Growing Up in the Genomic Era: Implications of Whole-Genome Sequencing for Children, Families, and Pediatric Practice

Technical report: ethical and policy issues in genetic testing and screening of children

(2013) Laine Friedman Ross et al.   GENETICS IN MEDICINE

Ethical and Policy Issues in Genetic Testing and Screening of Children

(2013) et al.   PEDIATRICS

Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms

(2012) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

“I want to know what's in Pandora's box”: Comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing

(2012) Anne Townsend et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

An Evidence Integration Triangle for Aligning Science with Policy and Practice

(2012) Russell E. Glasgow et al.   AMERICAN JOURNAL OF PREVENTIVE MEDICINE

Ethical Issues with Newborn Screening in the Genomics Era

(2012) Beth A. Tarini et al.   Annual Review of Genomics and Human Genetics

Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

(2012) Flavia M Facio et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

(2012) William A. Gahl et al.   GENETICS IN MEDICINE

Taxonomizing, sizing and overcoming the incidentalome

(2012) Isaac S. Kohane et al.   GENETICS IN MEDICINE

Improving the efficiency and relevance of evidence-based recommendations in the era of whole-genome sequencing: an EGAPP methods update

(2012) David L. Veenstra et al.   GENETICS IN MEDICINE

Association between health-service use and multiplex genetic testing

(2012) Robert J. Reid et al.   GENETICS IN MEDICINE

Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project

(2012) Leslie G. Biesecker   GENETICS IN MEDICINE

Exploring concordance and discordance for return of incidental findings from clinical sequencing

(2012) Robert C. Green et al.   GENETICS IN MEDICINE

Communicating inherited genetic risk between parent and child: A meta-thematic synthesis

(2012) Emma Rowland et al.   INTERNATIONAL JOURNAL OF NURSING STUDIES

The Ethical Hazards and Programmatic Challenges of Genomic Newborn Screening

(2012) Aaron J. Goldenberg et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Clinical application of exome sequencing in undiagnosed genetic conditions

(2012) Anna C Need et al.   JOURNAL OF MEDICAL GENETICS

The Pediatric Cancer Genome Project

(2012) James R Downing et al.   NATURE GENETICS

Incidental Medical Information in Whole-Exome Sequencing

(2012) B. D. Solomon et al.   PEDIATRICS

A public resource facilitating clinical use of genomes

(2012) Madeleine P. Ball et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Preferences among Diseases on a Genetic Susceptibility Test for Common Health Conditions: An Ancillary Study of the Multiplex Initiative

(2012) C.H. Wade et al.   Public Health Genomics

Genetic Service Delivery: Infrastructure, Assessment and Information

(2012) C.I. Kaye   Public Health Genomics

The Ultimate Genetic Test

(2012) R. Drmanac   SCIENCE

Whole-Genome Sequencing: The New Standard of Care?

(2012) L. R. Brunham et al.   SCIENCE

Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units

(2012) C. J. Saunders et al.   Science Translational Medicine

Chromosomal Haplotypes by Genetic Phasing of Human Families

(2011) Jared C. Roach et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Whole exome and whole genome sequencing

(2011) David Bick et al.   CURRENT OPINION IN PEDIATRICS

Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time

(2011) Jonathan S Berg et al.   GENETICS IN MEDICINE

Genomics Education for Health Care Professionals in the 21st Century

(2011) W. Gregory Feero et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Family Physicians’ Awareness and Knowledge of the Genetic Information Non-Discrimination Act (GINA)

(2011) Amanda L. Laedtke et al.   Journal of Genetic Counseling

Personalized genomic medicine: Lessons from the exome

(2011) Benjamin D. Solomon et al.   MOLECULAR GENETICS AND METABOLISM

Charting a course for genomic medicine from base pairs to bedside

(2011) Eric D. Green et al.   NATURE

Effect of Direct-to-Consumer Genomewide Profiling to Assess Disease Risk

(2011) Cinnamon S. Bloss et al.   NEW ENGLAND JOURNAL OF MEDICINE

Parents' Attitudes Toward Pediatric Genetic Testing for Common Disease Risk

(2011) K. P. Tercyak et al.   PEDIATRICS

Public Attitudes and Beliefs About Genetics

(2010) Celeste M. Condit   Annual Review of Genomics and Human Genetics

Application of genomics for risk stratification of childhood acute lymphoblastic leukaemia: from bench to bedside?

(2010) Shai Izraeli   BRITISH JOURNAL OF HAEMATOLOGY

Effects of genetic risk information on children's psychosocial wellbeing: A systematic review of the literature

(2010) Christopher H Wade et al.   GENETICS IN MEDICINE

The Prospect of Genome-guided Preventive Medicine: A Need and Opportunity for Genetic Counselors

(2010) Julianne M. O’Daniel   Journal of Genetic Counseling

Stakeholder Perspectives on a Risk-Benefit Framework for Genetic Testing

(2010) Joshua A. Roth et al.   Public Health Genomics

Ensuring the Safe Use of Genomic Medicine in Children

(2009) Susanne B. Haga et al.   CLINICAL PEDIATRICS

Health-related direct-to-consumer genetic testing: a review of companies’ policies with regard to genetic testing in minors

(2009) Pascal Borry et al.   Familial Cancer

Primary care providers’ willingness to recommend BRCA1/2 testing to adolescents

(2009) Suzanne C. O’Neill et al.   Familial Cancer

On the development of a decision support intervention for mothers undergoing BRCA1/2 cancer genetic testing regarding communicating test results to their children

(2009) Beth N. Peshkin et al.   Familial Cancer

A Systematic Review of Literature About the Genetic Testing of Adolescents

(2009) Lynn Rew et al.   Journal for Specialists in Pediatric Nursing

Parents' Interest in Predictive Genetic Testing for Their Children When a Disease Has No Treatment

(2009) B. A. Tarini et al.   PEDIATRICS

Consent for Newborn Screening: The Attitudes of Health Care Providers

(2009) F.A. Miller et al.   Public Health Genomics

Revisting wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years

(2008) Anne Andermann   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Too Many Referrals of Low-Risk Women for BRCA1/2 Genetic Services by Family Physicians

(2008) D. B. White et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research

(2008) Alison Metcalfe et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Differential use of available genetic tests among primary care physicians in the United States: results of a national survey

(2008) Alexandra E Shields et al.   GENETICS IN MEDICINE

Delivery of Genomic Medicine for Common Chronic Adult Diseases

(2008) Maren T. Scheuner et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Minors and informed consent in carrier testing: a survey of European clinical geneticists

(2008) P Borry et al.   JOURNAL OF MEDICAL ETHICS

Predictive genetic testing of children for adult-onset diseases and psychological harm

(2008) P J Malpas   JOURNAL OF MEDICAL ETHICS

Predictive genetic testing in minors for adult-onset genetic diseases

(2008) Pascal Borry et al.   MOUNT SINAI JOURNAL OF MEDICINE

Sisters in hereditary breast and ovarian cancer families: communal coping, social integration, and psychological well-being

(2008) Laura M. Koehly et al.   PSYCHO-ONCOLOGY