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Innovative Implementation Strategies for Familial Hypercholesterolemia Cascade Testing: The Impact of Genetic Counseling.
- Published in:
- Journal of Personalized Medicine, 2024, v. 14, n. 8, p. 841, doi. 10.3390/jpm14080841
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- Publication type:
- Article
Investigating Psychological Impact after Receiving Genetic Risk Results—A Survey of Participants in a Population Genomic Screening Program.
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- Journal of Personalized Medicine, 2022, v. 12, n. 12, p. 1943, doi. 10.3390/jpm12121943
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- Publication type:
- Article
Understanding the Patient Experience of Receiving Clinically Actionable Genetic Results from the MyCode Community Health Initiative, a Population-Based Genomic Screening Initiative.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 9, p. N.PAG, doi. 10.3390/jpm12091511
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- Publication type:
- Article
Collaborative Approach to Reach Everyone with Familial Hypercholesterolemia: CARE-FH Protocol.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 606, doi. 10.3390/jpm12040606
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- Publication type:
- Article
Acceptability, Appropriateness, and Feasibility of Automated Screening Approaches and Family Communication Methods for Identification of Familial Hypercholesterolemia: Stakeholder Engagement Results from the IMPACT-FH Study.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 6, p. 587, doi. 10.3390/jpm11060587
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- Publication type:
- Article
Pharmacogenomic (PGx) Counseling: Exploring Participant Questions about PGx Test Results.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 2, p. 29, doi. 10.3390/jpm10020029
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- Publication type:
- Article
Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program.
- Published in:
- Journal of Personalized Medicine, 2020, v. 10, n. 1, p. 7, doi. 10.3390/jpm10010007
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- Publication type:
- Article
Barriers and Facilitators to Genetic Testing for Familial Hypercholesterolemia in the United States: A Review.
- Published in:
- Journal of Personalized Medicine, 2019, v. 9, n. 3, p. 32, doi. 10.3390/jpm9030032
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- Publication type:
- Article
Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health.
- Published in:
- Journal of Personalized Medicine, 2018, v. 8, n. 3, p. 25, doi. 10.3390/jpm8030025
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- Publication type:
- Article
Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease.
- Published in:
- Journal of Personalized Medicine, 2014, v. 4, n. 1, p. 1, doi. 10.3390/jpm4010001
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- Publication type:
- Article
Use of a chatbot to increase uptake of cascade genetic testing.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 5, p. 1219, doi. 10.1002/jgc4.1592
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- Publication type:
- Article
Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first.
- Published in:
- Journal of Genetic Counseling, 2021, v. 30, n. 3, p. 634, doi. 10.1002/jgc4.1386
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- Publication type:
- Article
Impact of variant reclassification in the clinical setting of cardiovascular genetics.
- Published in:
- Journal of Genetic Counseling, 2021, v. 30, n. 2, p. 503, doi. 10.1002/jgc4.1336
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- Publication type:
- Article
Patient assessment of chatbots for the scalable delivery of genetic counseling.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 6, p. 1166, doi. 10.1002/jgc4.1169
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- Publication type:
- Article
Perspectives from individuals with familial hypercholesterolemia on direct contact in cascade screening.
- Published in:
- Journal of Genetic Counseling, 2020, v. 29, n. 6, p. 1142, doi. 10.1002/jgc4.1266
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- Publication type:
- Article
Genetic testing preferences and intentions in patients with clinically diagnosed familial hypercholesterolemia.
- Published in:
- Journal of Genetic Counseling, 2020, v. 29, n. 6, p. 919, doi. 10.1002/jgc4.1194
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- Publication type:
- Article
Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 6, p. 1087, doi. 10.1002/jgc4.1159
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- Publication type:
- Article
2019 National Society of Genetic Counselors Presidential Address.
- Published in:
- 2019
- By:
- Publication type:
- Editorial
Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
- Published in:
- Journal of Genetic Counseling, 2018, v. 27, n. 5, p. 1111, doi. 10.1007/s10897-018-0230-z
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- Publication type:
- Article
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
- Published in:
- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 56, doi. 10.1186/1750-1172-7-56
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- Publication type:
- Article
Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia.
- Published in:
- BMC Health Services Research, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12913-023-09304-y
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- Publication type:
- Article
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran Program.
- Published in:
- JAMIA Open, 2024, v. 7, n. 1, p. 1, doi. 10.1093/jamiaopen/ooae020
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- Publication type:
- Article
Imerslund-Gräsbeck syndrome: New mutation in amnionless.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
Imerslund-Gräsbeck syndrome: New mutation in amnionless.
- Published in:
- Pediatrics International, 2012, v. 54, n. 3, p. e19, doi. 10.1111/j.1442-200X.2011.03482.x
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- Publication type:
- Article
How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family HealthLink.
- Published in:
- Public Health Genomics, 2018, v. 21, n. 1/2, p. 53, doi. 10.1159/000493847
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- Publication type:
- Article
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions.
- Published in:
- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01246-8
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- Publication type:
- Article
Population genomic screening of young adults for familial hypercholesterolaemia: a cost-effectiveness analysis.
- Published in:
- European Heart Journal, 2022, v. 43, n. 34, p. 3243, doi. 10.1093/eurheartj/ehab770
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- Publication type:
- Article
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death.
- Published in:
- European Heart Journal, 2022, v. 43, n. 15, p. 1500, doi. 10.1093/eurheartj/ehab687
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- Publication type:
- Article
Genetic Testing for Familial Hypercholesterolemia in Clinical Practice.
- Published in:
- Current Atherosclerosis Reports, 2023, v. 25, n. 5, p. 197, doi. 10.1007/s11883-023-01094-2
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- Publication type:
- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
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- Publication type:
- Article
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0078-7
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- Publication type:
- Article
Barriers, facilitators, and solutions to familial hypercholesterolemia treatment.
- Published in:
- PLoS ONE, 2020, v. 15, n. 12, p. 1, doi. 10.1371/journal.pone.0244193
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- Publication type:
- Article
Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort.
- Published in:
- BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02375-4
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- Publication type:
- Article
Outcomes of a Randomized Controlled Trial of Genomic Counseling for Patients Receiving Personalized and Actionable Complex Disease Reports.
- Published in:
- Journal of Genetic Counseling, 2017, v. 26, n. 5, p. 980, doi. 10.1007/s10897-017-0073-z
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- Publication type:
- Article
Counselees' Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study.
- Published in:
- Journal of Genetic Counseling, 2017, v. 26, n. 4, p. 738, doi. 10.1007/s10897-016-0044-9
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- Publication type:
- Article
Direct-to-Consumer Personal Genomic Testing: A Case Study and Practical Recommendations for 'Genomic Counseling'.
- Published in:
- Journal of Genetic Counseling, 2012, v. 21, n. 3, p. 402, doi. 10.1007/s10897-012-9489-7
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- Publication type:
- Article
Tools for Assessing Readability and Quality of Health-Related Web Sites.
- Published in:
- Journal of Genetic Counseling, 2009, v. 18, n. 1, p. 49
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- Publication type:
- Article
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 3, p. e242388, doi. 10.1001/jamanetworkopen.2024.2388
- By:
- Publication type:
- Article
Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data Screening.
- Published in:
- Journal of the American Heart Association, 2023, v. 12, n. 13, p. 1, doi. 10.1161/JAHA.123.030073
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- Publication type:
- Article
Racial Disparities in Modifiable Risk Factors and Statin Usage in Black Patients With Familial Hypercholesterolemia.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Hidden Burden of Electronic Health Record-Identified Familial Hypercholesterolemia: Clinical Outcomes and Cost of Medical Care.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapy.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-020-00854-2
- By:
- Publication type:
- Article
A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.883073
- By:
- Publication type:
- Article
Implementation strategies to improve statin utilization in individuals with hypercholesterolemia: a systematic review and meta-analysis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.
- Published in:
- 2020
- By:
- Publication type:
- journal article