Incorporating personalized gene sequence variants, molecular genetics knowledge, and health knowledge into an EHR prototype based on the Continuity of Care Record standard

Journal of Biomedical Informatics

Volumn 45, Issue 1, 2012, Pages 82-92

  Jing, Xia ^a   Kay, Stephen ^b   Marley, Thomas ^c   Hardiker, Nicholas R ^b   Cimino, James J ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b UNIVERSITY OF SALFORD   (United Kingdom)

^c Independent Consultant   (United Kingdom)

Author keywords

Electronic health record; Information filters; Molecular Genetic Information; Personalized information; Sequence variants; Standards

Indexed keywords

ELECTRONIC HEALTH RECORD; INFORMATION FILTER; MOLECULAR GENETICS; PERSONALIZED INFORMATION; SEQUENCE VARIANTS;

GENES; HEALTH; HOSPITAL DATA PROCESSING; KNOWLEDGE BASED SYSTEMS; RECORDS MANAGEMENT; SOFTWOODS; STANDARDS; TESTING;

MOLECULAR BIOLOGY;

ADULT; AGE; ARTICLE; CHEMICAL STRUCTURE; CLINICAL ARTICLE; CYSTIC FIBROSIS; DIAGNOSTIC PROCEDURE; ELECTRONIC MEDICAL RECORD; ETHNICITY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HEALTH; HUMAN; KNOWLEDGE; LABORATORY TEST; MALE; MEDICAL INFORMATICS; MOLECULAR GENETICS; PRIORITY JOURNAL; SEX;

ELECTRONIC HEALTH RECORDS; GENOTYPE; HUMANS; INDIVIDUALIZED MEDICINE; MOLECULAR BIOLOGY; PHENOTYPE;

EID: 84856384897     PISSN: 15320464     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbi.2011.09.001     Document Type: Article

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