Dr Samantha Wake
SNR Lecturer Genetic Counselling Genomics Health
Department of Paediatrics
38 Scholarly works
0 Projects
HIGHLIGHTS
2019
Journal article
Family communication following a diagnosis of myotonic dystrophy: To tell or not to tell?
DOI: 10.1002/jgc4.11562018
Journal article
Genetics, insurance and professional practice: Survey of the Australasian clinical genetics workforce
DOI: 10.3389/fpubh.2018.003332018
Journal article
Genetic Counsellors and Private Practice: Professional Turbulence and Common Values
DOI: 10.1007/s10897-017-0201-92016
Journal article
“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
DOI: 10.1007/s12687-016-0262-82016
Journal article
Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practice
DOI: 10.1038/ejhg.2016.1352015
Journal article
"It's good to know": Experiences of gene identification and result disclosure in familial epilepsies
DOI: 10.1016/j.eplepsyres.2015.02.0112015
Journal article
Connecting patients, researchers and clinical genetics services: The experiences of participants in the Australian ovarian cancer study (AOCS)
DOI: 10.1038/ejhg.2014.86
RECENT SCHOLARLY WORKS
2013
Journal article
Genetic counseling training and certification in Australasia
DOI: 10.1007/s10897-012-9567-x2013
Journal article
Educating genetic counselors in Australia - Developing a masters program
DOI: 10.1007/s10897-013-9575-52013
Journal article
"It's about having the choice": Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome
DOI: 10.1002/ajmg.a.35674