GenomeConnect: Matchmaking Between Patients, Clinical Laboratories, and Researchers to Improve Genomic Knowledge

Human Mutation

Volumn 36, Issue 10, 2015, Pages 974-978

  Kirkpatrick, Brianne E ^a   Riggs, Erin Rooney ^a   Azzariti, Danielle R ^b   Miller, Vanessa Rangel ^c   Ledbetter, David H ^a   Miller, David T ^d,e   Rehm, Heidi ^b,f,g,h   Martin, Christa Lese ^a   Faucett, W Andrew ^a  

^a GEISINGER HEALTH SYSTEM   (United States)

^b Partners Health Care Center for Personalized Medicine   (United States)

^c Innolyst   (United States)

^d BOSTON CHILDREN S HOSPITAL   (United States)

^e Claritas Genomics   (United States)

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

^g HARVARD MEDICAL SCHOOL   (United States)

^h BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Data sharing; Genotype phenotype; Matchmaker exchange; Patient portal; Patient registry

Indexed keywords

ARTICLE; CLINICAL LABORATORY; CLINICAL RESEARCH; GENETIC VARIABILITY; GENOMICS; GENOTYPE PHENOTYPE CORRELATION; HUMAN; KNOWLEDGE BASE; PATIENT CARE; PRIORITY JOURNAL; COMPUTER INTERFACE; DISEASES; FACTUAL DATABASE; GENETIC PREDISPOSITION; GENETICS; HUMAN GENOME; INFORMATION DISSEMINATION; PATIENT PARTICIPATION; PERSONALIZED MEDICINE; PHENOTYPE; PROCEDURES;

DATABASES, FACTUAL; DISEASE; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; INFORMATION DISSEMINATION; PATIENT PARTICIPATION; PHENOTYPE; PRECISION MEDICINE; USER-COMPUTER INTERFACE;

EID: 84941878200     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22838     Document Type: Article

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