Literature DB >> 33597540

Please give me a copy of my child's raw genomic data.

Lauren Chad1,2,3, Michael J Szego4,5,6.   

Abstract

Entities:  

Year:  2021        PMID: 33597540      PMCID: PMC7889911          DOI: 10.1038/s41525-021-00175-y

Source DB:  PubMed          Journal:  NPJ Genom Med        ISSN: 2056-7944            Impact factor:   8.617


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  30 in total

Review 1.  Return of genetic testing results in the era of whole-genome sequencing.

Authors:  Bartha Maria Knoppers; Ma'n H Zawati; Karine Sénécal
Journal:  Nat Rev Genet       Date:  2015-08-04       Impact factor: 53.242

2.  Predictive genomic testing of children for adult onset disorders: a Canadian perspective.

Authors:  Michael J Szego; M Stephen Meyn; James A Anderson; Robin Hayeems; Cheryl Shuman; Nasim Monfared; Sarah Bowdin; Randi Zlotnik Shaul
Journal:  Am J Bioeth       Date:  2014       Impact factor: 11.229

3.  Information access. Raw personal data: providing access.

Authors:  Jeantine E Lunshof; George M Church; Barbara Prainsack
Journal:  Science       Date:  2014-01-24       Impact factor: 47.728

4.  Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?

Authors:  J A Anderson; M S Meyn; C Shuman; R Zlotnik Shaul; L E Mantella; M J Szego; S Bowdin; N Monfared; R Z Hayeems
Journal:  J Med Ethics       Date:  2016-11-25       Impact factor: 2.903

5.  The best-interests standard as threshold, ideal, and standard of reasonableness.

Authors:  L M Kopelman
Journal:  J Med Philos       Date:  1997-06

6.  Variation among Consent Forms for Clinical Whole Exome Sequencing.

Authors:  Sara A Fowler; Carol J Saunders; Mark A Hoffman
Journal:  J Genet Couns       Date:  2017-07-08       Impact factor: 2.537

7.  Genomic Sequencing Capacity, Data Retention, and Personal Access to Raw Data in Europe.

Authors:  Shaman Narayanasamy; Varvara Markina; Adrian Thorogood; Adriana Blazkova; Mahsa Shabani; Bartha M Knoppers; Barbara Prainsack; Robert Koesters
Journal:  Front Genet       Date:  2020-05-06       Impact factor: 4.599

8.  ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Authors:  Robert C Green; Jonathan S Berg; Wayne W Grody; Sarah S Kalia; Bruce R Korf; Christa L Martin; Amy L McGuire; Robert L Nussbaum; Julianne M O'Daniel; Kelly E Ormond; Heidi L Rehm; Michael S Watson; Marc S Williams; Leslie G Biesecker
Journal:  Genet Med       Date:  2013-06-20       Impact factor: 8.822

Review 9.  Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.

Authors:  Michael P Mackley; Benjamin Fletcher; Michael Parker; Hugh Watkins; Elizabeth Ormondroyd
Journal:  Genet Med       Date:  2016-09-01       Impact factor: 8.822

Review 10.  APPLaUD: access for patients and participants to individual level uninterpreted genomic data.

Authors:  Adrian Thorogood; Jason Bobe; Barbara Prainsack; Anna Middleton; Erick Scott; Sarah Nelson; Manuel Corpas; Natasha Bonhomme; Laura Lyman Rodriguez; Madeleine Murtagh; Erika Kleiderman
Journal:  Hum Genomics       Date:  2018-02-17       Impact factor: 4.639

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  1 in total

1.  Returning raw genomic data: rights of research participants and obligations of health care professionals.

Authors:  Jane L Nielsen; Carolyn Johnston; Tracey O'Brien; Vanessa J Tyrrell
Journal:  Med J Aust       Date:  2022-05-29       Impact factor: 12.776

  1 in total

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