Literature DB >> 2953913

The decision to be tested for Huntington's disease.

K A Quaid, J Brandt, S E Folstein.   

Abstract

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Year:  1987        PMID： 2953913

Source DB:  PubMed          Journal:  JAMA        ISSN： 0098-7484            Impact factor:   56.272


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  5 in total

1.  Disclosing Secondary Findings from Pediatric Sequencing to Families: Considering the "Benefit to Families".

Authors:  Benjamin S Wilfond; Conrad V Fernandez; Robert C Green
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

2.  Factors related to genetic testing in adults at risk for Huntington disease: the prospective Huntington at-risk observational study (PHAROS).

Authors:  K A Quaid; S W Eberly; E Kayson-Rubin; D Oakes; I Shoulson
Journal:  Clin Genet       Date:  2016-11-24       Impact factor: 4.438

3.  Attitudes of healthcare professionals and parents regarding genetic testing for violent traits in childhood.

Authors:  E Campbell; L F Ross
Journal:  J Med Ethics       Date:  2004-12       Impact factor: 2.903

Review 4.  Huntington's disease and the ethics of genetic prediction.

Authors:  G Terrenoire
Journal:  J Med Ethics       Date:  1992-06       Impact factor: 2.903

Review 5.  Predictive Genetic Counseling for Neurodegenerative Diseases: Past, Present, and Future.

Authors:  Jill S Goldman
Journal:  Cold Spring Harb Perspect Med       Date:  2020-07-01       Impact factor: 5.159
  5 in total

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