| Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool |
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| The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay |
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| Feasibility of establishing a network of community health workers to support care of people with sickle cell disease in Kumasi, Ghana |
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| Recruiting for diversity: a pilot test of recruitment strategies for a national alcohol survey with mail-in genetic data collection |
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| Correction to: Treatment decision‑making in sickle cell disease patients |
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| Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community |
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Ashkenazi Jewish community |
| Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care |
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| A collaborative genetic carrier screening model for the British Ashkenazi Jewish community |
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| Comprehension of skin cancer genetic risk feedback in primary care patients |
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| Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia |
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| Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS) |
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| IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy |
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| Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants |
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| Treatment decision-making in sickle cell disease patients |
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| Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study |
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| “Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice |
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| Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study |
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| When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country |
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| Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification |
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| Awareness of paternal age effect disorders among Japanese pregnant women: implications for prenatal genetic counseling for advanced paternal age |
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| Evaluating genetic and genomic tests for heritable conditions in Australia: lessons learnt from health technology assessments |
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| Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinics |
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| Costs, burdens and the prevention of genetic disorders: what role for professional influence? |
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| Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology |
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| Developing genetic counselling services in an underdeveloped healthcare setting |
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| Diagnostic yield and recognized barriers of an adult neurogenetics clinic |
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| Continuing the sequence? Towards an economic evaluation of whole genome sequencing for the diagnosis of rare diseases in Scotland |
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| “Being proactive, not reactive”: exploring perceptions of genetic testing among White, Latinx, and Pacific Islander Populations |
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| Genetic counselling as a route to enhanced autonomy: using a sequential mixed methods research approach to develop a theory regarding presymptomatic genetic testing for young adults at risk of inherit |
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| Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissection |
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| Anticipating the primary care role in genomic medicine: expectations of genetics health professionals |
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| Participation in genetic research among Latinx populations by Latin America birth-residency concordance: a global study |
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| Investigating the reasons for marriage among couples with thalassemia minor, in Iran |
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| Premarital genetic screening and care of Tanzanian children with sickle cell disease: a qualitative study on parents’ views and experiences |
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| Return of research results (RoRR) to the healthy CHRIS cohort: designing a policy with the participants |
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| Opportunities and barriers for genetic service delivery in Kenya from a health personnel perspective |
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| Fatal fetal abnormality Irish live-born survival—an observational study |
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| Demographic and socioeconomic trends in DNA banking utilization in the USA |
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| Understanding genomic health information: how to meet the needs of the culturally and linguistically diverse community—a mixed methods study |
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| Pilot investigation into the need and feasibility of a psychoeducation and support group for male caregivers of those with Huntington’s disease |
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| Modernizing family health history: achievable strategies to reduce implementation gaps |
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| Students’ attitudes towards somatic genome editing versus genome editing of the germline using an example of familial leukemia |
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| Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer |
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| Shaping national plans and strategies for rare diseases in Europe: past, present, and future |
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| Rare diseases: past achievements and future prospects |
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| Baseline knowledge and receptiveness to genetic testing for hereditary breast and ovarian cancer syndromes in Chinese high-risk females |
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| Our greatest untapped resource: our patients |
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| Healthcare providers attitudes towards risk stratification of adopted patients with limited family history information: a cross-sectional survey |
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| A content analysis of direct-to-consumer DNA testing on TikTok |
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| Public attitudes towards the genetic testing in Georgia |
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| Birth prevalence of congenital anomalies in Argentina, according to socioeconomic level |
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| Role of older generations in the family’s adjustment to Huntington disease |
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| Preconception expanded carrier screening: a focus group study with relatives of mucopolysaccharidosis type III patients and the general population |
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general Dutch population |
| European Reference Networks: challenges and opportunities |
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| Rare disease care pathways in the EU: from odysseys and labyrinths towards highways |
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| The ethics of resource allocation in translational genomic medicine |
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| Clinical and community genetics services in the Dutch Caribbean |
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| Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands |
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| Modelled epidemiological data for selected congenital disorders in South Africa |
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| Correction to: Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017 |
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| Hereditary diseases and child wish: exploring motives, considerations, and the (joint) decision-making process of genetically at-risk couples |
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| Interpretation and management of genetic test results by Canadian family physicians: a multiple choice survey of performance |
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| Knowledge and perceptions of BRCA1/2 genetic testing and needs of diverse women with a personal or family history of breast cancer in South Florida |
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| Barriers and strategies to integrate medical genetics and primary care in underserved populations: a scoping review |
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| Undiagnosed haemoglobinopathies among pregnant women attending antenatal care clinics in Pune, India |
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| Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017 |
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| Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication |
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| Electronic informed consent information for residual newborn specimen research: findings from focus groups with diverse populations |
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| Valuing genetic and genomic testing in France: current challenges and latest evidence |
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| Neonatal screening program for five conditions in Honduras |
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| Improving diagnostics of rare genetic diseases with NGS approaches |
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