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Jason Reuter - Publications

Affiliations: 
Stanford University, Palo Alto, CA 
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9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Rappoport N, Toung J, Hadley D, Wong RJ, Fujioka K, Reuter J, Abbott CW, Oh S, Hu D, Eng C, Huntsman S, Bodian DL, Niederhuber JE, Hong X, Zhang G, et al. A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. Scientific Reports. 8: 226. PMID 29317701 DOI: 10.1038/S41598-017-18246-5  0.697
2017 Li AS, Reuter JA, Cenik C, Synder MP. Abstract 2457: Investigating the functional significance of novel, recurrent noncoding mutations of TBC1D12 in bladder cancer Cancer Research. 77: 2457-2457. DOI: 10.1158/1538-7445.Am2017-2457  0.7
2016 Reuter JA, Spacek DV, Pai RK, Snyder MP. Simul-seq: combined DNA and RNA sequencing for whole-genome and transcriptome profiling. Nature Methods. PMID 27723755 DOI: 10.1038/nmeth.4028  0.756
2015 Araya CL, Cenik C, Reuter JA, Kiss G, Pande VS, Snyder MP, Greenleaf WJ. Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations. Nature Genetics. PMID 26691984 DOI: 10.1038/Ng.3471  0.724
2015 Ungewickell A, Bhaduri A, Rios E, Reuter J, Lee CS, Mah A, Zehnder A, Ohgami R, Kulkarni S, Armstrong R, Weng WK, Gratzinger D, Tavallaee M, Rook A, Snyder M, et al. Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2. Nature Genetics. PMID 26258847 DOI: 10.1038/Ng.3370  0.523
2015 Melton C, Reuter JA, Spacek DV, Snyder M. Recurrent somatic mutations in regulatory regions of human cancer genomes. Nature Genetics. PMID 26053494 DOI: 10.1038/Ng.3332  0.757
2015 Reuter JA, Spacek DV, Snyder MP. High-Throughput Sequencing Technologies. Molecular Cell. 58: 586-597. PMID 26000844 DOI: 10.1016/j.molcel.2015.05.004  0.716
2015 Araya CL, Cenik C, Reuter J, Snyder M, Greenleaf W. 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. DOI: 10.1158/1538-7445.Compsysbio-B2-42  0.726
2013 Jahaniani F, Rao V, Nevins S, Spacek D, Bharadwaj N, Reuter J, Snyder M. Emerging technologies to study long non-coding RNAs Molecular Biology of Long Non-Coding Rnas. 163-195. DOI: 10.1007/978-1-4614-8621-3_7  0.656
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