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32199 publications found in the database

*2012 (1980)

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

2012 Publications

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
Wapner, R. J. et al. New England Journal of Medicine 367(23), 2175-84, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia
Yang, J. J. et al. Blood 120(20), 4197-204, 2012  PubMed

BMP9 regulates endoglin-dependent chemokine responses in endothelial cells
Young, K. et al. Blood 120(20), 4263-73, 2012, Human Genome U133 Plus 2.0 Array  PubMed

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)
Shimazaki, H. et al. Journal of Medical Genetics 49(12), NPG, 2012  PubMed

Joint Effect of Genetic and Lifestyle Risk Factors on Type 2 Diabetes Risk among Chinese Men and Women
Villegas, R. et al. Plos One 7(11), NPG, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Karyotype versus Microarray Testing for Genetic Abnormalities after Stillbirth
Reddy, U. M. et al. New England Journal of Medicine 367(23), 2185-93, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Fucose sensing regulates bacterial intestinal colonization
Pacheco, A. R. et al. Nature 492(7427), NPG, 2012, E. coli Genome 2.0 Array  PubMed

Sequential genetic change at the TP53 and chemokine receptor CXCR4 locus during transformation of human ovarian surface epithelium
Archibald, K. M. et al. Oncogene 31(48), 4987-95, 2012  PubMed

Profiles of Genomic Instability in High-Grade Serous Ovarian Cancer Predict Treatment Outcome
Wang, Z. G. C. et al. Clinical Cancer Research 18(20), 5806-15, 2012  PubMed

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