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21.
Cheng, Y.S.* et al.: PPP2R5C couples hepatic glucose and lipid homeostasis. PLoS Genet. 11:e1005561 (2015)
22.
Horikoshi, M.* et al.: Discovery and fine-mapping of glycaemic and obesity-related trait loci using high-density imputation. PLoS Genet. 11:e1005230 (2015)
23.
Huan, T.* et al.: A meta-analysis of gene expression signatures of blood pressure and hypertension. PLoS Genet. 11:e1005035 (2015)
24.
Kluth, O.* et al.: Identification of four mouse diabetes candidate genes altering β-cell proliferation. PLoS Genet. 11:e1005506 (2015)
25.
Lagouge, M.* et al.: SLIRP regulates the rate of mitochondrial protein synthesis and protects LRPPRC from degradation. PLoS Genet. 11:e1005423 (2015)
26.
Lal, D.* et al.: Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS Genet. 11:e1005226 (2015)
27.
Lutz, U.* et al.: Modulation of ambient temperature-dependent flowering in Arabidopsis thaliana by natural variation of FLOWERING LOCUS M. PLoS Genet. 11:e1005588 (2015)
28.
Mahajan, A.* et al.: Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 11:e1004876 (2015)
29.
Moutsianas, L.* et al.: The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease. PLoS Genet. 11:e1005165 (2015)
30.
Raffler, J. et al.: Genome-wide association study with targeted and non-targeted NMR metabolomics identifies 15 novel loci of urinary human metabolic individuality. PLoS Genet. 11:e1005487 (2015)
31.
Tönjes, A.* et al.: Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin. PLoS Genet. 10:e1004854 (2015)
32.
Westra, H.J.* et al.: Cell specific eQTL analysis without sorting cells. PLoS Genet. 11:e1005223 (2015)
33.
Winkler, T.W.* et al.: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 11:e1005378 (2015)
34.
Hoggart, C.J.* et al.: Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index. PLoS Genet. 10, 1-12:e1004508 (2014)
35.
Medici, M.* et al.: Identification of novel genetic loci associated with thyroid peroxidase antibodies and clinical thyroid disease. PLoS Genet. 10:e1004123 (2014)
36.
Ng, M.C.Y.* et al.: Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. PLoS Genet. 10:e100451 (2014)
37.
Qanbari, S.* et al.: Classic selective sweeps revealed by massive sequencing in cattle. PLoS Genet. 10:e1004148 (2014)
38.
Cevik, S.* et al.: Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain. PLoS Genet. 9:e1003977 (2013)
39.
Evans, D.M.* et al.: Mining the human phenome using allelic scores that index biological intermediates. PLoS Genet. 9:e1003919 (2013)
40.
Faraco, J.* et al.: ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS Genet. 9:e1003270 (2013)