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32199 publications found in the database

*2013 (2117)

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

2013 Publications

Partial Uniparental Disomy With Mosaic Deletion 13q in an Infant With Multiple Congenital Anomalies
Jobanputra, V. et al. American Journal of Medical Genetics Part a 161(9), 2393-5, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Single-cell mutational profiling and clonal phylogeny in cancer
Potter, N. E. et al. Genome Research 23(12), 2115-25, 2013, Genome-Wide Human SNP Array 6.0  PubMed

MicroRNA-99 Family Members Suppress Homeobox A1 Expression in Epithelial Cells
Chen, D. et al. Plos One 8(12), NPG, 2013, Human Gene 1.0 ST Array  PubMed

Down-Regulation of OsSPX1 Causes High Sensitivity to Cold and Oxidative Stresses in Rice Seedlings
Wang, C. et al. Plos One 8(12), NPG, 2013, Rice Genome Array  PubMed

CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly
Hussain, M. S. et al. Human Molecular Genetics 22(25), 5199-214, 2013, Human Mapping 500K Array SetMapping 500K  PubMed

A comprehensive molecular study on Coffin-Siris and Nicolaides- Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Wieczorek, D. et al. Human Molecular Genetics 22(25), 5121-35, 2013, Genome-Wide Human SNP Array 6.0  PubMed

WT1 regulates the expression of inhibitory chemokines during heart development
Velecela, V. et al. Human Molecular Genetics 22(25), 5083-95, 2013, Mouse Genome 430 2.0 Array  PubMed

Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis
Connelly, J. J. et al. Human Molecular Genetics 22(25), 5107-20, 2013  PubMed

KDM2A promotes lung tumorigenesis by epigenetically enhancing ERK1/2 signaling
Wagner, K. W. et al. Journal of Clinical Investigation 123(12), 5231-46, 2013  PubMed

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