| “Before Facebook and before social media…we did not know anybody else that had this”: parent perspectives on internet and social media use during the pediatric clinical genetic testing process |
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| Cultivating inclusivity in precision medicine research: disability, diversity, and cultural competence |
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| A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia |
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| Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2 |
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| Perceptions of parents of children with hearing loss of genetic origin in South Africa |
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| Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors |
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| Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors’ and counselees’ views |
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| “This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers |
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| What do people think about genetics? A systematic review |
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| Correction to: EUROCAT: an update on its functions and activities |
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| An integrative review of factors that influence reproductive decisions in women with sickle cell disease |
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| Risk perception and screening behavior of Filipino women at risk for breast cancer: implications for cancer genetic counseling |
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| “A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening |
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| Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome |
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| Value of sharing and networking among birth defects surveillance programs: an ICBDSR perspective |
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| Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation |
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| Congenital disorders: epidemiological methods for answering calls for action |
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| Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide |
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| Historical overview of development in methods to estimate burden of disease due to congenital disorders |
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| Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility? |
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| Barriers to the identification of familial hypercholesterolemia among primary care providers |
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| Exploring the perceived self-efficacy of genetic counselors as teachers |
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| Family health history and genetic services—the East Baltimore community stakeholder interview project |
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| Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM) |
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| Rare single gene disorders: estimating baseline prevalence and outcomes worldwide |
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| High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information |
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| Experiences of patients seeking to participate in variant of uncertain significance reclassification research |
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| Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo |
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| Genetic counseling in an indigenous Filipino community with a high prevalence of A2ML1-related otitis media |
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| Parents’ views of genetic testing and treatment of familial hypercholesterolemia in children: a qualitative study |
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| Ethics in genetic counselling |
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| Genetics and ethics |
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| Clusters of genetic diseases in Brazil |
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| Assessing patient readiness for personalized genomic medicine |
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| Inequities in genetic testing for hereditary breast cancer: implications for public health practice |
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| EUROCAT: an update on its functions and activities |
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| Property and human genetic information |
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| Primary care providers’ lived experiences of genetics in practice |
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| New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated |
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| Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders |
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| Evaluating and improving the implementation of a community-based hereditary cancer screening program |
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| 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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| Coming to terms with the imperfectly normal child: attitudes of Israeli parents of screen-positive infants regarding subsequent prenatal diagnosis |
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| An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis |
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| Risk stratification, genomic data and the law |
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| Reproductive decision making: interviews with mothers of children with undiagnosed developmental delay |
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| Desiderata for digital consent in genomic research |
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| “I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings |
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| Experience of Asian males communicating cardiac genetic risk within the family |
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| Correction to: Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results:a systematic review and meta-analysis |
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