Mumps
What's New
Last Posted: Oct 09, 2023
- Genome-wide determinants of cellular immune responses to mumps vaccine.
Inna G Ovsyannikova, et al. Vaccine 2023 0 - Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases.
Zhu Xiaobo, et al. Frontiers in genetics 2023 0 1164274 - FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort.
Azad Meghan B, et al. Wellcome open research 2018 0 65 - Vaccines and the risk of acute disseminated encephalomyelitis.
Chen Yong, et al. Vaccine 2018 0 (26) 3733-3739 - Vaccinomics and Adversomics in the Era of Precision Medicine: A Review Based on HBV, MMR, HPV, and COVID-19 Vaccines.
Omersel Jasna et al. Journal of clinical medicine 2020 Nov 9(11) - Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines.
Scepanovic Petar, et al. Genome medicine 2018 0 (1) 59 - An Inactivated Virus Candidate Vaccine to Prevent COVID-19
MJ Mulligan, JAMA, August 13, 2020 - Genetic Variants in the IL-4/IL-13 Pathway Influence Measles Vaccine Responses and Vaccine Failure in Children from Mozambique.
Clifford Holly D, et al. Viral immunology 2017 0 (7) 472-478 - Maternal Vaccines: Part of a Healthy Pregnancy
CDC, 2019 - Measles: Make Sure Your Child is Fully Immunized
CDC, 2019
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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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