Genetics in Medicine contents: Volume 15, Issue 6

TABLE OF CONTENTS Volume 15, Issue 6 (June 2013) In this issue Research Highlights Reviews Commentary Editorial Special Article Original Research Article Education Report Brief Reports ACMG Policy Statement ACMG Standards and Guidelines Podcast Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Take part in our reader survey for a chance to win a MacBook Air As a reader of NPG's clinical and society-owned journals, we invite you to take part in a survey on your use of our journals and their associated websites. Take the survey and be entered into a prize draw for a MacBook Air* *Terms & conditions apply   Research Highlights Top In This Issue Genet Med 2013 15: 413-414; 10.1038/gim.2013.70 Full Text News Briefs Genet Med 2013 15: 413-414; 10.1038/gim.2013.81 Full Text Reviews Top Achieving the “triple aim” for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework Open Beth K. Potter, Pranesh Chakraborty, Jonathan B. Kronick, Kumanan Wilson, Doug Coyle, Annette Feigenbaum, Michael T. Geraghty, Maria D. Karaceper, Julian Little, Aizeddin Mhanni, John J. Mitchell, Komudi Siriwardena, Brenda J. Wilson and Ania Syrowatka ; on behalf of the Canadian Inherited Metabolic Diseases Research Network Genet Med 2013 15: 415-422; advance online publication, December 6, 2012; 10.1038/gim.2012.153 Abstract | Full Text Incorporating genomics into breast and prostate cancer screening: assessing the implications Open Susmita Chowdhury, Tom Dent, Nora Pashayan, Alison Hall, Georgios Lyratzopoulos, Nina Hallowell, Per Hall, Paul Pharoah and Hilary Burton Genet Med 2013 15: 423-432; advance online publication, February 14, 2013; 10.1038/gim.2012.167 Abstract | Full Text Commentary Top Cell-free fetal DNA testing: who is driving implementation? Jessica Mozersky and Michael T. Mennuti Genet Med 2013 15: 433-434; advance online publication, December 6, 2012; 10.1038/gim.2012.156 Full Text Editorial Top Return of results to the families of children in genomic sequencing: tallying risks and benefits James P. Evans Genet Med 2013 15: 435-436; 10.1038/gim.2013.54 Full Text Special Article Top How can polygenic inheritance be used in population screening for common diseases? Muin J. Khoury, A. Cecile J.W. Janssens and David F. Ransohoff Genet Med 2013 15: 437-443; advance online publication, February 14, 2013; 10.1038/gim.2012.182 Abstract | Full Text Original Research Articles Top Effective communication of molecular genetic test results to primary care providers Maren T. Scheuner, Maria Orlando Edelen, Lee H. Hilborne and Ira M. Lubin ; for the members of the RAND Molecular Genetic Test Report Advisory Board Genet Med 2013 15: 444-449; advance online publication, December 6, 2012; 10.1038/gim.2012.151 Abstract | Full Text Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era? Weimin Bi, Caroline Borgan, Amber N. Pursley, Patricia Hixson, Chad A. Shaw, Carlos A. Bacino, Seema R. Lalani, Ankita Patel, Pawel Stankiewicz, James R. Lupski, Arthur L. Beaudet and Sau Wai Cheung Genet Med 2013 15: 450-457; advance online publication, December 13, 2012; 10.1038/gim.2012.152 Abstract | Full Text The responses of research participants and their next of kin to receiving feedback of genetic test results following participation in the Australian Ovarian Cancer Study The Australian Ovarian Cancer Study Group:  Nina Hallowell, Kathryn Alsop, Margaret Gleeson, Ashley Crook, Loren Plunkett, David Bowtell and Gillian Mitchell Mary-Anne Young Genet Med 2013 15: 458-465; advance online publication, February 28, 2013; 10.1038/gim.2012.154 Abstract | Full Text Education Report Top Developing a comprehensive, effective patient-friendly website to enhance decision making in predictive testing for Huntington disease Alice K. Hawkins Virani, S.M. Creighton and M.R. Hayden Genet Med 2013 15: 466-472; advance online publication, December 6, 2012; 10.1038/gim.2012.149 Abstract | Full Text Brief Reports Top Informatics-based, highly accurate, noninvasive prenatal paternity testing Open Allison Ryan, Johan Baner, Zachary Demko, Matthew Hill, Styrmir Sigurjonsson, Michael L. Baird and Matthew Rabinowitz Genet Med 2013 15: 473-477; advance online publication, December 20, 2012; 10.1038/gim.2012.155 Abstract | Full Text Estimates of penetrance for recurrent pathogenic copy-number variations Open Jill A. Rosenfeld, Bradley P. Coe, Evan E. Eichler, Howard Cuckle and Lisa G. Shaffer Genet Med 2013 15: 478-481; advance online publication, December 20, 2012; 10.1038/gim.2012.164 Abstract | Full Text ACMG Policy Statement Top ACMG position statement on prenatal/preconception expanded carrier screening Wayne W. Grody, Barry H. Thompson, Anthony R. Gregg, Lora H. Bean, Kristin G. Monaghan, Adele Schneider and Roger V. Lebo Genet Med 2013 15: 482-483; advance online publication, April 25, 2013; 10.1038/gim.2013.47 Abstract | Full Text ACMG Standards and Guidelines Top American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders A Working Group of the American College of Medical Genetics and Genomics (ACMG) Laboratory Quality Assurance Committee Genet Med 2013 15: 484-494; advance online publication, April 25, 2013; 10.1038/gim.2013.49 Abstract | Full Text Podcast Top Podcast Advertisement Take part in our reader survey for a chance to win a MacBook Air As a reader of NPG's clinical and society-owned journals, we invite you to take part in a survey on your use of our journals and their associated websites. Take the survey and be entered into a prize draw for a MacBook Air* *Terms & conditions apply Please note that you need to be a subscriber or site-license holder to enjoy full-text access to Clinical Pharmacology & Therapeutics. In order to do so, please purchase a subscription. 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 print subscription enquiries, please contact our subscription department. For other enquiries, please contact our customer feedback department. 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