Inclusion Body Myositis
What's New
Last Posted: Dec 11, 2023
- High-resolution HLA genotyping in inclusion body myositis refines 8.1 ancestral haplotype association to DRB1*03:01:01 and highlights pathogenic role of arginine-74 of DR?1 chain.
Nataliya Slater, et al. Journal of autoimmunity 2023 0 103150 - Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies.
Rothwell Simon, et al. Arthritis & rheumatology (Hoboken, N.J.) 2022 0 - Genetics in inclusion body myositis.
Rothwell Simon, et al. Current opinion in rheumatology 2017 0 (6) 639-644 - Inclusion-body myositis and primary Sjögren syndrome: mechanisms for shared etiologies.
Limaye Vidya S, et al. Muscle & nerve 2020 0 (5) 570-574 - Anti-mitochondrial autoantibodies are associated with cardiomyopathy, dysphagia, and features of more severe disease in adult-onset myositis.
Sabbagh Sara E, et al. Clinical rheumatology 2021 0 (10) 4095-4100 - 47XXY and 47XXX in Scleroderma and Myositis.
Scofield R Hal, et al. ACR open rheumatology 2022 0 (6) 528-533 - HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis.
Oyama Munenori, et al. PloS one 2020 0 (8) e0237890 - Association study reveals novel risk loci for sporadic inclusion body myositis.
Johari M, et al. European journal of neurology 2017 2 - Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum.
Rothwell Simon, et al. Arthritis & rheumatology (Hoboken, N.J.) 2017 1 - Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
Gang Qiang, et al. Neurobiology of aging 2016 11 218.e1-218.e9
More
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
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
- Page last updated:May 03, 2024
- Content source: