Literature DB >> 23751019

Commercial clinical genetic sequencing panels for evaluating patients with familial disease--are they ready for prime time?

Arthur Feldman.   

Abstract

Entities:  

Mesh:

Year:  2013        PMID: 23751019      PMCID: PMC5350849          DOI: 10.1111/cts.12069

Source DB:  PubMed          Journal:  Clin Transl Sci        ISSN: 1752-8054            Impact factor:   4.689


× No keyword cloud information.
  4 in total

1.  Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.

Authors:  Alexander G Bick; Jason Flannick; Kaoru Ito; Susan Cheng; Ramachandran S Vasan; Michael G Parfenov; Daniel S Herman; Steven R DePalma; Namrata Gupta; Stacey B Gabriel; Birgit H Funke; Heidi L Rehm; Emelia J Benjamin; Jayashri Aragam; Herman A Taylor; Ervin R Fox; Christopher Newton-Cheh; Sekar Kathiresan; Christopher J O'Donnell; James G Wilson; David M Altshuler; Joel N Hirschhorn; J G Seidman; Christine Seidman
Journal:  Am J Hum Genet       Date:  2012-09-07       Impact factor: 11.025

Review 2.  Genetic testing in cardiovascular medicine: current landscape and future horizons.

Authors:  Amy C Sturm; Ray E Hershberger
Journal:  Curr Opin Cardiol       Date:  2013-05       Impact factor: 2.161

3.  Prognostic impact of familial screening in dilated cardiomyopathy.

Authors:  Michele Moretti; Marco Merlo; Giulia Barbati; Andrea Di Lenarda; Francesca Brun; Bruno Pinamonti; Dario Gregori; Luisa Mestroni; Gianfranco Sinagra
Journal:  Eur J Heart Fail       Date:  2010-06-04       Impact factor: 15.534

4.  Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.

Authors:  Ray E Hershberger; Joann Lindenfeld; Luisa Mestroni; Christine E Seidman; Matthew R G Taylor; Jeffrey A Towbin
Journal:  J Card Fail       Date:  2009-03       Impact factor: 5.712

  4 in total
  1 in total

1.  Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus.

Authors:  M Grandis; L Obici; M Luigetti; C Briani; F Benedicenti; G Bisogni; M Canepa; F Cappelli; C Danesino; G M Fabrizi; S Fenu; G Ferrandes; C Gemelli; F Manganelli; A Mazzeo; L Melchiorri; F Perfetto; L G Pradotto; P Rimessi; G Tini; S Tozza; L Trevisan; D Pareyson; P Mandich
Journal:  Orphanet J Rare Dis       Date:  2020-12-14       Impact factor: 4.123

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.