| Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach |
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| Thalassemia: a prevalent disease yet unknown term among college students in Saudi Arabia |
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| Cancer genetic counseling communication with low-income Chinese immigrants |
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| The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study |
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| Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services |
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| Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape |
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| A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings |
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| The effect of parental age on NF1 patients in Turkey |
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| Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk |
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| From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals |
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| Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives |
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| Genuine participation in participant-centred research initiatives: the rhetoric and the potential reality |
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| Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study |
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| The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages |
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| An overview of concepts and approaches used in estimating the burden of congenital disorders globally |
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| Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families |
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| Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening |
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| The challenges of the expanded availability of genomic information: an agenda-setting paper |
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| Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide |
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| How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF) |
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| Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen’s health through public-private initiatives |
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| A rare disorder or not? How a child with jaundice changed a nationwide regimen in the Netherlands |
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| The clinical and genetic Spectrum of Maroteaux-Lamy syndrome (Mucopolysaccharidosis VI) in the Eastern Province of Saudi Arabia |
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| Genomics for all in the 21st century? |
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| Blame—a novel by Tony Holtzman |
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| Increasing the involvement of diverse populations in genomics-based health care—lessons from haemoglobinopathies |
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| Referral to cancer genetic counseling: do migrant status and patients’ educational background matter? |
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| Racial minority group interest in direct-to-consumer genetic testing: findings from the PGen study |
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| Readability of informed consent forms for whole-exome and whole-genome sequencing |
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| Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership |
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| Association of DD genotype of angiotensin-converting enzyme gene (I/D) polymorphism with hypertension among a North Indian population |
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| Inclusion of diverse populations in genomic research and health services: Genomix workshop report |
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| Genetics in an isolated population like Finland: a different basis for genomic medicine? |
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| Diagnosis of rare diseases under focus: impacts for Canadian patients |
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| Health, wealth and behavioural change: an exploration of role responsibilities in the wake of epigenetics |
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| Diversity and inclusion in genomic research: why the uneven progress? |
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| Leveraging community-based participatory research capacity to recruit Pacific Islanders into a genetics study |
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| Focusing attention on ancestral diversity within genomics research: a potential means for promoting equity in the provision of genomics based healthcare services in developing countries |
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| Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results |
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| 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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| Exploring Asian Indian and Pakistani views about cancer and participation in cancer genetics research: toward the development of a community genetics intervention |
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| Self-reported race and ethnicity of US biobank participants compared to the US Census |
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| Brazilian legal and bioethical approach about donation for research and patents of human body parts |
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| With expanded carrier screening, founder populations run the risk of being overlooked |
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| Identifying opportunities for collaboration and growth of genetic counseling services in the Asia Region |
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| Education for fathers about newborn screening and leftover dried blood spots |
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| Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups |
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| Engaging rural communities in genetic research: challenges and opportunities |
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| Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India |
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| De-identified genomic data sharing: the research participant perspective |
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| Engaging a state: Facebook comments on a large population biobank |
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| The case for the genetic nurse in South Africa |
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| Does personal genome testing drive service utilization in an adult preventive medicine clinic? |
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| Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations |
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| The effect of a celebrity health disclosure on demand for health care: trends in BRCA testing and subsequent health services use |
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| Implementing genetic education in primary care: the Gen-Equip programme |
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| Frequency of single nucleotide platelet receptor gene polymorphism (P2Y12-i744T>C) in coronary artery disease patients among Tamilian population |
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✓ |
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Tamilian population |
| Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work? |
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| Breast cancer genetic counseling among Dutch patients from Turkish and Moroccan descent: participation determinants and perspectives of patients and healthcare professionals |
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| Engaging Hmong adults in genomic and pharmacogenomic research: Toward reducing health disparities in genomic knowledge using a community-based participatory research approach |
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| Survey of family history taking and genetic testing in pediatric practice |
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| Evaluation of cortisol and telomere length measurements in ethnically diverse women with breast cancer using culturally sensitive methods |
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| Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes |
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