Finding the missing heritability of complex diseases

TA Manolio, FS Collins, NJ Cox, DB Goldstein… - Nature, 2009 - nature.com
Genome-wide association studies have identified hundreds of genetic variants associated
with complex human diseases and traits, and have provided valuable insights into their …

STrengthening the REporting of Genetic Association Studies (STREGA)—an extension of the STROBE statement

J Little, JPT Higgins, JPA Ioannidis… - … Official Publication of …, 2009 - Wiley Online Library
Making sense of rapidly evolving evidence on genetic associations is crucial to making
genuine advances in human genomics and the eventual integration of this information in the …

American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility

ME Robson, CD Storm, J Weitzel… - Journal of clinical …, 2010 - ascopubs.org
As the leading professional organization representing physicians who are involved in
cancer treatment and research, the American Society of Clinical Oncology (ASCO) has long …

[HTML][HTML] From public health genomics to precision public health: a 20-year journey

MJ Khoury, MS Bowen, M Clyne, WD Dotson… - Genetics in …, 2018 - Elsevier
In this paper, we review the evolution of the field of public health genomics in the United
States in the past two decades. Public health genomics focuses on effective and responsible …

Genomic medicine: a decade of successes, challenges, and opportunities

JJ McCarthy, HL McLeod, GS Ginsburg - Science translational …, 2013 - science.org
Genomic medicine—an aspirational term 10 years ago—is gaining momentum across the
entire clinical continuum from risk assessment in healthy individuals to genome-guided …

The emergence of translational epidemiology: from scientific discovery to population health impact

MJ Khoury, M Gwinn… - American journal of …, 2010 - academic.oup.com
Recent emphasis on translational research (TR) is highlighting the role of epidemiology in
translating scientific discoveries into population health impact. The authors present …

Personalized medicine: new genomics, old lessons

K Offit - Human genetics, 2011 - Springer
Personalized medicine uses traditional, as well as emerging concepts of the genetic and
environmental basis of disease to individualize prevention, diagnosis and treatment …

Non-genetic risk and protective factors and biomarkers for neurological disorders: a meta-umbrella systematic review of umbrella reviews

AFA Mentis, E Dardiotis, V Efthymiou, GP Chrousos - BMC medicine, 2021 - Springer
Background The etiologies of chronic neurological diseases, which heavily contribute to
global disease burden, remain far from elucidated. Despite available umbrella reviews on …

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants

SE Gollust, ES Gordon, C Zayac, G Griffin… - Public health …, 2011 - karger.com
Abstract Background/Aims: To predict the potential public health impact of personal
genomics, empirical research on public perceptions of these services is needed. In this …

Development and evaluation of a genetic risk score for obesity

DW Belsky, TE Moffitt, K Sugden… - … and social biology, 2013 - Taylor & Francis
Multi-locus profiles of genetic risk, so-called “genetic risk scores,” can be used to translate
discoveries from genome-wide association studies into tools for population health research …