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32199 publications found in the database

*2012 (1980)

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

2012 Publications

BAP1 loss defines a new class of renal cell carcinoma
Pena-Llopis, S. et al. Nature Genetics 44(7), NPG, 2012  PubMed

Embryonic stem cell potency fluctuates with endogenous retrovirus activity
Macfarlan, T. S. et al. Nature 487(7405), NPG, 2012, Mouse Gene 1.0 ST array  PubMed

Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness
Wortmann, S. B. et al. Nature Genetics 44(7), NPG, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus
Santen, G. W. E. et al. Journal of Medical Genetics 49(6), 366-72, 2012  PubMed

Joint Bayesian inference of condition-specific miRNA and transcription factor activities from combined gene and microRNA expression data
Zacher, B. et al. Bioinformatics 28(13), 1714-20, 2012, Human Genome U133 Plus 2.0 Array  PubMed

Deregulated MicroRNAs in Myotonic Dystrophy Type 2
Greco, S. et al. Plos One 7(6), NPG, 2012, Human Exon Array  PubMed

Berry Flesh and Skin Ripening Features in Vitis vinifera as Assessed by Transcriptional Profiling
Lijavetzky, D. et al. Plos One 7(6), NPG, 2012  PubMed

Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency
Meimaridou, E. et al. Nature Genetics 44(7), 740-2, 2012  PubMed

The Chromosome 9p21.3 Coronary Heart Disease Risk Allele Is Associated with Altered Gene Expression in Normal Heart and Vascular Tissues
Pilbrow, A. P. et al. Plos One 7(6), NPG, 2012  PubMed

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