| Mothers of children with Down syndrome: a clinical and epidemiological study |
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| Ethical, legal, and social implications of genetic risk prediction for multifactorial disease: a narrative review identifying concerns about interpretation and use of polygenic scores |
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| Evaluating visual imagery for participant understanding of research concepts in genomics research |
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| Lost in print: difficulty in reading online information pertaining to phenylketonuria |
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| Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington’s disease |
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| Understanding how educational interventions improve treatment adherence in patients with familial hypercholesterolaemia: a systematic review |
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| Human genetics education as part of the Japanese Cancer Education Comprehensive Support Project |
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| Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK |
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| Cost-effectiveness of a gene sequencing test for Alzheimer’s disease in Ontario |
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| Telehealth in genetic counselling consultations: the impact of COVID-19 in a Portuguese genetic healthcare service |
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| Service provision of genetics health care in Portugal |
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| Cross-sectional survey on genetic testing utilization and perceptions in Wisconsin Amish and Mennonite communities |
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| Ophthalmic genetic counselling: emerging trends in practice perspectives in Asia |
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| Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: a web-based panel discussion |
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| Interest in genetic testing and risk-reducing behavioral changes: results from a community health assessment in New York City |
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| Sickle cell disease-related knowledge and perceptions of traditional healers in tribal communities in India: implications on sickle cell disease programme |
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| Direct-to-consumer genetic testing in the news: a descriptive analysis |
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| Parents’ perspectives on the use of children’s facial images for research and diagnosis: a survey |
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| Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner’s office referrals to a multi-disciplinary cardiogenetics program |
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| The perception of parents with a child with sickle cell disease in Ghana towards prenatal diagnosis |
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| Knowledge and awareness of sickle cell disease: a cross sectional study amongst unmarried adults in Nigeria’s capital city |
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| Resource allocation in genetic and genomic medicine |
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| Stakeholder knowledge and attitudes toward the use of predictive genetic testing in South Africa |
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| Experiences of individuals receiving a sex chromosome multisomy diagnosis |
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| Genes, exposures, and interactions on preterm birth risk: an exploratory study in an Argentine population |
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| Insight into how patients with prostate cancer interpret and communicate genetic test results: implications for families |
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| Short Communication: Restrictions in care following the COVID-19 pandemic severely impacted Machado-Joseph disease patients: a study in the Azores Islands, Portugal |
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| Variation among DNA banking consent forms: points for clinicians to bank on |
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| Experiences of individuals with a variant of uncertain significance on genetic testing for hereditary cancer risks: a mixed method systematic review |
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| Comparison of willingness and preference for genetic counseling via telemedicine: before vs. during the COVID-19 pandemic |
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| Telemedicine in the Amish and Mennonite communities of Wisconsin |
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| Correction to: Co‑designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom |
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| OBGYN providers’ lack of knowledge and management of genetic risks due to advanced paternal age underscore the need for updated practice guidance |
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| Multisite assessment of the impact of a prenatal testing educational App on patient knowledge and preparedness for prenatal testing decision making |
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| Carrier detection probabilities for autosomal recessive variants in unrelated and consanguineous couples — an evaluation of the 86 genes of the ACMG ‘Tier 3’ panel |
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non-Finnish Europeans |
| Attitudes of Filipino parents of children with Down syndrome on noninvasive prenatal testing |
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| Cancer patients’ understandings of genetic variants of uncertain significance in clinical care |
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| Comparing the attitudes of physicians and non-physicians toward communicating a patient’s BRCA1 mutation to a first-degree relative against a patient’s wishes |
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| Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom |
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| Attitudes and interest in incorporating BRCA1/2 cancer susceptibility testing into reproductive carrier screening for Ashkenazi Jewish men and women |
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| Parenthood among individuals with Turner syndrome: results of an online survey of attitudes towards pregnancy, adoption, and surrogacy |
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| Families with complex needs: an inside perspective from young people, their carers, and healthcare providers |
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| QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa |
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| Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who? |
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| Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program |
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| Patient-facing genetic and genomic mobile apps in the UK: a systematic review of content, functionality, and quality |
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| Correction to: Mothers’ knowledge and attitudes about newborn screening in Jordan |
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| Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period |
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| Considerations for developing regulations for direct-to-consumer genetic testing: a scoping review using the 3-I framework |
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| Psychiatric symptoms in a Spanish sample with hereditary cancer risk |
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| Peripheral health workers’ knowledge and experience related to sickle cell disease: an in-depth interview study in six tribal-dominated districts of India |
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tribal-dominated |
| Simulating the Genetics Clinic of the Future — whether undergoing whole-genome sequencing shapes professional attitudes |
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| Development and pilot testing of an online decision aid for women considering risk-stratified breast screening |
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| Public interest in unexpected genomic findings: a survey study identifying aspects of sequencing attitudes that influence preferences |
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| A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing |
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| YouTube as an information source on BRCA mutations: implications for patients and professionals |
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| The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes |
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| Opinions and experiences of recontacting patients: a survey of Australasian genetic health professionals |
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| Mothers’ knowledge and attitudes about newborn screening in Jordan |
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| Colorectal Cancer Survivors’ Receptivity toward Genomic Testing and Targeted Use of Non-Steroidal Anti-Inflammatory Drugs to Prevent Cancer Recurrence |
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| Beliefs on the causes of birth defects as perceived by mothers of children with birth defects in a tertiary care hospital in the Philippines |
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