Oral Cancer
What's New
Last Posted: May 07, 2024
- Survival estimation of oral cancer using fuzzy deep learning.
Rachasak Somyanonthanakul et al. BMC Oral Health 2024 24(1) 519 - Deep learning in oral cancer- a systematic review.
Kritsasith Warin et al. BMC Oral Health 2024 24(1) 212 - Identification of gene profiles related to the development of oral cancer using a deep learning technique.
Leili Tapak et al. BMC medical genomics 2023 16(1) 35 - Liquid Biopsy for Oral Cancer Diagnosis: Recent Advances and Challenges
Y Naito et al, J Per Med, February 8, 2023 - Deep learning-based pathology image analysis predicts cancer progression risk in patients with oral leukoplakia.
Xinyi Zhang et al. Cancer medicine 2023 - Explainable ensemble learning model improves identification of candidates for oral cancer screening.
Adeoye John et al. Oral oncology 2022 136106278 - Novel Machine Learning Model to Predict Interval of Oral Cancer Recurrence for Surveillance Stratification.
Bourdillon Alexandra T et al. The Laryngoscope 2022 - Cytogenetics in Oral Cancer: A Comprehensive Update.
Sv Sowmya et al. The journal of contemporary dental practice 2022 23(1) 123-131 - The Fagerström and AUDIT Tests as Probable Screening Tools in Oral Cancer and Their Correlation with CYP1A1, GSTM1, GSTP1, and GSTT1 Gene Expression.
Bandeira Celso Muller et al. International journal of environmental research and public health 2022 19(7) - Artificial intelligence - can it be used to outsmart oral cancer?
Baniulyte G et al. Evidence-based dentistry 2022 23(1) 12-13
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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
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 Public Health Genomics Branch 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:Feb 1, 2024
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