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61.
Kuechler, A.* et al.: Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. Eur. J. Hum. Genet. 23, 753-760 (2014)
62.
Malzahn, D.* et al.: Controversial association results for INSIG2 on body mass index may be explained by interactions with age and with MC4R. Eur. J. Hum. Genet. 22, 1217-1224 (2014)
63.
Rogowski, W.H. ; Grosse, S.D.* ; Schmidtke, J.* & Marckmann, G.*: Criteria for fairly allocating scarce health-care resources to genetic tests: Which matter most? Eur. J. Hum. Genet. 22, 25-31 (2014)
64.
Severin, F. et al.: Points to consider for prioritizing clinical genetic testing services:  European consensus process oriented at accountability for reasonableness. Eur. J. Hum. Genet. 23, 729-735 (2014)
65.
Broer, L.* et al.: Meta-analysis of telomere length in 19713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. Eur. J. Hum. Genet. 21, 1163-1168 (2013)
66.
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)
67.
Hedberg, C.* ; Melberg, A.* ; Kuhl, A.* ; Jenne, D. & Oldfors, A.*: Functional characterization of desmin mutant p.P419S Reply. Eur. J. Hum. Genet. 21, 590 (2013)
68.
Mehta, D. et al.: Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood. Eur. J. Hum. Genet. 21, 48-54 (2013)
69.
Oexle, K.* et al.: Dilution of candidates: The case of iron-related genes in restless legs syndrome. Eur. J. Hum. Genet. 21, 410-414 (2013)
70.
Rebala, K.* et al.: Contemporary paternal genetic landscape of Polish and German populations: From early medieval Slavic expansion to post-World War II resettlements. Eur. J. Hum. Genet. 21, 415-422 (2013)
71.
Severin, F. ; Schmidtke, J.* ; Mühlbacher, A.* & Rogowski, W.H.: Eliciting preferences for priority setting in genetic testing: A pilot study comparing best-worst scaling and discrete-choice experiments. Eur. J. Hum. Genet. 21, 1202-1208 (2013)
72.
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)
73.
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)
74.
Demirkan, A.* et al.: Genetic architecture of circulating lipid levels. Eur. J. Hum. Genet. 19, 813-819 (2011)
75.
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)
76.
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)
77.
O'Dushlaine, C.* et al.: Genes predict village of origin in rural Europe. Eur. J. Hum. Genet. 18, 1269-1270 (2010)
78.
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)
79.
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)
80.
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)
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