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Issue DateTitleAuthor(s)
2023-07-27Special Issue: "Genetic Counseling and Genetic Testing in Precision Medicine".Turbitt, E; Jacobs, C; McEwen, A
2022-06Predictive genetic testing for Motor neuron disease: time for a guideline?McNeill, A; Amador, M-D-M; Bekker, H; Clarke, A; Crook, A; Cummings, C; McEwen, A; McDermott, C; Quarrell, O; Renieri, A; Roggenbuck, J; Salmon, K; Volk, A; Weishaupt, J; International Alliance of ALS/MND Associations,
2021-06-01Advancing precision public health using human genomics: examples from the field and future research opportunitiesRoberts, MC; Fohner, AE; Landry, L; Olstad, DL; Smit, AK; Turbitt, E; Allen, CG
2023-08-02Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness.Freeman, L; Bristowe, L; Kirk, EP; Delatycki, MB; Scully, JL
2023-05Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening.Freeman, L; Delatycki, MB; Scully, JL; Briggs, N; Kirk, EP
2023-07-31Scaling-up and future sustainability of a national reproductive genetic carrier screening program.Fehlberg, Z; Best, S; Long, JC; Theodorou, T; Pope, C; Hibbert, P; Williams, S; Freeman, L; Righetti, S; Archibald, AD; Braithwaite, J
2023-02Young-onset dementia: A systematic review of the psychological and social impact on relatives.Wiggins, M; McEwen, A; Sexton, A
2023-03Consistency of What? Appropriately Contextualizing Ethical Analysis of Non-Invasive Prenatal Testing.Newson, AJ; Deans, Z; Dive, L; Holmes, IC
2023-04-01Family Communication about Diagnostic Genetic Testing for Younger-Onset Dementia.Poulton, A; Curnow, L; Eratne, D; Sexton, A
2023-12-18Parents' preferences for receiving and discussing prognostic genetic information regarding their children's neurodevelopmental condition: A qualitative study.Turbitt, E; Bourne, M; McEwen, A; Amor, DJ
Results 61-70 of 70 (Search time: 0.01 seconds).

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