| Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population |
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| Carrier screening in preconception consultation in primary care |
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| Preconception care and genetic risk: ethical issues |
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| A profile of the genetic counsellor and genetic nurse profession in European countries |
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| Biobank governance: heterogeneous modes of ordering and democratization |
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| Consanguineous marriages |
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| Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making |
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| Evaluation findings from genetics and family health history community-based workshops for African Americans |
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| Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry |
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West African Ancestry |
| Erratum to: A short history of the first three years of the Community Genetics Network and its Newsletter |
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| Is there a doctor in the house? |
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| Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands |
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| Patients' experiences and views of cascade screening for familial hypercholesterolemia (FH): a qualitative study |
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| Breast cancer genetic counselling referrals: how comparable are the findings between the UK and the Netherlands? |
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| Power, expertise and the limits of representative democracy: genetics as scientific progress or political legitimation in carcinogenic risk assessment of pharmaceuticals? |
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| 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 |
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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 |
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| Establishing a community partnership to optimize recruitment of African American pedigrees for a genetic epidemiology study |
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| The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy |
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| Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States—lessons learned |
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| Young smokers’ views of genetic susceptibility testing for lung cancer risk: minding unintended consequences |
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| Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives |
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| Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem |
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| Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study |
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| A short history of the first 3 years of the Community Genetics Network and its newsletter |
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| Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories |
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| Access to genetic testing and genetic counseling in vulnerable populations: the d/Deaf and hard of hearing population |
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| Newborn screening education on the internet: a content analysis of North American newborn screening program websites |
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| Funding of rare disease research in Germany: a pilot study |
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| Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany |
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| The impact of single gene and chromosomal disorders on hospital admissions in an adult population |
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| A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010 |
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| Quality issues in clinical genetic services edited by Ulf Kristofferson, Jörg Schmidtke, and Jean-Jacques Cassiman |
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| A holistic approach to education programs in thalassemia for a multi-ethnic population: consideration of perspectives, attitudes, and perceived needs |
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| Prevalence of Bardet–Biedl syndrome in Tunisia |
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| Hypothesis: epigenetic effects will require a review of the genetics of child development |
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| Genetic testing and counseling for hereditary neurological diseases in Mali |
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| Some considerations about a report on ‘Public health in an era of genomic-based and personalized medicine’ from the Public Health Foundation, Cambridge |
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| 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 |
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| Factors influencing consultation to discuss family history of cancer by asymptomatic patients in primary care |
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| 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 |
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