Literature DB >> 23990543

Call for prudence in whole-genome testing.

C G van El, W J Dondorp, G M W R de Wert, M C Cornel.   

Abstract

Mesh:

Year:  2013        PMID: 23990543     DOI: 10.1126/science.341.6149.958-b

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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  4 in total

1.  Towards a European consensus for reporting incidental findings during clinical NGS testing.

Authors:  Jayne Y Hehir-Kwa; Mireille Claustres; Ros J Hastings; Conny van Ravenswaaij-Arts; Gabrielle Christenhusz; Maurizio Genuardi; Béla Melegh; Anne Cambon-Thomsen; Philippos Patsalis; Joris Vermeesch; Martina C Cornel; Beverly Searle; Aarno Palotie; Ettore Capoluongo; Borut Peterlin; Xavier Estivill; Peter N Robinson
Journal:  Eur J Hum Genet       Date:  2015-06-03       Impact factor: 4.246

2.  Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing.

Authors:  Elli G Gourna; Natalie Armstrong; Susan E Wallace
Journal:  Eur J Hum Genet       Date:  2015-06-10       Impact factor: 4.246

3.  A protocol for the identification and validation of novel genetic causes of kidney disease.

Authors:  Andrew Mallett; Chirag Patel; Barbara Maier; Julie McGaughran; Michael Gabbett; Minoru Takasato; Anne Cameron; Peter Trnka; Stephen I Alexander; Gopala Rangan; Michel C Tchan; Georgina Caruana; George John; Cathy Quinlan; Hugh J McCarthy; Valentine Hyland; Wendy E Hoy; Ernst Wolvetang; Ryan Taft; Cas Simons; Helen Healy; Melissa Little
Journal:  BMC Nephrol       Date:  2015-09-15       Impact factor: 2.388

4.  Incidental findings from clinical sequencing in Greece: reporting experts' attitudes.

Authors:  E G Gourna; N Armstrong; S E Wallace
Journal:  J Community Genet       Date:  2014-07-22
  4 in total

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