Genética de Enfermedades Complejas
GENOME
University of Innsbruck
Innsbruck, AustriaPublications in collaboration with researchers from University of Innsbruck (11)
2022
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
American Journal of Human Genetics, Vol. 109, Núm. 8, pp. 1366-1387
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A saturated map of common genetic variants associated with human height
Nature, Vol. 610, Núm. 7933, pp. 704-712
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome Biology, Vol. 23, Núm. 1
2021
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Polymorphisms within the TNFSF4 and mapkapk2 loci influence the risk of developing invasive aspergillosis: A two-stage case control study in the context of the aspbiomics consortium
Journal of Fungi, Vol. 7, Núm. 1, pp. 1-17
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The power of genetic diversity in genome-wide association studies of lipids
Nature, Vol. 600, Núm. 7890, pp. 675-679
2020
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Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium
Blood Cancer Journal, Vol. 10, Núm. 7
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Polymorphisms within the ARNT2 and CX3CR1 genes are associated with the risk of developing invasive aspergillosis
Infection and Immunity, Vol. 88, Núm. 4
2017
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IL-10 overexpression predisposes to invasive aspergillosis by suppressing antifungal immunity
Journal of Allergy and Clinical Immunology, Vol. 140, Núm. 3, pp. 867-870.e9
2016
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Common genetic polymorphisms within NFκB-related genes and the risk of developing invasive aspergillosis
Frontiers in Microbiology, Vol. 7, Núm. AUG
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Polymorphisms in host immunity-modulating genes and risk of invasive aspergillosis: Results from the AspBIOmics Consortium
Infection and Immunity, Vol. 84, Núm. 3, pp. 643-657