Literature DB >> 19796327

A systematic review of literature about the genetic testing of adolescents.

Lynn Rew1, Michael Mackert, Daniel Bonevac.   

Abstract

PURPOSE: Mapping of the human genome raises interest in and concern about the genetic testing of adolescents. Our purpose was to determine the attitudes and knowledge adolescents and their parents have about genetic testing. DESIGN AND
METHOD: This paper is a report of a systematic review of the research literature (n = 56) about the attitudes and knowledge adolescents and their parents have about genetic testing.
RESULTS: The majority of studies, which were descriptive in design, focused on a specific heritable disorder, were conducted in the United States, and over-sampled well-educated White females. PRACTICE IMPLICATIONS: Results suggest that adolescents and their families have relatively positive attitudes about genetic testing and may experience both harms and benefits from testing. Nurses may be in positions to assist adolescents and their families in making decisions about genetic testing, remaining sensitive to family dynamics and issues of privacy and autonomy.

Entities:  

Mesh:

Year:  2009        PMID: 19796327     DOI: 10.1111/j.1744-6155.2009.00210.x

Source DB:  PubMed          Journal:  J Spec Pediatr Nurs        ISSN: 1539-0136            Impact factor:   1.260


  9 in total

1.  Genetic testing and counseling for hereditary neurological diseases in Mali.

Authors:  Katherine Gloria Meilleur; Souleymane Coulibaly; Moussa Traoré; Guida Landouré; Alison La Pean; Modibo Sangaré; Fanny Mochel; Siona Traoré; Kenneth H Fischbeck; Hae-Ra Han
Journal:  J Community Genet       Date:  2011-02-22

Review 2.  Impact of presymptomatic genetic testing on young adults: a systematic review.

Authors:  Lea Godino; Daniela Turchetti; Leigh Jackson; Catherine Hennessy; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2015-07-15       Impact factor: 4.246

Review 3.  Outcomes of support groups for carriers of BRCA 1/2 pathogenic variants and their relatives: a systematic review.

Authors:  Benedetta Bertonazzi; Daniela Turchetti; Lea Godino
Journal:  Eur J Hum Genet       Date:  2022-01-26       Impact factor: 4.246

Review 4.  Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.

Authors:  Christopher H Wade; Beth A Tarini; Benjamin S Wilfond
Journal:  Annu Rev Genomics Hum Genet       Date:  2013-07-15       Impact factor: 8.929

5.  Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample.

Authors:  Jarle Johannessen; Terje Nærland; Sigrun Hope; Tonje Torske; Anne Lise Høyland; Jana Strohmaier; Arvid Heiberg; Marcella Rietschel; Srdjan Djurovic; Ole A Andreassen
Journal:  Int J Mol Sci       Date:  2017-05-18       Impact factor: 5.923

6.  Young adults' attitudes to sharing whole-genome sequencing information: a university-based survey.

Authors:  Pepita Barnard; Sarah Sharples; Brian J Thomson; Jonathan M Garibaldi
Journal:  BMC Med Genomics       Date:  2019-04-16       Impact factor: 3.063

7.  Development of a measure of genome sequencing knowledge for young people: The kids-KOGS.

Authors:  Celine Lewis; Bao S Loe; Chris Sidey-Gibbons; Christine Patch; Lyn S Chitty; Saskia C Sanderson
Journal:  Clin Genet       Date:  2019-07-30       Impact factor: 4.438

8.  Attitudes among parents of persons with autism spectrum disorder towards information about genetic risk and future health.

Authors:  Jarle Johannessen; Terje Nærland; Sigrun Hope; Tonje Torske; Anett Kaale; Katrine V Wirgenes; Eva Malt; Srdjan Djurovic; Marcella Rietschel; Ole A Andreassen
Journal:  Eur J Hum Genet       Date:  2021-11-15       Impact factor: 5.351

9.  Attitudes toward Genetic Testing for Hypertension among African American Women and Girls.

Authors:  Jacquelyn Y Taylor; Bronwen Peternell; Jennifer A Smith
Journal:  Nurs Res Pract       Date:  2013-11-02
  9 in total

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