Journal of Community Genetics - 2011

41 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population
Carrier screening in preconception consultation in primary care
Preconception care and genetic risk: ethical issues
A profile of the genetic counsellor and genetic nurse profession in European countries
Biobank governance: heterogeneous modes of ordering and democratization
Consanguineous marriages
Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making
Evaluation findings from genetics and family health history community-based workshops for African Americans
Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry West African Ancestry
Erratum to: A short history of the first three years of the Community Genetics Network and its Newsletter
Is there a doctor in the house?
Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands
Patients' experiences and views of cascade screening for familial hypercholesterolemia (FH): a qualitative study
Breast cancer genetic counselling referrals: how comparable are the findings between the UK and the Netherlands?
Power, expertise and the limits of representative democracy: genetics as scientific progress or political legitimation in carcinogenic risk assessment of pharmaceuticals?
Tay-Sachs disease preconception screening in Australia: self-knowledge of being an Ashkenazi Jew predicts carrier state better than does ancestral origin, although there is an increased risk for c.142 Ashkenazi Jew; ancestral origin; South African heritage
A pilot study of knowledge and interest of genetic counseling and testing for hereditary breast and ovarian cancer syndrome among Puerto Rican women
Establishing a community partnership to optimize recruitment of African American pedigrees for a genetic epidemiology study
The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy
Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States—lessons learned
Young smokers’ views of genetic susceptibility testing for lung cancer risk: minding unintended consequences
Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives
Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem
Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study
A short history of the first 3 years of the Community Genetics Network and its newsletter
Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories
Access to genetic testing and genetic counseling in vulnerable populations: the d/Deaf and hard of hearing population
Newborn screening education on the internet: a content analysis of North American newborn screening program websites
Funding of rare disease research in Germany: a pilot study
Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
The impact of single gene and chromosomal disorders on hospital admissions in an adult population
A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010
Quality issues in clinical genetic services edited by Ulf Kristofferson, Jörg Schmidtke, and Jean-Jacques Cassiman
A holistic approach to education programs in thalassemia for a multi-ethnic population: consideration of perspectives, attitudes, and perceived needs
Prevalence of Bardet–Biedl syndrome in Tunisia
Hypothesis: epigenetic effects will require a review of the genetics of child development
Genetic testing and counseling for hereditary neurological diseases in Mali
Some considerations about a report on ‘Public health in an era of genomic-based and personalized medicine’ from the Public Health Foundation, Cambridge
Frequency distribution of the single-nucleotide -108C/T polymorphism at the promoter region of the PON1 gene in Asian Indians and its relationship with coronary artery disease
Factors influencing consultation to discuss family history of cancer by asymptomatic patients in primary care
Frequency of sickle cell genotype among the Yorubas in Lagos: implications for the level of awareness and genetic counseling for sickle cell disease in Nigeria