Last Posted: May 18, 2021
- Antineutrophil Cytoplasmic Antibody-Associated Vasculitis Update: Genetic Pathogenesis.
Li Weiran, et al. Frontiers in immunology 2021 0 624848
- A shared motif of hla-dpb1 affecting the susceptibility to pr3-anca positive granulomatosis with polyangiitis: comparative analysis of a Turkish cohort with matched healthy controls.
Ince Burak, et al. Rheumatology international 2021 2
- Association of TERT and DSP variants with microscopic polyangiitis and myeloperoxidase-ANCA positive vasculitis in a Japanese population: a genetic association study.
Kawasaki Aya, et al. Arthritis research & therapy 2020 10 (1) 246
- Gene variants and treatment outcomes in antineutrophil cytoplasmic antibody-associated vasculitis.
Hessels Arno C et al. The pharmacogenomics journal 2020 Jul
- Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.
Lyons Paul A, et al. Nature communications 2019 11 (1) 5120
- Association of NCF1 polymorphism with systemic lupus erythematosus and systemic sclerosis but not with ANCA-associated vasculitis in a Japanese population.
Yokoyama Nozomi, et al. Scientific reports 2019 11 (1) 16366
- Risk HLA class II alleles and amino acid residues in myeloperoxidase-ANCA-associated vasculitis.
Wang Huai-Yu, et al. Kidney international 2019 7
- Association of PTPN22 1858C/T Polymorphism with Autoimmune Diseases: A Systematic Review and Bayesian Approach.
Tizaoui Kalthoum, et al. Journal of clinical medicine 2019 3 (3)
- Thiopurine methyltransferase genotype and activity cannot predict outcomes of azathioprine maintenance therapy for antineutrophil cytoplasmic antibody associated vasculitis: A retrospective cohort study.
Hessels Arno C, et al. PloS one 2018 0 (4) e0195524
- Clinical outcome in anti-neutrophil cytoplasmic antibody-associated vasculitis and gene variants of 11ß-hydroxysteroid dehydrogenase type 1 and the glucocorticoid receptor.
Hessels Arno C, et al. Rheumatology (Oxford, England) 2018 11
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.