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1000 Titel
  • EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer
1000 Autor/in
  1. McDevitt, Trudi |
  2. Durkie, Miranda |
  3. Arnold, Norbert |
  4. Burghel, George J |
  5. Butler, Samantha |
  6. Claes, Kathleen |
  7. Logan, Peter |
  8. Robinson, Rachel |
  9. Sheils, Katie |
  10. Wolstenholme, Nicola |
  11. Hanson, Helen |
  12. Turnbull, Clare |
  13. Hume, Stacey |
1000 Verlag Springer International Publishing
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-03-05
1000 Erschienen in
1000 Quellenangabe
  • 32(5):479-488
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41431-023-01507-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11061103/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>Hereditary Breast and Ovarian Cancer (HBOC) is a genetic condition associated with increased risk of cancers. The past decade has brought about significant changes to hereditary breast and ovarian cancer (HBOC) diagnostic testing with new treatments, testing methods and strategies, and evolving information on genetic associations. These best practice guidelines have been produced to assist clinical laboratories in effectively addressing the complexities of HBOC testing, while taking into account advancements since the last guidelines were published in 2007. These guidelines summarise cancer risk data from recent studies for the most commonly tested high and moderate risk HBOC genes for laboratories to refer to as a guide. Furthermore, recommendations are provided for somatic and germline testing services with regards to clinical referral, laboratory analyses, variant interpretation, and reporting. The guidelines present recommendations where ‘<jats:bold>must</jats:bold>’ is assigned to advocate that the recommendation is essential; and ‘<jats:bold>should</jats:bold>’ is assigned to advocate that the recommendation is highly advised but may not be universally applicable. Recommendations are presented in the form of shaded italicised statements throughout the document, and in the form of a table in supplementary materials (Table S4). Finally, for the purposes of encouraging standardisation and aiding implementation of recommendations, example report wording covering the essential points to be included is provided for the most common HBOC referral and reporting scenarios. These guidelines are aimed primarily at genomic scientists working in diagnostic testing laboratories.</jats:p>
1000 Sacherschließung
lokal Genetic Predisposition to Disease [MeSH]
lokal /631/67/68
lokal Female [MeSH]
lokal Humans [MeSH]
lokal Breast Neoplasms/genetics [MeSH]
lokal Practice Guidelines as Topic [MeSH]
lokal Review Article
lokal /45/47
lokal Hereditary Breast and Ovarian Cancer Syndrome/diagnosis [MeSH]
lokal /45/41
lokal Ovarian Neoplasms/diagnosis [MeSH]
lokal Genetic Testing/standards [MeSH]
lokal Ovarian Neoplasms/genetics [MeSH]
lokal /631/208/69
lokal review-article
lokal /45/23
lokal Breast Neoplasms/diagnosis [MeSH]
lokal Genetic Testing/methods [MeSH]
lokal /45/56
lokal Hereditary Breast and Ovarian Cancer Syndrome/genetics [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0009-0008-2425-5194|https://orcid.org/0000-0001-7071-7048|https://frl.publisso.de/adhoc/uri/QXJub2xkLCBOb3JiZXJ0|https://orcid.org/0000-0001-9360-8194|https://frl.publisso.de/adhoc/uri/QnV0bGVyLCBTYW1hbnRoYQ==|https://orcid.org/0000-0003-0841-7372|https://frl.publisso.de/adhoc/uri/TG9nYW4sIFBldGVy|https://frl.publisso.de/adhoc/uri/Um9iaW5zb24sIFJhY2hlbA==|https://orcid.org/0000-0002-1649-1495|https://frl.publisso.de/adhoc/uri/V29sc3RlbmhvbG1lLCBOaWNvbGE=|https://orcid.org/0000-0002-3303-8713|https://frl.publisso.de/adhoc/uri/VHVybmJ1bGwsIENsYXJl|https://orcid.org/0000-0002-3217-3032
1000 Hinweis
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1000 Erstellt am 2025-02-03T14:15:37.055+0100
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