Associated Papers
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
Human genetic polymorphism and Leishmaniasis.
Bharati K
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases, 2022
Novel FCN2 Variants and Haplotypes are Associated with Rheumatic Heart Disease.
Badarukhiya JA et al.
Dna and Cell Biology, 2021
Hepatitis B Virus Infection Among Leprosy Patients: A Case for Polymorphisms Compromising Activation of the Lectin Pathway and Complement Receptors.
Boldt ABW et al.
Frontiers in Immunology, 2020
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
The prevalence of the variants of the L-ficolin gene (FCN2) in the arctic populations of East Siberia.
Smolnikova MV et al.
Immunogenetics, 2017
Mannose-binding lectin and l-ficolin polymorphisms in patients with community-acquired pneumonia caused by intracellular pathogens.
van Kempen G et al.
Immunology, 2017
FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not -4 A>G and -602 G>A.
Erkan AN et al.
International Journal of Pediatric Otorhinolaryngology, 2016
Low ficolin-2 levels in common variable immunodeficiency patients with bronchiectasis.
Metzger ML et al.
Clinical and Experimental Immunology, 2015
Association of Ficolin-2 Serum Levels and FCN2 Genetic Variants with Indian Visceral Leishmaniasis.
Mishra A et al.
Plos One, 2015
Multiple Infectious Complications in a Severely Injured Patient with Single Nucleotide Polymorphisms in Important Innate Immune Response Genes.
Bronkhorst MW et al.
The Open Orthopaedics Journal, 2015
Association of the FCN2 Gene Single Nucleotide Polymorphisms with Susceptibility to Pulmonary Tuberculosis.
Xu DD et al.
Plos One, 2015
Risk of infection and sepsis in severely injured patients related to single nucleotide polymorphisms in the lectin pathway.
Bronkhorst MW et al.
The British Journal of Surgery, 2013
Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China.
Zhang DF et al.
Human Genetics, 2013
Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.
Szala A et al.
Immunogenetics, 2013
Association of L-ficolin levels and FCN2 genotypes with chronic Chagas disease.
Luz PR et al.
Plos One, 2013
Ficolin-2 levels and genetic polymorphisms of FCN2 in malaria.
Faik I et al.
Human Immunology, 2011
Ficolin-2 levels and FCN2 haplotypes influence hepatitis B infection outcome in Vietnamese patients.
Hoang TV et al.
Plos One, 2011
MBL2, FCN1, FCN2 and FCN3-The genes behind the initiation of the lectin pathway of complement.
Garred P et al.
Molecular Immunology, 2009
Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.
Ruskamp JM et al.
Clinical and Experimental Immunology, 2009
Host genetic susceptibility to pneumococcal and meningococcal disease: a systematic review and meta-analysis.
Brouwer MC et al.
The Lancet. Infectious Diseases, 2009
Functional SNPs in the human ficolin (FCN) genes reveal distinct geographical patterns.
Hummelshøj T et al.
Molecular Immunology, 2008
Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.
Cedzynski M et al.
Clinical and Experimental Immunology, 2007
Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease.
Chapman SJ et al.
Molecular Immunology, 2007
Coding and non-coding polymorphisms in the lectin pathway activator L-ficolin gene in 188 Dutch blood bank donors.
Herpers BL et al.
Molecular Immunology, 2006
Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2.
Hummelshoj T et al.
Human Molecular Genetics, 2005