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32199 publications found in the database

*2015 (1336)

*Starting in 2010, coverage has been refocused on core journals.

2015 Publications

The senescent methylome and its relationship with cancer, ageing and germline genetic variation in humans
Lowe, R. et al. Genome Biology 16(), NPG, 2015, Genome-Wide Human SNP Array 6.0  PubMed

Cell-fate determination by ubiquitin-dependent regulation of translation
Werner, A. et al. Nature 525(7570), 523-7, 2015, Human Gene 1.0 ST Array  PubMed

SEGEL: A Web Server for Visualization of Smoking Effects on Human Lung Gene Expression
Xu, Y. et al. Plos One 10(5), NPG, 2015, Human Genome U133 Plus 2.0 Array  PubMed

The Role of the Immune Response in the Pathogenesis of Thyroid Eye Disease: A Reassessment
Rosenbaum, J. T. et al. Plos One 10(9), NPG, 2015, Human Genome U133 Plus 2.0 Array  PubMed

Leveraging existing data sets to generate new insights into Alzheimer's disease biology in specific patient subsets
Fowler, K. D. et al. Scientific Reports 5(), NPG, 2015  PubMed

Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses
Farhan, S. M. K. et al. Journal of Medical Genetics 52(10), 666-75, 2015, Genome-Wide Human SNP Array 6.0  PubMed

RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement
Janer, A. et al. European Journal of Human Genetics 23(10), 1301-7, 2015, Genome-Wide Human SNP Array 6.0  PubMed

Identification and functional annotation of lncRNA genes with hypermethylation in colorectal cancer
Liao, Q. et al. Gene 572(2), 259-65, 2015, Human Genome U133 Plus 2.0 Array  PubMed

Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants
Duan, J. et al. Human Molecular Genetics 24(16), 4674-85, 2015, Genome-Wide Human SNP Array 6.0  PubMed

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