Related references
Note: Only part of the references are listed.Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background
Kelly E. Ormond et al.
GENETICS IN MEDICINE (2019)
Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions
Sulev Reisberg et al.
GENETICS IN MEDICINE (2019)
Consumer use and response to online third-party raw DNA interpretation services
Catharine Wang et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2018)
The dawn of consumer-directed testing
Erica Ramos et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2018)
Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years
Michael D. Linderman et al.
BMC MEDICAL GENOMICS (2018)
Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization
Devanshi Patel et al.
JOURNAL OF GENETIC COUNSELING (2018)
The personal and clinical utility of polygenic risk scores
Ali Torkamani et al.
NATURE REVIEWS GENETICS (2018)
The impact of genetic counselors' use of facilitative strategies on cognitive and emotional processing of genetic risk disclosure for Alzheimer's disease
Yue Guan et al.
PATIENT EDUCATION AND COUNSELING (2018)
Effect of the Apolipoprotein E Genotype on Cognitive Change During a Multidomain Lifestyle Intervention A Subgroup Analysis of a Randomized Clinical Trial
Alina Solomon et al.
JAMA NEUROLOGY (2018)
Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations
Amit V. Khera et al.
NATURE GENETICS (2018)
Ancestry Testing and the Practice of Genetic Counseling
Brianne E. Kirkpatrick et al.
JOURNAL OF GENETIC COUNSELING (2017)
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
Julie Lecarpentier et al.
JOURNAL OF CLINICAL ONCOLOGY (2017)
Genetic prediction of male pattern baldness
Saskia P. Hagenaars et al.
PLOS GENETICS (2017)
Potentially modifiable lifestyle factors, cognitive reserve, and cognitive function in later life: A cross-sectional study
Linda Clare et al.
PLOS MEDICINE (2017)
Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score
Rahul S. Desikan et al.
PLOS MEDICINE (2017)
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients A Pilot Randomized Trial
Jason L. Vassy et al.
ANNALS OF INTERNAL MEDICINE (2017)
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
Alicia R. Martin et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
Are physicians prepared for whole genome sequencing? a qualitative analysis
K. D. Christensen et al.
CLINICAL GENETICS (2016)
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public
Saskia C. Sanderson et al.
GENETICS IN MEDICINE (2016)
A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research
Andrew J. Darnell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Advancing Pharmacogenomics Education in the Core PharmD Curriculum through Student Personal Genomic Testing
Solomon M. Adams et al.
AMERICAN JOURNAL OF PHARMACEUTICAL EDUCATION (2016)
The Relationship Between Burnout and Occupational Stress in Genetic Counselors
Brittney Johnstone et al.
JOURNAL OF GENETIC COUNSELING (2016)
Company disclosure and consumer perceptions of the privacy implications of direct-to-consumer genetic testing
Emily Christofides et al.
NEW GENETICS AND SOCIETY (2016)
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR Study
Frederick E. Dewey et al.
SCIENCE (2016)
Beyond clinical utility: The multiple values of DTC genetics
Mauro Turrini et al.
APPLIED AND TRANSLATIONAL GENOMICS (2016)
Identification of type 2 diabetes subgroups through topological analysis of patient similarity
Li Li et al.
SCIENCE TRANSLATIONAL MEDICINE (2015)
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases
Neil A. Miller et al.
GENOME MEDICINE (2015)
Who is at Risk for Compassion Fatigue? An Investigation of Genetic Counselor Demographics, Anxiety, Compassion Satisfaction, and Burnout
Whiwon Lee et al.
JOURNAL OF GENETIC COUNSELING (2015)
Personal utility in genomic testing: is there such a thing?
Eline M. Bunnik et al.
JOURNAL OF MEDICAL ETHICS (2015)
The growth and gaps of genetic data sharing policies in the United States
Jalayne J. Arias et al.
JOURNAL OF LAW AND THE BIOSCIENCES (2015)
Translational research is a key to nongeneticist physicians' genomics education
W. Gregory Feero et al.
GENETICS IN MEDICINE (2014)
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Ali Amin Al Olama et al.
NATURE GENETICS (2014)
Physicians' Preparedness for Integration of Genomic and Pharmacogenetic Testing into Practice Within a Major Healthcare System
Christina G. Selkirk et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS (2013)
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Robert C. Green et al.
GENETICS IN MEDICINE (2013)
Seven new loci associated with age-related macular degeneration
Lars G. Fritsche et al.
NATURE GENETICS (2013)
Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy
Chia-Chan Liu et al.
NATURE REVIEWS NEUROLOGY (2013)
Evidence That Personal Genome Testing Enhances Student Learning in a Course on Genomics and Personalized Medicine
Keyan Salari et al.
PLOS ONE (2013)
Identifying Personal Genomes by Surname Inference
Melissa Gymrek et al.
SCIENCE (2013)
Broadening research consent in the era of genome-informed medicine
Courtney Kronenthal et al.
GENETICS IN MEDICINE (2012)
Association of Cytochrome P450 2C19 Genotype With the Antiplatelet Effect and Clinical Efficacy of Clopidogrel Therapy
Alan R. Shuldiner et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2009)
Estimating local ancestry in admixed populations
Sriram Sankararaman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
The Psychic Costs of Empathic Engagement: Personal and Demographic Predictors of Genetic Counselor Compassion Fatigue
Sharanya Udipi et al.
Journal of Genetic Counseling (2008)
The HCP5 single-nucleotide polymorphism:: A simple screening tool for prediction of hypersensitivity reaction to abacavir
Sara Colombo et al.
JOURNAL OF INFECTIOUS DISEASES (2008)
Personal genomes: The case of the missing heritability
Brendan Maher
NATURE (2008)
Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays
Nils Homer et al.
PLOS GENETICS (2008)
Data and theory point to mainly additive genetic variance for complex traits
William G. Hill et al.
PLOS GENETICS (2008)
Share Paper
