“Unnatural resources?”: parallels and distinctions between the Newfoundland Genome and traditional resource sectors Janelle Skeard Research 19 June 2024
Knowledge of genetics and attitudes toward genetic testing among university students in Indonesia Iskandar HermantoCindy Kurniawati ChandraFerdy Kurniawan Cayami Research 08 June 2024
Prevalence of congenital anomalies and prenatal diagnosis by birth institution (public vs. non-public): indicators of inequality in access to elective termination of pregnancy for fetal anomalies Paloma BrunBoris GroismanRosa Liascovich Research 01 June 2024
Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients Rachel HodanMiles PicusGregory E. Idos Research 30 May 2024
Health-related roles of older generations in families with inherited genetic conditions: a scoping review Carla Roma OliveiraCatarina SeidiÁlvaro Mendes Research 25 May 2024
Caregiver-reported barriers to care for children and adults with Williams Syndrome Elizabeth W. BarnhardtMarilee MartensJennifer Walton Research Open access 22 May 2024
The acceptability and clinical impact of using polygenic scores for risk-estimation of common cancers in primary care: a systematic review Faye C. DannhauserLily C. TaylorJuliet A. Usher-Smith Review Open access 21 May 2024
The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis Luiza M. NevesMárcia PintoZilton F. M. Vasconcelos Research Open access 10 May 2024
The need to set explicit goals for human germline gene editing public dialogues Wendy P. GeuverinkDiewertje Houtmanthe ‘De DNA dialogen’ consortium Research Open access 08 May 2024
Comparative assessment of quality of life among adolescents with sickle cell disease and sickle cell trait: evidence from Odisha, India Basanta Kumar BindhaniJayanta Kumar Nayak Research 08 April 2024
Patient perspectives on pharmacogenomic (PGx) testing for antidepressant prescribing in primary care: a qualitative description study Alexandra CernatZainab SamaanMeredith Vanstone Research 08 April 2024
A collaborative model for Medical Genetics services delivery in Portugal: a multidisciplinary perspective Catarina CostaJoão SilvaMilena Paneque Correspondence 07 March 2024
Research biobank participants attitudes towards genetic exceptionalism and health record confidentiality Victoria DortenzioRosamond RhodesHetanshi Naik Research 05 March 2024
The urgency for a change in genetics healthcare provision: views from Portuguese medical geneticists Catarina CostaLídia GuimarãesMilena Paneque Research Open access 01 March 2024
Understanding perceptions of tumor genomic profile testing in Black/African American cancer patients in a qualitative study: the role of medical mistrust, provider communication, and family support Caseem C. LuckSarah Bauerle BassMichael J. Hall Research 16 February 2024
Public participation in human genome editing research governance: what do scientists think? Margaret WaltzMichael A. FlattR. Jean Cadigan Research 14 February 2024
Development of a culturally targeted chatbot to inform living kidney donor candidates of African ancestry about APOL1 genetic testing: a mixed methods study Elisa J. GordonJessica Gacki-SmithCatherine Wicklund Research Open access 13 February 2024 Pages: 205 - 216
Endline assessment of knowledge about sickle cell disease among the tribal community of Chhotaudepur district of Gujarat Shaily B. SurtiAnkita ParmarShubhangi Patel Research 09 February 2024 Pages: 187 - 194
Attitudes of medical professionals toward fragile X carrier screening and genetic counseling in China Yingbao ZhuJia LiRanhui Duan Research 26 January 2024 Pages: 177 - 185
Advertisement by medical facilities as an opportunity route of APOE genetic testing in Japan: a website analysis Kenichiro SatoYoshiki NiimiTakeshi Iwatsubo Research Open access 16 January 2024 Pages: 195 - 204
Empowerment of genetic information by women at-risk of being carriers of Duchenne and Becker muscular dystrophies Alice Maria Luderitz HoefelCesar Augusto WeschenfelderJonas Alex Morales Saute Research 02 January 2024 Pages: 163 - 175
Wikipedia as an academic service-learning tool in science and technology: higher education case from Siberia Ayla ArslanMarko Turk Research 21 December 2023 Pages: 147 - 161
Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population Chen Gafni-AmsalemOlfat Aboleil-ZoubiStavit A. Shalev Research 20 December 2023 Pages: 137 - 146
Training of community health agents — a strategy for earlier recognition of mucopolysaccharidoses Diane Bressan PedriniLarissa Pozzebon da SilvaRoberto Giugliani Research 20 December 2023 Pages: 129 - 135
Patient experiences in receiving telegenetics care for inherited cardiovascular diseases Dani S. TemaresLusha W. LiangIsha Kalia Research 14 December 2023 Pages: 119 - 127
A qualitative exploration of interprofessional collaborative practice between genetic counselors and mental health providers Claire Lily Martha NusbaumMegan WirthAllison L. Cirino Research 08 December 2023 Pages: 103 - 117
Latina immigrants’ breast and colon cancer causal attributions: genetics is key Katie FiallosJill OwczarzakLori H. Erby Research 30 November 2023 Pages: 59 - 73
Survey of attitude to human genome modification in Nigeria Maryam JibrillaHayatu RajiMalachy Ifeanyi Okeke Research 23 November 2023 Pages: 1 - 11
Genetic risk prediction in Hispanics/Latinos: milestones, challenges, and social-ethical considerations Betzaida L. MaldonadoDaniel G. PiquéChristopher R. Gignoux Review Open access 14 November 2023 Pages: 543 - 553
The impact of the Journal of Community Genetics: Good Health and Wellbeing, Quality Education, and Reduced Inequalities Martina C CornelAngus Clarke Editorial 03 November 2023 Pages: 503 - 504
Retrospective chart analysis to determine the impact of a patient-facing digital risk stratification tool combined with a clinical screener for hereditary cancer genetic risk assessment triage in a community oncology clinic Kate P. Shane-CarsonDouglas SmithCaroline Seeley Research 27 October 2023 Pages: 25 - 31
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY Nivedita AhlawatKathryn ElliottKirsten A. Riggan Research 21 October 2023 Pages: 75 - 83
“There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry J. HynesL. DawsonH. Etchegary Research Open access 21 October 2023 Pages: 49 - 58
Prevalence of beta thalassemia carriers in India: a systematic review and meta-analysis Dharmarajan SumedhaKar Anita Review 20 October 2023 Pages: 527 - 541
The CPT1A Arctic variant: perspectives of community members and providers in two Alaska tribal health settings Julie A. BeansSusan Brown TrinidadDenise A. Dillard Research 17 October 2023 Pages: 613 - 620
Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions Robert KlitzmanEkaterina BezborodkoPaul S. Appelbaum Research 16 October 2023 Pages: 85 - 96
Benefits and concerns of expanded carrier screening: what do pregnant Latina women in Texas think? Embedzayi MadhiriHaocen WangLei-Shih Chen Research 14 October 2023 Pages: 605 - 612
A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments Maria Mabyalwa MudauHeather SeymourNadia Carstens Research Open access 10 October 2023 Pages: 39 - 48
Relationship satisfaction in adults with phenylketonuria is positively associated with following recommended treatment, having a partner involved in management, and maintaining good health Rachel SundstromLeah WetherillMelissa Lah Research 06 October 2023 Pages: 627 - 638
Ethics of artificial intelligence in prenatal and pediatric genomic medicine Simon CoghlanChristopher GyngellDanya F Vears Research Open access 05 October 2023 Pages: 13 - 24
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening Christina A. HansenAaron W. ReiterRobert S. Wildin Research 04 October 2023 Pages: 33 - 37
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease Mallorie T. TamAlonso DaboubJulie M. Robillard Research Open access 03 October 2023 Pages: 97 - 101
Big advocacy, little recognition: the hidden work of Black patients in precision medicine Lynette Hammond GeridoKenneth ResnicowZhe He Research Open access 29 September 2023 Pages: 657 - 665
Are we nearly there yet? Starts and stops on the road to use of polygenic scores Sowmiya MoorthieDaphne Oluwasen MartschenkoSegun Fatumo Editorial Open access 27 September 2023 Pages: 439 - 440
Factors associated with adherence to BRCA1/2 mutation testing after oncogenetic counseling in long-surviving patients with a previous diagnosis of breast or ovarian cancer Silvia ActisMarta D’AlonzoNicoletta Biglia Research Open access 19 September 2023 Pages: 649 - 656
When and how to enlighten citizens on genetics and hereditary cancer: a web survey of online video viewers Reimi SogawaTakahito WadaAkira Hirasawa Research 16 September 2023 Pages: 575 - 581
Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity Michael SetzerJia YanMorgan Similuk Research 15 September 2023 Pages: 639 - 647
The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies Sara AbudahabNancy HakoozRana Dajani Review 13 September 2023 Pages: 505 - 517
Population diversity and equity in the genomic era: going global to return to the local Anahí Ruderman Review 05 September 2023 Pages: 519 - 525
Experiences of cystic fibrosis newborn screening and genetic counseling Kimberly FoilLillian ChristonSylvia Szentpetery Research 01 September 2023 Pages: 621 - 626