counseling.

Educational Needs and Preferred Methods of Learning Among Florida Practitioners Who Order Genetic Testing for Hereditary Breast and Ovarian Cancer

S. Vadaparampil, T. Pal, D. Cragun, 2013, Journal of Cancer Education.

Impact of Genetic Testing on Risk-Management Behavior of Black Breast Cancer Survivors: A Longitudinal, Observational Study

S. Vadaparampil, C. Knott, Jongphil Kim, 2019, Annals of Surgical Oncology.

Racial and ethnic differences in genetic counseling experiences and outcomes in the United States: A systematic review

D. Cragun, K. Redlinger-Grosse, H. Zierhut, 2020, Journal of genetic counseling.

Genetic Testing Across Young Hispanic and Non-Hispanic White Breast Cancer Survivors: Facilitators, Barriers, and Awareness of the Genetic Information Nondiscrimination Act.

T. Pal, D. Cragun, A. Weidner, 2019, Genetic testing and molecular biomarkers.

A Delphi study to prioritize genetic counseling outcomes: What matters most

Ian M. MacFarlane, D. Cragun, K. Redlinger-Grosse, 2020, Journal of genetic counseling.

Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts

Alanna Kulchak Rahm, Pamala A. Pawloski, Ilene G. Ladd, 2018, BMC Health Services Research.

Coincidence analysis: a new method for causal inference in implementation science

Edward J. Miech, L. Damschroder, E. Miech, 2020, Implementation Science.

Motivational interviewing for genetic counseling: A unified framework for persuasive and equipoise conversations

Lynette Hammond Gerido, J. Griggs, K. Resnicow, 2022, Journal of genetic counseling.

A Mixed-Methods Protocol to Identify Best Practices for Implementing Pharmacogenetic Testing in Clinical Settings

S. Haga, Megan C. Roberts, D. Cragun, 2022, Journal of personalized medicine.

Developing and pretesting case studies in dental and dental hygiene education: using the diffusion of innovations model.

S. Christiansen, W. Hendricson, L. Tedesco, 2012, Journal of dental education.

Evaluate, assess, treat: development and evaluation of the EAT framework to increase effective communication regarding sensitive oral-systemic health issues.

S. Christiansen, W. Hendricson, L. Tedesco, 2012, European journal of dental education : official journal of the Association for Dental Education in Europe.

Qualitative Methods for Refining a Web-Based Educational Tool for Patients Focused on Inherited Cancer Predisposition

T. Pal, D. Cragun, A. Tezak, 2021, Journal of Cancer Education.

Cytochrome P450 Oxidoreductase Deficiency

R. Hopkin, D. Cragun, 2009 .

Proportion of BRCA mutation frequency in young black women with breast cancer.

S. Vadaparampil, S. Narod, D. Bonner, 2014 .

A success of a genetics educational intervention for nursing and dietetic students: A model for incorporating genetics into nursing and allied health curricula.

C. Prows, D. Cragun, S. Couch, 2005, Journal of allied health.

Revising the FOCUS framework through a qualitative study assessing self‐reported counseling skills of genetic counselors

D. Cragun, Marleah Dean, H. Zierhut, 2022, Journal of genetic counseling.

Views on Abortion: A Comparison of Female Genetic Counselors and Women from the General Population

Ryan T. Cragun, M. Myers, D. Cragun, 2009, Journal of Genetic Counseling.

Randomized trial of two e-learning programs for oral health students on secondary prevention of eating disorders.

S. Christiansen, W. Hendricson, L. Tedesco, 2014, Journal of dental education.

Evaluation of a theory-driven e-learning intervention for future oral healthcare providers on secondary prevention of disordered eating behaviors.

S. Christiansen, W. Hendricson, L. Tedesco, 2013, Health education research.

Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley–Bixler syndrome

N. Leslie, R. Hopkin, R. Kelley, 2004, American journal of medical genetics. Part A.

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

M. Dattani, P. Hindmarsh, M. Kempers, 2011, The Journal of clinical endocrinology and metabolism.

Use of the term "Antley-Bixler syndrome": minimizing confusion.

R. Hopkin, D. Cragun, 2005, American journal of human genetics.

Development of FOCUS-GC: Framework for Outcomes of Clinical Communication Services in Genetic Counseling

D. Cragun, H. Zierhut, 2018, Journal of Genetic Counseling.

BRCA sequencing and large rearrangement testing in young Black women with breast cancer

S. Vadaparampil, S. Narod, D. Bonner, 2014, Journal of Community Genetics.

Outcomes from a pilot genetic counseling intervention using motivational interviewing and the extended parallel process model to increase cascade cholesterol screening

Ian M. MacFarlane, J. Steinberger, S. Walters, 2021, Journal of genetic counseling.

Psychosocial impact of BRCA testing in young Black breast cancer survivors

S. Vadaparampil, C. Holt, Jongphil Kim, 2018, Psycho-oncology.

Personas of pregnant and parenting women with substance use and their barriers and pathways to system engagement.

D. Cragun, Megan Bell, J. Marshall, 2023, Birth.

Factors associated with genetic counseling and BRCA testing in a population-based sample of young Black women with breast cancer

Tuya Pal, S. Vadaparampil, S. Narod, 2015, Breast Cancer Research and Treatment.

Pre‐test genetic counseling services for hereditary breast and ovarian cancer delivered by non‐genetics professionals in the state of Florida

S. Vadaparampil, T. Pal, C. Scherr, 2015, Clinical genetics.

Identification, Evaluation, and Treatment of Patients with Hereditary Cancer Risk within the United States

T. Pal, D. Cragun, 2013, ISRN oncology.

Educational Needs and Preferred Methods of Learning Among Florida Practitioners Who Order Genetic Testing for Hereditary Breast and Ovarian Cancer

S. Vadaparampil, T. Pal, D. Cragun, 2013, Journal of Cancer Education.

Applying the framework for developing and evaluating complex interventions to increase family communication about hereditary cancer

T. Pal, D. Cragun, Marleah Dean, 2023, PEC innovation.

Application of motivational interviewing strategies with the extended parallel process model to improve risk communication for parents of children with familial hypercholesterolemia

S. Walters, D. Cragun, K. Redlinger-Grosse, 2022, Journal of genetic counseling.

Development of a motivational interviewing genetic counseling intervention to increase cascade cholesterol screening in families of children with familial hypercholesterolemia

S. Walters, D. Cragun, P. McCarthy Veach, 2019, Journal of genetic counseling.

Care delivery considerations for widespread and equitable implementation of inherited cancer predisposition testing

T. Pal, A. Kinney, D. Cragun, 2017, Expert review of molecular diagnostics.

Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

T. Pal, E. Chao, D. Cragun, 2014, Clinical genetics.

Universal Tumor Screening for Lynch Syndrome: Identification of system-level implementation factors influencing patient reach

D. Cragun, 2013 .

False Alarms in Consumer Genomics Add to Public Fear and Potential Health Care Burden

Xiaoming Liu, R. Jiang, D. Cragun, 2020, Journal of personalized medicine.

DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.

A. Rope, H. Saal, R. Hopkin, 2009, The Journal of pediatrics.

Comparing universal Lynch syndrome tumor-screening programs to evaluate associations between implementation strategies and patient follow-through

Heather Hampel, Deborah Cragun, Tuya Pal, 2014, Genetics in Medicine.

Factors for increasing adoption of e-courses among dental and dental hygiene faculty members.

S. Christiansen, W. Hendricson, L. Tedesco, 2011, Journal of dental education.

Applying Public Health Screening Criteria: How Does Universal Newborn Screening Compare to Universal Tumor Screening for Lynch Syndrome in Adults with Colorectal Cancer?

T. Pal, R. DeBate, D. Cragun, 2015, Journal of Genetic Counseling.

Sharing genetic test results with family members of BRCA, PALB2, CHEK2, and ATM carriers.

T. Pal, D. Cragun, Marleah Dean, 2021, Patient education and counseling.

Qualitative Comparative Analysis

Julie Baldwin, Heather Hampel, Deborah Cragun, 2016, Journal of mixed methods research.

Elucidating Genetic Counseling Outcomes from the Perspective of Genetic Counselors

Stephanie A Cohen, D. Cragun, K. Shannon, 2016, Journal of Genetic Counseling.

Creation of a Network to Promote Universal Screening for Lynch Syndrome: The Lynch Syndrome Screening Network

H. Hampel, K. Jasperson, D. Cragun, 2015, Journal of Genetic Counseling.

Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing.

S. Vadaparampil, D. Cragun, 2018, Translational behavioral medicine.

Evaluation of Clinical Practices Related to Variants of Uncertain Significance Results in Inherited Cardiac Arrhythmia and Inherited Cardiomyopathy Genes

D. Cragun, T. McDonald, Kathleen Pope, 2020, Circulation. Genomic and precision medicine.

Bridging the Chasm: Challenges, Opportunities, and Resources for Integrating a Dissemination and Implementation Science Curriculum into Medical Education

David A. Chambers, T. Skolarus, R. Brownson, 2018, Journal of medical education and curricular development.

Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?

S. Vadaparampil, T. Pal, C. Scherr, 2016, Genetic testing and molecular biomarkers.

Qualitative Methods for Refining a Web-Based Educational Tool for Patients Focused on Inherited Cancer Predisposition

T. Pal, D. Cragun, A. Tezak, 2021, Journal of Cancer Education.

Recruitment of a Population‐Based Sample of Young Black Women with Breast Cancer through a State Cancer Registry

S. Vadaparampil, D. Bonner, T. Pal, 2016, The breast journal.

Proposed Outcomes Measures for State Public Health Genomic Programs

M. Clyne, D. Chambers, Kee Chan, 2018, Genetics in Medicine.

Gender comparisons of unhealthy weight-control behaviors among sixth-Graders.

J. Thompson, R. DeBate, D. Cragun, 2013, Journal of nutrition education and behavior.

Psychometric properties of the Body Esteem Scale for Adolescents and Adults in an early adolescent sample

J. Thompson, R. DeBate, D. Cragun, 2013, Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity.

“Be Prepared if I Bring It Up:” Patients’ Perceptions of the Utility of Religious and Spiritual Discussion During Genetic Counseling

Ryan T. Cragun, A. Trepanier, D. Cragun, 2016, Journal of Genetic Counseling.

Knowledge and perceptions of the genetic counseling profession among a national cross‐sectional sample of U.S. adults

Ryan T. Cragun, D. Cragun, Christina Pasca, 2021, Journal of genetic counseling.

Inherited Cancer Knowledge Among Black Females with Breast Cancer Before and After Viewing a Web-Based Educational Video.

T. Pal, D. Cragun, A. Tezak, 2023, Genetic testing and molecular biomarkers.

Do religiosity and spirituality really matter for social, mental, and physical health?: A tale of two samples

Ryan T. Cragun, D. Cragun, J. Sumerau, 2016 .

Healthcare decision makers' perspectives on the creation of new genetic counselor positions in North America: Exploring the case for psychiatric genetic counseling

D. Cragun, C. Hoell, J. Austin, 2022, Journal of genetic counseling.

Piloting a Spanish-Language Web-Based Tool for Hereditary Cancer Genetic Testing

D. Cragun, Brenda Zuniga, Gretter Manso, 2023, Current Oncology.

Comment on “Can Breast Surgeons Provide Breast Cancer Genetic Testing? An American Society of Breast Surgeons Survey”

S. Vadaparampil, T. Pal, C. Scherr, 2017, Annals of Surgical Oncology.

Cytochrome P450 Oxidoreductase Deficiency

R. Hopkin, D. Cragun, 2009 .

Iron Hack - A symposium/hackathon focused on porphyrias, Friedreich’s ataxia, and other rare iron-related diseases [version 1; peer review: 2 approved]

S. Fatumo, Chengqi Wang, G. C. Ferreira, 2020 .

Frames of Reference

D. Cragun, J. Sumerau, 2016 .

BRCA sequencing and large rearrangement testing in young Black women with breast cancer

S. Vadaparampil, S. Narod, D. Bonner, 2013, Journal of Community Genetics.

The development and preliminary evaluation of the Genetic Counseling Skills Checklist

D. Cragun, Marleah Dean, H. Zierhut, 2023, Journal of genetic counseling.

Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline.

S. Domchek, H. Rana, G. Idos, 2024, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.

A. Rope, H. Saal, R. Hopkin, 2009, Jornal de Pediatria.

Proposed Outcomes Measures for State Public Health Genomic Programs

David A. Chambers, M. Clyne, Kee Chan, 2018, Genetics in Medicine.

Configurational comparative methods

D. Cragun, 2020, Handbook on Implementation Science.