Smallpox
What's New
Last Posted: Jan 11, 2024
- Utility of Cytochrome P450 4F2 Genotyping to Assess Drug Interaction Risk for Brincidovovir, a Cytochrome P450 4F2 Substrate.
Tim Tippin, et al. Clinical pharmacology in drug development 2024 0 - Genomic associations with antibody response to an oral cholera vaccine.
Vijay Laxmi Roy, et al. Vaccine 2023 0 - BRCA1 and BRCA2 founder mutations account for 78% of germline carriers among hereditary breast cancer families in Chile.
Alvarez Carolina, et al. Oncotarget 2017 0 (43) 74233-74243 - High risk genotypes for schizophrenia may have been adaptive in the context of smallpox.
Block Janice, et al. Medical hypotheses 2020 0 109556 - COVID-19: endemic doesn’t mean harmless
A Katzourakis, Nature, January 24, 2022 - Polymorphisms in STING Affect Human Innate Immune Responses to Poxviruses.
Kennedy Richard B, et al. Frontiers in immunology 2020 0 567348 - Vaccines: Life savers against infectious diseases
Wellcome Trust Sanger Blog, August 2, 2019 - Did CRISPR help - or harm - the first-ever gene-edited babies?
J Cohen, Science, August 1, 2019 - As D.I.Y. Gene Editing Gains Popularity, 'Someone Is Going to Get Hurt'
E Baumgaertner, NY Times, May 14, 2018 - Gene Editing for Good: How CRISPR Could Transform Global Development
B Gates, Foreign Affairs, Apr 10, 2018
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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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