Instituto Universitario de Tecnologías Biomédicas
Instituto de investigación
Hannover Medical School
Hanóver, AlemaniaPublicaciones en colaboración con investigadores/as de Hannover Medical School (18)
2023
-
A second update on mapping the human genetic architecture of COVID-19
Nature
-
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
Nature, Vol. 623, Núm. 7988, pp. 803-813
2022
-
Multi-ancestry genome-wide association study of asthma exacerbations
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, Vol. 33, Núm. 6, pp. e13802
2021
-
ADRB2 haplotypes and asthma exacerbations in children and young adults: An individual participant data meta-analysis
Clinical and Experimental Allergy, Vol. 51, Núm. 9, pp. 1157-1171
-
Combined analysis of transcriptomic and genetic data for the identification of loci involved in glucocorticosteroid response in asthma
Allergy: European Journal of Allergy and Clinical Immunology, Vol. 76, Núm. 4, pp. 1238-1243
-
Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use
European Respiratory Journal, Vol. 57, Núm. 5
-
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
-
Identification of robo2 as a potential locus associated with inhaled corticosteroid response in childhood asthma
Journal of Personalized Medicine, Vol. 11, Núm. 8
2019
-
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
Nature Communications, Vol. 10, Núm. 1
-
Genome-wide association study of inhaled corticosteroid response in admixed children with asthma
Clinical and Experimental Allergy, Vol. 49, Núm. 6, pp. 789-798
2018
-
17q21 variant increases the risk of exacerbations in asthmatic children despite inhaled corticosteroids use
Allergy: European Journal of Allergy and Clinical Immunology
2017
-
Rationale and design of the multiethnic Pharmacogenomics in Childhood Asthma consortium
Pharmacogenomics, Vol. 18, Núm. 10, pp. 931-943
2016
2013
-
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
European Journal of Human Genetics, Vol. 21, Núm. 2, pp. 162-172
2012
-
Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
2011
-
Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
Annals of the Rheumatic Diseases
2009
-
Etiology, management, and outcome of the Budd-Chiari syndrome
Annals of Internal Medicine, Vol. 151, Núm. 3, pp. 167-175