Associated Papers
Polymorphisms in FCN genes and their influence on systemic lupus erythematosus susceptibility: a report from Western India.
Rai K et al.
Immunohorizons, 2025
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
38585811 (PubMed )
Supplement: media-3.xlsx › Sheet1
Association of ficolin-1 and ficolin-3 gene variation and pulmonary tuberculosis susceptibility in a Chinese population.
Li Y et al.
Journal of Clinical Laboratory Analysis, 2021
Associations of Ficolins With Hematological Malignancies in Patients Receiving High-Dose Chemotherapy and Autologous Hematopoietic Stem Cell Transplantations.
Świerzko AS et al.
Frontiers in Immunology, 2019
Association of the FCN2 Gene Single Nucleotide Polymorphisms with Susceptibility to Pulmonary Tuberculosis.
Xu DD et al.
Plos One, 2015
Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.
Szala A et al.
Immunogenetics, 2013
Genetic evidence of functional ficolin-2 haplotype as susceptibility factor in cutaneous leishmaniasis.
Assaf A et al.
Plos One, 2012
Ficolin-2 levels and FCN2 haplotypes influence hepatitis B infection outcome in Vietnamese patients.
Hoang TV et al.
Plos One, 2011
Single nucleotide polymorphisms of Ficolin 2 gene in Behçet's disease.
Chen X et al.
Journal of Dermatological Science, 2006
Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2.
Hummelshoj T et al.
Human Molecular Genetics, 2005
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