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Public Health Genomics and Precision Health Knowledge Base (v8.2)
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The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.
Laurie Steven et al. Human mutation 2022
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Genome Nexus: A Comprehensive Resource for the Annotation and Interpretation of Genomic Variants in Cancer.
de Bruijn Ino et al. JCO clinical cancer informatics 2022 6e2100144
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hGLUTEN Tool: Measuring Its Social Impact Indicators.
Moreno Antonia et al. International journal of environmental research and public health 2021 18(23)
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An update on the CHDGKB for the systematic understanding of risk factors associated with non-syndromic congenital heart disease.
Yang Lan et al. Computational and structural biotechnology journal 2021 195741-5751
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Assessing the Robustness and Performance of Artificial Intelligence Powered Planning Tools in Clinical Settings.
Hito M et al. International journal of radiation oncology, biology, physics 2021 111(3S) e91
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Neptune: an environment for the delivery of genomic medicine
V Eric et al, Genetics in Medicine, June 13, 2021
GEInter: an R package for robust gene-environment interaction analysis.
Wu Mengyun et al. Bioinformatics (Oxford, England) 2021
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Aging Atlas: a multi-omics database for aging biology.
et al. Nucleic acids research 2020 Oct
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Variation in cancer risk among families with genetic susceptibility.
Huang Theodore et al. Genetic epidemiology 2020 Oct
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COCOA: coordinate covariation analysis of epigenetic heterogeneity.
Lawson John T et al. Genome biology 2020 Sep 21(1) 240
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A Big Data Platform for Real Time Analysis of Signs of Depression in Social Media.
Martínez-Castaño Rodrigo et al. International journal of environmental research and public health 2020 Jul 17(13)
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CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease.
Yang Lan et al. Database : the journal of biological databases and curation 2020 Jan 2020
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genoDraw: A Web Tool for Developing Pedigree Diagrams Using the Standardized Human Pedigree Nomenclature Integrated with Biomedical Vocabularies.
Garcia-Giordano Luciano et al. AMIA ... Annual Symposium proceedings. AMIA Symposium 2019 2019457-466
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The National Gene Vector Biorepository. Eleven Years of Providing Resources to the Gene Therapy Community.
Cornetta Kenneth G et al. Human gene therapy 2020 Jan
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Precision health research and implementation reviewed through the conNECT framework.
Menon Usha et al. Nursing outlook 2019 May
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Interactive Narrative in a Mobile Health Behavioral Intervention (Tumaini): Theoretical Grounding and Structure of a Smartphone Game to Prevent HIV Among Young Africans.
Winskell Kate et al. JMIR serious games 2019 May 7(2) e13037
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The Transcriptomic Toolbox: Resources for Interpreting Large Gene Expression Data within a Precision Medicine Context for Metabolic Disease Atherosclerosis.
Marín de Evsikova Caralina et al. Journal of personalized medicine 2019 Apr 9(2)
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A Unified Model for the Analysis of Gene-Environment Interaction.
Gauderman W James et al. American journal of epidemiology 2019 Apr 188(4) 760-767
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Introduction to Genomics: A Primer.
Flynn Sharon et al. Seminars in oncology nursing 2019 Jan
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Distributed gene clinical decision support system based on cloud computing.
Xu Bo et al. BMC medical genomics 2018 Nov 11(Suppl 5) 100
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Polygenic approaches to detect gene-environment interactions when external information is unavailable.
Lin Wan-Yu et al. Briefings in bioinformatics 2018 Sep
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Management of Individuals at Increased Hereditary Risk
ASCO, 2018
Genetic testing and autism: Tutorial for communication sciences and disorders.
DeThorne Laura S et al. Journal of communication disorders 2018 May 7461-73
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SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.
Dayem Ullah Abu Z et al. Nucleic acids research 2018 May
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Standard measures for sickle cell disease research: the PhenX Toolkit sickle cell disease collections.
Eckman James R et al. Blood advances 2017 Dec 1(27) 2703-2711
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Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.
Brody Jennifer A et al. Nature genetics 2017 Oct 49(11) 1560-1563
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Simplifying the Use of Pharmacogenomics in Clinical Practice: Building the Genomic Prescribing System.
Danahey Keith et al. Journal of biomedical informatics 2017 Sep
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ArrayTrack: An FDA and Public Genomic Tool.
Fang Hong et al. Methods in molecular biology (Clifton, N.J.) 2017 1613333-353
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A combination test for detection of gene-environment interaction in cohort studies.
Coombes Brandon et al. Genetic epidemiology 2017 Jul 41(5) 396-412
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The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data.
Wong Kira M et al. Nucleic acids research 2017 Jan 45(D1) D819-D826
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Page last reviewed:
Jul 25, 2022
Page last updated:
Jan 31, 2023
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