Journal Article (123)
21.
Journal Article
154 (6), pp. 1190 - 1193 (2013)
Long noncoding RNAs usher in a new era in the biology of enhancers. Cell 22.
Journal Article
5, p. 5:34 - 5:34 (2013)
DNA sequencing methods in human genetics and disease research. F1000Prime Rep 23.
Journal Article
91 (9), pp. 1095 - 1107 (2013)
The enzymatic activity of the VEGFR2-receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine 24.
Journal Article
45 (9), pp. 984 - 995 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 25.
Journal Article
5 (9), pp. 1431 - 1442 (2013)
Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation. EMBO Molecular Medicine 26.
Journal Article
10 (3), pp. 303 - 315 (2013)
Zebrafish Expression Ontology of Gene Sets (ZEOGS): a tool to analyze enrichment of zebrafish anatomical terms in large gene sets. Zebrafish 27.
Journal Article
20 (8), pp. 1044 - 1054 (2013)
Synaptic MAGUK multimer formation is mediated by PDZ domains and promoted by ligand binding. Chemistry & Biology 28.
Journal Article
14 (8), p. R84 - R84 (2013)
PROmiRNA: a new miRNA promoter recognition method uncovers the complex regulation of intronic miRNAs. Genome Biology 29.
Journal Article
22 (16), pp. 3306 - 3314 (2013)
Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. Human Molecular Genetics 30.
Journal Article
2 (8), pp. 771 - 778 (2013)
An integrative computational analysis provides evidence for FBN1-associated network de-regulation in trisomy 21. Biology Open 31.
Journal Article
23 (8), pp. 1307 - 1318 (2013)
Comprehensive prediction in 78 human cell lines reveals rigidity and compactness of transcription factor dimers. Genome Research 32.
Journal Article
161A (8), pp. 1915 - 1922 (2013)
A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. American Journal of Medical Genetics Part A 33.
Journal Article
21 (8), pp. 887 - 890 (2013)
A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 34.
Journal Article
10 (4), pp. 305 - 307 (2013)
Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 35.
Journal Article
56 (8), pp. 1802 - 1812 (2013)
Amorfrutin B is an efficient natural peroxisome proliferator-activated receptor gamma (PPARgamma) agonist with potent glucose-lowering properties. Diabetologia 36.
Journal Article
4, 4:2156 (2013)
Genome sequence and functional genomic analysis of the oil-degrading bacterium Oleispira antarctica. Nature Communications 37.
Journal Article
8 (6) (2013)
Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS One 38.
Journal Article
8 (7), p. e67461 - e67461 (2013)
High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications. PLoS One 39.
Journal Article
45 (7), pp. 767 - 775 (2013)
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. Nature Genetics 40.
Journal Article
12 (7), pp. 659 - 668 (2013)
Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study. Lancet Neurology