| Wikipedia as an academic service-learning tool in science and technology: higher education case from Siberia |
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| Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population |
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| Training of community health agents — a strategy for earlier recognition of mucopolysaccharidoses |
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| Patient experiences in receiving telegenetics care for inherited cardiovascular diseases |
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| A qualitative exploration of interprofessional collaborative practice between genetic counselors and mental health providers |
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| Latina immigrants’ breast and colon cancer causal attributions: genetics is key |
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| Survey of attitude to human genome modification in Nigeria |
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| Genetic risk prediction in Hispanics/Latinos: milestones, challenges, and social-ethical considerations |
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non-European ancestry |
| The impact of the Journal of Community Genetics: Good Health and Wellbeing, Quality Education, and Reduced Inequalities |
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| Retrospective chart analysis to determine the impact of a patient-facing digital risk stratification tool combined with a clinical screener for hereditary cancer genetic risk assessment triage in a co |
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| “There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry |
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| Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY |
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| Prevalence of beta thalassemia carriers in India: a systematic review and meta-analysis |
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| The CPT1A Arctic variant: perspectives of community members and providers in two Alaska tribal health settings |
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| Benefits and concerns of expanded carrier screening: what do pregnant Latina women in Texas think? |
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| Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions |
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| A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments |
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| Relationship satisfaction in adults with phenylketonuria is positively associated with following recommended treatment, having a partner involved in management, and maintaining good health |
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| Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening |
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| Ethics of artificial intelligence in prenatal and pediatric genomic medicine |
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| Short Communication: Lived experience perspectives on genetic testing for a rare eye disease |
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| Big advocacy, little recognition: the hidden work of Black patients in precision medicine |
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Black |
| Are we nearly there yet? Starts and stops on the road to use of polygenic scores |
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| Factors associated with adherence to BRCA1/2 mutation testing after oncogenetic counseling in long-surviving patients with a previous diagnosis of breast or ovarian cancer |
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| When and how to enlighten citizens on genetics and hereditary cancer: a web survey of online video viewers |
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| The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies |
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| Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity |
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| Population diversity and equity in the genomic era: going global to return to the local |
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| Experiences of cystic fibrosis newborn screening and genetic counseling |
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| Developing and assessing a kin keeping scale with application to identifying central influencers in African American family networks |
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African American |
| Genetic services survey—experience of people with rare diseases and their families accessing genetic services in the Irish Republic |
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Irish; Irish Republic; Irish patients; Irish families; Irish Health Service |
| Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive study |
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| Psychosocial impacts of caring for a child with a genetic disorder in Accra, Ghana |
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| Genetic counseling in sickle cell disease: Insights from the Indian tribal population |
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| Identification of maternal attitudes and knowledge about newborn screenings: a Turkey sample |
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| Nigerian parents’ perspectives on genetic testing in their children with genetic eye diseases |
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| A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington’s disease |
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| Adolescents’ experiences and views of the national school-based thalassaemia screening programme in Malaysia: a qualitative study |
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| The beta thalassaemia trait in Jamaica |
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| “What if” should precede “whether” and “how” in the social conversation around human germline gene editing |
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| The role of polygenic risk scores in breast cancer risk perception and decision-making |
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| Life story of Iranian parents of a child with phenylketonuria: a qualitative study |
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| “Fruits of our past karma”: a qualitative study on knowledge and attitudes about congenital anomalies among women in Pune district, India |
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| Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review |
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| The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation |
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| Knowledge, attitude, and perceptions about cancer genetic testing in clinical practice in Karachi, Pakistan |
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| Clinical utility of polygenic risk scores: a critical 2023 appraisal |
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| Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project |
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| A review of key terminology and definitions used for birth defects globally |
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| Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition |
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| Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study |
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| Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community |
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| Communicating risk and the landscape of cancer prevention — an exploratory study that examines perceptions of cancer-related genetic counseling and testing among African Americans and Latinos in the M |
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African American (AA) and Latino populations |
| An exemplary model of genetic counselling for highly specialised services |
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| Fundamental knowledge taught in compulsory education for effective genetic counseling: a qualitative study of descriptions in textbooks |
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| Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC |
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| New year, new goals for the journal? |
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| Re-envisioning community genetics: community empowerment in preventive genomics |
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| What makes a good life: using theatrical performance to enhance communication about polygenic risk scores research in patient and public involvement |
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| Correction to: Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling |
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| Interventions addressing genetic disease burdens within selected countries in the MENA region: a scoping review |
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| Public’s awareness of biobanks and willingness to participate in biobanking: the moderating role of social value orientation |
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| Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities |
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| Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling |
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| Assessing patient-level knowledge of precision medicine in a community health center setting |
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