Associated Papers
Polymorphic pseudogenes in the human genome - a comprehensive assessment.
Lopes-Marques M et al.
Human Genetics, 2024
39488654 (PubMed )
Supplement: 439_2024_2715_MOESM7_ESM.xlsx › Additional_table_1
In search of a function for human type III interferons: insights from inherited and acquired deficits.
Zhang Q et al.
Current Opinion in Immunology, 2024
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells.
Nassir N et al.
Human Genomics, 2021
34802461 (PubMed )
Supplement: 40246_2021_368_MOESM2_ESM.xlsx › DbLOF
Polymorphisms in mitochondrial ribosomal protein S5 (MRPS5) are associated with leprosy risk in Chinese.
Xing Y et al.
Plos Neglected Tropical Diseases, 2020
33362202 (PubMed )
Supplement: pntd.0008883.s010.xlsx › S9-rare_variants_in_8_families
Associations between Familial Rates of Psychiatric Disorders and De Novo Genetic Mutations in Autism.
Luhrs K et al.
Autism Research and Treatment, 2017
29250444 (PubMed )
Supplement: 9371964.f1.xlsx › SI_Table3
Relationship between IFNA1, IFNA5, IFNA10, and IFNA17 gene polymorphisms and Crimean-Congo hemorrhagic fever prognosis in a Turkish population range.
Elaldi N et al.
Journal of Medical Virology, 2016
Exome sequencing identifies novel compound heterozygous IFNA4 and IFNA10 mutations as a cause of impaired function in Crohn's disease patients.
Xiao CX et al.
Scientific Reports, 2015
Evolutionary genetic dissection of human interferons.
Manry J et al.
The Journal of Experimental Medicine, 2011
Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients.
Makrythanasis P et al.
Genetic Testing and Molecular Biomarkers, 2010
Variation in the type I interferon gene cluster on 9p21 influences susceptibility to asthma and atopy.
Chan A et al.
Genes and Immunity, 2006
Association between IFNA genotype and the risk of sarcoidosis.
Akahoshi M et al.
Human Genetics, 2004
A rare form of narcolepsy (HLA-DR2-) shows possible association with (functionally relevant) alpha-interferon gene polymorphisms.
Wieczorek S et al.
Psychiatric Genetics, 2004
Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data.
Böhringer S et al.
European Journal of Human Genetics : Ejhg, 2003
Cytokine gene polymorphism in human disease: on-line databases, supplement 1.
Bidwell J et al.
Genes and Immunity, 2001
The interferon gene cluster: a candidate region for MS predisposition? Multiple Sclerosis Study Group.
Miterski B et al.
Genes and Immunity, 1999
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