Whole-genome sequencing in critically ill infants and emerging ethical challenges

被引:7
作者
Char, Danton S. [1 ]
机构
[1] Stanford Univ, Dept Anesthesiol, Med Ctr, Stanford, CA 94305 USA
关键词
D O I
10.1016/S2213-2600(15)00151-4
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
引用
收藏
页码:333 / 335
页数:3
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共 10 条
[1]   Whole-Genome Sequencing for Optimized Patient Management [J].
Bainbridge, Matthew N. ;
Wiszniewski, Wojciech ;
Murdock, David R. ;
Friedman, Jennifer ;
Gonzaga-Jauregui, Claudia ;
Newsham, Irene ;
Reid, Jeffrey G. ;
Fink, John K. ;
Morgan, Margaret B. ;
Gingras, Marie-Claude ;
Muzny, Donna M. ;
Hoang, Linh D. ;
Yousaf, Shahed ;
Lupski, James R. ;
Gibbs, Richard A. .
SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (87)
[2]   Exome sequencing as a tool for Mendelian disease gene discovery [J].
Bamshad, Michael J. ;
Ng, Sarah B. ;
Bigham, Abigail W. ;
Tabor, Holly K. ;
Emond, Mary J. ;
Nickerson, Deborah A. ;
Shendure, Jay .
NATURE REVIEWS GENETICS, 2011, 12 (11) :745-755
[3]   Whole genome sequencing in critically ill children [J].
Char, Danton S. ;
Cho, Mildred ;
Magnus, David .
LANCET RESPIRATORY MEDICINE, 2015, 3 (04) :264-266
[4]   Annual Summary of Vital Statistics: 2009 [J].
Kochanek, Kenneth D. ;
Kirmeyer, Sharon E. ;
Martin, Joyce A. ;
Strobino, Donna M. ;
Guyer, Bernard .
PEDIATRICS, 2012, 129 (02) :338-348
[5]  
Priest JR, 2014, HEART RHYTHM, V11, P1707, DOI [10.1016/j.hrthm.20l4.06.030, 10.1016/j.hrthm.2014.06.030]
[6]   Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units [J].
Saunders, Carol Jean ;
Miller, Neil Andrew ;
Soden, Sarah Elizabeth ;
Dinwiddie, Darrell Lee ;
Noll, Aaron ;
Abu Alnadi, Noor ;
Andraws, Nevene ;
Patterson, Melanie LeAnn ;
Krivohlavek, Lisa Ann ;
Fellis, Joel ;
Humphray, Sean ;
Saffrey, Peter ;
Kingsbury, Zoya ;
Weir, Jacqueline Claire ;
Betley, Jason ;
Grocock, Russell James ;
Margulies, Elliott Harrison ;
Farrow, Emily Gwendolyn ;
Artman, Michael ;
Safina, Nicole Pauline ;
Petrikin, Joshua Erin ;
Hall, Kevin Peter ;
Kingsmore, Stephen Francis .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (154)
[7]   Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders [J].
Soden, Sarah E. ;
Saunders, Carol J. ;
Willig, Laurel K. ;
Farrow, Emily G. ;
Smith, Laurie D. ;
Petrikin, Josh E. ;
LePichon, Jean-Baptiste ;
Miller, Neil A. ;
Thiffault, Isabelle ;
Dinwiddie, Darrell L. ;
Twist, Greyson ;
Noll, Aaron ;
Heese, Bryce A. ;
Zellmer, Lee ;
Atherton, Andrea M. ;
Abdelmoity, Ahmed T. ;
Safina, Nicole ;
Nyp, Sarah S. ;
Zuccarelli, Britton ;
Larson, Ingrid A. ;
Modrcin, Ann ;
Herd, Suzanne ;
Creed, Mitchell ;
Ye, Zhaohui ;
Yuan, Xuan ;
Brodsky, Robert A. ;
Kingsmore, Stephen F. .
SCIENCE TRANSLATIONAL MEDICINE, 2014, 6 (265)
[8]   Genomic medicine: evolving science, evolving ethics [J].
Soden, Sarah E. ;
Farrow, Emily G. ;
Saunders, Carol J. ;
Lantos, John D. .
PERSONALIZED MEDICINE, 2012, 9 (05) :523-528
[9]  
Willig LK, 2015, LANCET RESPIR MED
[10]   Managing incidental findings in human subjects research: Analysis and recommendations [J].
Wolf, Susan M. ;
Lawrenz, Frances P. ;
Nelson, Charles A. ;
Kahn, Jeffrey P. ;
Cho, Mildred K. ;
Clayton, Ellen Wright ;
Fletcher, Joel G. ;
Georgieff, Michael K. ;
Hammerschmidt, Dale ;
Hudson, Kathy ;
Illes, Judy ;
Kapur, Vivek ;
Keane, Moira A. ;
Koenig, Barbara A. ;
LeRoy, Bonnie S. ;
McFarland, Elizabeth G. ;
Paradise, Jordan ;
Parker, Lisa S. ;
Terry, Sharon F. ;
Van Ness, Brian ;
Wilfond, Benjamin S. .
JOURNAL OF LAW MEDICINE & ETHICS, 2008, 36 (02) :219-248