Genetic Testing for Inherited Cardiac Diseases in Underserved Populations of Non-European Ancestry Double Disparity

被引：12
作者：
Gerhard, Glenn S. [1 ]
Fisher, Susan G. [2 ,3 ]
Feldman, Arthur M. [4 ]
机构：
[1] Temple Univ, Dept Med Genet & Mol Biochem, Lewis Katz Sch Med, 960 Med Educ & Res Bldg,3500 N Broad St, Philadelphia, PA 19140 USA
[2] Temple Univ, Dept Clin Sci, Lewis Katz Sch Med, Philadelphia, PA 19140 USA
[3] Temple Univ, Temple Clin Res Inst, Lewis Katz Sch Med, Philadelphia, PA 19140 USA
[4] Temple Univ, Dept Med, Lewis Katz Sch Med, Philadelphia, PA 19140 USA
来源：
JAMA CARDIOLOGY | 2018年 / 3卷 / 04期
关键词：
HEALTH;
D O I：
10.1001/jamacardio.2017.5345
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：273 / 274
页数：2
相关论文
共 10 条
[1]   Genetic testing in cardiovascular diseases [J].
Arndt, Anne-Karin ;
MacRae, Calum A. .
CURRENT OPINION IN CARDIOLOGY, 2014, 29 (03) :235-240
[2]   Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology [J].
Brody, Jennifer A. ;
Morrison, Alanna C. ;
Bis, Joshua C. ;
O'Connell, Jeffrey R. ;
Brown, Michael R. ;
Huffman, Jennifer E. ;
Ames, Darren C. ;
Carroll, Andrew ;
Conomos, Matthew P. ;
Gabriel, Stacey ;
Gibbs, Richard A. ;
Gogarten, Stephanie M. ;
Gupta, Namrata ;
Jaquish, Cashell E. ;
Johnson, Andrew D. ;
Lewis, Joshua P. ;
Liu, Xiaoming ;
Manning, Alisa K. ;
Papanicolaou, George J. ;
Pitsillides, Achilleas N. ;
Rice, Kenneth M. ;
Salerno, William ;
Sitlani, Colleen M. ;
Smith, Nicholas L. ;
Heckbert, Susan R. ;
Laurie, Cathy C. ;
Mitchell, Braxton D. ;
Vasan, Ramachandran S. ;
Rich, Stephen S. ;
Rotter, Jerome I. ;
Wilson, James G. ;
Boerwinkle, Eric ;
Psaty, Bruce M. ;
Cupples, L. Adrienne .
NATURE GENETICS, 2017, 49 (11) :1560-1563
[3]   A fast and cost-effective molecular diagnostic tool for genetic diseases involved in sudden cardiac death [J].
Chanavat, Valerie ;
Janin, Alexandre ;
Millat, Gilles .
CLINICA CHIMICA ACTA, 2016, 453 :80-85
[4]   Million Veteran Program: A mega-biobank to study genetic influences on health and disease [J].
Gaziano, John Michael ;
Concato, John ;
Brophy, Mary ;
Fiore, Louis ;
Pyarajan, Saiju ;
Breeling, James ;
Whitbourne, Stacey ;
Deen, Jennifer ;
Shannon, Colleen ;
Humphries, Donald ;
Guarino, Peter ;
Aslan, Mihaela ;
Anderson, Daniel ;
LaFleur, Rene ;
Hammond, Timothy ;
Schaa, Kendra ;
Moser, Jennifer ;
Huang, Grant ;
Muralidhar, Sumitra ;
Przygodzki, Ronald ;
O'Leary, Timothy J. .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2016, 70 :214-223
[5]  
Konski AF, 2017, PERSONALIZED MED B F
[6]   Implementing genomics and pharmacogenomics in the clinic: The National Human Genome Research Institute's genomic medicine portfolio [J].
Manolio, Teri A. .
ATHEROSCLEROSIS, 2016, 253 :225-236
[7]   Genetic Misdiagnoses and the Potential for Health Disparities [J].
Manrai, Arjun K. ;
Funke, Birgit H. ;
Rehm, Heidi L. ;
Olesen, Morten S. ;
Maron, Bradley A. ;
Szolovits, Peter ;
Margulies, David M. ;
Loscalzo, Joseph ;
Kohane, Isaac S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (07) :655-665
[8]  
Palmetto GBA, 2017, ARRHYTHMOGENIC RIGHT
[9]   Who Pays? coverage challenges for cardiovascular Genetic testing-in U.S. Patients [J].
Spoonamore, Katherine G. ;
Johnson, Nicole M. .
FRONTIERS IN CARDIOVASCULAR MEDICINE, 2016, 3
[10]   Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions [J].
Tan, Tiong Yang ;
Dillon, Oliver James ;
Stark, Zornitza ;
Schofield, Deborah ;
Alam, Khurshid ;
Shrestha, Rupendra ;
Chong, Belinda ;
Phelan, Dean ;
Brett, Gemma R. ;
Creed, Emma ;
Jarmolowicz, Anna ;
Yap, Patrick ;
Walsh, Maie ;
Downie, Lilian ;
Amor, David J. ;
Savarirayan, Ravi ;
McGillivray, George ;
Yeung, Alison ;
Peters, Heidi ;
Robertson, Susan J. ;
Robinson, Aaron J. ;
Macciocca, Ivan ;
Sadedin, Simon ;
Bell, Katrina ;
Oshlack, Alicia ;
Georgeson, Peter ;
Thorne, Natalie ;
Gaff, Clara ;
White, Susan M. .
JAMA PEDIATRICS, 2017, 171 (09) :855-862
1