Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study

Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project

(2017) Saskia C Sanderson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients

(2017) Heidi S. Lumish et al.   Journal of Genetic Counseling

Patient preferences regarding incidental genomic findings discovered during tumor profiling

(2016) Melinda L. Yushak et al.   CANCER

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

(2016) Sarah S. Kalia et al.   GENETICS IN MEDICINE

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

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases

(2016) Lotte Krabbenborg et al.   Journal of Genetic Counseling

Research Participants’ Preferences for Hypothetical Secondary Results from Genomic Research

(2016) Julia Wynn et al.   Journal of Genetic Counseling

Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment

(2015) Dean A. Regier et al.   CANADIAN MEDICAL ASSOCIATION JOURNAL

Participant use and communication of findings from exome sequencing: a mixed-methods study

(2015) Katie L. Lewis et al.   GENETICS IN MEDICINE

Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research

(2015) Julia Wynn et al.   Journal of Genetic Counseling

Illustrative case studies in the return of exome and genome sequencing results

(2015) Laura M Amendola et al.   Personalized Medicine

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

(2014) Gail P. Jarvik et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Managing the ethical challenges of next-generation sequencing in genomic medicine

(2014) A. J. Clarke   BRITISH MEDICAL BULLETIN

Attitudes of parents toward the return of targeted and incidental genomic research findings in children

(2014) Conrad V. Fernandez et al.   GENETICS IN MEDICINE

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

Self-guided management of exome and whole-genome sequencing results: changing the results return model

(2013) Joon-Ho Yu et al.   GENETICS IN MEDICINE

Return of incidental findings in genomic medicine: measuring what patients value—development of an instrument to measure preferences for information from next-generation testing (IMPRINT)

(2013) Caroline Savage Bennette et al.   GENETICS IN MEDICINE

Researchers’ views on return of incidental genomic research results: qualitative and quantitative findings

(2013) Robert Klitzman et al.   GENETICS IN MEDICINE

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

(2013) Robert C. Green et al.   GENETICS IN MEDICINE

Return of Secondary Genomic Findings vs Patient Autonomy

(2013) Robert Klitzman et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Reporting Genomic Sequencing Results to Ordering Clinicians

(2013) Robert C. Green et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

“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

What factors may influence psychological well being at three months and one year post BRCA genetic result disclosure?

(2012) Nina Bosch et al.   BREAST

Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study

(2012) Juli Murphy Bollinger et al.   GENETICS IN MEDICINE

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

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

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

(2012) Susan M. Wolf et al.   GENETICS IN MEDICINE

Next-generation sequencing in the clinic: are we ready?

(2012) Leslie G. Biesecker et al.   NATURE REVIEWS GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++

(2010) Eugene V. Davydov et al.   PLoS Computational Biology

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

What Can Interest Tell Us about Uptake of Genetic Testing? Intention and Behavior amongst Smokers Related to Patients with Lung Cancer

(2009) S.C. Sanderson et al.   Public Health Genomics