| Participation of low-income women in genetic cancer risk assessment and BRCA 1/2 testing: the experience of a safety-net institution |
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| Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica |
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| Wide disparity of clinical genetics services and EU rare disease research funding across Europe |
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| Components of genetic counsellor education: A systematic review of the peer-reviewed literature |
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| Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis |
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| Life experiences of individuals with hereditary hemorrhagic telangiectasia and disclosing outside the family: a qualitative analysis |
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| A review of 5-HT transporter linked promoter region (5-HTTLPR) polymorphism and associations with alcohol use problems and sexual risk behaviors |
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| Differences in preferences for models of consent for biobanks between Black and White women |
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| Primary prevention of neural tube defects in Brazil: insights into anencephaly |
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| Genetic professionals’ views on genetic counsellors: a French survey |
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| Social determinants of family health history collection |
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| Erratum to: Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil |
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| Parents’ experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study |
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| Rural Mexican-Americans’ perceptions of family health history, genetics, and disease risk: implications for disparities-focused research dissemination |
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| Discussion of photoprotection, screening, and risk behaviors with children and grandchildren after melanoma genetic testing |
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| Ethical problems in health research with indigenous or originary peoples in Peru |
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| Challenges for providing genetic counselling in Colombian genetic clinics: the viewpoint of the physicians providing genetic consultations |
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| Genetic information and biobanking: a Brazilian perspective on biological and biographical issues |
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| Genetics and ethics in Latin America |
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| Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil |
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| Genetics and ethics: a possible and necessary dialogue |
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| Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm |
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| Neurogenetics in Peru: clinical, scientific and ethical perspectives |
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| Timing and context: important considerations in the return of genetic results to research participants |
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| The Latin American School of Human and Medical Genetics: promoting education and collaboration in genetics and ethics applied to health sciences across the continent |
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| Between personal and relational privacy: understanding the work of informed consent in cancer genetics in Brazil |
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| Analysis of pre-test interviews in a cohort of Brazilian patients with movement disorders |
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| Confidentiality and data sharing: vulnerabilities of the Mexican Genomics Sovereignty Act |
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| Project REENCONTRO: ethical aspects of genetic identification in families separated by the compulsory isolation of leprosy patients in Brazil |
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| General Practitioners’ knowledge and use of genetic counselling in managing patients with genetic cardiac disease in non-specialised settings |
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| Patentability of human genes: the conceptual differences between the industrialised and Latin American countries |
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| SCA2 predictive testing in Cuba: challenging concepts and protocol evolution |
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| Genetics in primary health care and the National Policy on Comprehensive Care for People with Rare Diseases in Brazil: opportunities and challenges for professional education |
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| Knowledge and awareness of personal sickle cell genotype among parents of children with sickle cell disease in southeast Nigeria |
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| Identification of the hot-spot areas for sickle cell disease using cord blood screening at a district hospital: an Indian perspective |
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| The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem |
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| John MacMillan, M.D. (1959–2014): an inspiring example of a community clinical geneticist |
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| Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases |
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| Ethical, legal and social issues in restoring genetic identity after forced disappearance and suppression of identity in Argentina |
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| Ethical issues in genetics and public health in Latin America with a focus on Argentina |
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| Variants of unknown significance on chromosomal microarray analysis: parental perspectives |
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| UK Pakistani views on the adverse health risks associated with consanguineous marriages |
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| Public attitudes regarding the use of electronic health information and residual clinical tissues for research |
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| Awareness of risks of biobank research may affect public attitudes toward consent |
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| A study of consanguineous marriage as a risk factor for developing comitant strabismus |
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| “Awakening to” a new meaning of being at-risk for arrhythmogenic right ventricular cardiomyopathy: a grounded theory study |
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| Bioethics, population studies, and geneticophobia |
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| Variation in healthcare services for specialist genetic testing and implications for planning genetic services: the example of inherited retinal dystrophy in the English NHS |
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| Public health approach to birth defects: the Argentine experience |
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| Evaluation of two-year Jewish genetic disease screening program in Atlanta: insight into community genetic screening approaches |
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