Journal of Community Genetics - 2023

65 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
Wikipedia as an academic service-learning tool in science and technology: higher education case from Siberia
Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population
Training of community health agents — a strategy for earlier recognition of mucopolysaccharidoses
Patient experiences in receiving telegenetics care for inherited cardiovascular diseases
A qualitative exploration of interprofessional collaborative practice between genetic counselors and mental health providers
Latina immigrants’ breast and colon cancer causal attributions: genetics is key
Survey of attitude to human genome modification in Nigeria
Genetic risk prediction in Hispanics/Latinos: milestones, challenges, and social-ethical considerations non-European ancestry
The impact of the Journal of Community Genetics: Good Health and Wellbeing, Quality Education, and Reduced Inequalities
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
“There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY
Prevalence of beta thalassemia carriers in India: a systematic review and meta-analysis
The CPT1A Arctic variant: perspectives of community members and providers in two Alaska tribal health settings
Benefits and concerns of expanded carrier screening: what do pregnant Latina women in Texas think?
Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions
A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments
Relationship satisfaction in adults with phenylketonuria is positively associated with following recommended treatment, having a partner involved in management, and maintaining good health
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening
Ethics of artificial intelligence in prenatal and pediatric genomic medicine
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease
Big advocacy, little recognition: the hidden work of Black patients in precision medicine Black
Are we nearly there yet? Starts and stops on the road to use of polygenic scores
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
When and how to enlighten citizens on genetics and hereditary cancer: a web survey of online video viewers
The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies
Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity
Population diversity and equity in the genomic era: going global to return to the local
Experiences of cystic fibrosis newborn screening and genetic counseling
Developing and assessing a kin keeping scale with application to identifying central influencers in African American family networks African American
Genetic services survey—experience of people with rare diseases and their families accessing genetic services in the Irish Republic 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
Psychosocial impacts of caring for a child with a genetic disorder in Accra, Ghana
Genetic counseling in sickle cell disease: Insights from the Indian tribal population
Identification of maternal attitudes and knowledge about newborn screenings: a Turkey sample
Nigerian parents’ perspectives on genetic testing in their children with genetic eye diseases
A pilot evaluation of an 8-week mindfulness-based stress reduction program for people with pre-symptomatic Huntington’s disease
Adolescents’ experiences and views of the national school-based thalassaemia screening programme in Malaysia: a qualitative study
The beta thalassaemia trait in Jamaica
“What if” should precede “whether” and “how” in the social conversation around human germline gene editing
The role of polygenic risk scores in breast cancer risk perception and decision-making
Life story of Iranian parents of a child with phenylketonuria: a qualitative study
“Fruits of our past karma”: a qualitative study on knowledge and attitudes about congenital anomalies among women in Pune district, India
Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review
The qualitative experiences of otolaryngologists with genetic services in pediatric hearing loss evaluation
Knowledge, attitude, and perceptions about cancer genetic testing in clinical practice in Karachi, Pakistan
Clinical utility of polygenic risk scores: a critical 2023 appraisal
Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project
A review of key terminology and definitions used for birth defects globally
Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
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 African American (AA) and Latino populations
An exemplary model of genetic counselling for highly specialised services
Fundamental knowledge taught in compulsory education for effective genetic counseling: a qualitative study of descriptions in textbooks
Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC
New year, new goals for the journal?
Re-envisioning community genetics: community empowerment in preventive genomics
What makes a good life: using theatrical performance to enhance communication about polygenic risk scores research in patient and public involvement
Correction to: Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling
Interventions addressing genetic disease burdens within selected countries in the MENA region: a scoping review
Public’s awareness of biobanks and willingness to participate in biobanking: the moderating role of social value orientation
Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities
Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling
Assessing patient-level knowledge of precision medicine in a community health center setting