Genetics in Medicine contents: Volume 15, Issue 10

Advertisement Circulation: Cardiovascular Genetics is the #1 journal dedicated to cardiovascular genetics, genomics, and systems biology.  Join an esteemed roster of your peers - submit your manuscript for publication in Circulation: Cardiovascular Genetics today. Visit the journal's Information for Authors to learn about preferred article types and how to submit. TABLE OF CONTENTS Volume 15, Issue 10 (October 2013) In this issue Research Highlights Introduction Reviews Invited Commentary Original Research Article Special Article Epilogue Glossary Corrigenda Podcast Advertisement Don't miss out! If you haven't had a chance to read the following NutDi articles access them today. - Insulin stimulation regulates AS160 and TBC1D1 phosphorylation sites in human skeletal muscle OPEN - The relationship between family and child weight status by household structure in South Korea: 2007-2010 OPEN - A simple scoring method using cardiometabolic risk measurements in pregnancy to determine 10-year risk of type 2 diabetes in women with gestational diabetes OPEN   Research Highlights Top In this Issue Genet Med 2013 15: 755-756; 10.1038/gim.2013.152 Full Text News Briefs Genet Med 2013 15: 756; 10.1038/gim.2013.156 Full Text Introduction Top Integration of genomics into the electronic health record: mapping terra incognita Joseph M. Kannry and Marc S. Williams Genet Med 2013 15: 757-760; 10.1038/gim.2013.102 Full Text Reviews Top The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future OPEN Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W. Andrew Faucett, Rongling Li, Teri A. Manolio, Saskia C. Sanderson, Joseph Kannry, Randi Zinberg, Melissa A. Basford, Murray Brilliant, David J. Carey, Rex L. Chisholm, Christopher G. Chute, John J. Connolly, David Crosslin, Joshua C. Denny, Carlos J. Gallego, Jonathan L. Haines, Hakon Hakonarson, John Harley, Gail P. Jarvik, Isaac Kohane, Iftikhar J. Kullo, Eric B. Larson, Catherine McCarty, Marylyn D. Ritchie, Dan M. Roden, Maureen E. Smith, Erwin P. Böttinger and Marc S. Williams and The eMERGE Network Genet Med 2013 15: 761-771; advance online publication, June 6, 2013; 10.1038/gim.2013.72 Abstract | Full Text Practical challenges in integrating genomic data into the electronic health record Abel N. Kho, Luke V. Rasmussen, John J. Connolly, Peggy L. Peissig, Justin Starren, Hakon Hakonarson and M. Geoffrey Hayes Genet Med 2013 15: 772-778; advance online publication, September 26, 2013; 10.1038/gim.2013.131 Abstract | Full Text Storing and interpreting genomic information in widely deployed electronic health record systems Andrew G. Ury Genet Med 2013 15: 779-785; advance online publication, August 15, 2013; 10.1038/gim.2013.111 Abstract | Full Text Clinical genomics in the world of the electronic health record Keith Marsolo and S. Andrew Spooner Genet Med 2013 15: 786-791; advance online publication, July 11, 2013; 10.1038/gim.2013.88 Abstract | Full Text Stakeholder engagement: a key component of integrating genomic information into electronic health records Andrea Hartzler, Catherine A. McCarty, Luke V. Rasmussen, Marc S. Williams, Murray Brilliant, Erica A. Bowton, Ellen Wright Clayton, William A. Faucett, Kadija Ferryman, Julie R. Field, Stephanie M. Fullerton, Carol R. Horowitz, Barbara A. Koenig, Jennifer B. McCormick, James D. Ralston, Saskia C. Sanderson, Maureen E. Smith and Susan Brown Trinidad Genet Med 2013 15: 792-801; advance online publication, September 12, 2013; 10.1038/gim.2013.127 Abstract | Full Text Some experiences and opportunities for big data in translational research Christopher G. Chute, Mollie Ullman-Cullere, Grant M. Wood, Simon M. Lin, Min He and Jyotishman Pathak Genet Med 2013 15: 802-809; advance online publication, September 5, 2013; 10.1038/gim.2013.121 Abstract | Full Text Ethical, legal, and social implications of incorporating genomic information into electronic health records Ribhi Hazin, Kyle B. Brothers, Bradley A. Malin, Barbara A. Koenig, Saskia C. Sanderson, Mark A. Rothstein, Marc S. Williams, Ellen W. Clayton and Iftikhar J. Kullo Genet Med 2013 15: 810-816; advance online publication, September 12, 2013; 10.1038/gim.2013.117 Abstract | Full Text Invited Commentary Top Opportunities for genomic clinical decision support interventions Casey Lynnette Overby, Isaac Kohane, Joseph L Kannry, Marc S Williams, Justin Starren, Erwin Bottinger, Omri Gottesman, Joshua C Denny, Chunhua Weng, Peter Tarczy-Hornoch and George Hripcsak Genet Med 2013 15: 817-823; advance online publication, September 19, 2013; 10.1038/gim.2013.128 Full Text Original Research Article Top A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record Peter Tarczy-Hornoch, Laura Amendola, Samuel J. Aronson, Levi Garraway, Stacy Gray, Robert W. Grundmeier, Lucia A Hindorff, Gail Jarvik, Dean Karavite, Matthew Lebo, Sharon E. Plon, Eliezer Van Allen, Karen E. Weck, Peter S. White and Yaping Yang Genet Med 2013 15: 824-832; advance online publication, September 26, 2013; 10.1038/gim.2013.120 Abstract | Full Text Special Article Top Electronic health record design and implementation for pharmacogenomics: a local perspective Josh F. Peterson, Erica Bowton, Julie R. Field, Marc Beller, Jennifer Mitchell, Jonathan Schildcrout, William Gregg, Kevin Johnson, Jim N. Jirjis, Dan M. Roden, Jill M. Pulley and Josh C. Denny Genet Med 2013 15: 833-841; advance online publication, September 5, 2013; 10.1038/gim.2013.109 Abstract | Full Text Epilogue Top The undiscovered country: the future of integrating genomic information into the EHR Joseph Kannry and Marc S. Williams Genet Med 2013 15: 842-845; advance online publication, September 26, 2013; 10.1038/gim.2013.130 Full Text Glossary Top Glossary Genet Med 2013 15: 846-848; 10.1038/gim.2013.167 Full Text Corrigenda Top CORRIGENDUM: The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders Genet Med 2013 15: 849; 10.1038/gim.2013.147 Full Text CORRIGENDUM: Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome Joseph Muenzer, Michael Beck, Christine M Eng, Roberto Giugliani, Paul Harmatz, Rick Martin, Uma Ramaswami, Ashok Vellodi, James E Wraith, Maureen Cleary, Muge Gucsavas-Calikoglu, Ana Cristina Puga, Marwan Shinawi, Birgit Ulbrich, Suresh Vijayaraghavan, Susanne Wendt, Anne Marie Conway, Alexandra Rossi, David A H Whiteman and Alan Kimura Genet Med 2013 15: 849; 10.1038/gim.2013.132 Full Text Podcast Top Podcast Advertisement Genepod - the monthly podcast from Genetics in Medicine Join us as we delve into the latest research in medical genetics and genomics, featuring highlighted content from this leading journal. Genepod and the contents of GIM should be of interest to anyone who uses genetics or genomics in medical practice or in medically-related research. Listen now at www.nature.com/gim/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. Nature Publishing Group | 75 Varick Street, 9th Floor | New York | NY 10013-1917 | USA Nature Publishing Group's worldwide offices: London - Paris - Munich - New Delhi - Tokyo - Melbourne San Diego - San Francisco - Washington - New York - Boston Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at Brunel Road, Houndmills, Basingstoke, Hampshire RG21 6XS. © 2013 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.