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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Inorganic Arsenic-induced cellular transformation is coupled with genome wide changes in chromatin structure, transcriptome and splicing patterns
Riedmann, C. et al. BMC Genomics 16(), NPG, 2015, Human Transcriptome Array 2.0  PubMed

Susceptibility allele-specific loss of miR-1324-mediated silencing of the INO80B chromatin-assembly complex gene in pre-eclampsia
Oudejans, C. B. M. et al. Human Molecular Genetics 24(1), 118-27, 2015, CytoScan  PubMed

The Quorum Sensing Peptides PhrG, CSP and EDF Promote Angiogenesis and Invasion of Breast Cancer Cells In Vitro
De Spiegeleer, B. et al. Plos One 10(3), NPG, 2015, Human Transcriptome Array 2.0  PubMed

Investigation of Associations between NR1D1, RORA and RORB Genes and Bipolar Disorder
Lai, Y. C. et al. Plos One 10(3), NPG, 2015, Axiom Genome-Wide Population-Optimized Human Arrays  PubMed

Absence of Heterozygosity Due to Template Switching during Replicative Rearrangements
Carvalho, C. M. B. et al. American Journal of Human Genetics 96(4), 555-64, 2015  PubMed

Dose-Dependent Effects of Morphine Exposure on mRNA and microRNA (miR) Expression in Hippocampus of Stressed Neonatal Mice
McAdams, R. M. et al. Plos One 10(4), NPG, 2015, miRNA Array  PubMed

The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes
Challis, D. et al. BMC Genomics 16(), NPG, 2015, Axiom Exome Genotyping Array  PubMed

Submicroscopic Deletions at 13q32.1 Cause Congenital Microcoria
Fares-Taie, L. et al. American Journal of Human Genetics 96(4), 631-9, 2015  PubMed

Interstitial Duplication of Chromosome Region 1q25.1q25.3: Report of a Patient With Mild Cognitive Deficits, Tall Stature and Facial Dysmorphisms
Kehrer, M. et al. American Journal of Medical Genetics Part a 167A(3), 653-6, 2015  PubMed

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