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Rappoport N, Toung J, Hadley D, et al. (2018) A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. Scientific Reports. 8: 226 |
Li AS, Reuter JA, Cenik C, et al. (2017) Abstract 2457: Investigating the functional significance of novel, recurrent noncoding mutations of TBC1D12 in bladder cancer Cancer Research. 77: 2457-2457 |
Reuter JA, Spacek DV, Pai RK, et al. (2016) Simul-seq: combined DNA and RNA sequencing for whole-genome and transcriptome profiling. Nature Methods |
Araya CL, Cenik C, Reuter JA, et al. (2015) Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations. Nature Genetics |
Ungewickell A, Bhaduri A, Rios E, et al. (2015) Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2. Nature Genetics |
Melton C, Reuter JA, Spacek DV, et al. (2015) Recurrent somatic mutations in regulatory regions of human cancer genomes. Nature Genetics |
Reuter JA, Spacek DV, Snyder MP. (2015) High-Throughput Sequencing Technologies. Molecular Cell. 58: 586-597 |
Araya CL, Cenik C, Reuter J, et al. (2015) Abstract B2-42: Systematic dissection of multi-scale mutational hotspots across 21 cancer types reveals a rich landscape of functionally targeted oncogenic disruptions Cancer Research. 75 |
Jahaniani F, Rao V, Nevins S, et al. (2013) Emerging technologies to study long non-coding RNAs Molecular Biology of Long Non-Coding Rnas. 163-195 |