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Paper Details

Perspectives on Genetic Testing and Return of Results from the First Cohort of Presymptomatically Tested Individuals At Risk of Huntington Disease.
J Genet Couns
3
2018
HD, Huntington Disease, Huntington's disease, exome, expanded, genome, participants, people
Aged, Decision Making, Direct-To-Consumer Screening and Testing, Female, Follow-Up Studies, Genetic Testing, Health Knowledge, Attitudes, Practice, Humans, Huntington Disease, Male, Middle Aged, Patient Preference, Qualitative Research
Author NameAffiliation
Kelsey StuttgenBerman Institute of Bioethics, Johns Hopkins University
Kelsey StuttgenInstitute of Genetic Medicine, Johns Hopkins University School of Medicine
Juli BollingerBerman Institute of Bioethics, Johns Hopkins University
Rachel DvoskinBerman Institute of Bioethics, Johns Hopkins University
Allison F McCagueBerman Institute of Bioethics, Johns Hopkins University
Allison F McCagueInstitute of Genetic Medicine, Johns Hopkins University School of Medicine
Barnett ShpritzJohns Hopkins University School of Medicine
Jason BrandtJohns Hopkins University School of Medicine
Jason BrandtJohns Hopkins University School of Medicine
Debra J H MathewsBerman Institute of Bioethics, Johns Hopkins University
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Release 1.2