Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelines
暂无分享,去创建一个
Gil Alterovitz | Guilherme Del Fiol | Stanley M. Huff | Brian R. Jackson | Jennifer H. Garvin | Aly Khalifa | Steven B. Bleyl | Clinton C. Mason | Marc S. Williams | Marc S. Williams | G. Fiol | S. Huff | G. Alterovitz | S. Bleyl | J. Garvin | B. Jackson | C. Mason | A. Khalifa | C. C. Mason
[1] Alex H. Wagner,et al. FHIR Genomics: enabling standardization for precision medicine use cases , 2020, npj Genomic Medicine.
[2] H. Kearney,et al. Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization , 2011, Genetics in Medicine.
[3] S. South,et al. American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities , 2011, Genetics in Medicine.
[4] Bale,et al. Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology , 2015, Genetics in Medicine.
[5] Ros Hastings,et al. European guidelines for constitutional cytogenomic analysis , 2018, European Journal of Human Genetics.
[6] S. South,et al. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants , 2011, Genetics in Medicine.
[7] Marc S. Williams,et al. The interface of genomic information with the electronic health record: a points to consider statement of the American College of Medical Genetics and Genomics (ACMG) , 2020, Genetics in Medicine.
[8] Acmg Board Of Directors. Laboratory and clinical genomic data sharing is crucial to improving genetic health care: a position statement of the American College of Medical Genetics and Genomics , 2017, Genetics in Medicine.
[9] Katrina Rack,et al. Cytogenetic Nomenclature and Reporting. , 2017, Methods in molecular biology.
[10] S. South,et al. Technical standards for the interpretation and reporting of constitutional copy number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) , 2019, Genetics in Medicine.
[11] Borut Peterlin,et al. Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic) , 2013, European Journal of Human Genetics.
[12] Gil Alterovitz,et al. SMART on FHIR Genomics: facilitating standardized clinico-genomic apps , 2015, J. Am. Medical Informatics Assoc..
[13] H. Kearney,et al. American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing , 2013, Genetics in Medicine.
[14] N. Heerema,et al. Section E6.1–6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow–acquired chromosomal abnormalities , 2016, Genetics in Medicine.
[15] Simon M. Lin,et al. Clinical exome sequencing reports: current informatics practice and future opportunities , 2017, J. Am. Medical Informatics Assoc..