Literature DB >> 25813238

The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine.

S C Bowdin1,2,3, R Z Hayeems2,4,5, N Monfared2, R D Cohn1,2,6,3,7, M S Meyn1,2,6,3,7.   

Abstract

Our increasing knowledge of how genomic variants affect human health and the falling costs of whole-genome sequencing are driving the development of individualized genomic medicine. This new clinical paradigm uses knowledge of an individual's genomic variants to anticipate, diagnose and manage disease. While individualized genetic medicine offers the promise of transformative change in health care, it forces us to reconsider existing ethical, scientific and clinical paradigms. The potential benefits of pre-symptomatic identification of at-risk individuals, improved diagnostics, individualized therapy, accurate prognosis and avoidance of adverse drug reactions coexist with the potential risks of uninterpretable results, psychological harm, outmoded counseling models and increased health care costs. Here we review the challenges, opportunities and limits of integrating genomic analysis into pediatric clinical practice and describe a model for implementing individualized genomic medicine. Our multidisciplinary team of bioinformaticians, health economists, health services and policy researchers, ethicists, geneticists, genetic counselors and clinicians has designed a 'Genome Clinic' research project that addresses multiple challenges in pediatric genomic medicine--ranging from development of bioinformatics tools for the clinical assessment of genomic variants and the discovery of disease genes to health policy inquiries, assessment of clinical care models, patient preference and the ethics of consent.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  individualized genomic medicine; next-generation sequencing; pediatrics; whole exome; whole genome

Mesh:

Year:  2015        PMID: 25813238     DOI: 10.1111/cge.12579

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  12 in total

1.  The clinical utility of next-generation sequencing in the neonatal intensive care unit.

Authors:  Sarah C Bowdin
Journal:  CMAJ       Date:  2016-05-30       Impact factor: 8.262

2.  Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.

Authors:  Robin Z Hayeems; Jasmin Bhawra; Kate Tsiplova; M Stephen Meyn; Nasim Monfared; Sarah Bowdin; D James Stavropoulos; Christian R Marshall; Raveen Basran; Cheryl Shuman; Shinya Ito; Iris Cohn; Courtney Hum; Marta Girdea; Michael Brudno; Ronald D Cohn; Stephen W Scherer; Wendy J Ungar
Journal:  Eur J Hum Genet       Date:  2017-11-20       Impact factor: 4.246

Review 3.  Clinical application of next-generation sequencing to the practice of neurology.

Authors:  Jessica Rexach; Hane Lee; Julian A Martinez-Agosto; Andrea H Németh; Brent L Fogel
Journal:  Lancet Neurol       Date:  2019-05       Impact factor: 44.182

4.  Genome-wide sequencing technologies: A primer for paediatricians.

Authors:  Robin Z Hayeems; Kym M Boycott
Journal:  Paediatr Child Health       Date:  2017-12-02       Impact factor: 2.253

5.  Ethical Considerations on Pediatric Genetic Testing Results in Electronic Health Records.

Authors:  Shibani Kanungo; Jayne Barr; Parker Crutchfield; Casey Fealko; Neelkamal Soares
Journal:  Appl Clin Inform       Date:  2020-11-11       Impact factor: 2.342

6.  A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.

Authors:  Kate Tsiplova; Richard M Zur; Christian R Marshall; Dimitri J Stavropoulos; Sergio L Pereira; Daniele Merico; Edwin J Young; Wilson W L Sung; Stephen W Scherer; Wendy J Ungar
Journal:  Genet Med       Date:  2017-05-04       Impact factor: 8.822

7.  Clinical care models in the era of next-generation sequencing.

Authors:  Anne Slavotinek
Journal:  Mol Genet Genomic Med       Date:  2016-05-12       Impact factor: 2.183

8.  Genetic Testing among Children in a Complex Care Program.

Authors:  Krista Oei; Robin Z Hayeems; Wendy J Ungar; Ronald D Cohn; Eyal Cohen
Journal:  Children (Basel)       Date:  2017-05-22

9.  My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.

Authors:  Holly K Tabor; Seema M Jamal; Joon-Ho Yu; Julia M Crouch; Aditi G Shankar; Karin M Dent; Nick Anderson; Damon A Miller; Brett T Futral; Michael J Bamshad
Journal:  Genet Med       Date:  2016-09-15       Impact factor: 8.822

Review 10.  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

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