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Publications

Preserved DNA Damage Checkpoint Pathway Protects against Complications in Long-Standing Type 1 Diabetes.

Bhatt S, Gupta MK, Khamaisi M, et al. Preserved DNA Damage Checkpoint Pathway Protects against Complications in Long-Standing Type 1 Diabetes. Cell Metab. 2015;22(2):239-52. doi:10.1016/j.cmet.2015.07.015

Improved canine exome designs, featuring ncRNAs and increased coverage of protein coding genes.

Broeckx BJG, Hitte C, Coopman F, et al. Improved canine exome designs, featuring ncRNAs and increased coverage of protein coding genes. Sci Rep. 2015;5:12810. doi:10.1038/srep12810

Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck.

Balick DJ, Do R, Cassa CA, Reich D, Sunyaev SR. Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck. PLoS Genet. 2015;11(8):e1005436. doi:10.1371/journal.pgen.1005436

ERBB2 emerges as a new target for colorectal cancer.

Pectasides E, Bass AJ. ERBB2 emerges as a new target for colorectal cancer. Cancer Discov. 2015;5(8):799-801. doi:10.1158/2159-8290.CD-15-0730

Rapid Intraoperative Molecular Characterization of Glioma.

Shankar GM, Francis JM, Rinne ML, et al. Rapid Intraoperative Molecular Characterization of Glioma. JAMA Oncol. 2015;1(5):662-7. doi:10.1001/jamaoncol.2015.0917

Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk.

Hu X, Deutsch AJ, Lenz TL, et al. Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk. Nat Genet. 2015;47(8):898-905. doi:10.1038/ng.3353

Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use.

Clark SL, Aberg KA, Nerella S, et al. Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use. Alcohol Clin Exp Res. 2015;39(8):1396-405. doi:10.1111/acer.12790

Rare Coding Variation and Risk of Intracerebral Hemorrhage.

Radmanesh F, Falcone GJ, Anderson CD, et al. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke. 2015;46(8):2299-301. doi:10.1161/STROKEAHA.115.009838

Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity.

Usher CL, Handsaker RE, Esko T, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Nat Genet. 2015;47(8):921-5. doi:10.1038/ng.3340

Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk.

Jansen H, Loley C, Lieb W, et al. Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis. 2015;241(2):419-26. doi:10.1016/j.atherosclerosis.2015.05.033