PuSH - Publication Server of Helmholtz Zentrum München

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61.
Ellinghaus, D.* et al.: Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4. Hepatology 58, 1074-1083 (2013)
62.
Ellinghaus, D.* et al.: Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. Gastroenterology 145, 339-347 (2013)
63.
Enciso-Mora, V.* et al.: Deciphering the 8q24.21 association for glioma. Hum. Mol. Genet. 22, 2293-2302 (2013)
64.
Enciso-Mora, V.* et al.: Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. Br. J. Cancer 108, 2178-2185 (2013)
65.
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)
66.
Lal, D.* et al.: Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia 54, 265-271 (2013)
67.
Liu, J.Z.* et al.: Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat. Genet. 45, 670-675 (2013)
68.
Møller, R.S.* et al.: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia 54, 256-264 (2013)
69.
Pandey, R.C.* et al.: Genetic variation in the toll-like receptor signaling pathway is associated with childhood asthma. J. Allergy Clin. Immunol. 131, 602-605 (2013)
70.
Pandey, R.C.* et al.: Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma. J. Allergy Clin. Immunol. 131, 1245-1247 (2013)
71.
Parsa, A.* et al.: Common variants in mendelian kidney disease genes and their association with renal function. J. Am. Soc. Nephrol. 24, 2105-2117 (2013)
72.
Weidinger, S.* et al.: A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Hum. Mol. Genet. 22, 4841-4856 (2013)
73.
Arnold, M. et al.: Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases. BMC Genomics 13:490 (2012)
74.
Chasman, D.I.* et al.: Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Hum. Mol. Genet. 21, 5329-5343 (2012)
75.
Ellinghaus, D.* et al.: Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. Am. J. Hum. Genet. 90, 636-647 (2012)
76.
Ellinghaus, E.* et al.: Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. J. Invest. Dermatol. 132, 1133-1140 (2012)
77.
Fischer, A.* et al.: A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1. Am. J. Respir. Crit. Care Med. 186, 877-885 (2012)
78.
Folseraas, T.* et al.: Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci. J. Hepatol. 57, 366-375 (2012)
79.
Jacobs, D.I.* et al.: Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: A novel candidate SNP approach. Front. Genet. 3:203 (2012)
80.
Jostins, L.* et al.: Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491, 119-124 (2012)