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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Alterations in hepatic one-carbon metabolism and related pathways following a high-fat dietary intervention
Rubio-Aliaga, I. et al. Physiological Genomics 43(8), 408-16, 2011  PubMed

Deciphering the luteal transcriptome: potential mechanisms mediating stage-specific luteolytic response of the corpus luteum to prostaglandin F2alpha
Mondal, M. et al. Physiological Genomics 43(8), 447-56, 2011, Bovine Genome Array  PubMed

Common variation in GPC5 is associated with acquired nephrotic syndrome
Okamoto, K. et al. Nature Genetics 43(5), NPG, 2011  PubMed

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Sulem, P. et al. Human Molecular Genetics 20(10), 2071-7, 2011  PubMed

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1
Jensen, L. R. et al. European Journal of Human Genetics 19(6), 717-20, 2011  PubMed

Comparative genomic analyses identify common molecular pathways modulated upon exposure to low doses of arsenic and cadmium
Benton, M. A. et al. BMC Genomics 12(), NPG, 2011, Human Gene 1.0 ST Array  PubMed

Prognostic gene-expression signature of carcinoma-associated fibroblasts in non-small cell lung cancer
Navab, R. et al. Proceedings of the National Academy of Sciences of the United States of America 108(17), 7160-5, 2011  PubMed

Gene expression profiling in multipotent DFAT cells derived from mature adipocytes
Ono, H. et al. Biochemical and Biophysical Research Communications 407(3), 562-7, 2011, Porcine  PubMed

Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions
Joseph-George, A. M. et al. Journal of Medical Genetics 48(5), 317-22, 2011, Genome-Wide Human SNP Array 6.0  PubMed

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