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41.
Cheng, T.H.* et al.: Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP. Eur. J. Hum. Genet. 23, 260-263 (2015)
42.
Collet, M.* et al.: High incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhood. Eur. J. Hum. Genet., DOI: 10.1038/ejhg.2015.264 (2015)
43.
Dondorp, W.* et al.: Non-invasive prenatal testing for aneuploidy and beyond: Challenges of responsible innovation in prenatal screening. Eur. J. Hum. Genet. 23, 1438-1450 (2015)
44.
Dondorp, W.* et al.: Non-invasive prenatal testing for aneuploidy and beyond: Challenges of responsible innovation in prenatal screening. Summary and recommendations. Eur. J. Hum. Genet., DOI: 10.1038/ejhg.2015.56 (2015)
45.
Oláhová, M.* et al.: A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency. Eur. J. Hum. Genet. 23, 935-939 (2015)
46.
Schulte, E.C. et al.: Rare variants in β-Amyloid Precursor Protein (APP) and Parkinson's disease. Eur. J. Hum. Genet. 23, 1328-1333 (2015)
47.
Spjuth, O.* et al.: Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research. Eur. J. Hum. Genet. 24, 521-528 (2015)
48.
Budin-Ljosne, I.* et al.: Data sharing in large research consortia: Experiences and recommendations from ENGAGE. Eur. J. Hum. Genet. 22, 317-321 (2014)
49.
Huckins, L.M.* et al.: Using ancestry-informative markers to identify fine structure across 15 populations of European origin. Eur. J. Hum. Genet. 22, 1190-1200 (2014)
50.
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)
51.
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)
52.
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)
53.
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)
54.
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)
55.
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)
56.
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)
57.
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)
58.
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)
59.
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)
60.
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)