Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy

Author:

Christian SusanORCID,Atallah Joseph,Clegg Robin,Giuffre Michael,Huculak Cathleen,Dzwiniel Tara,Parboosingh Jillian,Taylor Sherryl,Somerville Martin

Publisher

Wiley

Subject

Genetics (clinical)

Reference15 articles.

1. Ackerman, M. J., Priori, S. G., Willems, S., Berul, C., Brugada, R., Calkins, H., Camm, J., Ellinor, P. T., Gollob, M., Hamilton, R., Hershberger, R. E., Judge, D. P., Le Marec, H., McKenna, W. J., Schulze-Bahr, E., Semsarian, C., Towbin, J. A., Watkins, H., Wilde, A., Wolpert, C., & Zipes, D. P. (2011). HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the heart rhythm society (HRS) and the european heart rhythm association (EHRA). Heart Rhythm: The Official Journal of the Heart Rhythm Society, 8(8), 1308–1339.

2. Alderfer, M. A., Zelley, K., Lindell, R. B., Novokmet, A., Mai, P. L., Garber, J. E., Nathan, D., Scollon, S., Chun, N. M., Patenaude, A. F., Ford, J. M., Plon, S. E., Schiffman, D., Diller, L. R., Savage, S. A., Malkin, D., Ford, C. A., & Nichols, K. E. (2015). Parent decision-making around the genetic testing of children for germline TP53 mutations. Cancer, 121(2), 286–293.

3. Botkin, J. R., Belmont, J. W., Berg, J. S., Berkman, B. E., Bombard, Y., Holm, I. A., Levy, H. P., Ormond, K. E., Saal, H. M., Spinner, N. B., Wilfond, B. S., & McInerney, J. D. (2015). Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Journal of Human Genetics, 97(1), 6–21.

4. Charron, P., Arad, M., Arbustini, E., Basso, C., Bilinska, Z., Elliott, P., Helio, T., Keren, A., McKenna, W. J., Monserrat, L., Seggewiss, H., van Langen, I., Tavazzi, L., & European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. (2010). Genetic counselling and testing in cardiomyopathies: A position statement of the european society of cardiology working group on myocardial and pericardial diseases. European Heart Journal, 31(22), 2715–2726.

5. Christiaans, I., Birnie, E., Bonsel, G. J., Wilde, A. A., & van Langen, I. M. (2008). Uptake of genetic counselling and predicitive DNA testing in hypertrophic cardiomyopathy. European Journal of Human Genetics : EJHG, 16(10), 1201–1207.

Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3