| Online BRCA1/2 screening in the Australian Jewish community: a qualitative study |
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| A new decade of community genetics: old and new challenges |
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| Expanded universal carrier screening and its implementation within a publicly funded healthcare service |
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| Contentious ethical issues in community genetics: let’s talk about them |
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| African American mothers’ attitudes towards genetic testing in the InterGEN study |
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| Haemoglobin disorders—a point of entry for community genetics services in India? |
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| Willingness of women to participate in obstetrical and pediatric research involving biobanks |
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| A large family with CYLD cutaneous syndrome: medical genetics at the community level |
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| Determining accurate costs for genomic sequencing technologies—a necessary prerequisite |
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| Correction to: Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience |
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| A framework for youth-friendly genetic counseling |
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| Survey of primary care physicians’ views about breast and ovarian cancer screening for true BRCA1/2 non-carriers |
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| Exploring Asian Indian views about cancer and participation in cancer research: an evaluation of a culturally tailored educational intervention |
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| Human genome editing and the identity politics of genetic disability |
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| Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience |
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| Patients’ views on variants of uncertain significance across indications |
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| Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community? |
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| Consanguinity and genetic diseases among the Bedouin population in the Negev |
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| Population structure and inherited genetic disorders in the Bedouin of the Negev |
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| Correction to: Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey |
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| Exploring perceptions of consanguineous unions with women from an East London community: analysis of discussion groups |
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| Allocating healthcare resources to genomic testing in Canada: latest evidence and current challenges |
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| Applying theory to characterize impediments to dissemination of community-facing family health history tools: a review of the literature |
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| Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing |
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| Developing a national certification pathway for genetic counselors in Sweden—a short report |
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| Co-creating a knowledge base in the “22q11.2 deletion syndrome” community |
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| Developing a culturally targeted video to enhance the use of genetic counseling in Latina women at increased risk for hereditary breast and ovarian cancer |
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| Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review |
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| Attitudes and experiences regarding genetic research among persons of African descent |
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| Improving access to cancer genetic services: perspectives of high-risk clients in a community-based setting |
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| Health and lifestyle behaviors in colorectal cancer survivors with and without Lynch syndrome |
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| Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session |
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| Experiences and interpretations of BRCA1/2 testing among women affected by breast or ovarian cancer who received a negative result |
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| Evaluation of the template letter regarding the disclosure of genetic information within the family in France |
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| Perinatal mortality associated with congenital defects of the central nervous system in Colombia, 2005–2014 |
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| Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network |
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| Does family communication matter? Exploring knowledge of breast cancer genetics in cancer families |
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| Factors associated with willingness to provide biospecimens for genetics research among African American cancer survivors |
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| “It would be so much easier”: health system-led genetic risk notification—feasibility and acceptability of cascade screening in an integrated system |
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| Psychosocial, attitudinal, and demographic correlates of cancer-related germline genetic testing in the 2017 Health Information National Trends Survey |
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| Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017–2026 |
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| Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result |
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| Perspectives on communication and engagement with regard to collecting biospecimens and family health histories for cancer research in a rural Alaska Native community |
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| The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies |
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| Knowledge, attitudes, and perceived barriers towards genetic testing across three rural Illinois communities |
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| Factors influencing use of telegenetic counseling: perceptions of health care professionals in Sweden |
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| Responsiveness and adaptability in community engaged biobanking research: experiences from a Hispanic community |
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| Birth defects surveillance: experiences in Argentina and Colombia |
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