Literature DB >> 30991113

Point of View: An evolution from genetic counselling to genomic counselling.

Christine Patch1, Anna Middleton2.   

Abstract

The highly specialist, hub and spoke model of Clinical Genetics, as described by the Royal College of Physicians in the UK in 1991, is under the spotlight. Whilst this has underpinned the successful delivery of genetics services historically, it may not be able to deliver genomic healthcare on its own, at scale, simply because genomic testing is no longer contained - any clinician can now order a genomic test, irrespective of their discipline. The professional group of genomic counsellors are now questioning whether there is need for an evolution of their roles. Do we persist in being attached to past models, or do we embrace new models of care and take a direct role in 'mainstreaming' the skills of genomic counselling?. We conclude the genomic counsellor profession and the translated skills of genomic counselling have much to offer in shaping the future of medicine as genomic technologies become part of routine clinical practice.
Copyright © 2019. Published by Elsevier Masson SAS.

Entities:  

Mesh:

Year:  2019        PMID: 30991113     DOI: 10.1016/j.ejmg.2019.04.010

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  5 in total

Review 1.  Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review.

Authors:  Alison Luk Young; Aalya Imran; Michael J Spoelma; Rachel Williams; Katherine M Tucker; Jane Halliday; Laura E Forrest; Claire E Wakefield; Phyllis N Butow
Journal:  Eur J Hum Genet       Date:  2022-10-17       Impact factor: 5.351

2.  Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents' associations.

Authors:  Gregorio Serra; Luigi Memo; Alessandra Coscia; Mario Giuffré; Ambra Iuculano; Mariano Lanna; Diletta Valentini; Anna Contardi; Sauro Filippeschi; Tiziana Frusca; Fabio Mosca; Luca A Ramenghi; Corrado Romano; Annalisa Scopinaro; Alberto Villani; Giuseppe Zampino; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2021-04-19       Impact factor: 2.638

3.  Genomic sequencing in oncology: Considerations for integration in routine cancer care.

Authors:  Belinda Rahman; Alastair Lamb; Andrew Protheroe; Ketan Shah; Joyce Solomons; Jonathan Williams; Elizabeth Ormondroyd
Journal:  Eur J Cancer Care (Engl)       Date:  2022-04-05       Impact factor: 2.328

4.  The experiences of UK-based genetic counsellors working in mainstream settings.

Authors:  Ellie Quinn; Katherine Mazur
Journal:  Eur J Hum Genet       Date:  2022-08-02       Impact factor: 5.351

5.  Molecular diagnostic challenges for non-retinal developmental eye disorders in the United Kingdom.

Authors:  Daniel Jackson; Samantha Malka; Philippa Harding; Juliana Palma; Hannah Dunbar; Mariya Moosajee
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-08-23       Impact factor: 3.908

  5 in total

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