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©
Terkko 2005-2021
Interpretation and management of genetic test results by Canadian family physicians: a multiple choice survey of performance
Journal of Community Genetics
6 days
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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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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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Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017
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Undiagnosed haemoglobinopathies among pregnant women attending antenatal care clinics in Pune, India
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Electronic informed consent information for residual newborn specimen research: findings from focus groups with diverse populations
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38 days
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Neonatal screening program for five conditions in Honduras
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Valuing genetic and genomic testing in France: current challenges and latest evidence
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Improving diagnostics of rare genetic diseases with NGS approaches
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42 days
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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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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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Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals
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Genetic epidemiology of hemoglobinopathies among Iraqi Kurds
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99 days
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Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate’s primary healthcare centers in 2018
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Attitudes among South African university staff and students towards disclosing secondary genetic findings
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100 days
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In memoriam Prof. Dr. Leo P. ten Kate
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Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences?
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Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England
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Sickle cell trait newborn screen results: disclosure and management
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Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide
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133 days
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Birth defect mortality in India 1990–2017: estimates from the Global Burden of Disease data
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Home testing for COVID-19: lessons from direct to consumer genetics
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The language and values of genetics: invited editorial on“letter to the editor: time to update the language of genetics from the 19th to the twenty-first century. A response to Schmidtke and Cornel” \by Small, Mason and Wright) (DOI: 10.1007/s12687-0
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Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making
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180 days
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Public engagement with genomic medicine: a summary of town hall discussions
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Building awareness on genetic counselling: the launch of Italian Association of Genetic Counsellors (AIGeCo)
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195 days
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Curative gene therapies for rare diseases
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198 days
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Impacts of personal DNA ancestry testing
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200 days
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Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania
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