Gulvir Gill, Catherine Beard, Kirsty Storey, Shelby Taylor, Adrienne Sexton. Psychooncology 2020
Times Cited: 2
Times Cited: 2
Times Cited
Times Co-cited
Similarity
Comprehension and personal value of negative non-diagnostic genetic panel testing.
Christin Hoell, Sharon Aufox, Nora Nashawaty, Melanie F Myers, Maureen E Smith. J Genet Couns 2021
Christin Hoell, Sharon Aufox, Nora Nashawaty, Melanie F Myers, Maureen E Smith. J Genet Couns 2021
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Economic Evaluation of Population-Based BRCA1/BRCA2 Mutation Testing across Multiple Countries and Health Systems.
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BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study.
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Genetic susceptibility testing from a stress and coping perspective.
Holly C Gooding, Kurt Organista, Jeffrey Burack, Barbara Bowles Biesecker. Soc Sci Med 2006
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A systematic review of interventions to improve recall of medical advice in healthcare consultations.
Philip W B Watson, Brian McKinstry. J R Soc Med 2009
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Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
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Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
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New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study.
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Population screening in the age of genomic medicine.
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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
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Using Genetic Technologies To Reduce, Rather Than Widen, Health Disparities.
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PUGS: A novel scale to assess perceptions of uncertainties in genome sequencing.
B B Biesecker, S W Woolford, W M P Klein, K B Brothers, K L Umstead, K L Lewis, L G Biesecker, P K J Han. Clin Genet 2017
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A state-based approach to genomics for rare disease and population screening.
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Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines.
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Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
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Coming full circle: a reciprocal-engagement model of genetic counseling practice.
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Identifying Primary Care Physicians Continuing Education Needs by Examining Clinical Practices, Attitudes, and Barriers to Screening Across Multiple Cancers.
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Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature.
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The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research.
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Experiences and attitudes of hereditary cancer screening patients in a consumer directed testing model.
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Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
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Using the common sense model to understand perceived cancer risk in individuals testing for BRCA1/2 mutations.
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The dawn of consumer-directed testing.
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Recruiting diversity where it exists: The Alabama Genomic Health Initiative.
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Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology.
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Primary care providers' cancer genetic testing-related knowledge, attitudes, and communication behaviors: A systematic review and research agenda.
Jada G Hamilton, Ekland Abdiwahab, Heather M Edwards, Min-Lin Fang, Andrew Jdayani, Erica S Breslau. J Gen Intern Med 2017
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Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
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Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives.
Chris Jacobs, Caroline Dancyger, Jonathan A Smith, Susan Michie. Eur J Hum Genet 2015
Chris Jacobs, Caroline Dancyger, Jonathan A Smith, Susan Michie. Eur J Hum Genet 2015
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Adherence to NCCN Guidelines for Genetic Testing in Breast Cancer Patients: Who Are We Missing?
J Jaime Alberty-Oller, Sarah Weltz, Antonio Santos, Kereeti Pisapati, Meng Ru, Christina Weltz, Hank Schmidt, Elisa Port. Ann Surg Oncol 2021
J Jaime Alberty-Oller, Sarah Weltz, Antonio Santos, Kereeti Pisapati, Meng Ru, Christina Weltz, Hank Schmidt, Elisa Port. Ann Surg Oncol 2021
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Engaging Patients in Precision Oncology: Development and Usability of a Web-Based Patient-Facing Genomic Sequencing Report.
Ilana B Solomon, Sarah McGraw, Jenny Shen, Adem Albayrak, Gil Alterovitz, Melanie Davies, Catherine Del Vecchio Fitz, Rachel A Freedman, Lisa N Lopez, Lynette M Sholl,[...]. JCO Precis Oncol 2020
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The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure.
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Sharing genetic test results with family members of BRCA, PALB2, CHEK2, and ATM carriers.
Marleah Dean, Ann L Tezak, Sabrina Johnson, Joy K Pierce, Anne Weidner, Kate Clouse, Tuya Pal, Deborah Cragun. Patient Educ Couns 2021
Marleah Dean, Ann L Tezak, Sabrina Johnson, Joy K Pierce, Anne Weidner, Kate Clouse, Tuya Pal, Deborah Cragun. Patient Educ Couns 2021
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A regional population-based hereditary breast cancer screening tool in Italy: First 5-year results.
Laura Cortesi, Bruna Baldassarri, Stefano Ferretti, Elisabetta Razzaboni, Mariangela Bella, Lauro Bucchi, Debora Canuti, Pierandrea De Iaco, Giorgio De Santis, Fabio Falcini,[...]. Cancer Med 2020
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Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
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30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.
Emma R Woodward, Kate Green, George J Burghel, Michael Bulman, Tara Clancy, Fiona Lalloo, Helene Schlecht, Andrew J Wallace, D Gareth Evans. Eur J Hum Genet 2022
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An Update on Immune Checkpoint Therapy for the Treatment of Lynch Syndrome.
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Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer.
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Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the Mark.
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Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.
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Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort.
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Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.