Genetics in Medicine contents: Volume 19, Issue 3

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Discover the difference today!   TABLE OF CONTENTS Volume 19, Issue 3 (March 2017) In this issue Research Highlights Review Systematic Review Commentary Original Research Article Education Report Brief Report Letter to the Editor Addendum Podcast Sign in for free ACMG member access Facebook Twitter Subscribe Recommend to your library RSS ACMG Research Highlights Top In This Issue Genet Med 2017 19: 265; 10.1038/gim.2017.5 Full Text News Briefs Genet Med 2017 19: 266; 10.1038/gim.2017.13 Full Text Review Top Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians Jennifer Roggenbuck, Adam Quick and Stephen J. Kolb Genet Med 2017 19: 267-274; advance online publication, August 18, 2016; 10.1038/gim.2016.107 Abstract | Full Text Systematic Review Top Switch to agalsidase alfa after shortage of agalsidase beta in Fabry disease: a systematic review and meta-analysis of the literature Antonio Pisani, Dario Bruzzese, Massimo Sabbatini, Letizia Spinelli, Massimo Imbriaco and Eleonora Riccio Genet Med 2017 19: 275-282; advance online publication, September 8, 2016; 10.1038/gim.2016.117 Abstract | Full Text Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies OPEN Michael P. Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins and Elizabeth Ormondroyd Genet Med 2017 19: 283-293; advance online publication, September 1, 2016; 10.1038/gim.2016.109 Abstract | Full Text Commentary Top Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics Frederick R. Bieber, Athena M. Cherry, Beverly S. Emanuel, Uta Francke, H. Eugene Hoyme, Laird G. Jackson, Cynthia C. Morton, Maximillian Muenke, Cynthia M. Powell, Hope H. Punnett, P. Nagesh Rao, Stuart Schwartz, Roger E. Stevenson and Daniel L. Van Dyke Genet Med 2017 19: 294-296; advance online publication, November 17, 2016; 10.1038/gim.2016.171 Abstract | Full Text Original Research Article Top A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome Christopher A. Wassif, Lisa Kratz, Susan E. Sparks, Courtney Wheeler, Simona Bianconi, Andrea Gropman, Karim A. Calis, Richard I. Kelley, Elaine Tierney and Forbes D. Porter Genet Med 2017 19: 297-305; advance online publication, August 11, 2016; 10.1038/gim.2016.102 Abstract | Full Text Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, Jessica M.E. van den Oever, Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koen Devriendt and Joris R. Vermeesch Genet Med 2017 19: 306-313; advance online publication, September 1, 2016; 10.1038/gim.2016.113 Abstract | Full Text Modeling the prevention of colorectal cancer from the combined impact of host and behavioral risk factors OPEN Matthew Frampton and Richard S. Houlston Genet Med 2017 19: 314-321; advance online publication, August 4, 2016; 10.1038/gim.2016.101 Abstract | Full Text Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores OPEN Kristi Läll, Reedik Mägi, Andrew Morris, Andres Metspalu and Krista Fischer Genet Med 2017 19: 322-329; advance online publication, August 11, 2016; 10.1038/gim.2016.103 Abstract | Full Text Effect of decision aid for breast cancer prevention on decisional conflict in women with a BRCA1 or BRCA2 mutation: a multisite, randomized, controlled trial Kelly A. Metcalfe, Cindy-Lee Dennis, Aletta Poll, Susan Armel, Rochelle Demsky, Lindsay Carlsson, Sonia Nanda, Alexander Kiss and Steven A. Narod Genet Med 2017 19: 330-336; advance online publication, September 1, 2016; 10.1038/gim.2016.108 Abstract | Full Text Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results Kyle B. Brothers, Kelly M. East, Whitley V. Kelley, M. Frances Wright, Matthew J. Westbrook, Carla A. Rich, Kevin M. Bowling, Edward J. Lose, E. Martina Bebin, Shirley Simmons, John A. Myers, Greg Barsh, Richard M. Myers, Greg M. Cooper, Jill M. Pulley, Mark A. Rothstein and Ellen Wright Clayton Genet Med 2017 19: 337-344; advance online publication, August 25, 2016; 10.1038/gim.2016.110 Abstract | Full Text Engaging Māori in biobanking and genomic research: a model for biobanks to guide culturally informed governance, operational, and community engagement activities Angela Beaton, Maui Hudson, Moe Milne, Ramari Viola Port, Khyla Russell, Barry Smith, Valmaine Toki, Lynley Uerata, Phillip Wilcox, Karen Bartholomew and Helen Wihongi Genet Med 2017 19: 345-351; advance online publication, September 15, 2016; 10.1038/gim.2016.111 Abstract | Full Text Education Report Top Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population Ashley Kuhl, Sandra van Calcar, Mei Baker, Christine M. Seroogy, Gregory Rice and Jessica Scott Schwoerer Genet Med 2017 19: 352-356; advance online publication, August 11, 2016; 10.1038/gim.2016.104 Abstract | Full Text Brief Report Top Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening David Ng, Celine S. Hong, Larry N. Singh, Jennifer J. Johnston, James C. Mullikin and Leslie G. Biesecker ; on behalf of the NISC Comparative Sequencing Program Genet Med 2017 19: 357-361; advance online publication, August 18, 2016; 10.1038/gim.2016.105 Abstract | Full Text Letter to the Editor Top The ABMGG’s response to a commentary on the decision to create a 24-month specialty of Laboratory Genetics and Genomics V. Reid Sutton and Miriam G. Blitzer ; on behalf of the Board of Directors of the American Board of Medical Genetics and Genomics Genet Med 2017 19: 362-363; advance online publication, November 17, 2016; 10.1038/gim.2016.179 Full Text Addendum Top ADDENDUM: Reviewer Acknowledgment 2016 Genet Med 2017 19: 364; 10.1038/gim.2017.6 Full Text Podcast Top Podcast FREE Podcast You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/nams/svc/myaccount (You will need to log in to be recognised as a nature.com registrant). For further technical assistance, please contact our registration department. For other enquiries, please contact our customer feedback department. 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