Terkko Navigator / Journal of Community Genetics

Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom

Attitudes and interest in incorporating BRCA1/2 cancer susceptibility testing into reproductive carrier screening for Ashkenazi Jewish men and women

Parenthood among individuals with Turner syndrome: results of an online survey of attitudes towards pregnancy, adoption, and surrogacy

Families with complex needs: an inside perspective from young people, their carers, and healthcare providers

QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa

Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?

Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program

Correction to: Mothers’ knowledge and attitudes about newborn screening in Jordan

Patient-facing genetic and genomic mobile apps in the UK: a systematic review of content, functionality, and quality

Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period

Considerations for developing regulations for direct-to-consumer genetic testing: a scoping review using the 3-I framework

Psychiatric symptoms in a Spanish sample with hereditary cancer risk

Simulating the Genetics Clinic of the Future— whether undergoing whole-genome sequencing shapes professional attitudes

Development and pilot testing of an online decision aid for women considering risk-stratified breast screening

A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing

YouTube as an information source on BRCA mutations: implications for patients and professionals

Opinions and experiences of recontacting patients: a survey of Australasian genetic health professionals

The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes

Mothers’ knowledge and attitudes about newborn screening in Jordan

Colorectal Cancer Survivors’ Receptivity toward Genomic Testing and Targeted Use of Non-Steroidal Anti-Inflammatory Drugs to Prevent Cancer Recurrence

Beliefs on the causes of birth defects as perceived by mothers of children with birth defects in a tertiary care hospital in the Philippines

Correction to: Treatment decision‑making in sickle cell disease patients

Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community

A collaborative genetic carrier screening model for the British Ashkenazi Jewish community

Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care

Comprehension of skin cancer genetic risk feedback in primary care patients

Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia

Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS)

IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy

Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants

Treatment decision-making in sickle cell disease patients

Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study

“Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice

Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study

When guidelines face reality— Lynch syndrome screening in the setting of public health system in a developing country

Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification

Awareness of paternal age effect disorders among Japanese pregnant women: implications for prenatal genetic counseling for advanced paternal age

Evaluating genetic and genomic tests for heritable conditions in Australia: lessons learnt from health technology assessments

Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinics

Costs, burdens and the prevention of genetic disorders: what role for professional influence?

Supporting teachers to use genomics as a context in the classroom: an evaluation of learning resources for high school biology

Developing genetic counselling services in an underdeveloped healthcare setting

Diagnostic yield and recognized barriers of an adult neurogenetics clinic

Continuing the sequence? Towards an economic evaluation of whole genome sequencing for the diagnosis of rare diseases in Scotland

“Being proactive, not reactive”: exploring perceptions of genetic testing among White, Latinx, and Pacific Islander Populations

Genetic counselling as a route to enhanced autonomy: using a sequential mixed methods research approach to develop a theory regarding presymptomatic genetic testing for young adults at risk of inherited cancer syndromes

Psychological distress in response to physical activity restrictions in patients with non-syndromic thoracic aortic aneurysm/dissection

Anticipating the primary care role in genomic medicine: expectations of genetics health professionals

Participation in genetic research among Latinx populations by Latin America birth-residency concordance: a global study

Does electrifying organic synthesis pay off? The energy efficiency of electro-organic conversions