Associated Papers
Sequence variants influencing the regulation of serum IgG subclass levels.
Olafsdottir TA et al.
Nature Communications, 2024
39277589 (PubMed )
Supplement: 41467_2024_52470_MOESM4_ESM.xlsx › SD3
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.
Emdin CA et al.
Nature Communications, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T2
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Huang H et al.
Nature, 2017
28658209 (PubMed )
Supplement: NIHMS72714-supplement-Supplementary_Table_1.xlsx › annotation__summary
Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma.
Igartua C et al.
Nature Communications, 2015
25591454 (PubMed )
Supplement: NIHMS645116-supplement-1.pdf
Select a paper to view details