Matthew Betts, PhD

Affiliations: 
Bioquant Ruprecht-Karls-University Heidelberg, Heidelberg, Baden-Württemberg, Germany 
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"Matthew Betts"
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Publications

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Betts MJ, Wichmann O, Utz M, et al. (2017) Systematic identification of phosphorylation-mediated protein interaction switches. Plos Computational Biology. 13: e1005462
Boldt K, van Reeuwijk J, Lu Q, et al. (2016) An organelle-specific protein landscape identifies novel diseases and molecular mechanisms. Nature Communications. 7: 11491
López C, Bergmann AK, Paul U, et al. (2016) Genes encoding members of the JAK-STAT pathway or epigenetic regulators are recurrently mutated in T-cell prolymphocytic leukaemia. British Journal of Haematology
Kretzmer H, Bernhart SH, Wang W, et al. (2015) DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control. Nature Genetics
Wagener R, Aukema SM, Schlesner M, et al. (2015) The PCBP1 gene encoding poly(rC) binding protein I is recurrently mutated in Burkitt lymphoma. Genes, Chromosomes & Cancer. 54: 555-64
Betts MJ, Lu Q, Jiang Y, et al. (2015) Mechismo: predicting the mechanistic impact of mutations and modifications on molecular interactions. Nucleic Acids Research. 43: e10
Wagener R, Aukema SM, Schlesner M, et al. (2015) The PCBP1 gene encoding poly(rC) binding protein I is recurrently mutated in Burkitt lymphoma Genes Chromosomes and Cancer. 54: 555-564
Suratanee A, Schaefer MH, Betts MJ, et al. (2014) Characterizing protein interactions employing a genome-wide siRNA cellular phenotyping screen. Plos Computational Biology. 10: e1003814
Hasselblatt M, Nagel I, Oyen F, et al. (2014) SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis. Acta Neuropathologica. 128: 453-6
Rohde M, Richter J, Schlesner M, et al. (2014) Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols. Genes, Chromosomes & Cancer. 53: 911-6
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