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Journal of Community Genetics|November 22, 2022
Service provision of genetics health care in PortugalC Costa, M S Lemos, L F Azevedo, et al.Journal of Community Genetics|December 11, 2022
Lost in print: difficulty in reading online information pertaining to phenylketonuriaLalitha Samuel, Joseph Fera, Corey H BaschJournal of Community Genetics|December 10, 2022
Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington's diseaseCathy Gluyas, Lisa Mottram, Rosanne Gibb, et al.Journal of Community Genetics|October 27, 2020
Sickle cell trait newborn screen results: disclosure and managementMargaret Lilley, Stephanie Hoang, Pamela Blumenschein, et al.Journal of Community Genetics|January 7, 2023
Assessing patient-level knowledge of precision medicine in a community health center settingSarah C Stallings, Jennifer Richmond, Juan R Canedo, et al.Journal of Community Genetics|December 18, 2022
Ethical, legal, and social implications of genetic risk prediction for multifactorial disease: a narrative review identifying concerns about interpretation and use of polygenic scoresCarolyn Riley ChapmanJournal of Community Genetics|May 23, 2012
Public-private partnership as a solution for integrating genetic services into health care of countries with low and middle incomesFlorian Meier, Oliver Schöffski, Jörg SchmidtkeJournal of Community Genetics|July 23, 2017
Diagnosis of rare diseases under focus: impacts for Canadian patientsDaphne Esquivel-Sada, Minh Thu NguyenJournal of Community Genetics|September 27, 2017
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwideSowmiya Moorthie, Hannah Blencowe, Matthew W Darlison, et al.Journal of Community Genetics|September 28, 2017
The challenges of the expanded availability of genomic information: an agenda-setting paperPascal Borry, Heidi Beate Bentzen, Isabelle Budin-Ljøsne, et al.Pageof 82