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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)
Momozawa, Y.* et al.: IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes. Nat. Commun. 9:2427 (2018)
Manousaki, D.* et al.: Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study. PLoS Med. 14:e1002294 (2017)
Melin, B.S.* et al.: Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat. Genet. 49, 789-794 (2017)
Cheng, Y.C.* et al.: Genome-wide association analysis of young onset stroke identifies a locus on chromosome 10q25 near HABP2. Stroke 47, 307-316 (2016)
Jun, G.* et al.: A novel Alzheimer disease locus located near the gene encoding tau protein. Mol. Psychiatry 21, 108–117 (2016)
Brenner, D.R.* et al.: Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. Carcinogenesis 36, 1314-1326 (2015)
Debette, S.* et al.: Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. Nat. Genet. 47, 78-83 (2015)
Kinnersley, B.* et al.: Genome-wide association study identifies multiple susceptibility loci for glioma. Nat. Commun. 6:8559 (2015)
Kinnersley, B.* et al.: Quantifying the heritability of glioma using genome-wide complex trait analysis. Sci. Rep. 5:17267 (2015)
Siroux, V.* et al.: Genetic heterogeneity of asthma phenotypes identified by a clustering approach. Eur. Respir. J. 43, 439-452 (2014)
Enciso-Mora, V.* et al.: Deciphering the 8q24.21 association for glioma. Hum. Mol. Genet. 22, 2293-2302 (2013)
Enciso-Mora, V.* et al.: Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. Br. J. Cancer 108, 2178-2185 (2013)
Esko, T.* et al.: Genetic characterization of Northeastern Italian population isolates in the context of broader European genetic diversity. Eur. J. Hum. Genet. 21, 659-665 (2013)
International Multiple Sclerosis Genetics Consortium (Illig, T. ; Lichtner, P.) et al.: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353-1360 (2013)
Melka, M.G.* et al.: FTO, obesity and the adolescent brain. Hum. Mol. Genet. 22, 1050-1058 (2013)
Billings, L.K.* et al.: Impact of common variation in bone-related genes on type 2 diabetes and related traits. Diabetes 61, 2176-2186 (2012)
Clarke, R.* et al.: Homocysteine and coronary heart disease: Meta-analysis of MTHFR case-control studies, avoiding publication bias. PLoS Med. 9:e1001177 (2012)
Ghoussaini, M.* et al.: Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat. Genet. 44, 312-319 (2012)
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)