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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Heart, Lung, Blood, and Sleep Disorders

Last data update: Jul 07, 2022. (Total: 48091 Documents since 2012)
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Records 1 - 12 (of 12 Records)

Query Trace: Lung Diseases[original query]>>Tools/Methods [Product Type]
A Framework for Augmented Intelligence in Allergy and Immunology Practice and Research-A Work Group Report of the AAAAI Health Informatics, Technology and Education Committee.
Khoury Paneez et al. The journal of allergy and clinical immunology. In practice 2022
Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisation.
King Charlotte et al. The pharmacogenomics journal 2020 Jan
High-throughput phenotyping with electronic medical record data using a common semi-supervised approach (PheCAP).
Zhang Yichi et al. Nature protocols 2019 Nov
New CRISPR tool has the potential to correct almost all disease-causing DNA glitches, scientists report
S Begley. Stat News, October 21, 2019
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
2019 Digital Toolkit: NATIONAL BIRTH DEFECTS PREVENTION MONTH
A Comprehensive Human Gastric Cancer Organoid Biobank Captures Tumor Subtype Heterogeneity and Enables Therapeutic Screening.
Yan Helen H N et al. Cell stem cell 2018 Oct
ILDgenDB: integrated genetic knowledge resource for interstitial lung diseases (ILDs).
Mishra Smriti et al. Database : the journal of biological databases and curation 2018 2018
Prioritizing complex disease risk genes by integrating multiple data.
Guo Shanshan et al. Genomics 2018 Apr
Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening.
Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.
CFTR2: How will it help care?
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