From variant to function in human disease genetics

• Over the next decade, the primary challenge in human genetics will be to understand the biological mechanisms by which genetic variants influence phenotypes, including disease risk. Although the scale of this challenge is daunting, better methods for functional variant interpretation will have transformative consequences for disease diagnosis, risk prediction, and the development of new therapies. An array of new methods for characterizing variant impact at scale, using patient tissue samples as well as in vitro models, are already being applied to dissect variant mechanisms across a range of human cell types and environments. These approaches are also increasingly being deployed in clinical settings. We discuss the rationale, approaches, applications, and future outlook for characterizing the molecular and cellular effects of genetic variants.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)

MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Nyckelord

Disease

Gene Expression Regulation

Genetic Diseases

Inborn

Genetic Predisposition to Disease

Genetic Techniques

Genetic Variation

Genome

Human

Genome-Wide Association Study

Genomics

Humans

Molecular Sequence Annotation

Multifactorial Inheritance

Phenotype

Quantitative Trait Loci

Publikations- och innehållstyp

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