| Translation and adaptation of skin cancer genomic risk education materials for implementation in primary care |
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| A novel approach to screening for familial hypercholesterolemia in a large public venue |
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| A qualitative study of patients’ perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH) |
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| Leaves imitate trees: Minnesota Hmong concepts of heredity and applications to genomics research |
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| Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples |
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| Erratum to: Development and validation of the biobanking attitudes and knowledge survey-Spanish (BANKS-SP) |
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| Challenges in the management of patients with maple syrup urine disease diagnosed by newborn screening in a developing country |
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| Development and validation of the biobanking attitudes and knowledge survey-Spanish (BANKS-SP) |
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| Community engagement and education: addressing the needs of South Asian families with genetic disorders |
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South Asian |
| Biobank participant support of newborn screening for disorders with variable treatment and intervention options |
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| Population-level diversity in the association of genetic polymorphisms of one-carbon metabolism with breast cancer risk |
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| Geographic clusters of congenital anomalies in Argentina |
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| Within and beyond the communal turn to informed consent in industry-sponsored pharmacogenetics research: merits and challenges of community advisory boards |
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| Engaging diverse populations in biospecimen donation: results from the Hoy y Mañana study |
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| Why do pregnant women accept or decline prenatal diagnosis for Down syndrome? |
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| Carrier screening for beta-thalassemia in the Maldives: perceptions of parents of affected children who did not take part in screening and its consequences |
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| Successful implementation of Lynch syndrome screening in a safety net institution |
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| Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information |
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| Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England |
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| Swedish healthcare providers’ perceptions of preconception expanded carrier screening (ECS)—a qualitative study |
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| Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana |
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| Relevant ethical consideration in research with indigenous people in Peru |
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| A cost analysis of a cancer genetic service model in the UK |
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| Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection |
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| Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine |
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| “It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare |
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| Health research: working with Indigenous People in Peru |
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| Participant views on consent in cancer genetics research: preparing for the precision medicine era |
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