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
Whole exome sequencing characterization of individuals presenting extreme phenotypes of high and low risk of developing tobacco-induced lung adenocarcinoma.
Patiño-García A et al.
Translational Lung Cancer Research, 2021
A functional splice variant associated with decreased asthma risk abolishes the ability of gasdermin B to induce epithelial cell pyroptosis.
Panganiban RA et al.
The Journal of Allergy and Clinical Immunology, 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
Detection and interpretation of shared genetic influences on 42 human traits.
Pickrell JK et al.
Nature Genetics, 2016
27182965 (PubMed )
Supplement: NIHMS780506-supplement-5.pdf
Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma.
Igartua C et al.
Nature Communications, 2015
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