Zeitschriftenartikel (162)
21.
Zeitschriftenartikel
10 (11), e1004788 (2014)
Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genetics 22.
Zeitschriftenartikel
10 (11), e1004788 (2014)
Lack of Replication of the GRIN2A-by-Coffee Interaction in Parkinson Disease. PLoS Genetics 23.
Zeitschriftenartikel
9 (11), e112112 (2014)
Upk3b is dispensable for development and integrity of urothelium and mesothelium. PLoS One 24.
Zeitschriftenartikel
2014, bau101 (2014)
A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools. Database: The Journal of Biological Databases and Curation 25.
Zeitschriftenartikel
86 (2), S. 151 - 157 (2014)
Activation of AMP-activated protein kinase sensitizes lung cancer cells and H1299 xenografts to erlotinib. Lung Cancer 26.
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164A (11), S. 2753 - 2763 (2014)
NDST1 missense mutations in autosomal recessive intellectual disability. American Journal of Medical Genetics Part A 27.
Zeitschriftenartikel
53 (4), S. 659 - 670 (2014)
Expression of blood serum proteins and lymphocyte differentiation clusters after chronic occupational exposure to ionizing radiation. Radiation and Environmental Biophysics 28.
Zeitschriftenartikel
76 (5), S. 758 - 764 (2014)
Absent CNKSR2 causes seizures and intellectual, attention, and language deficits. Annals of Neurology 29.
Zeitschriftenartikel
24 (11), S. 1894 - 1904 (2014)
The landscape of human STR variation. Genome Research 30.
Zeitschriftenartikel
9 (10), e111006 (2014)
Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains. PLoS One 31.
Zeitschriftenartikel
9 (2), S. 542 - 554 (2014)
Microprocessor activity controls differential miRNA biogenesis In Vivo. Cell Reports 32.
Zeitschriftenartikel
23 (20), S. 5536 - 5544 (2014)
Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Human Molecular Genetics 33.
Zeitschriftenartikel
10 (10), e1003884 (2014)
Reconstruction of the Gene Regulatory Network Involved in the Sonic Hedgehog Pathway with a Potential Role in Early Development of the Mouse Brain. PLoS Computational Biology 34.
Zeitschriftenartikel
83 (15), S. 1353 - 1358 (2014)
The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology 35.
Zeitschriftenartikel
86 (4), S. 318 - 325 (2014)
Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas-type polysyndactyly and Laurin-Sandrow syndrome. Clinical Genetics: an international journal of genetics in medicine 36.
Zeitschriftenartikel
9 (9), e108777 (2014)
An Image-Based Genetic Assay Identifies Genes in T1D Susceptibility Loci Controlling Cellular Antiviral Immunity in Mouse. PLoS One 37.
Zeitschriftenartikel
4, e454 (2014)
No association between CTNNBL1 and episodic memory performance. Translational Psychiatry 38.
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289 (39), S. 26817 - 26828 (2014)
Architecture of polyglutamine-containing fibrils from time-resolved fluorescence decay. The Journal of Biological Chemistry 39.
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426 (19), S. 3221 - 3231 (2014)
Molecular analysis of two novel missense mutations in the GDF5 proregion that reduce protein activity and are associated with brachydactyly type C. Journal of Molecular Biology 40.
Zeitschriftenartikel
5, 5:4675 (2014)
Immunochip SNP array identifies novel genetic variants conferring susceptibility to candidaemia. Nature Communications