Journal of Community Genetics - 2019

48 articles | Last updated: 2025-12-03 14:12:57
Caucasian
0
White
0
European
0
Other
0
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Online BRCA1/2 screening in the Australian Jewish community: a qualitative study
A new decade of community genetics: old and new challenges
Expanded universal carrier screening and its implementation within a publicly funded healthcare service
Contentious ethical issues in community genetics: let’s talk about them
African American mothers’ attitudes towards genetic testing in the InterGEN study
Haemoglobin disorders—a point of entry for community genetics services in India?
Willingness of women to participate in obstetrical and pediatric research involving biobanks
A large family with CYLD cutaneous syndrome: medical genetics at the community level
Determining accurate costs for genomic sequencing technologies—a necessary prerequisite
Correction to: Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
A framework for youth-friendly genetic counseling
Survey of primary care physicians’ views about breast and ovarian cancer screening for true BRCA1/2 non-carriers
Exploring Asian Indian views about cancer and participation in cancer research: an evaluation of a culturally tailored educational intervention
Human genome editing and the identity politics of genetic disability
Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
Patients’ views on variants of uncertain significance across indications
Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community?
Consanguinity and genetic diseases among the Bedouin population in the Negev
Population structure and inherited genetic disorders in the Bedouin of the Negev
Correction to: Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey
Exploring perceptions of consanguineous unions with women from an East London community: analysis of discussion groups
Allocating healthcare resources to genomic testing in Canada: latest evidence and current challenges
Applying theory to characterize impediments to dissemination of community-facing family health history tools: a review of the literature
Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing
Developing a national certification pathway for genetic counselors in Sweden—a short report
Co-creating a knowledge base in the “22q11.2 deletion syndrome” community
Developing a culturally targeted video to enhance the use of genetic counseling in Latina women at increased risk for hereditary breast and ovarian cancer
Effectiveness of interventions to identify and manage patients with familial cancer risk in primary care: a systematic review
Attitudes and experiences regarding genetic research among persons of African descent
Improving access to cancer genetic services: perspectives of high-risk clients in a community-based setting
Health and lifestyle behaviors in colorectal cancer survivors with and without Lynch syndrome
Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
Experiences and interpretations of BRCA1/2 testing among women affected by breast or ovarian cancer who received a negative result
Evaluation of the template letter regarding the disclosure of genetic information within the family in France
Perinatal mortality associated with congenital defects of the central nervous system in Colombia, 2005–2014
Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network
Does family communication matter? Exploring knowledge of breast cancer genetics in cancer families
Factors associated with willingness to provide biospecimens for genetics research among African American cancer survivors
“It would be so much easier”: health system-led genetic risk notification—feasibility and acceptability of cascade screening in an integrated system
Psychosocial, attitudinal, and demographic correlates of cancer-related germline genetic testing in the 2017 Health Information National Trends Survey
Haemoglobinopathies in India: estimates of blood requirements and treatment costs for the decade 2017–2026
Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result
Perspectives on communication and engagement with regard to collecting biospecimens and family health histories for cancer research in a rural Alaska Native community
The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies
Knowledge, attitudes, and perceived barriers towards genetic testing across three rural Illinois communities
Factors influencing use of telegenetic counseling: perceptions of health care professionals in Sweden
Responsiveness and adaptability in community engaged biobanking research: experiences from a Hispanic community
Birth defects surveillance: experiences in Argentina and Colombia