| Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals |
|
|
|
|
|
|
✓ |
✓ |
migrant background |
| Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate’s primary healthcare centers in 2018 |
|
|
|
|
|
|
|
|
|
| Genetic epidemiology of hemoglobinopathies among Iraqi Kurds |
|
|
|
|
|
|
|
|
|
| Attitudes among South African university staff and students towards disclosing secondary genetic findings |
|
|
|
|
|
|
|
|
|
| In memoriam Prof. Dr. Leo P. ten Kate |
|
|
|
|
|
|
|
|
|
| Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences? |
|
|
|
|
|
|
|
|
|
| Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England |
|
|
|
|
|
|
|
|
|
| Sickle cell trait newborn screen results: disclosure and management |
|
|
|
|
|
|
|
|
|
| Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide |
|
|
|
|
|
|
|
|
|
| Birth defect mortality in India 1990–2017: estimates from the Global Burden of Disease data |
|
|
|
|
|
|
|
|
|
| Knowing, relationships and trust—citizens’ perceptions of whole genome sequencing for the Genetics Clinic of the Future |
|
|
|
|
|
|
|
|
|
| Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making |
|
|
|
|
|
|
|
|
|
| Public engagement with genomic medicine: a summary of town hall discussions |
|
|
|
|
|
|
|
|
|
| Curative gene therapies for rare diseases |
|
|
|
|
|
|
|
|
|
| Building awareness on genetic counselling: the launch of Italian Association of Genetic Counsellors (AIGeCo) |
|
|
|
|
|
|
|
|
|
| Impacts of personal DNA ancestry testing |
|
|
|
|
|
|
|
|
|
| Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania |
|
|
|
|
|
|
|
|
|
| Patients’ decision to contribute to a biobank in the light of the patient-recruiter relationship—a qualitative study of broad consent in a hospital setting |
|
|
|
|
|
|
|
|
|
| Hmong participants’ reactions to return of individual and community pharmacogenetic research results: “A positive light for our community” |
|
|
|
|
|
|
|
|
|
| Is family history still underutilised? Exploring the views and experiences of primary care doctors in Malaysia |
|
|
|
|
|
|
|
|
|
| Utilization of clinical genetic counseling among childhood and young adult cancer survivors in a registry trial |
|
|
|
|
|
|
|
|
|
| Genetic counselling in sickle cell disease: views of single young adults in Ghana |
|
|
|
|
|
|
|
|
|
| Awareness of genetic testing for children with autism spectrum disorder among caregivers in an autism support group |
|
|
|
|
|
|
|
|
|
| The language and values of genetics: invited editorial on “letter to the editor: time to update the language of genetics from the 19th to the twenty-first century. A response to Schmidtke and Cornel” |
|
|
|
|
|
|
|
|
|
| Perspectives regarding family disclosure of genetic research results in three racial and ethnic minority populations |
|
|
|
|
|
|
|
|
|
| Home testing for COVID-19: lessons from direct to consumer genetics |
|
|
|
|
|
|
|
|
|
| Knowledge, awareness, and attitude of premarital screening with special focus on sickle cell disease: a study from Odisha |
|
|
|
|
|
|
|
|
|
| The implementation of pharmacogenomics into UK general practice: a qualitative study exploring barriers, challenges and opportunities |
|
|
|
|
|
|
|
|
|
| Empowering newborn screening programs in African countries through establishment of an international collaborative effort |
|
|
|
|
|
|
|
|
|
| Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals |
|
|
|
|
|
|
|
|
|
| Parental experiences and genetic counsellor roles in Pierre Robin sequence |
|
|
|
|
|
|
|
|
|
| Letter to the Editor: Time to update the language of genetics from the nineteenth to the twenty-first century: a response to Schmidtke and Cornel |
|
|
|
|
|
|
|
|
|
| Letter to the editor. Gene editing and disabled people: a response to Iñigo de Miguel Beriain |
|
|
|
|
|
|
|
|
|
| Attitudes towards genetic testing and information: does parenthood shape the views? |
|
|
|
|
|
|
|
|
|
| Gene editing and disabled people: a response to Felicity Boardman |
|
|
|
|
|
|
|
|
|
| The readability of online health resources for phenylketonuria |
|
|
|
|
|
|
|
|
|
| “It’s being part of the big picture, even though you’re a tiny jigsaw piece”—motivations and expectations of individuals participating in the Enroll-HD observational study |
|
|
|
|
|
|
|
|
|
| How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners |
|
|
|
|
|
|
|
|
|
| Applying Rogers’ framework to evaluate public awareness and knowledge of medical genetics in a developing country |
|
|
|
|
|
|
|
|
|
| Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan |
|
|
|
|
|
|
|
|
|
| Quality of life and comprehensive health supervision for children with Down syndrome in Thailand |
|
|
|
|
|
|
|
|
|
| Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment |
|
|
|
|
|
|
|
|
|
| Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care |
|
|
|
|
|
|
|
|
|
| Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor children |
|
|
|
|
|
|
|
|
|
| Birth prevalence of congenital anomalies in the City of Buenos Aires, Argentina, according to socioeconomic level |
|
|
|
|
|
|
|
|
|
| Prenatal detection of congenital anomalies and related factors in Argentina |
|
|
|
|
|
|
|
|
|