Friday, July 6, 2012

Genetics in Medicine contents: Volume 14, Issue 7


TABLE OF CONTENTS

Volume 14, Issue 7 (July 2012)

In this issue
Research Highlights
Review
Special Article
Original Research Article
ACMG College News
In Memoriam
Corrigendum

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Research Highlights

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Enhanced interpretation of newborn screening results without analyte cutoff values

Genet Med 2012 14: 631; 10.1038/gim.2012.69

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News Briefs

Genet Med 2012 14: 631-632; 10.1038/gim.2012.70

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Review

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Building the evidence base for decision making in cancer genomic medicine using comparative effectiveness research

Katrina A.B. Goddard, William A. Knaus, Evelyn Whitlock, Gary H. Lyman, Heather Spencer Feigelson, Sheri D. Schully, Scott Ramsey, Sean Tunis, Andrew N. Freedman, Muin J. Khoury and David L. Veenstra

Genet Med 2012 14: 633-642; advance online publication, April 19, 2012; 10.1038/gim.2012.16

Abstract | Full Text

Special Article

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Knowledge integration at the center of genomic medicine

Muin J. Khoury, Marta Gwinn, W. David Dotson and Sheri D. Schully

Genet Med 2012 14: 643-647; advance online publication, May 3, 2012; 10.1038/gim.2012.43

Abstract | Full Text

Original Research Articles

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Enhanced interpretation of newborn screening results without analyte cutoff values

Gregg Marquardt, Robert Currier, David M.S. McHugh, Dimitar Gavrilov, Mark J. Magera, Dietrich Matern, Devin Oglesbee, Kimiyo Raymond, Piero Rinaldo, Emily H. Smith, Silvia Tortorelli, Coleman T. Turgeon, Fred Lorey, Bridget Wilcken, Veronica Wiley, Lawrence C. Greed, Barry Lewis, François Boemer, Roland Schoos, Sandrine Marie, Marie-Françoise Vincent, Yuri Cleverthon Sica, Mouseline Torquado Domingos, Khalid Al-Thihli, Graham Sinclair, Osama Y. Al-Dirbashi, Pranesh Chakraborty, Mark Dymerski, Cory Porter, Adrienne Manning, Margretta R. Seashore, Jonessy Quesada, Alejandra Reuben, Petr Chrastina, Petr Hornik, Iman Atef Mandour, Sahar Abdel Atty Sharaf, Olaf Bodamer, Bonifacio Dy, Jasmin Torres, Roberto Zori, David Cheillan, Christine Vianey-Saban, David Ludvigson, Adrya Stembridge, Jim Bonham, Melanie Downing, Yannis Dotsikas, Yannis L. Loukas, Vagelis Papakonstantinou, Georgios S.A. Zacharioudakis, Ákos Baráth, Eszter Karg, Leifur Franzson, Jon J. Jonsson, Nancy N. Breen, Barbara G. Lesko, Stanton L. Berberich, Kimberley Turner, Margherita Ruoppolo, Emanuela Scolamiero, Italo Antonozzi, Claudia Carducci, Ubaldo Caruso, Michela Cassanello, Giancarlo la Marca, Elisabetta Pasquini, Iole Maria Di Gangi, Giuseppe Giordano, Marta Camilot, Francesca Teofoli, Shawn M. Manos, Colleen K. Peterson, Stephanie K. Mayfield Gibson, Darrin W. Sevier, Soo-Youn Lee, Hyung-Doo Park, Issam Khneisser, Phaidra Browning, Fizza Gulamali-Majid, Michael S. Watson, Roger B. Eaton, Inderneel Sahai, Consuelo Ruiz, Rosario Torres, Mary A. Seeterlin, Eleanor L. Stanley, Amy Hietala, Mark McCann, Carlene Campbell, Patrick V. Hopkins, Monique G. de Sain–Van der Velden, Bert Elvers, Mark A. Morrissey, Sherlykutty Sunny, Detlef Knoll, Dianne Webster, Dianne M. Frazier, Julie D. McClure, David E. Sesser, Sharon A. Willis, Hugo Rocha, Laura Vilarinho, Catharine John, James Lim, S. Graham Caldwell, Kathy Tomashitis, Daisy E. Castiñeiras Ramos, Jose Angel Cocho de Juan, Inmaculada Rueda Fernández, Raquel Yahyaoui Macías, José María Egea-Mellado, Inmaculada González-Gallego, Carmen Delgado Pecellin, Maria Sierra García-Valdecasas Bermejo, Yin-Hsiu Chien, Wuh-Liang Hwu, Thomas Childs, Christine D. McKeever, Tijen Tanyalcin, Mahera Abdulrahman, Cecilia Queijo, Aída Lemes, Tim Davis, William Hoffman, Mei Baker and Gary L. Hoffman

Genet Med 2012 14: 648-655; advance online publication, February 16, 2012; 10.1038/gim.2012.2

Abstract | Full Text

Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies

Patricia A. Deverka, Sheri D. Schully, Naoko Ishibe, Josh J. Carlson, Andrew Freedman, Katrina A.B. Goddard, Muin J. Khoury and Scott D. Ramsey

Genet Med 2012 14: 656-662; advance online publication, April 5, 2012; 10.1038/gim.2012.3

Abstract | Full Text

Toward modernizing the systematic review pipeline in genetics: efficient updating via data mining

Byron C. Wallace, Kevin Small, Carla E. Brodley, Joseph Lau, Christopher H. Schmid, Lars Bertram, Christina M. Lill, Joshua T. Cohen and Thomas A. Trikalinos

Genet Med 2012 14: 663-669; advance online publication, April 5, 2012; 10.1038/gim.2012.7

Abstract | Full Text

Performance of PREMM1,2,6, MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases

Rowena C. Mercado, Heather Hampel, Fay Kastrinos, Ewout Steyerberg, Judith Balmana, Elena Stoffel, David E. Cohn, Floor J. Backes, John L. Hopper, Mark A. Jenkins, Noralane M. Lindor, Graham Casey, Robert Haile, Subha Madhavan, Albert de la Chapelle and Sapna Syngal and the Colon Cancer Family Registry

Genet Med 2012 14: 670-680; advance online publication, March 8, 2012; 10.1038/gim.2012.18

Abstract | Full Text

Patients’ understanding of and responses to multiplex genetic susceptibility test results

Kimberly A. Kaphingst, Colleen M. McBride, Christopher Wade, Sharon Hensley Alford, Robert Reid, Eric Larson, Andreas D. Baxevanis and Lawrence C. Brody

Genet Med 2012 14: 681-687; advance online publication, April 5, 2012; 10.1038/gim.2012.22

Abstract | Full Text

BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening

Shiri Shkedi-Rafid, Efrat Gabai-Kapara, Julia Grinshpun-Cohen and Ephrat Levy-Lahad

Genet Med 2012 14: 688-694; advance online publication, April 5, 2012; 10.1038/gim.2012.31

Abstract | Full Text

ACMG College News

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ACMG College news

Genet Med 2012 14: 695-696; 10.1038/gim.2012.75

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In Memoriam

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David L. Rimoin, MD, PhD 1936–2012

Reed E. Pyeritz

Genet Med 2012 14: 697-698; 10.1038/gim.2012.79

Full Text

Corrigendum

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CORRIGENDUM: Biobanking: shifting the analogy from consent to surrogacy

Genet Med 2012 14: 699; 10.1038/gim.2012.17

Full Text

Podcast

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Podcast

 
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1 comment:

Anonymous said...

Great post! I came across your article while I was reading up on sample management software. I'm happy I did because you have shared some great information about biobanking. I really think that biobanking has become very important in this day and age, thank you for sharing this with us.