scispace - formally typeset
Open AccessJournal ArticleDOI

Musings on genome medicine: the value of family history

Angus John Clarke
- 03 Aug 2009 - 
- Vol. 1, Iss: 8, pp 75-75
TLDR
It is argued that the routine availability of genome sequence information on individuals will not render family history information obsolete, both because the taking of a family history has other uses for the health professional, and because genome sequence data on their own omit the effects of numerous factors important for modifying risks of disease.
Abstract
Will the routine availability of genome sequence information on individuals render family history information obsolete? I argue that it will not, both because the taking of a family history has other uses for the health professional, and because genome sequence data on their own omit the effects of numerous factors important for modifying risks of disease. These include information derived from factors downstream of genetic variants and from upstream epigenetic effects. Further difficulties arise with uncertainties relating to gene-gene and gene-environment interactions, which may take decades to resolve if their resolution is even possible.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Desde la Genética Médica hacia la Medicina Genómica

TL;DR: The conocimiento de los fundamentos de Genetica ya no es una necesidad para una especialidad medica concreta, sino que es obligado para todas las profesiones sanitarias as discussed by the authors.
Journal ArticleDOI

User experience of self‐reported computerized medical history taking for acute chest pain: The Clinical Expert Operating System Chest Pain Danderyd Study

TL;DR: The findings suggest that CHT programmes can be integrated as a standard process for collecting self-reported medical history data in the ED setting and adjusted to better suit the context of the clinical use.
Reference EntryDOI

Children in Genetic Research

TL;DR: In this article, the authors review the Declaration of Helsinki and other ethical guidance, as well as differing standards for research with children between Britain and the USA, and discuss the benefits of genetic research in richer and in poorer countries.
References
More filters
Journal ArticleDOI

Systems genetics of complex traits in Drosophila melanogaster.

TL;DR: The authors quantified genome-wide transcript abundance and phenotypes for six ecologically relevant traits in D. melanogaster wild-derived inbred lines and observed 10,096 genetically variable transcripts and high heritabilities for all organismal phenotypes.
Journal ArticleDOI

A Critical Appraisal of the Scientific Basis of Commercial Genomic Profiles Used to Assess Health Risks and Personalize Health Interventions

TL;DR: There is insufficient scientific evidence to conclude that genomic profiles are useful in measuring genetic risk for common diseases or in developing personalized diet and lifestyle recommendations for disease prevention.
Journal ArticleDOI

Family history: A comprehensive genetic risk assessment method for the chronic conditions of adulthood

TL;DR: Family history reports of common, chronic disease are prevalent among the population at large, and collection and interpretation of comprehensive family history data is a feasible, initial method for risk stratification for many preventable, chronic conditions.
Journal ArticleDOI

The genetic architecture of quantitative traits: lessons from Drosophila

TL;DR: Studies in Drosophila have revealed large numbers of pleiotropic genes that interact epistatically to regulate quantitative traits, and large number of QTLs with sex-, environment- and genotype-specific effects, which offer valuable lessons for understanding the genetic basis of variation for complex traits in other organisms, including humans.
Journal ArticleDOI

Gene-environment interactions for complex traits: Definitions, methodological requirements and challenges

TL;DR: This review discusses methodological issues involved in investigating gene–environment (G × E) interactions in genetic–epidemiological studies of complex diseases and their potential relevance for clinical application and attempts to clarify conceptual differences of the term ‘interaction’ in the statistical and biological sciences.
Related Papers (5)