Tuberculosis
What's New
Last Posted: Jul 07, 2022
- Making cough count in tuberculosis care
AJ Zimmer et al, Comm Medicine, July 6, 2022 - Artificial Intelligence Assisting the Early Detection of Active Pulmonary Tuberculosis From Chest X-Rays: A Population-Based Study.
Nijiati Mayidili et al. Frontiers in molecular biosciences 2022 9874475 - TB-Net: A Tailored, Self-Attention Deep Convolutional Neural Network Design for Detection of Tuberculosis Cases From Chest X-Ray Images.
Wong Alexander et al. Frontiers in artificial intelligence 2022 5827299 - Infectious diseases prevention and control using an integrated health big data system in China.
Zhou Xudong et al. BMC infectious diseases 2022 22(1) 344 - A systematic review on the cost effectiveness of pharmacogenomics in developing countries: implementation challenges.
Sukri Asif et al. The pharmacogenomics journal 2022 - A treatment recommender clinical decision support system for personalized medicine: method development and proof-of-concept for drug resistant tuberculosis.
Verboven Lennert et al. BMC medical informatics and decision making 2022 22(1) 56 - AutoCellANLS: An Automated Analysis System for Mycobacteria-Infected Cells Based on Unstained Micrograph.
Zhuang Yan et al. Biomolecules 2022 12(2) - Using Pharmacogenetics to Enhance Tuberculosis (TB) Treatment
M Moore et al, CDC Blog Post, February 22, 2022 - Precision Public Health in Action: New CDC Pilot Projects Integrating Human Genomics into Public Health Surveillance and Applied Research
M Clyne et al, CDC Blog Post, February 14, 2022 - Integrating landmark modeling framework and machine learning algorithms for dynamic prediction of tuberculosis treatment outcomes.
Kheirandish Maryam et al. Journal of the American Medical Informatics Association : JAMIA 2022
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
- CDC Information (21)
- NIH Information (5)
- COVID-19 (178)
- CDC Publications (88)
- Human Genome Epidemiologic Studies (1316)
- GWAS Studies (19)
- Human Genomics Translation/Implementation Studies (50)
- Genomic Tests Evidence Synthesis (3)
- Genomic Tests Guidelines (1)
- Non-Genomics Precision Health (53)
- Pathogen Advanced Molecular Detection (716)
- Reviews/Commentaries (30)
- Ethical/Legal and Social Issues (ELSI) (2)
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Jul 25, 2022
- Page last updated:Dec 07, 2022
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