Design and user experience testing of a polygenic score report: a qualitative study of prospective users

Validation of an Integrated Risk Tool, Including Polygenic Risk Score, for Atherosclerotic Cardiovascular Disease in Multiple Ethnicities and Ancestries

(2021) Michael E. Weale et al.   AMERICAN JOURNAL OF CARDIOLOGY

Improving reporting standards for polygenic scores in risk prediction studies

(2021) Hannah Wand et al.   NATURE

Polygenic risk scores in the clinic: new perspectives needed on familiar ethical issues

(2021) Anna C. F. Lewis et al.   Genome Medicine

Recommendations for designing genetic test reports to be understood by patients and non-specialists

(2020) George D. Farmer et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Polygenic Scores to Assess Atherosclerotic Cardiovascular Disease Risk

(2020) Krishna G. Aragam et al.   CIRCULATION RESEARCH

Polygenic risk scores: from research tools to clinical instruments

(2020) Cathryn M. Lewis et al.   Genome Medicine

Hidden in Plain Sight — Reconsidering the Use of Race Correction in Clinical Algorithms

(2020) Darshali A. Vyas et al.   NEW ENGLAND JOURNAL OF MEDICINE

Impute.me: An Open-Source, Non-profit Tool for Using Data From Direct-to-Consumer Genetic Testing to Calculate and Interpret Polygenic Risk Scores

(2020) Lasse Folkersen et al.   Frontiers in Genetics

Association of a Polygenic Risk Score With Breast Cancer Among Women Carriers of High- and Moderate-Risk Breast Cancer Genes

(2020) Shannon Gallagher et al.   JAMA Network Open

Validation of a prostate cancer polygenic risk score

(2020) Mary H. Black et al.   PROSTATE

Clinical use of current polygenic risk scores may exacerbate health disparities

(2019) Alicia R. Martin et al.   NATURE GENETICS

CLINICAL CHARACTERISTICS AND TREATMENT PATTERNS OF PATIENTS AT HIGH POLYGENIC RISK FOR CORONARY ARTERY DISEASE

(2019) Krishna G. Aragam et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A comparison of genomic laboratory reports and observations that may enhance their clinical utility for providers and patients

(2019) Kyle Walter Davis et al.   Molecular Genetics & Genomic Medicine

Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer

(2019) et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

(2019) Julian R. Homburger et al.   Genome Medicine

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

(2018) Amit V. Khera et al.   NATURE GENETICS

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults

(2018) Michael Inouye et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients

(2017) Galen Joseph et al.   Journal of Genetic Counseling

Impact of a Patient-Facing Enhanced Genomic Results Report to Improve Understanding, Engagement, and Communication

(2017) Janet L. Williams et al.   Journal of Genetic Counseling

Enhancing genomic laboratory reports: A qualitative analysis of provider review

(2016) Janet L. Williams et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

(2016) Johan T. den Dunnen et al.   HUMAN MUTATION

Beyond Memorability: Visualization Recognition and Recall

(2016) Michelle A. Borkin et al.   IEEE TRANSACTIONS ON VISUALIZATION AND COMPUTER GRAPHICS

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

(2016) Amit V. Khera et al.   NEW ENGLAND JOURNAL OF MEDICINE

Enhancing genomic laboratory reports from the patients' view: A qualitative analysis

(2015) Heather Stuckey et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Guidelines for diagnostic next-generation sequencing

(2015) Gert Matthijs et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

More Than Telling a Story: Transforming Data into Visually Shared Stories

(2015) Bongshin Lee et al.   IEEE COMPUTER GRAPHICS AND APPLICATIONS

Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding

(2014) Susanne B Haga et al.   Genome Medicine

2013 ACC/AHA Guideline on the Assessment of Cardiovascular Risk

(2013) David C. Goff et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies

(2011) Catherine A McCarty et al.   BMC Medical Genomics

Points of view: Color blindness

(2011) Bang Wong   NATURE METHODS

Using Monochromatic Design Views to Avoid a Premature Fixation on Design Solutions

(2010) Amod Damle   HUMAN FACTORS