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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Environmental Health

Last data update: Jan 31, 2023. (Total: 52373 Documents since 2012)
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Query Trace: all[original query]>>Tools/Methods [Product Type]
The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.
Laurie Steven et al. Human mutation 2022
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
hGLUTEN Tool: Measuring Its Social Impact Indicators.
Moreno Antonia et al. International journal of environmental research and public health 2021 18(23)
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
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
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
Aging Atlas: a multi-omics database for aging biology.
et al. Nucleic acids research 2020 Oct
Variation in cancer risk among families with genetic susceptibility.
Huang Theodore et al. Genetic epidemiology 2020 Oct
COCOA: coordinate covariation analysis of epigenetic heterogeneity.
Lawson John T et al. Genome biology 2020 Sep 21(1) 240
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)
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
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
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
Precision health research and implementation reviewed through the conNECT framework.
Menon Usha et al. Nursing outlook 2019 May
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
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)
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
Introduction to Genomics: A Primer.
Flynn Sharon et al. Seminars in oncology nursing 2019 Jan
Distributed gene clinical decision support system based on cloud computing.
Xu Bo et al. BMC medical genomics 2018 Nov 11(Suppl 5) 100
Polygenic approaches to detect gene-environment interactions when external information is unavailable.
Lin Wan-Yu et al. Briefings in bioinformatics 2018 Sep
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
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
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
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
Simplifying the Use of Pharmacogenomics in Clinical Practice: Building the Genomic Prescribing System.
Danahey Keith et al. Journal of biomedical informatics 2017 Sep
ArrayTrack: An FDA and Public Genomic Tool.
Fang Hong et al. Methods in molecular biology (Clifton, N.J.) 2017 1613333-353
A combination test for detection of gene-environment interaction in cohort studies.
Coombes Brandon et al. Genetic epidemiology 2017 Jul 41(5) 396-412
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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