Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics
出版年份 2022 全文链接
标题
Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics
作者
关键词
-
出版物
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume -, Issue -, Pages -
出版商
Wiley
发表日期
2022-01-04
DOI
10.1002/ajmg.a.62619
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Taking an antiracist posture in scientific publications in human genetics and genomics
- (2021) Kyle B. Brothers et al. GENETICS IN MEDICINE
- Toward the diagnosis of rare childhood genetic diseases: what do parents value most?
- (2021) Samantha Pollard et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Family-level impact of genetic testing: integrating health economics and ethical, legal, and social implications
- (2021) Hadley Stevens Smith et al. Personalized Medicine
- Personal utility of genomic sequencing for infants with congenital deafness
- (2021) Erin Tutty et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Opportunities and pitfalls of social media research in rare genetic diseases: a systematic review
- (2021) Emily G. Miller et al. GENETICS IN MEDICINE
- “Doctors can read about it, they can know about it, but they've never lived with it”: How parents use social media throughout the diagnostic odyssey
- (2021) Natalie T. Deuitch et al. Journal of Genetic Counseling
- A qualitative study of Latinx parents' experiences of clinical exome sequencing
- (2020) Daniel Luksic et al. Journal of Genetic Counseling
- Diversity and inclusion for the All of Us research program: A scoping review
- (2020) Brandy M. Mapes et al. PLoS One
- Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science
- (2020) Kelly Schoch et al. GENETICS IN MEDICINE
- Racial and ethnic differences in knowledge and attitudes about genetic testing in the US: Systematic review
- (2019) Juan R. Canedo et al. Journal of Genetic Counseling
- Spillover Effects on Caregivers’ and Family Members’ Utility: A Systematic Review of the Literature
- (2019) Eve Wittenberg et al. PHARMACOECONOMICS
- On What We Have Learned and Still Need to Learn about the Psychosocial Impacts of Genetic Testing
- (2019) Erik Parens et al. HASTINGS CENTER REPORT
- Exome sequencing: value is in the eye of the beholder
- (2019) Scott D. Grosse et al. GENETICS IN MEDICINE
- Parents’ perceptions of personal utility of exome sequencing results
- (2019) Lonna Mollison et al. GENETICS IN MEDICINE
- Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results
- (2018) Allison Werner-Lin et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project
- (2018) J Scott Roberts et al. GENETICS IN MEDICINE
- A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network
- (2018) Chloe M. Reuter et al. JOURNAL OF PEDIATRICS
- Communication of cancer-related genetic and genomic information: A landscape analysis of reviews
- (2018) Emily B Peterson et al. Translational Behavioral Medicine
- Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease
- (2018) Kimberly Splinter et al. NEW ENGLAND JOURNAL OF MEDICINE
- Defining the Value of Treatments of Rare Pediatric Conditions
- (2018) Lisa A. Prosser JAMA Pediatrics
- Family Spillover Effects in Pediatric Cost-Utility Analyses
- (2018) Tara A. Lavelle et al. Applied Health Economics and Health Policy
- Personal utility in genomic testing: a systematic literature review
- (2017) Jennefer N Kohler et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders
- (2016) Allyn McConkie Rosell et al. Journal of Genetic Counseling
- The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine
- (2016) William A. Gahl et al. MOLECULAR GENETICS AND METABOLISM
- Genomics is failing on diversity
- (2016) Alice B. Popejoy et al. NATURE
- Health as a Family Affair
- (2016) Eve Wittenberg et al. NEW ENGLAND JOURNAL OF MEDICINE
- Patients’ perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project
- (2016) Philip J Lupo et al. Personalized Medicine
- Implicit Racial/Ethnic Bias Among Health Care Professionals and Its Influence on Health Care Outcomes: A Systematic Review
- (2015) William J. Hall et al. AMERICAN JOURNAL OF PUBLIC HEALTH
- Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
- (2015) S.L. Sawyer et al. CLINICAL GENETICS
- FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project
- (2014) Chandree L. Beaulieu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Personal utility in genomic testing: is there such a thing?
- (2014) Eline M Bunnik et al. JOURNAL OF MEDICAL ETHICS
- The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders
- (2013) Vandana Shashi et al. GENETICS IN MEDICINE
- Personal utility and genomic information: Look before you leap
- (2009) Scott D Grosse et al. GENETICS IN MEDICINE
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