Genetic Counselors’ Views and Experiences with the Clinical Integration of Genome Sequencing

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

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

Identifying Personal Genomes by Surname Inference

(2013) M. Gymrek et al.   SCIENCE

Ethics and Genomic Incidental Findings

(2013) A. L. McGuire et al.   SCIENCE

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

Whole-Genome and Whole-Exome Sequencing in Hereditary Cancer

(2012) Julianne M. O’Daniel et al.   CANCER JOURNAL

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

(2012) Ros Hastings et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Points to consider in the clinical application of genomic sequencing

(2012)   GENETICS IN MEDICINE

Santorini mutation detection meeting 2011: Rapid advance in sequencing technology poses challenges for interpretation of genetic variations

(2012) Eleana F. Stavrou et al.   HUMAN MUTATION

Iodotyrosine Deiodinase Defect Identified via Genome-Wide Approach

(2012) Agnès Burniat et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders

(2012) Bahareh Rabbani et al.   JOURNAL OF HUMAN GENETICS

The clinical implementation of whole genome sequencing: a conversation with seven scientific experts

(2012) Jordan P. Lerner-Ellis   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical application of exome sequencing in undiagnosed genetic conditions

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

Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease

(2012) Jose Bras et al.   NATURE REVIEWS NEUROSCIENCE

Human Genetic Variation, Shared and Private

(2012) F. Casals et al.   SCIENCE

Whole-Genome Sequencing: The New Standard of Care?

(2012) L. R. Brunham et al.   SCIENCE

Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research

(2011) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Human Genome Sequencing in Health and Disease

(2011) Claudia Gonzaga-Jauregui et al.   Annual Review of Medicine

Strategies for exome and genome sequence data analysis in disease-gene discovery projects

(2011) PN Robinson et al.   CLINICAL GENETICS

Performance comparison of whole-genome sequencing platforms

(2011) Hugo Y K Lam et al.   NATURE BIOTECHNOLOGY

Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

(2010) Elizabeth A Worthey et al.   GENETICS IN MEDICINE

Challenges in the clinical application of whole-genome sequencing

(2010) Kelly E Ormond et al.   LANCET

Clinical assessment incorporating a personal genome

(2010) Euan A Ashley et al.   LANCET

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

Sequencing technologies — the next generation

(2009) Michael L. Metzker   NATURE REVIEWS GENETICS