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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Activation of nuclear factor-kappa B signalling promotes cellular senescence
Rovillain, E. et al. Oncogene 30(20), 2356-66, 2011, Human Genome U133 Plus 2.0 Array  PubMed

A cluster of coregulated genes determines TGF-beta-induced regulatory T-cell (Treg) dysfunction in NOD mice
D'Alise, A. M. et al. Proceedings of the National Academy of Sciences of the United States of America 108(21), 8737-42, 2011, Mouse Gene 1.0 ST array  PubMed

An autosomal locus that controls chromosome-wide replication timing and mono-allelic expression
Stoffregen, E. P. et al. Human Molecular Genetics 20(12), 2366-78, 2011  PubMed

The MYH9/APOL1 region and chronic kidney disease in European-Americans
O'Seaghdha, C. M. et al. Human Molecular Genetics 20(12), 2450-6, 2011  PubMed

Common genetic variants associated with open-angle glaucoma
Ramdas, W. D. et al. Human Molecular Genetics 20(12), 2464-71, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

Genome-wide meta-analysis for severe diabetic retinopathy
Grassi, M. A. et al. Human Molecular Genetics 20(12), 2472-81, 2011  PubMed

Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
Fingert, J. H. et al. Human Molecular Genetics 20(12), 2482-94, 2011  PubMed

The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis
Bakircioglu, M. et al. American Journal of Human Genetics 88(5), 523-35, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome
O'Sullivan, J. et al. American Journal of Human Genetics 88(5), 616-20, 2011, Genome-Wide Human SNP Array 6.0  PubMed

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