From genetic discovery to future personalized health research

New Biotechnology

Volumn 30, Issue 3, 2013, Pages 291-295

  Palotie, Aarno ^a,b,c   Widén, Elisabeth ^b   Ripatti, Samuli ^a,b  

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b UNIVERSITY OF HELSINKI   (Finland)

^c BROAD INSTITUTE OF MIT AND HARVARD   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOME-WIDE ASSOCIATION; HUMAN GENOME PROJECT; NEW TECHNOLOGIES; NEXT-GENERATION SEQUENCING; PERSONALIZED HEALTHS; RESEARCH QUESTIONS; STATISTICAL INFERENCE; SYSTEMATIC PLANNING;

DNA SEQUENCES; RESEARCH;

GENES;

ALZHEIMER DISEASE; ARTICLE; EVIDENCE BASED MEDICINE; EXOME; GENE EXPRESSION; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC DRIFT; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; GOUT; HAPLOTYPE; HAPLOTYPE MAP; HUMAN; HUMAN GENOME; HUMAN GENOME PROJECT; MUTATION RATE; MUTATIONAL ANALYSIS; PERSONALIZED MEDICINE; PRIORITY JOURNAL; SICK SINUS SYNDROME;

BIOMEDICAL RESEARCH; DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HUMANS; INDIVIDUALIZED MEDICINE; PERSONAL HEALTH SERVICES;

EID: 84878107677     PISSN: 18716784     EISSN: 18764347     Source Type: Journal    
DOI: 10.1016/j.nbt.2012.11.013     Document Type: Article

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