Associated Papers
Genomic characterization of lymphomas in patients with inborn errors of immunity.
Ye X et al.
Blood Advances, 2022
35687490 (PubMed )
Supplement: advancesADV2021006654-suppl4.xlsx › PL21__PON_in_red_
Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.
Jäger S et al.
Scientific Reports, 2017
28729637 (PubMed )
Supplement: 41598_2017_6158_MOESM1_ESM.pdf
Evaluation of Toll-like-receptor gene family variants as prognostic biomarkers in rheumatoid arthritis.
Torices S et al.
Immunology Letters, 2017
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Henmyr V et al.
Bmc Medical Genetics, 2017
28228119 (PubMed )
Supplement: 12881_2017_379_MOESM8_ESM.xlsx › TabS4
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
27490946 (PubMed )
Supplement: pone.0159609.s002.xlsx › Results_Discovery_phase_I
A probabilistic model to predict clinical phenotypic traits from genome sequencing.
Chen YC et al.
Plos Computational Biology, 2014
25188385 (PubMed )
Supplement: pcbi.1003825.s014.xlsx › TableS12
Multiple sclerosis and polymorphisms of innate pattern recognition receptors TLR1-10, NOD1-2, DDX58, and IFIH1.
Enevold C et al.
Journal of Neuroimmunology, 2009
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeII_
Characterization and functional investigation of single nucleotide polymorphisms (SNPs) in the human TLR5 gene.
Merx S et al.
Human Mutation, 2006
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