Galonska C, Ziller MJ, Karnik R, Meissner A. Ground State Conditions Induce Rapid Reorganization of Core Pluripotency Factor Binding before Global Epigenetic Reprogramming. Cell Stem Cell. 2015;17(4):462-70. doi:10.1016/j.stem.2015.07.005
Publications
Mather KJ, Kim C, Christophi CA, et al. Steroid Sex Hormones, Sex Hormone-Binding Globulin, and Diabetes Incidence in the Diabetes Prevention Program. J Clin Endocrinol Metab. 2015;100(10):3778-86. doi:10.1210/jc.2015-2328
Kirkpatrick BE, Riggs ER, Azzariti DR, et al. GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge. Hum Mutat. 2015;36(10):974-8. doi:10.1002/humu.22838
Pringle PL, Stewart KO, Peloquin JM, et al. Body Mass Index, Genetic Susceptibility, and Risk of Complications Among Individuals with Crohn’s Disease. Inflamm Bowel Dis. 2015;21(10):2304-10. doi:10.1097/MIB.0000000000000498
Crago AM, Chmielecki J, Rosenberg M, et al. Near universal detection of alterations in CTNNB1 and Wnt pathway regulators in desmoid-type fibromatosis by whole-exome sequencing and genomic analysis. Genes Chromosomes Cancer. 2015;54(10):606-15. doi:10.1002/gcc.22272
Kroksveen AC, Jaffe JD, Aasebø E, et al. Quantitative proteomics suggests decrease in the secretogranin-1 cerebrospinal fluid levels during the disease course of multiple sclerosis. Proteomics. 2015;15(19):3361-9. doi:10.1002/pmic.201400142
Chuquiyauri R, Molina DM, Moss EL, et al. Genome-Scale Protein Microarray Comparison of Human Antibody Responses in Plasmodium vivax Relapse and Reinfection. Am J Trop Med Hyg. 2015;93(4):801-9. doi:10.4269/ajtmh.15-0232
Kim K, Jiang X, Cui J, et al. Interactions between amino acid-defined major histocompatibility complex class II variants and smoking in seropositive rheumatoid arthritis. Arthritis Rheumatol. 2015;67(10):2611-23. doi:10.1002/art.39228
Replogle JM, De Jager PL. Reply: To PMID 25545807. Ann Neurol. 2015;78(4):659-60. doi:10.1002/ana.24456
Kim J, Won HH, Kim Y, Choi JR, Yu N, Lee KA. Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement. J Med Genet. 2015;52(10):706-9. doi:10.1136/jmedgenet-2015-103001