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Demenais, F.* et al.: Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Nat. Genet. 50, 42-53 (2018)
Vasileiou, G.* et al.: Mutations in the BAF-complex subunit DPF2 are associated with coffin-siris syndrome. Am. J. Hum. Genet. 102, 468-479 (2018)
Bramswig, N.C.* et al.: Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability. Hum. Genet. 136, 821-834 (2017)
Imboden, M.* et al.: Genome-wide association study of lung function decline in adults with and without asthma. J. Allergy Clin. Immunol. 129, 1218-1228 (2012)
Halapi, E.* et al.: A sequence variant on 17q21 is associated with age at onset and severity of asthma. Eur. J. Hum. Genet. 18, 902-908 (2010)
Gudbjartsson, D.F.* et al.: Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009)
Wjst, M. ; Altmüller, J. ; Braig, C. ; Bahnweg, M. & André, E.: A genome-wide linkage scan for 25-OH-D3 and 1,25-(OH)2-D3 serum levels in asthma families. J. Steroid Biochem. Mol. Biol. 103, 799-802 (2007)
Wjst, M. et al.: Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway. Respir. Res. 7, 1-11 (2006)
Altmüller, J. et al.: Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families. BMC Pulm. Med. 5:1 (2005)
Gohlke, H. et al.: Association of the Interleukin-1 Receptor Antagonist Gene with Asthma. Am. J. Respir. Crit. Care Med. 169, 1217-1223 (2004)
Vollmert, C. et al.: Single nucleotide polymorphism screening and association analysis - exclusion of integrin ß7 and vitamin D receptor (chromosome 12q) as candidate genes for asthma. Clin. Exp. Allergy 34, 1841-1850 (2004)
Werner, M. et al.: Asthma is associated with single-nucleotide polymorphisms in ADAM33. Clin. Exp. Allergy 34, 26-31 (2004)
Herbon, N. et al.: High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. Genomics 81, 510-518 (2003)
Duetsch, G. et al.: STAT6 as an asthma candidate gene : Polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study. Hum. Mol. Genet. 11, 613-621 (2002)
Altmüller, J. ; Palmer, L.J.* ; Fischer, G. ; Scherb, H. & Wjst, M.: Genomewide Scans of Complex Human Diseases : True Linkage is Hard to Find. Am. J. Hum. Genet. 69, 936-950 (2001)