Literature DB >> 25099850

Mainstreaming genetic testing of cancer predisposition genes.

Nazneen Rahman1.   

Abstract

Entities:  

Keywords:  BRCA1; BRCA2; Cancer predisposition genes; gene testing; next-generation sequencing

Mesh:

Year:  2014        PMID: 25099850      PMCID: PMC4312836          DOI: 10.7861/clinmedicine.14-4-436

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


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  18 in total

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Review 3.  RB1 gene mutations in retinoblastoma.

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Review 5.  Exploring the genomes of cancer cells: progress and promise.

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Journal:  Science       Date:  2011-03-25       Impact factor: 47.728

6.  RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.

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7.  DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome.

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Journal:  J Med Genet       Date:  2011-01-25       Impact factor: 6.318

8.  Results of a phase II open-label, non-randomized trial of cisplatin chemotherapy in patients with BRCA1-positive metastatic breast cancer.

Authors:  Tomasz Byrski; Rebecca Dent; Pawel Blecharz; Malgorzata Foszczynska-Kloda; Jacek Gronwald; Tomasz Huzarski; Cezary Cybulski; Elzbieta Marczyk; Robert Chrzan; Andrea Eisen; Jan Lubinski; Steven A Narod
Journal:  Breast Cancer Res       Date:  2012-07-20       Impact factor: 6.466

9.  Platinum chemotherapy for BRCA1-related breast cancer: do we need more evidence?

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10.  Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers.

Authors:  Peter C Fong; David S Boss; Timothy A Yap; Andrew Tutt; Peijun Wu; Marja Mergui-Roelvink; Peter Mortimer; Helen Swaisland; Alan Lau; Mark J O'Connor; Alan Ashworth; James Carmichael; Stan B Kaye; Jan H M Schellens; Johann S de Bono
Journal:  N Engl J Med       Date:  2009-06-24       Impact factor: 91.245

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1.  An Association of Cancer Physicians' strategy for improving services and outcomes for cancer patients.

Authors:  Richard Baird; Ian Banks; David Cameron; John Chester; Helena Earl; Mark Flannagan; Adam Januszewski; Richard Kennedy; Sarah Payne; Emlyn Samuel; Hannah Taylor; Roshan Agarwal; Samreen Ahmed; Caroline Archer; Ruth Board; Judith Carser; Ellen Copson; David Cunningham; Rob Coleman; Adam Dangoor; Graham Dark; Diana Eccles; Chris Gallagher; Adam Glaser; Richard Griffiths; Geoff Hall; Marcia Hall; Danielle Harari; Michael Hawkins; Mark Hill; Peter Johnson; Alison Jones; Tania Kalsi; Eleni Karapanagiotou; Zoe Kemp; Janine Mansi; Ernie Marshall; Alex Mitchell; Maung Moe; Caroline Michie; Richard Neal; Tom Newsom-Davis; Alison Norton; Richard Osborne; Gargi Patel; John Radford; Alistair Ring; Emily Shaw; Rod Skinner; Dan Stark; Sam Turnbull; Galina Velikova; Jeff White; Alison Young; Johnathan Joffe; Peter Selby
Journal:  Ecancermedicalscience       Date:  2016-01-05

Review 2.  Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects.

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3.  Recommendations for the implementation of genetic testing for metastatic prostate cancer patients in Canada.

Authors:  Shamini Selvarajah; Kasmintan A Schrader; Michael P Kolinsky; Ricardo A Rendon; Soufiane El Hallani; Neil E Fleshner; Sebastien J Hotte; Justin Lorentz; Karen Panabaker; Renée Perrier; Frédéric Pouliot; Alan Spatz; Stephen Yip; Kim N Chi
Journal:  Can Urol Assoc J       Date:  2022-10       Impact factor: 2.052

Review 4.  CRISPR/Cas9: A revolutionary genome editing tool for human cancers treatment.

Authors:  Fatima Akram; Ikram Ul Haq; Sania Sahreen; Narmeen Nasir; Waqas Naseem; Memoona Imitaz; Amna Aqeel
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5.  The integration of BRCA testing into oncology clinics.

Authors:  Natalie Percival; Angela George; Jennifer Gyertson; Monica Hamill; Andreia Fernandes; Emily Davies; Nazneen Rahman; Susana Banerjee
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Review 6.  Genetic causes of cancer predisposition in children and adolescents.

Authors:  Federica Saletta; Luciano Dalla Pozza; Jennifer A Byrne
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7.  Genetic counselors and Genomic Counseling in the United Kingdom.

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Journal:  Mol Genet Genomic Med       Date:  2015-03       Impact factor: 2.183

8.  Using family history forms in pediatric oncology to identify patients for genetic assessment.

Authors:  A Hamilton; E Smith; J Hamon; E Tomiak; M Bassal; S L Sawyer
Journal:  Curr Oncol       Date:  2017-12-20       Impact factor: 3.677

9.  CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting.

Authors:  Márton Münz; Elise Ruark; Anthony Renwick; Emma Ramsay; Matthew Clarke; Shazia Mahamdallie; Victoria Cloke; Sheila Seal; Ann Strydom; Gerton Lunter; Nazneen Rahman
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10.  Development of cancer genetic services in the UK: A national consultation.

Authors:  Ingrid Slade; Daniel Riddell; Clare Turnbull; Helen Hanson; Nazneen Rahman
Journal:  Genome Med       Date:  2015-02-02       Impact factor: 11.117

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