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Genomics and Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB
Last data update: Dec 06, 2019. (Total: 27371 Documents since 2012)
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Records 1-28 (of 28 Record(s))
Query Trace: Genomic medicine[orginal query]>>Tools/Methods[Product Type]
Publication
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
Horowitz Carol R, et al. American journal of human genetics 2019 5 0.
Gene discovery informatics toolkit defines candidate genes for unexplained infertility and prenatal or infantile mortality.
Dawes Ruebena, et al. NPJ genomic medicine 2019 0 0. 8
DMD Open-access Variant Explorer (DOVE): A scalable, open-access, web-based tool to aid in clinical interpretation of genetic variants in the DMD gene.
Bailey Mitchell et al. Molecular genetics & genomic medicine 2018 Nov
ClinVar database of global familial hypercholesterolemia-associated DNA variants.
Iacocca Michael A et al. Human mutation 2018 Nov 39(11) 1631-1640
Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M).
Woolley J Patrick, et al. NPJ genomic medicine 2018 0 0. 17
Considerations for Design, Development, and Analytical Validation of Next Generation Sequencing (NGS) – Based In Vitro Diagnostics (IVDs) Intended to Aid in the Diagnosis of Suspected Germline Diseases
FDA, April 13, 2018
The Forefront of Genomics
Watch a video from the National Human Genome Research Institute, Feb 2018
gnomAD browser beta | genome Aggregation Database
Jan 25, 2018
PharmCAT: A Pharmacogenomics Clinical Annotation Tool.
Klein Teri E et al. Clinical pharmacology and therapeutics 2017 Dec
Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
Orlando Lori A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Sep
Massive-scale genomic data sharing to improve rare disease diagnosis
D MacArthur VIDEO presentation, Scripps Institute, Future of Genomic Medicine 2017
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies.
Viennas Emmanouil et al. Nucleic acids research 2016 Oct
A comprehensive global genotype-phenotype database for rare diseases.
Trujillano Daniel, et al. Molecular genetics & genomic medicine 2017 1 0. (1) 66-75
Ethical, Legal, and Social Implications of Personalized Genomic Medicine Research: Current Literature and Suggestions for the Future.
Callier Shawneequa L et al. Bioethics 2016 Nov 30(9) 698-705
Assessing multilevel determinants of adoption and implementation of genomic medicine: an organizational mixed-methods approach.
Oishi Sabine M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Nov 17(11) 919-26
GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge.
Kirkpatrick Brianne E et al. Human mutation 2015 Oct 36(10) 974-8
Translation and validation of a Spanish-language genetic health literacy screening tool.
Rodríguez Sally Ann et al. Health Psychol 2015 Feb (2) 120-9
An Alternative Methodological Approach for Cost-Effectiveness Analysis and Decision Making in Genomic Medicine.
Fragoulakis Vasilios et al. Omics : a journal of integrative biology 2016 Apr
Using a Team-Based Learning Approach at National Meetings to Teach Residents Genomic Pathology.
Haspel Richard L et al. Journal of graduate medical education 2016 Feb 8(1) 80-4
A model for integrating molecular-based testing in transfusion services.
Sandler S Gerald et al. Blood transfusion = Trasfusione del sangue 2015 Sep 1-7
Standards for Clinical Grade Genomic Databases.
Yohe Sophia L et al. Archives of pathology & laboratory medicine 2015 Nov 139(11) 1400-12
Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Korf Bruce R et al. Genet. Med. 2014 Nov 16(11) 804-9
Global implementation of genomic medicine: We are not alone
Manolio TA, et al. Sci Transl Med 3 June 2015: Vol. 7, Issue 290, p. 290ps13
The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).
Electronic health record design and implementation for pharmacogenomics: a local perspective.
The next controversy in genetic testing: clinical data as trade secrets?
Integration of genomic medicine into pathology residency training: the stanford open curriculum.
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