Stakeholder engagement: a key component of integrating genomic information into electronic health records. Read more about Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Ethical, legal, and social implications of incorporating genomic information into electronic health records. Read more about Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Factors influencing organizational adoption and implementation of clinical genetic services. Read more about Factors influencing organizational adoption and implementation of clinical genetic services.
A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians. Read more about A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians.
Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency. Read more about Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency.
Effective communication of molecular genetic test results to primary care providers. Read more about Effective communication of molecular genetic test results to primary care providers.
Managing incidental findings and research results in genomic research involving biobanks and archived data sets. Read more about Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Read more about Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling. Read more about Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling.
Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting. Read more about Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting.
