Stomach Cancer
What's New
Last Posted: Aug 08, 2023
- Spatial Clusters of Cancer Mortality in Brazil: A Machine Learning Modeling Approach.
Bruno Casaes Teixeira et al. Int J Public Health 2023 681604789 - Machine learning predicts cancer-associated venous thromboembolism using clinically available variables in gastric cancer patients.
Xu Qianjie et al. Heliyon 2023 9(1) e12681 - Survival Prediction of Stomach Cancer Using Expression Data and Deep Learning Models with Histopathological Image.
Wei Ting et al. Cancer science 2022 - Estimation of familial recurrence risk of malignancy: application of liability threshold model in genetic counseling.
Nagao Yoshiro et al. Clinical genetics 2022 - Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants.
Li Shuai et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 JCO2102112 - Automatic Recognition of Colon and Esophagogastric Cancer with Machine Learning and Hyperspectral Imaging.
Collins Toby et al. Diagnostics (Basel, Switzerland) 2021 11(10) - Artificial intelligence in gastric cancer: a translational narrative review.
Yu Chaoran et al. Annals of translational medicine 2021 9(3) 269 - Smoking, alcohol consumption, and cancer: A mendelian randomisation study in UK Biobank and international genetic consortia participants.
Larsson Susanna C et al. PLoS medicine 2020 Jul 17(7) e1003178 - Should All Breast Cancer Patients Undergo Genetic Testing?
V Hackenthal, Medscape, August 9, 2019 - CLINGEN Actionability Report for MUTYH-Associated Polyposis - MUTYH
ClinGen Actionability Working Group
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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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