Found: 21
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Genetic Testing Uptake among Ovarian Cancer Survivors in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study.
- Published in:
- Cancers, 2024, v. 16, n. 14, p. 2563, doi. 10.3390/cancers16142563
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- Publication type:
- Article
Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study.
- Published in:
- Public Health Genomics, 2024, v. 27, n. 1, p. 16, doi. 10.1159/000535610
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- Publication type:
- Article
"Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00270-4
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- Publication type:
- Article
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 18, p. 2330, doi. 10.3390/cells12182330
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- Publication type:
- Article
An Examination of the Ethical and Legal Limits in Implementing "Traceback Testing" for Deceased Patients.
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- Journal of Law, Medicine & Ethics, 2022, v. 50, n. 4, p. 818, doi. 10.1017/jme.2023.23
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- Publication type:
- Article
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00217-1
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- Publication type:
- Article
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>™) for lynch syndrome risk assessment in a diverse population.
- Published in:
- Familial Cancer, 2022, v. 21, n. 2, p. 167, doi. 10.1007/s10689-021-00243-3
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- Publication type:
- Article
Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.
- Published in:
- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00213-5
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- Publication type:
- Article
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 1, p. 230, doi. 10.1002/jgc4.1476
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- Publication type:
- Article
Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 11, p. 1194, doi. 10.3390/jpm11111194
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- Publication type:
- Article
Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation.
- Published in:
- Frontiers in Psychiatry, 2021, v. 12, p. 1, doi. 10.3389/fpsyt.2021.715922
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- Publication type:
- Article
Lessons learned about harmonizing survey measures for the CSER consortium.
- Published in:
- Journal of Clinical & Translational Science, 2020, v. 4, n. 6, p. 537, doi. 10.1017/cts.2020.41
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- Publication type:
- Article
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0130-8
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- Publication type:
- Article
The Healthcare Systems Research Network (HCSRN) as an Environment for Dissemination and Implementation Research: A Case Study of Developing a Multi-Site Research Study in Precision Medicine.
- Published in:
- eGEMS (Generating Evidence & Methods to Improve Patient Outcomes), 2019, v. 7, n. 1, p. 1, doi. 10.5334/egems.283
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- Publication type:
- Article
Evidence‐based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.
- Published in:
- Human Mutation, 2018, v. 39, n. 11, p. 1677, doi. 10.1002/humu.23631
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- Publication type:
- Article
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.
- Published in:
- 2018
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- Publication type:
- journal article
Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.
- Published in:
- Cancer (0008543X), 2015, v. 121, n. 18, p. 3281, doi. 10.1002/cncr.29470
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- Publication type:
- Article
Depression and Anxiety Symptoms Among Women Who Carry the FMR1 Premutation: Impact of Raising a Child With Fragile X Syndrome Is Moderated by CRHR1 Polymorphisms.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 5, p. 549, doi. 10.1002/ajmg.b.32061
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- Publication type:
- Article
Evaluating Gene Expression in C57BL/6J and DBA/2J Mouse Striatum Using RNA-Seq and Microarrays.
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- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017820
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- Publication type:
- Article
Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers.
- Published in:
- Behavior Genetics, 2008, v. 38, n. 5, p. 493, doi. 10.1007/s10519-008-9214-3
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- Publication type:
- Article
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.
- Published in:
- Genetic Epidemiology, 2008, v. 32, n. 6, p. 553, doi. 10.1002/gepi.20329
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- Publication type:
- Article