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61.
Zaboli, G.* et al.: Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits. Eur. J. Hum. Genet. 20, 77-83 (2012)
62.
Becker, F.* et al.: Genetic testing and common disorders in a public health framework: How to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders. Eur. J. Hum. Genet. 19, S6-S44 (2011)
63.
Demirkan, A.* et al.: Genetic architecture of circulating lipid levels. Eur. J. Hum. Genet. 19, 813-819 (2011)
64.
Bouzigon, E.* et al.: Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. Eur. J. Hum. Genet. 18, 700-706 (2010)
65.
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)
66.
O'Dushlaine, C.* et al.: Genes predict village of origin in rural Europe. Eur. J. Hum. Genet. 18, 1269-1270 (2010)
67.
Lu, T.T.* et al.: An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population. Eur. J. Hum. Genet. 17, 967-975 (2009)
68.
Wjst, M. ; Lichtner, P. ; Meitinger, T. & Grimbacher, B.*: STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families. Eur. J. Hum. Genet. 17, 352-356 (2009)
69.
Collin, R.W.* et al.: Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer. Eur. J. Hum. Genet. 16, 1430-1436 (2008)
70.
Wermter, A.K.* et al.: Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: First evidence of polar overdominance in humans. Eur. J. Hum. Genet. 16, 1126-1134 (2008)
71.
Yang, P.* et al.: Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity. Eur. J. Hum. Genet. 16, 350-357 (2008)
73.
Mackevics, V.* et al.: The adiponectin gene is associated with adiponectin levels but not with characteristics of the insulin resistance syndrome in healthy Caucasians. Eur. J. Hum. Genet. 14, 349-356 (2006)
74.
Grabowski, M. et al.: The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted. Eur. J. Hum. Genet. 11, 138-144 (2003)
75.
Golla, A. et al.: Chronic recurrent multifocal osteomyelitis (CRMO) : Evidence for a susceptibility gene located on chromosome 18q21.3-18q22. Eur. J. Hum. Genet. 10, 217-221 (2002)