Testicular Cancer
What's New
Last Posted: May 12, 2023
- Utility of polygenic risk scores in UK cancer screening: a modelling analysis
C Huntley et al, Lancet Oncology, May 2023 - Gender-specific counselling of patients with upper tract urothelial carcinoma and Lynch syndrome.
Clara Cerrato et al. World journal of urology 2023 - Genetic determinants for the racial disparities in the risk of prostate and testicular cancers
I Uzamere et al, Comm Med, November 2, 2022 - Prevalence of pathogenic germline cancer risk variants in testicular cancer patients: Identifying high risk groups.
Ramamurthy Chethan et al. Urologic oncology 2022 - Familial aggregation of testicular cancer among early-onset cancer survivors. A prospective observational cohort data from Finland.
Seikkula Heikki et al. Cancer epidemiology 2020 Oct 69101807 - Genome-wide association study of cardiovascular disease in testicular cancer patients treated with platinum-based chemotherapy.
Steggink Lars C et al. The pharmacogenomics journal 2020 Oct - Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors.
Trendowski Matthew R et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2020 Sep - Assessment of Polygenic Architecture and Risk Prediction based on Common Variants Across Fourteen Cancers
Y Zhan et al, BioRXIV preprint, August 9, 2019 - Lynch syndrome and urologic malignancies: a contemporary review.
Lim Amy et al. Current opinion in urology 2019 Apr - Testicular Cancer Biomarkers: A Role for Precision Medicine in Testicular Cancer.
Leão Ricardo et al. Clinical genitourinary cancer 2018 Oct
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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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