Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families

Whole-genome sequencing and the physician

(2012) A Thorogood et al.   CLINICAL GENETICS

Incidence and predictors of positive and negative effects of BRCA1/2 genetic testing on familial relationships: a 3-year follow-up study

(2012) Julie Lapointe et al.   GENETICS IN MEDICINE

“What does it mean?”: Uncertainties in understanding results of chromosomal microarray testing

(2012) Marian Reiff 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

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

(2012) Wybo Dondorp et al.   HUMAN MUTATION

Copy Number and SNP Arrays in Clinical Diagnostics

(2011) Christian P. Schaaf et al.   Annual Review of Genomics and Human Genetics

Why is genetic screening for autosomal dominant disorders underused in families? The case of hereditary hemorrhagic telangiectasia

(2011) Barbara A. Bernhardt et al.   GENETICS IN MEDICINE

Family communication matters: The impact of telling relatives about unclassified variants and uninformative DNA-test results

(2011) Joël Vos et al.   GENETICS IN MEDICINE

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

(2011) Hutton M Kearney et al.   GENETICS IN MEDICINE

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

Identification of incestuous parental relationships by SNP-based DNA microarrays

(2011) CP Schaaf et al.   LANCET

Varieties of Uncertainty in Health Care

(2011) Paul K. J. Han et al.   MEDICAL DECISION MAKING

The Coming Explosion in Genetic Testing — Is There a Duty to Recontact?

(2011) Reed E. Pyeritz   NEW ENGLAND JOURNAL OF MEDICINE

Molecular Technologies Open New Clinical Genetic Vistas

(2011) L. Jackson et al.   Science Translational Medicine

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

What is a meaningful result? Disclosing the results of genomic research in autism to research participants

(2010) Fiona Alice Miller et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The clinical context of copy number variation in the human genome

(2010) Charles Lee et al.   EXPERT REVIEWS IN MOLECULAR MEDICINE

A blueprint for maternal and child health primary care physician education in medical genetics and genomic medicine: Recommendations of the United States Secretary for Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children

(2010) Alex R Kemper et al.   GENETICS IN MEDICINE

What keeps you up at night? Genetics professionals' distressing experiences in patient care

(2010) Barbara A Bernhardt et al.   GENETICS IN MEDICINE

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

(2010) Melanie Manning et al.   GENETICS IN MEDICINE

Motivating Factors for Physician Ordering of Factor V Leiden Genetic Tests

(2009) Lucia A. Hindorff et al.   ARCHIVES OF INTERNAL MEDICINE

Beyond Information

(2009) Ronald M. Epstein et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Chromosomal Microarray Interpretation: What Is a Child Neurologist to Do?

(2009) Alex R. Paciorkowski et al.   PEDIATRIC NEUROLOGY

Whole Genome Scanning: Resolving Clinical Diagnosis and Management Amidst Complex Data

(2009) Sarah E Ali-Khan et al.   PEDIATRIC RESEARCH

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

(2008) Sandra Darilek et al.   GENETICS IN MEDICINE

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

Understanding Incidental Findings in the Context of Genetics and Genomics

(2008) Mildred K. Cho   JOURNAL OF LAW MEDICINE & ETHICS

Educational Needs in Genetic Medicine: Primary Care Perspectives

(2008) Susan B. Trinidad et al.   Public Health Genomics