| Genomic and molecular landscape of DNA damage repair deficiency across the cancer genome atlas TA Knijnenburg, L Wang, MT Zimmermann, N Chambwe, GF Gao, ... Cell reports 23 (1), 239-254. e6, 2018 | 925 | 2018 |
| Crystal structures of the CusA efflux pump suggest methionine-mediated metal transport F Long, CC Su, MT Zimmermann, SE Boyken, KR Rajashankar, ... Nature 467 (7314), 484-488, 2010 | 261 | 2010 |
| Crystal structure of the CusBA heavy-metal efflux complex of Escherichia coli CC Su, F Long, MT Zimmermann, KR Rajashankar, RL Jernigan, EW Yu Nature 470 (7335), 558-562, 2011 | 240 | 2011 |
| Bioaccumulation of therapeutic drugs by human gut bacteria M Klünemann, S Andrejev, S Blasche, A Mateus, P Phapale, ... Nature 597 (7877), 533-538, 2021 | 198 | 2021 |
| Mitochondrial metabolic reprogramming by CD36 signaling drives macrophage inflammatory responses Y Chen, M Yang, W Huang, W Chen, Y Zhao, ML Schulte, P Volberding, ... Circulation research 125 (12), 1087-1102, 2019 | 140 | 2019 |
| Understanding protein–nanoparticle interaction: a new gateway to disease therapeutics K Giri, K Shameer, MT Zimmermann, S Saha, PK Chakraborty, A Sharma, ... Bioconjugate chemistry 25 (6), 1078-1090, 2014 | 103 | 2014 |
| MACE: model based analysis of ChIP-exo L Wang, J Chen, C Wang, L Uusküla-Reimand, K Chen, A Medina-Rivera, ... Nucleic acids research 42 (20), e156-e156, 2014 | 85 | 2014 |
| Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction JL Theis, MT Zimmermann, JM Evans, BW Eckloff, ED Wieben, ... Circulation: Cardiovascular Genetics 8 (4), 564-571, 2015 | 83 | 2015 |
| Computational and experimental characterization of RNA cubic nanoscaffolds KA Afonin, W Kasprzak, E Bindewald, PS Puppala, AR Diehl, KT Hall, ... Therapeutic RNA Nanotechnology, 121-149, 2021 | 75 | 2021 |
| Whole-exome analysis reveals novel somatic genomic alterations associated with outcome in immunochemotherapy-treated diffuse large B-cell lymphoma AJ Novak, YW Asmann, MJ Maurer, C Wang, SL Slager, LS Hodge, ... Blood cancer journal 5 (8), e346-e346, 2015 | 71 | 2015 |
| Novel type of renal amyloidosis derived from apolipoprotein-CII SH Nasr, S Dasari, L Hasadsri, JD Theis, JA Vrana, MA Gertz, P Muppa, ... Journal of the American Society of Nephrology 28 (2), 439-445, 2017 | 66 | 2017 |
| Recurrent MSCE116K mutations in ALK-negative anaplastic large cell lymphoma RA Luchtel, MT Zimmermann, G Hu, S Dasari, M Jiang, N Oishi, ... Blood, The Journal of the American Society of Hematology 133 (26), 2776-2789, 2019 | 65 | 2019 |
| System-wide associations between DNA-methylation, gene expression, and humoral immune response to influenza vaccination MT Zimmermann, AL Oberg, DE Grill, IG Ovsyannikova, IH Haralambieva, ... PLoS One 11 (3), e0152034, 2016 | 64 | 2016 |
| Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine IH Haralambieva, IG Ovsyannikova, RB Kennedy, BR Larrabee, ... Human genetics 136, 421-435, 2017 | 63 | 2017 |
| Human telomerase model shows the role of the TEN domain in advancing the double helix for the next polymerization step K Steczkiewicz, MT Zimmermann, M Kurcinski, BA Lewis, D Dobbs, ... Proceedings of the National Academy of Sciences 108 (23), 9443-9448, 2011 | 59 | 2011 |
| Predict drug sensitivity of cancer cells with pathway activity inference X Wang, Z Sun, MT Zimmermann, A Bugrim, JP Kocher BMC medical genomics 12, 5-13, 2019 | 52 | 2019 |
| TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy JL Theis, MT Zimmermann, BT Larsen, IN Rybakova, PA Long, JM Evans, ... Human molecular genetics 23 (21), 5793-5804, 2014 | 52 | 2014 |
| Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses S Dasari, JD Theis, JA Vrana, RM Zenka, MT Zimmermann, JPA Kocher, ... Journal of proteome research 13 (5), 2352-2358, 2014 | 46 | 2014 |
| MAVENs: motion analysis and visualization of elastic networks and structural ensembles MT Zimmermann, A Kloczkowski, RL Jernigan BMC bioinformatics 12, 1-7, 2011 | 46 | 2011 |
| Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome MA Cousin, BA Creighton, KA Breau, RC Spillmann, E Torti, S Dontu, ... Nature genetics 53 (7), 1006-1021, 2021 | 45 | 2021 |
