Last Posted: Dec 25, 2019
- XRCC1 variants do not represent a risk for dermatomyositis and systemic lupus erythematosus in Bulgarian patients.
Kamenarska Zornitsa, et al. Acta dermatovenerologica Alpina, Pannonica, et Adriatica 2019 12 (4) 149-152
- Study Tests Immunotherapy in People with Cancer and Autoimmune Diseases
NCI, August 26, 2019
- Genetic association of HLA-DRB1 multiple polymorphisms with dermatomyositis in Chinese population.
Lin J M, et al. HLA 2017 0 (6) 354-359
- HLA-DRB1 Alleles as Genetic Risk Factors for the Development of Anti-MDA5 Antibodies in Patients with Dermatomyositis.
Chen Zhiyong, et al. The Journal of rheumatology 2017 9 (9) 1389-1393
- Genetically Determined TNF-a Secretion Influences the Development of Dermatomyositis and Systemic Lupus Erythematosus.
Dourmishev Lyubomir A, et al. Folia medica 2018 6 (2) 216-220
- Association of HLA-DRB1 alleles with susceptibility to mixed connective tissue disease in Polish patients.
Paradowska-Gorycka A, et al. HLA 2016 1 (1) 13-8
- Novel susceptibility alleles in HLA region for myositis and myositis specific autoantibodies in Korean patients.
Kang Eun Ha, et al. Seminars in arthritis and rheumatism 2019 3
- The spectrum and clinical significance of myositis-specific autoantibodies in Chinese patients with idiopathic inflammatory myopathies.
Li Shanshan, et al. Clinical rheumatology 2019 3
- The effect of cigarette smoking on the clinical and serological phenotypes of polymyositis and dermatomyositis.
Schiffenbauer Adam, et al. Seminars in arthritis and rheumatism 2018 0 (3) 504-512
- Association between the BANK1 rs3733197 polymorphism and polymyositis/dermatomyositis in a Chinese Han population.
Chen Si, et al. Clinical rheumatology 2018 8
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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics 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.