Literature DB >> 24270507

Policy challenges of clinical genome sequencing.

Caroline F Wright1, Anna Middleton, Hilary Burton, Fiona Cunningham, Steve E Humphries, Jane Hurst, Ewan Birney, Helen V Firth.   

Abstract

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Year:  2013        PMID： 24270507     DOI： 10.1136/bmj.f6845

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  21 in total

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Review 2.  Paediatric genomics: diagnosing rare disease in children.

Authors:  Caroline F Wright; David R FitzPatrick; Helen V Firth
Journal:  Nat Rev Genet       Date:  2018-02-05       Impact factor: 53.242

Review 3.  Risk-Adjusted Cancer Screening and Prevention (RiskAP): Complementing Screening for Early Disease Detection by a Learning Screening Based on Risk Factors.

Authors:  Rita K Schmutzler; Björn Schmitz-Luhn; Bettina Borisch; Peter Devilee; Diana Eccles; Per Hall; Judith Balmaña; Stefania Boccia; Peter Dabrock; Günter Emons; Wolfgang Gaissmaier; Jacek Gronwald; Stefanie Houwaart; Stefan Huster; Karin Kast; Alexander Katalinic; Sabine C Linn; Sowmiya Moorthie; Paul Pharoah; Kerstin Rhiem; Tade Spranger; Dominique Stoppa-Lyonnet; Johannes Jozef Marten van Delden; Marc van den Bulcke; Christiane Woopen
Journal:  Breast Care (Basel)       Date:  2021-08-12       Impact factor: 2.268

4.  Conceptual issues for screening in the genomic era - time for an update?

Authors:  Caroline F Wright; Ron L Zimmern
Journal:  Epidemiol Biostat Public Health       Date:  2014-12-11

5.  Return of Results from Genomic Sequencing: A Policy Discussion of Secondary Findings for Cancer Predisposition.

Authors:  Kimberly J Johnson; Sarah Gehlert
Journal:  J Cancer Policy       Date:  2014-09-01

6.  Evidence for penetrance in patients without a family history of disease: a systematic review.

Authors:  Heather Turner; Leigh Jackson
Journal:  Eur J Hum Genet       Date:  2020-01-14       Impact factor: 4.246

7.  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

8.  Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.

Authors:  Caroline F Wright; Tomas W Fitzgerald; Wendy D Jones; Stephen Clayton; Jeremy F McRae; Margriet van Kogelenberg; Daniel A King; Kirsty Ambridge; Daniel M Barrett; Tanya Bayzetinova; A Paul Bevan; Eugene Bragin; Eleni A Chatzimichali; Susan Gribble; Philip Jones; Netravathi Krishnappa; Laura E Mason; Ray Miller; Katherine I Morley; Vijaya Parthiban; Elena Prigmore; Diana Rajan; Alejandro Sifrim; G Jawahar Swaminathan; Adrian R Tivey; Anna Middleton; Michael Parker; Nigel P Carter; Jeffrey C Barrett; Matthew E Hurles; David R FitzPatrick; Helen V Firth
Journal:  Lancet       Date:  2014-12-17       Impact factor: 79.321

9.  The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.

Authors:  Caroline S Bennette; Carlos J Gallego; Wylie Burke; Gail P Jarvik; David L Veenstra
Journal:  Genet Med       Date:  2014-11-13       Impact factor: 8.822

Review 10.  Exome Sequencing in Fetuses with Structural Malformations.

Authors:  Fiona L Mackie; Keren J Carss; Sarah C Hillman; Matthew E Hurles; Mark D Kilby
Journal:  J Clin Med       Date:  2014-07-08       Impact factor: 4.241
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