Associated Papers
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc8.xlsx › Supplementary_Table_7C
Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe.
Kerner G et al.
Cell Genomics, 2023
Effects of Lipopolysaccharide-Binding Protein (LBP) Single Nucleotide Polymorphism (SNP) in Infections, Inflammatory Diseases, Metabolic Disorders and Cancers.
Meng L et al.
Frontiers in Immunology, 2021
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Ostrowski J et al.
Scientific Reports, 2016
28008999 (PubMed )
Supplement: srep39831-s2.xls › Table_S7
Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.
Carrera P et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartet.
Corpas M et al.
Bmc Genomics, 2015
26547235 (PubMed )
Supplement: 12864_2015_1973_MOESM3_ESM.xls › TableS2-57Variants
Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
van Schouwenburg PA et al.
Clinical Immunology (orlando, Fla.), 2015
26122175 (PubMed )
Supplement: NIHMS64345-supplement-Supplementary_tables.xlsx › Table_S15
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